# Kawasaki Disease Foundation

> KD Foundation

> Generated by All in One SEO v5.0.3, this is an llms.txt file, used by LLMs to index the site.

## Sitemaps

- [XML Sitemap](https://kdfoundation.org/sitemap.xml): Contains all public & indexable URLs for this website.

## Posts

- [Heart to Heart, Episode 2: What Is Kawasaki Disease?](https://kdfoundation.org/heart-to-heart-episode-2-what-is-kawasaki-disease/): What exactly is Kawasaki disease, and why is early recognition so important? In the second episode of Heart to Heart, we review Kawasaki disease—what it is, who it affects, and why timely diagnosis and treatment matter. Whether you're a newly diagnosed family, caregiver, or curious, this episode offers an accessible introduction. We discuss common symptoms,
- [Heart to Heart, Episode 1: A KDF Youth Podcast](https://kdfoundation.org/heart-to-heart-a-kdf-youth-podcast/): We are thrilled to announce the launch of Heart to Heart, the very first podcast created by our incredible KDF Youth interns! In Episode 1, the hosts open up about their own Kawasaki Disease journeys - sharing their diagnoses, challenges, and what motivates them to raise awareness and support the KD community. This powerful introduction
- [Heart to Heart, Episode 3: Breaking Down Language and Cultural Barriers in Kawasaki Disease Care](https://kdfoundation.org/heart-to-heart-breaking-down-language-and-cultural-barriers-in-kawasaki-disease-care/): When a child is diagnosed with Kawasaki disease, families face unfamiliar medical info, treatment decisions, and unanswered questions. For those in a different language, this can be overwhelming. In Heart to Heart, Noelle from Kawasaki Disease Korea (KDK) discusses challenges due to language and cultural barriers for families affected by Kawasaki disease. She emphasizes
- [Heart to Heart, Episode 4: Could AI Help Advance Kawasaki Disease Research?](https://kdfoundation.org/heart-to-heart-episode-4-could-ai-help-advance-kawasaki-disease-research/): What if existing medicines could help treat diseases with limited treatment options? Advances in artificial intelligence are helping researchers explore that possibility, opening new doors for rare disease research and innovation. In this episode of Heart to Heart, we examine how artificial intelligence and drug repurposing are being used to identify potential new treatments for
- [The Buckallew Family Story](https://kdfoundation.org/the-buckallew-family-story/): Morgan Buckallew shares her family's journey through IVIG-resistant Kawasaki Disease and how Infliximab helped change her son's outcome.
- [Celebrating Ava Quinn: A Meaningful Milestone for the KD Community](https://kdfoundation.org/celebrating-ava-quinn-a-meaningful-milestone-for-the-kd-community/): Celebrating Ava Quinn’s work on a Kawasaki Disease transition toolkit, helping young patients move from pediatric to adult care with confidence and support.
- [2025 KD Parent Symposium](https://kdfoundation.org/2025-kd-parent-symposium/): The 2025 KD Parent Symposium brought together leading clinicians, researchers, and families for a powerful day of education, research updates, and community connection. The program featured emerging AI developments, new insights into diagnosis and treatment, research on vulnerable patient populations, and long-term care for adults who had KD in childhood. Two expert-led Q&A sessions and
- [2025 Mount Sinai Kawasaki Disease Conference](https://kdfoundation.org/2025-mount-sinai-kawasaki-disease-conference/): Kawasaki Disease Across the Ages: What Parents and Families Should Know The 2025 Mount Sinai Kawasaki Disease Conference brought together leading clinicians and researchers to explore how Kawasaki Disease affects patients throughout their entire lifespan. This year’s theme, “Across the Ages,” emphasized long-term heart health, emerging research, and how families can stay informed and empowered
- [Founder Greg Chin Reflects on 25 Years of KDF](https://kdfoundation.org/founder-greg-chin-reflects-on-25-years-of-kdf/): As we celebrate 25 years of the Kawasaki Disease Foundation, we’re honored to look back on where it all began with one family’s determination to make sure no parent ever faced Kawasaki disease alone. Greg Chin, who founded KDF in 2000 after his son’s diagnosis, transformed his family’s experience into a mission that would unite
- [Thriving Beyond KD: A Father's Story](https://kdfoundation.org/thriving-beyond-kd-a-fathers-story/): My name is Loren Wheale, and I want to tell you about my daughter Mollie. I am telling this story for the parents who are right now sitting in a hospital room with a sick child, scared out of their minds, wondering if life will ever be normal again. I have been there. I know
- [KDF Youth's Standout Intern: Joshua & Charlotte Wei](https://kdfoundation.org/kdf-youths-standout-intern-joshua-charlotte-wei/): This month, we are so proud to shine our Intern Spotlight on siblings Joshua and Charlotte, who have brought incredible heart, dedication, and creativity to KDF Youth. Joshua’s experience with KD at a young age inspired him to share his voice and spread awareness so that other families would have the resources his didn’t have
- [Board Member Highlight: Sean King](https://kdfoundation.org/board-member-highlight-sean-king/): Q. How did you first become connected to Kawasaki Disease and the Kawasaki Disease Foundation? A. My journey with the Kawasaki Disease Foundation began in 2006 when my son, Chance, was diagnosed with Kawasaki Disease at the age of three. As a result of the illness, Chance developed two coronary artery aneurysms. This was an overwhelming
- [Mount Sinai Adult Congenital Heart Disease Symposium](https://kdfoundation.org/mount-sinai-symposium-nyc/): We’re excited to share the upcoming 4th Mount Sinai Adult Congenital Heart Disease Symposium: Kawasaki Disease Across the Ages, taking place September 12–13, 2025 in New York City. This state-of-the-art symposium will bring together pediatric and adult cardiologists, interventionalists, and imaging specialists to collaborate on optimizing care for Kawasaki Disease across the lifespan - from
- [Kawasaki Disease Foundation Quarterly Newsletter | Spring 2025](https://kdfoundation.org/kawasaki-disease-foundation-quarterly-newsletter-spring-2025/): KDF Newsletter, Spring 2025 In This Issue: 1. KD Specialist Highlight: Annette Baker 2. CalPlasma: Saving Lives 3. UCSD Research Study 4. Dr. Rowley's Breakthrough Study 5. KD Intern Highlight: Grace Choe 6. Dr. Tomisaku Kawasaki Scholarship 7. My Health Planner Toolkit 8. FAQs, Researched + Answered 9. Becoming a KDF Volunteer READ NEWSLETTER>>
- [KDF Youth’s Standout Intern: Grace Choe](https://kdfoundation.org/kdf-youths-standout-intern-grace-choe/): KDF Youth's Standout Intern 🎉 We’re proud to recognize Grace Choe as our Standout Intern for the Spring quarter! Grace has been an incredible asset to the Kawasaki Disease Foundation’s social media team, bringing her creativity and enthusiasm to content creation that informs, inspires, and uplifts our community. We deeply appreciate her can-do attitude, positive
- [Empowering the Next Generation: Ava Quinn’s Health Care Transition Toolkit](https://kdfoundation.org/empowering-the-next-generation/): We are excited to shine a light on Ava Quinn, an inspiring young advocate and passionate supporter of the Kawasaki Disease Foundation (KDF). Her recent project is already making a remarkable difference in the Kawasaki Disease (KD) community. As part of her master's program in Applied Developmental Psychology (ADP) at the University of Pittsburgh's School
- [Dr. Tomisaku Kawasaki Memorial Scholarship Recipient](https://kdfoundation.org/dr-tomisaku-kawasaki-memorial-scholarship-recipient_2025/): Dr. Tomisaku Kawasaki Memorial Scholarship Recipient: Kate Xu Scholarship Recipient: Kate Xu Scholarship Year: Fall 2025 - Spring 2026 Scholarship Type: High school student entering a university University Name: Massachusetts Institute of Technology (MIT) Scholarship Amount: $5,000 Kate Xu was diagnosed with Kawasaki Disease (KD) at the age of three after multiple misdiagnoses in the
- [Breakthrough in Kawasaki Disease Cause](https://kdfoundation.org/breakthrough-in-kawasaki-disease-cause/): Breakthrough Study Links Kawasaki Disease to a Single, Unknown Respiratory Virus After more than five decades of uncertainty, researchers at Stanley Manne Children’s Research Institute at Ann & Robert H. Lurie Children’s Hospital of Chicago have uncovered compelling evidence pointing to a single respiratory virus—still unidentified—as the cause of Kawasaki disease. This marks a major
- [Dr. Rowley Responds to KD Virus Study](https://kdfoundation.org/dr-rowley-responds-to-kd-virus-study/): After we shared a recent study exploring the possibility of an unidentified virus as the cause of Kawasaki Disease, we received many thoughtful comments, questions, and concerns from our community. We’re grateful for your engagement and curiosity. To provide clarity and context, Dr. Anne H. Rowley, who led the study, offered a detailed explanation addressing
- [Ask the KD Experts: 2024 UCSD KD Parent Symposium Q&A Session (Transcribed)](https://kdfoundation.org/2024-kawasaki-disease-parent-symposium-qa-questions-transcribed/): 2024 Kawasaki Disease Parent Symposium Q&A Questions (Transcribed) Q: How can families participate in the KD genetic studies? Who qualifies to enroll and how? A: Currently, DNA studies are focused on patients with aneurysms. Families with a child who has aneurysms and wish to participate can request a mouthwash kit for at-home testing; a swab
- [Ask the KD Experts: Why is Kawasaki disease less commonly treated with steroids?](https://kdfoundation.org/why-is-kawasaki-disease-less-commonly-treated-with-steroids/): Ask the KD Experts: Why is Kawasaki disease less commonly treated with steroids? While it’s not common for Rady Children’s Hospital to treat Kawasaki disease (KD) with steroids, the use of steroids in combination with IVIG continues to be used around the world for children with aneurysms and with treatment-resistant KD. In San Diego, many
- [Watch the 2020 KD Parent Symposium (Virtual Event)](https://kdfoundation.org/2020symposium/): Watch the 2020- UCSD KD Parent Symposium (Virtual Event) Annual Kawasaki Disease Parent Symposium hosted by the University of California San Diego, Kawasaki Disease Research Center. The event was held virtually via Zoom. Video Time Stamp Speaker Topic 0:05:15 Jane C. Burns, MD: A tribute to Dr. Kawasaki and his legacy 0:18:16 Prof. Michael Levin:
- [Ask the KD Experts: KD & COVID-19 FAQ (update: 5/8/2020)](https://kdfoundation.org/kd-covid-19-faq-update-5-8-2020/): Dear KD Parents, There has been a lot of recent media attention regarding a pediatric inflammatory shock syndrome linked to COVID-19 that appears to affect a few patients who share some features of Kawasaki Disease, including coronary artery aneurysms and favorable response to IVIG. Due to the flood of inquiries that we have been receiving
- [Ask the KD Experts: 2020 UCSD KD Parent Symposium Q&A Session](https://kdfoundation.org/2020-kd-parent-symposium-qa-session/): 2020 UCSD KD Parent Symposium (Virtual Event) Q&A Session Watch the annual Kawasaki Disease Parent Symposium hosted by the University of California San Diego, Kawasaki Disease Research Center via the link below, or scroll down to read the transcribed questions and answers asked during the Q&A sessions. WATCH VIDEO>> KD Parent Symposium 2020 – Transcript
- [Watch the 2021 KD Parent Symposium (Virtual Event)](https://kdfoundation.org/2021-kd-parent-symposium-virtual-event/): Watch the 2021- UCSD KD Parent Symposium (Virtual Event) Annual Kawasaki Disease Parent Symposium hosted by the University of California San Diego, Kawasaki Disease Research Center. The event was held virtually via Zoom. Video Time Stamp Speaker Topic 00:00:00 - 00:16:40 Jane C. Burns MD: Welcome and update on KD at Rady Children’s Hospital
- [Watch the 2022 UCSD KD Parent Symposium](https://kdfoundation.org/2022kdsymposium/): Watch the 2022- UCSD KD Parent Symposium (Virtual & In-Person Event) Annual Kawasaki Disease Parent Symposium hosted by the University of California San Diego, Kawasaki Disease Research Center. The event was held virtually and in-person. Video Time Stamp Speaker Topic 00:00:00 - 00:15:15 Jane C. Burns MD: Welcome and update on KD at Rady Children’s
- [Ask the KD Experts: 2022 UCSD KD Parent Symposium Q&A Session](https://kdfoundation.org/2022-ucsd-kd-parent-symposium-qa-session/): 2022 UCSD KD Parent Symposium Q&A Session Watch the annual Kawasaki Disease Parent Symposium hosted by the University of California San Diego, Kawasaki Disease Research Center via the link below, or scroll down to read the transcribed questions and answers asked during the Q&A session 1. WATCH VIDEO>> Q&A Session 1- Kawasaki Disease Parent Symposium,
- [Watch the 2023 UCSD KD Parent Symposium (Virtual Event)](https://kdfoundation.org/watch-the-2023-ucsd-kd-parent-symposium-virtual-event/): Watch the 2023 UCSD KD Parent Symposium (Virtual Event) Annual Kawasaki Disease Parent Symposium hosted by the University of California San Diego, Kawasaki Disease Research Center. The event was held virtually. Timestamps for presentations and sessions throughout the event 00:04:00 : Jane C Burns MD: Welcome and update on KD Rady Children's Hospital 00:19:00 :
- [[Watch On-Demand] Navigating Kawasaki Disease Together: A Dialogue with Experts for Patients and Caregivers](https://kdfoundation.org/watch-on-demand-navigating-kawasaki-disease-together-a-dialogue-with-experts-for-patients-and-caregivers/): [Watch On-Demand] Navigating Kawasaki Disease Together: A Dialogue with Experts for Patients and Caregivers The Kawasaki Disease Foundation teamed up with Kawasaki Disease Canada to host a symposium titled “Navigating Kawasaki Disease Together: A Dialogue with Experts for Patients and Caregivers”. This session brought together Kawasaki Disease specialists, parents, caregivers, patients, and worldwide KD organizations
- [[Watch On-Demand] 2024 Kawasaki Disease Parent Symposium](https://kdfoundation.org/kdsymposium24/): [Watch On-Demand] 2024 Kawasaki Disease Parent Symposium The annual Kawasaki Disease Parent Symposium, hosted by the Kawasaki Disease Research Center at the University of San Diego, California in partnership with the Kawasaki Disease Foundation, provided valuable updates on Kawasaki disease studies and research. This online event, held on Saturday, October 5, 2024, offered insights from
- [Kawasaki Disease Foundation Quarterly Newsletter | Winter 2025](https://kdfoundation.org/kawasaki-disease-foundation-quarterly-newsletter-winter-2025/): KDF Newsletter, Winter 2025 In This Issue: 1. "Lights On, Hearts Strong" — A Heartfelt Thank You for Your Support 2. Celebrating Dr. Tomisaku Kawasaki's 100th Birthday 3. Dr. Tomisaku Kawasaki 2025-2026 Scholarship — Now Accepting Applications! 4. KD Researchers Spotlight: Professor Kuo 5. Meet Emily Rodriguez: KDF Intern READ NEWSLETTER>>
- [Children with resistant KD may be treated with infliximab instead of a second dose of IVIG](https://kdfoundation.org/children-with-resistant-kd-may-be-treated-with-infliximab-instead-of-a-second-dose-of-ivig/): Children with resistant KD may be treated with infliximab instead of a second dose of IVIG In the treatment of Kawasaki disease (KD), intravenous immunoglobulin (IVIG) is the standard therapy used to reduce inflammation, lower the risk of coronary artery complications, and prevent long-term heart damage. However, a subset of children with KD may fail
- [Kawasaki disease is not an autoimmune disease](https://kdfoundation.org/kawasaki-disease-is-not-an-autoimmune-disease/): KD is not an autoimmune disease, and there is no evidence that it leads to autoimmunity later in life Kawasaki disease (KD) is not classified as an autoimmune disease, and there is no substantial evidence indicating that patients who have had KD are predisposed to autoimmunity later in life. Here’s an explanation that clarifies both
- [A high heart rate is a key symptom of acute Kawasaki disease used for diagnosis](https://kdfoundation.org/a-high-heart-rate-is-a-key-symptom-of-acute-kawasaki-disease-used-for-diagnosis/): A high heart rate is a key symptom of acute Kawasaki disease used for diagnosis A high heart rate, or tachycardia, is a key symptom observed in the acute phase of Kawasaki disease (KD) and plays a crucial role in the diagnostic process. Here's why tachycardia is part of the acute presentation of KD and
- [Celebrating Dr. Tomisaku Kawasaki: A Legacy of Dedication to Kawasaki Disease Research](https://kdfoundation.org/100thbday/): Celebrating Dr. Tomisaku Kawasaki: A Legacy of Dedication to Kawasaki Disease Research Read: The Legacy of Dr. Tomisaku Kawasaki, a manuscript recently published by the International Journal of Rheumatic Diseases. As we approach the 100th birthday of Dr. Tomisaku Kawasaki, the world reflects on the profound impact he has had on the medical community, particularly
- [Meet Emily Rodriguez: KDF Intern](https://kdfoundation.org/emilyrodriguez/): Meet Emily Rodriguez: KDF Intern Allow us to introduce Emily. At just four months old, she received a diagnosis of Kawasaki Disease. Her case was complex—her symptoms were unusual, confounding doctors back in 2005. After numerous misdiagnoses, including ear infection, meningitis, and scarlet fever, the right diagnosis was finally reached following days of uncertainty and
- [Give $26, Get Stickers, Spread KD Awareness](https://kdfoundation.org/give-26-get-stickers-spread-kd-awareness/): Give $26, Get Stickers, Spread KD Awareness From January 13th to 19th, the Kawasaki Disease Foundation is offering a special thank you to the first 150 people who make a $26 donation to our cause. When you donate, you’ll receive a Kawasaki Disease sticker pack as our way of showing gratitude for your support! Why
- [Kawasaki Disease: Understanding the Rare Illness in Children](https://kdfoundation.org/kawasaki-disease-understanding-the-rare-illness-in-children/): Kawasaki Disease: Understanding the Rare Illness in Children Kawasaki Disease (KD) is a rare but serious condition that primarily affects children under the age of five. Named after Dr. Tomisaku Kawasaki, who first described the illness in 1967, KD is now recognized worldwide as one of the leading causes of acquired heart disease in children.
- [Spotlight on Dedicated KD Researchers: Ho-Chang Kuo, MD, PhD, FAAAAI](https://kdfoundation.org/spotlight-on-dedicated-kd-researchers-ho-chang-kuo-md-phd-faaaai/): Spotlight on Dedicated KD Researchers: Ho-Chang Kuo, MD, PhD, FAAAAI Professor Ho-Chang Kuo, born in 1973, earned his M.D. degree from National Yang-Ming University in Taiwan in 1999, followed by a Ph.D. from the Graduate Institute of Clinical Medical Science at Chang Gung University in 2011. He serves as an attending pediatrician, physician-scientist, and
- [Together, We Shine Brighter – Lights On, Hearts Strong!](https://kdfoundation.org/together-we-shine-brighter-lights-on-hearts-strong/): Together, We Shine Brighter – Lights On, Hearts Strong As we kick off another exciting week in our Lights On, Hearts Strong campaign, we’re thrilled to share the incredible progress we’ve made together! Our social media is glowing! Thanks to your support, we’ve seen a big increase in followers across all platforms. Each new connection means another
- [The Jekums Family: Our KD Story](https://kdfoundation.org/jekumsfam/): The Jekums Family: Our KD Story Written by Sari Jekums Orange County, CA We began our journey with Kawasaki disease (KD) when my son was diagnosed four years ago. Even though my husband and I are both Registered Nurses, KD was not on our radar as we were taught many years ago that it
- [Twenty Six Years Post KD and Healthy!](https://kdfoundation.org/twenty-six-years-post-kd/): My Kawasaki Disease Journey | 26 Years Post KD and Healthy! Written by: Kate Davila My name is Kate Davila, and I had Kawasaki disease (KD) 26 years ago when I was 15 years old. I hope that my journey with this disease brings some comfort to your family. Even patients with heart complications can
- [Kawasaki Disease Stories: Calen Page](https://kdfoundation.org/kd-stories-calen-page/): Calen Page By: Jennifer Page A committed group of people in Big Rapids, Michigan, are working to raise funds to support KD Research in the Quest for a Diagnostic Test. For many children, having a diagnostic test is the difference between life and death. It would have been for my beautiful son Calen James Page.
- [Chance's KD Story/Union University College of Pharmacy Fundraiser](https://kdfoundation.org/chances-kd-story-union-university-college-of-pharmacy-fundraiser/): Chance’s Kawasaki Disease Story Chance was diagnosed with Kawasaki Disease when he was 3 years old. He developed a fever on May 31, 2006, and was treated for a viral infection at a local urgent care clinic. Over the next 24-hours Chance’s fever rose higher, the lymph glands in his neck became significantly swollen, and
- [Jamie Dukat's KD Strong Story | How I transitioned from pediatric to adult cardiology](https://kdfoundation.org/jamie-dukats-kd-strong-story/): Jamie Dukat's KD Strong Story | How I transitioned from pediatric to adult cardiology How old were you when you were diagnosed with KD? If you were old enough to remember, how did you feel? What was your reaction to being treated for KD? If you were not old enough, what have your parents or
- [Ask the KD Experts: KD & Vision Loss](https://kdfoundation.org/ask-the-kd-experts-kd-vision/): Ask the KD Experts: Kawasaki Disease and Vision Loss Question: I wanted to ask if you could please provide some feedback on vision loss due to KD. There's been a story surfacing these past few days of a blind Paralympian who lost his vision to KD as a child. A link was shared on the
- [Lights On, Hearts Strong | Kawasaki Disease Awareness](https://kdfoundation.org/lights-on-hearts-strong-kawasaki-disease-awareness/): Today marks the first day of Kawasaki Disease Awareness Month, and we are thrilled to officially launch our Lights On, Hearts Strong campaign! This January, we’re coming together to honor the strength, bravery, and resilience of children affected by Kawasaki Disease. “Lights On, Hearts Strong” is more than a campaign — it’s a movement to shine a light
- [Kawasaki Disease Foundation Quarterly Newsletter | Winter 2024](https://kdfoundation.org/kawasaki-disease-foundation-quarterly-newsletter-winter-2024/): KDF Newsletter, Winter 2024 In This Issue: 1. Kawasaki Disease Awareness Campaign: "Lights On, Hearts Strong" 2. Dr. Tomisaku Kawasaki 2025-2026 Scholarship 3. KD Patients Feedback Needed: Transition to Adult Healthcare 4. KD Parent Symposium Q&A Session (Transcribed) 5. Update on Diagnosis and Management of KD: A Scientific Statement from the American Heart Association 6.
- [Kawasaki Disease Research Center: Winter 2024 Newsletter](https://kdfoundation.org/kawasaki-disease-research-center-winter-2024-newsletter/)
- [Exciting News: Lights On, Hearts Strong Campaign](https://kdfoundation.org/exciting-news-lights-on-hearts-strong-campaign/): We are excited to announce the launch of our Lights On, Hearts Strong campaign this January, dedicated to raising awareness and funds for Kawasaki Disease! This campaign is an opportunity to illuminate the critical need for awareness about KD, and your support will make a powerful impact. Throughout the month, we’ll be sharing meaningful social
- [Health Care Transition (HCT) Survey](https://kdfoundation.org/hctsurvey/): **Your Input is Crucial! Help Shape a Toolkit for Pediatric Kawasaki Disease Patients Transitioning to Adult Cardiology Care** The KDF is reaching out to both youth and adult patients who are currently transitioning to adult healthcare or have successfully completed this journey. Our adult survey is designed to gather key insights from patients with Kawasaki
- [Dr. Tomisaku Kawasaki Memorial Scholarship – Call for Scholarship Applications Spring 2025](https://kdfoundation.org/dr-tomisaku-kawasaki-memorial-scholarship-call-for-scholarship-applications-spring-2025/): Dr. Tomisaku Kawasaki Memorial Scholarship – Call for Scholarship Applications Spring 2025 Deadline for Applications: February 28, 2025 The KD Foundation scholarship, established to honor Dr. Kawasaki’s contributions to pediatric medicine, will reopen on January 26, 2025, for the 2025-2026 school year. One (1) scholarship will be awarded to a graduating high school senior who has been
- [Update on Diagnosis and Management of Kawasaki Disease: A Scientific Statement From the American Heart Association](https://kdfoundation.org/update-on-diagnosis-and-management-of-kawasaki-disease-a-scientific-statement-from-the-american-heart-association/): Update on Diagnosis and Management of Kawasaki Disease: A Scientific Statement From the American Heart Association Kawasaki disease (KD) is an acute febrile illness mainly affecting children under 5 and is the leading cause of acquired heart disease in developed countries. It can result in coronary artery dilation and aneurysms in 25% of untreated cases.
- [Editorial: Fostering Global Collaboration Around Kawasaki Disease. Reflections From the 14th International Kawasaki Disease Symposium](https://kdfoundation.org/editorial-fostering-global-collaboration-around-kawasaki-disease-reflections-from-the-14th-international-kawasaki-disease-symposium/): Editorial: Fostering Global Collaboration Around Kawasaki Disease. Reflections From the 14th International Kawasaki Disease Symposium From August 26 to August 29, the 14th International Kawasaki Disease Symposium (IKDS) was held in Montreal, Canada. For the past 40 years, IKDS has brought together researchers and scientists dedicated to understanding Kawasaki Disease (KD). With new generations joining
- [Kawasaki Disease Foundation Quarterly Newsletter | Fall 2024](https://kdfoundation.org/kawasaki-disease-foundation-quarterly-newsletter-fall-2024/): KDF Newsletter, Fall 2024 In this issue: 1. Treating Resistant KD: Evidence Update for Parents and Clinicians 2. Recap: 14th International KD Symposium (IKDS) 3. Watch the 2024 IKDS Parent Conference: Navigating KD Together 4. Watch On-Demand: 2024 Annual KD Parent Symposium 5. Feedback Survey: 2024 Annual KD Parent Symposium 6. Meet Ava Quinn: KDF's
- [Comparing Two Treatments for IVIG-Resistant Kawasaki Disease – Evidence Update for Clinicians](https://kdfoundation.org/comparing-two-treatments-for-ivig-resistant-kawasaki-disease-evidence-update-for-clinicians/): Comparing Two Treatments for IVIG-Resistant Kawasaki Disease – Evidence Update for Clinicians Children with resistant KD who received infliximab were more likely to have their fever resolve within 24 hours than were children who received a second dose of IVIG. On average, children who received infliximab also had shorter fever duration, spent less time in
- [Comparing Two Treatments for Resistant Kawasaki Disease – Evidence Update for Parents](https://kdfoundation.org/comparing-two-treatments-for-resistant-kawasaki-disease-evidence-update-for-parents/): Comparing Two Treatments for Resistant Kawasaki Disease – Evidence Update for Parents Compared with children who received a second dose of IVIG, children who received infliximab were more likely to have their fever end within 24 hours. Children who received infliximab also had shorter fevers and spent less time in the hospital than children who
- [Meet Ava Quinn: KDF Graduate School Intern](https://kdfoundation.org/meet-ava-quinn-kdf-graduate-school-intern/): Meet Ava Quinn: KDF Graduate School Intern My name is Ava Quinn, and I currently reside in Pittsburgh, Pennsylvania, having relocated from Conshohocken in 2021. I recently completed my Bachelor's of Science in Applied Developmental Psychology at the University of Pittsburgh and am now pursuing a Master's degree in the same field through an accelerated
- [2024 Kawasaki Disease Parent Symposium Feedback Survey](https://kdfoundation.org/2024survey/): 2024 Kawasaki Disease Parent Symposium Feedback Survey We invite you to participate in the 2024 Kawasaki Disease Parent Symposium Feedback Survey. The symposium, hosted by the Kawasaki Disease Research Center at the University of San Diego, California in partnership with the Kawasaki Disease Foundation, provided valuable updates on Kawasaki disease studies and research. This online
- [Recap from the 14th International Kawasaki Disease Symposium (IKDS)](https://kdfoundation.org/ikds24_recap/): Recap from the 14th International Kawasaki Disease Symposium (IKDS) The board members of the Kawasaki Disease Foundation – USA attended the 14th International Kawasaki Disease Symposium (IKDS) in Montreal, Canada from August 26 to 29, 2024. The symposium brought together providers, researchers, pharmacists, foundations, patients, and families to discuss crucial advancements in Kawasaki Disease. Clinicians
- [See's Candies Fundraiser! Up to 50% of your purchase is donated to KDF!](https://kdfoundation.org/sees24/): See's Candies Fundraiser Indulge in See's Candies and support KDF! With up to 50% of your purchase donated to KDF, you can satisfy your sweet tooth while making a difference! SHOP NOW>>
- [Control Participants Needed: individuals with no history of KD and who are not first relatives of someone with a history of KD](https://kdfoundation.org/control-participants-needed-individuals-with-no-history-of-kd-and-who-are-not-first-relatives-of-someone-with-a-history-of-kd/): Control Participants Needed: individuals with no history of KD and who are not first relatives of someone with a history of KD The Kawasaki Disease Research Center at the University of California, San Diego, is looking for participants for its Adult Kawasaki Study. Participants with a history of KD and no history of KD are
- [Simposio Anual de Padres de la Enfermedad de Kawasaki](https://kdfoundation.org/simposio2024/): ¡Aproveche la oportunidad de unirse al Simposio anual para padres sobre la enfermedad de Kawasaki en línea a través de Zoom! Obtenga información valiosa sobre la enfermedad de Kawasaki, manténgase actualizado sobre las últimas investigaciones y tratamientos de KD e interactúe con expertos de KD para obtener respuestas a sus preguntas en tiempo real. Qué:
- [Kawasaki Disease Foundation Quarterly Newsletter | Summer 2024](https://kdfoundation.org/summer2024/): KDF Newsletter, Summer 2024 In This Issue: 1. UCSD Adult Kawasaki Disease Study Needs Control Participants 2. Cardiac Clinic at SickKids Needs Online Survey Participants 3. Announcing the Dr. Tomisaku Kawasaki Memorial Scholarship Recipients 4. Upcoming Virtual Events: Navigating Kawasaki Disease Together: A Dialogue with Experts for Patients and Caregivers UCSD Annual Kawasaki Disease Parent
- [2024 Virtual Kawasaki Disease Parent Symposium](https://kdfoundation.org/2024-virtual-kawasaki-disease-parent-symposium/): UCSD Annual Kawasaki Disease Parent Symposium What: UCSD Annual Kawasaki Disease Parent Symposium When: Saturday, October 5, 2024, from 9:00 am to 12:00 pm pst/12:00 pm to 3:00 pm est Where: Online via Zoom Click here to register>> Q&A session will be included to allow parents to ask their questions to the specialists. Spanish interpretation will be
- [Participate in KD Research | Complete Online Survey Today!](https://kdfoundation.org/participate-in-kd-research-complete-online-survey-today/): Dear Patient/Guardian, The Cardiac Clinic at SickKids is conducting a brief survey with Kawasaki Disease (KD) patients and families. As part of a quality improvement initiative, this survey has been provided to various online forums and organizations for distribution. The purpose of this survey: Your unique experiences living with a KD diagnosis are important to
- [New Rochelle, NY: Bringing awareness to KD](https://kdfoundation.org/new-rochelle-ny-bringing-awareness-to-kawasaki-disease/): New Rochelle, NY: Bringing awareness to Kawasaki disease During the KDF's 26 days of Kawasaki Disease Awareness campaign, KD mom, Danielle Foster contacted us for support in raising KD awareness. Danielle decided to host an awareness fundraiser for KD in her community, and her impromptu event was very successful. Here are her thoughts on
- [Qualifying for Disability Benefits with Kawasaki Disease](https://kdfoundation.org/disabilitybenefits/): Qualifying for Disability Benefits with Kawasaki Disease By: SSD Help Twitter: @DisabilityGuide If your child has Kawasaki disease (KD) and you are finding that he or she is having difficulty in school and medical bills are piling up, you may be eligible for assistance. The Social Security Administration (SSA) offers monthly resources to people in
- [First Annual Conference of the KD Society of India](https://kdfoundation.org/india/): The 6th KD Summit of India/ 1st Annual Conference of the Kawasaki Disease Society of India Written by Dana Bell Fairfield, CA The 6th Kawasaki Disease Summit of India and the First Annual Conference of the Kawasaki Disease Society of India took place in early November 2018 in beautiful Chandigarh, India and was hosted by
- [Join the Adult Kawasaki Disease Study via Online Health Questionnaires (18 years & over)](https://kdfoundation.org/join-the-adult-kawasaki-study/): Join the Adult Kawasaki Study The Kawasaki Disease Research Center at the University of California, San Diego, is looking for participants for its Adult Kawasaki Study. This longitudinal study aims to investigate the long-term effects of KD in adults. The information obtained from the health questionnaires could provide valuable insights into the long-term outcomes for
- [KD Foundation is Seeking Interns for the KDF Youth Fall Internship Program (Volunteer Position)](https://kdfoundation.org/fall24/): KDF Youth Fall Internship Program POSITION DESCRIPTION: The Kawasaki Disease Foundation (KDF) is accepting applications for three part-time positions for our KDF Youth Program. LOCATION: 100% Remote/Online, must reside in the United States. SCHEDULE/SHIFT: Flexible, 4-8 hours per week, with optional attendance at our monthly board meeting scheduled online on the last Monday of the month at 6
- [KD Foundation is Seeking Interns for the KDF Youth Summer Internship Program (Volunteer Position)](https://kdfoundation.org/summer24/): KDF Youth Summer Internship Program POSITION DESCRIPTION: The Kawasaki Disease Foundation (KDF) is accepting applications for three part-time positions for our KDF Youth Program. LOCATION: 100% Remote/Online, must reside in the United States. SCHEDULE/SHIFT: Flexible, 5-10 hours per week, with optional attendance at our monthly board meeting scheduled online on the last Monday of the month at 6
- [Safety of Apixaban on pediatric heart disease on the prevention of embolism](https://kdfoundation.org/saxophone-apixaban-vs-other-blood-thinners/): Safety of Apixaban on pediatric heart disease on the prevention of embolism People with certain types of heart disease may need to take medication to prevent their blood from clotting. That medication is called an anticoagulant or a blood thinner. The purpose of this study is to find out whether the medicine called Apixaban (commonly
- [New KD Study Examines Plasmablasts in KD Patients](https://kdfoundation.org/new-study-identifies-a-previously-unrecognized-virus-from-a-known-virus-family-that-has-caused-an-infection-in-kd-children-during-the-onset-of-symptoms/): New study identifies a previously unrecognized virus from a known virus family that has caused an infection in KD children during the onset of symptoms The results of a new study conducted by Dr. Anne Rowley and her team at Pediatrics, Northwestern University Feinberg School of Medicine, Ann & Robert H. Lurie Children’s Hospital of
- [Infliximab versus second IVIG for treatment of resistant KD in the USA (KIDCARE)](https://kdfoundation.org/infliximab-versus-second-ivig-for-treatment-of-resistant-kd-in-the-usa-kidcare/): Infliximab versus second intravenous immunoglobulin for treatment of resistant Kawasaki disease in the USA (KIDCARE): a randomised, multicentre comparative effectiveness trial Summary Background Although intravenous immunoglobulin (IVIG) is effective therapy for Kawasaki disease, 10–20% of patients have recrudescent fever as a sign of persistent inflammation and require additional treatment. We aimed to compare infliximab with
- [Lisa Connelly's Case Study (Lisa's Miles)](https://kdfoundation.org/lisasmiles/): Sudden cardiac death in adult with prior history of Kawasaki disease without coronary artery involvement: A case report Lisa Connelly was 37 when she passed away from a massive heart attack on November 29, 2015. The pathology report showed that she had 50-80% blockage in her coronary arteries due to muscle cell build-up. The pathologist
- [Tolerability of COVID-19 Infection and Messenger RNA Vaccination Among Patients With a History of Kawasaki Disease](https://kdfoundation.org/tolerability-of-covid-19-infection-and-messenger-rna-vaccination-among-patients-with-a-history-of-kawasaki-disease/): Tolerability of COVID-19 Infection and Messenger RNA Vaccination Among Patients With a History of Kawasaki Disease Study shows that mRNA vaccines may be safe, and COVID-19 may not be severe for patients with a history of KD. READ MORE HERE>>
- [Dr Michael Portman Explains How Cardiac Disease Differs Between Pediatric, Adult Patients](https://kdfoundation.org/dr-michael-portman-explains-how-cardiac-disease-differs-between-pediatric-adult-patients/): Dr Michael Portman Explains How Cardiac Disease Differs Between Pediatric, Adult Patients During an interview at the 2022 American Heart Association Scientific Sessions in Chicago, the different types of cardiac diseases that present in pediatric patients vs adult patients were addressed by Michael A. Portman, MD, FAHA, director, Pediatric Cardiovascular Research, Center for Integrative Brain
- [KD Aneurysm & Transition of Care](https://kdfoundation.org/kd-aneurysm-transition-of-care/): KD Aneurysm & Transition of Care A group of experts led by Dr. Tremoulet from the Kawasaki Disease Research Center at the University of California, San Diego has published a manuscript through the American Heart Association. The manuscript highlights the importance of a smooth transition of care for patients with aneurysms due to Kawasaki disease
- [Pharmacogenomics of intravenous immunoglobulin response in Kawasaki disease](https://kdfoundation.org/pharmacogenomics-of-intravenous-immunoglobulin-response-in-kawasaki-disease/): Pharmacogenomics of intravenous immunoglobulin response in Kawasaki disease Dr. Michael Portman recently presented findings from a groundbreaking study on Kawasaki disease (KD) at the Seattle Children's Hospital KD Clinic. The study involved a whole genome sequencing of hundreds of thousands of KD patients to identify the genes responsible for the non-response of 20-30% of children
- [Recap: KDF East Coast Gala](https://kdfoundation.org/recap-kdf-east-coast-gala/): Recap of the KDF's 'To Save a Child's Heart' East Coast Gala The first east coast KDF gala was one to remember! And quite unexpectedly, the memories began even before our guests arrived. As we were setting up in the rotunda of The Jefferson Hotel, a man stopped in his tracks when he saw a
- [Event Recap: International Kawasaki Disease Symposium, Yokohama, Japan](https://kdfoundation.org/event-recap-international-kawasaki-disease-symposium-yokohama-japan/): Event Recap: International Kawasaki Disease Symposium, Yokohama, Japan This past June 2018, 485 participants from 32 countries gathered in Yokohama, Japan for the 12th International Kawasaki Disease Symposium (IKDS). The 3 ½ day conference covered Kawasaki disease (KD) issues which included diagnosis and treatment, American Heart Association guidelines, KD epidemiology, genetics, pathology, pathogenesis, etiology, immunology,
- [Last 6 Recap - The Venice 6](https://kdfoundation.org/last-6-recap-the-venice-6/): The Venice 6 - Event Recap The Venice 6 fundraising event held on Sunday, November 13, 2022, at Venice Beach, CA, benefitting the Kawasaki Disease Foundation, was super fun for all those who attended and had a fantastic turnout. The event was hosted by The Last 6 Miles, an organization that educates and funds research
- [Cookies 4 Kawasaki - KDF Youth Donates Items for Kawasaki Patients at Rady Children's Hospital, San Diego](https://kdfoundation.org/cookies-4-kawasaki-kdf-youth-donates-items-for-kawasaki-patients-at-rady-childrens-hospital-san-diego/): Cookies 4 Kawasaki - KDF Youth Donates Items for Kawasaki Patients at Rady Children's Hospital, San Diego In 2022, the KD Foundation's KDF Youth organized Cookies4Kawasaki - a fundraiser raising money to make a difference in the lives of Kawasaki Disease patients. Two Pop-Up events were organized and hosted by the KDF Youth Board members
- [Join KDF Youth!](https://kdfoundation.org/join-kdf-youth/): The KDF Youth program of the Kawasaki Disease Foundation is searching for new members! If you are a young person passionate about raising awareness for KD, hosting online and in-person fundraisers, learning social media communication skills, and earning volunteer hours, you are invited to join KDF Youth! The hours are flexible, and all the work
- [Researchers Identify Potential Diagnostic Test for Kawasaki Disease](https://kdfoundation.org/researchers-identify-potential-diagnostic-test-for-kawasaki-disease/): This article was published by Jackie Carr via UC San Diego Health on August 6, 2018. Researchers Identify Potential Diagnostic Test for Kawasaki Disease For the first time, researchers at University of California San Diego School of Medicine and Imperial College London, with international collaborators, have determined that Kawasaki Disease (KD) can be accurately
- [KD SD Spike Likely Tied To Aerosol Particles](https://kdfoundation.org/kd-sd-spike-likely-tied-to-aerosol-particles/): Researcher: Kawasaki Disease Spike In San Diego Likely Tied To Aerosol Particles An unusual and potentially deadly disease is making a growing number of San Diego County children sick, and researchers say it’s caused by something in the air. When 3-year-old Amelia Hurvitz was admitted to Rady Children’s Hospital in February, the toddler, with curly
- [2019 Kawasaki Disease Awareness Challenge Participant Results](https://kdfoundation.org/2019kdacresults/): 2019 Kawasaki Disease Awareness Challenge Participant Results The Foundation thanks our 2019 KDAC challenge participants. We are grateful for YOUR support and appreciate the time and energy YOU dedicated to helping raise awareness and funds for Kawasaki disease. Together YOU raised $3,265 and ran, walked, biked or hiked 1,406.65 miles from June 21 to September
- [Ask the KD Experts: Kawasaki Disease & COVID-19](https://kdfoundation.org/covid19/): Ask the KD Experts: Kawasaki Disease and COVID-19 Question: Is my KD child more at risk to COVID-19 than the general population? Answer: Children who have had KD go on to be immunologically normal in their response to viruses, vaccines, and other reactions to their environment. While there are certain apparent genetic links to atopic
- [Kawasaki Disease & Coronavirus (NL63)](https://kdfoundation.org/nl63/): Kawasaki Disease & Coronavirus (HCoV-NL63) We've learned that some of our community members have expressed concerns about a past coronavirus and Kawasaki disease. Some of you may recall several years ago researchers, Esper et al.’s announced a link between a different coronavirus (HCoV-NL63) and KD (source 1). The study identified 53 children who had received
- [Ask the KD Experts: KD & COVID-19 Latest News](https://kdfoundation.org/430covid19/): Ask the KD Experts: KD & COVID-19 Latest News Dear KD Parents, We wanted to reach out to provide information and reassurance to our KD parents in light of new information that is emerging about children who develop a severe shock syndrome with some features of KD that appears related to the new coronavirus illness,
- [Statement to the Media following the 2 May Pediatric Intensive Care-COVID-19 International Collaborative Conference Call](https://kdfoundation.org/statement-to-the-media-following-the-2-may-pediatric-intensive-care-covid-19-international-collaborative-conference-call/): Statement to the Media following the 2 May Pediatric Intensive Care-COVID-19 International Collaborative Conference Call With many parents throughout the world wondering about the new information presented by mainstream media regarding COVID-19 and Kawasaki Disease, we wanted to share some more detailed information on what has been happening among the experts in related fields. We
- [Dr. Michael Portman - New Inflammatory Syndrome in Children Related to Virus](https://kdfoundation.org/dr-michael-portman-new-inflammatory-syndrome-in-children-related-to-virus/)
- [Rady Re-Evaluating Recent Kawasaki Cases For New Pediatric Illness Tied To Coronavirus](https://kdfoundation.org/rady-re-evaluating-recent-kawasaki-cases-for-new-pediatric-illness-tied-to-coronavirus/): Rady Re-Evaluating Recent Kawasaki Cases For New Pediatric Illness Tied To Coronavirus San Diego's Children's Hospital is reviewing patients it recently treated for Kawasaki disease to determine if they were actually suffering from a similar but rare new illness connected to the novel coronavirus. Doctors around the world, often in regions hit hardest by the pandemic,
- [Ask the KD Experts: KD & COVID-19 Update](https://kdfoundation.org/ask-the-kd-experts-kd-covid-19-update/): Ask the KD Experts: KD & COVID-19 Update The following update was provided by Jane Burns, M.D. Professor and Director, Kawasaki Disease Research Center. June 23, 2020 1. KD patients who are well, healthy people, with normal functioning hearts are at no increased risk over the general population of any complication of SARS-CoV-2 infection. 2.
- [The Diagnosis and Management of MIS-C with Dr. Tremoulet](https://kdfoundation.org/mis-c/): THE DIAGNOSIS AND MANAGEMENT OF MULTISYSTEM INFLAMMATORY SYNDROME IN CHILDREN (MIS-C) WITH DR. ADRIANA TREMOULET Summary Four weeks after a COVID exposure, children may not be entirely in the clear. MIS-C is a post-infectious inflammatory state that affects pediatric patients and can lead to heart failure, acute abdomen, and a new Kawasaki-like syndrome in older
- [Thank you for your support](https://kdfoundation.org/kdday21/): To ALL our KD Community who helped raise Kawasaki disease awareness on the 11th National KD Awareness Day, January 26, 2021 - THANK YOU! Together, we helped raise awareness of KD by sharing symptoms and KD facts posts, sharing our personal stories and experiences with KD, which is not always an easy thing to do,
- [Ask the KD Experts: Are there any updates on the safety of the COVID-19 vaccine for children and adults with a history of Kawasaki disease?](https://kdfoundation.org/ask-the-kd-experts-are-there-any-updates-on-the-safety-of-the-covid-19-vaccine-for-children-and-adults-with-a-history-of-kawasaki-disease/): Ask the KD Experts: Are there any updates on the safety of the COVID-19 vaccine for children and adults with a history of Kawasaki disease? New inquiries regarding updates on the safety of the COVID-19 vaccine in children and adults with a history of Kawasaki disease (KD) have been submitted to the KD Foundation over
- [Ask the KD Experts: Is the COVID-19 vaccine safe for children and adults with a history of Kawasaki disease?](https://kdfoundation.org/ask-the-kd-experts-is-the-covid-19-vaccine-safe-for-children-and-adults-with-a-history-of-kawasaki-disease/): Ask the KD Experts: Is the COVID-19 vaccine safe for children and adults with a history of Kawasaki disease? The following update was provided by Jane Burns, M.D. Professor and Director, Kawasaki Disease Research Center. We understand that there may be concerns over the safety of the COVID-19 vaccine in children and adults with a
- [KD Summer Newsletter from Dr. Jane Burns](https://kdfoundation.org/kd-summer-newsletter-from-dr-jane-burns/): KD Newsletter from Dr. Jane Burns The KD Summer Newsletter from Dr. Jane C. Burns addresses updates on the Covid-19 vaccine, KD Cases in San Diego during Covid-19, and new research opportunities. Read the complete newsletter here: KD Newsletter-Summer2021. Jane C. Burns, M.D. Professor and Director, Kawasaki Disease Research Center Dept. of Pediatrics MC 0641
- [2021 Virtual Kawasaki Disease Parent Symposium](https://kdfoundation.org/2021kdsymposium/): What: UCSD 2021 Virtual Kawasaki Disease Parent Symposium When: Saturday, October 2, 2021, from 9 am to 12 pm PST Who: Jane C. Burns, M.D. Director, UCSD KD Research Center | Adriana Tremoulet, M.D. Associate Director, UCSD KD Research Center Why: Learn about Kawasaki Disease Hear KD experts give research updates Learn about new KD
- [2021 Virtual KD Parent Symposium - Agenda](https://kdfoundation.org/2021-virtual-kawasaki-disease-parent-symposium-agenda/): What: UCSD 2021 Virtual Kawasaki Disease Parent Symposium When: Saturday, October 2, 2021, from 9 am to 12 pm PST Who: Jane C. Burns, M.D. Director, UCSD KD Research Center | Adriana Tremoulet, M.D. Associate Director, UCSD KD Research Center Why: Learn about Kawasaki Disease Hear KD experts give research updates Learn about new KD
- [Same Treatment Tested for Kids with KD and Rare COVID-19 Reaction](https://kdfoundation.org/same-treatment-tested-for-kids-with-kd-and-rare-covid-19-reaction/): Same Treatment Tested for Kids with Kawasaki Disease and Rare COVID-19 Reaction In a pair of new studies, published online October 26 and August 31, 2021, two collaborating teams of researchers at University of California San Diego School of Medicine examined the use of IVIG in two groups; one group used a second dose of
- [Six Ways to Raise KD Awareness on KD Day 2022](https://kdfoundation.org/six-ways-to-raise-kd-awareness-on-kd-day-2022/): January 26th is National Kawasaki Disease Awareness Day Join the Kawasaki Disease Foundation in raising awareness for Kawasaki Disease from January 1st to 26th, 2022 How YOU can HELP: Be a part of the Wear Your Heart on Your Sleeve Campaign Wear a heart on your sleeve on January 26th. Purchase a t-shirt, hoodie, or
- [Kawasaki Disease Awareness Day is Today - January 26, 2022](https://kdfoundation.org/kdday22/): Kawasaki Disease Awareness Day is Today - Wednesday, January 26, 2022! Twelve years ago, the Kawasaki Disease Foundation requested to have January 26th designated as KD Awareness Day. Senator Jim Webb of Virginia and Daniel Inouye of Hawaii sponsored the official declaration and presented it before the 111th Congress, 2nd session. This day is significant
- [Spread KD Awareness & Give - January 26, 2022](https://kdfoundation.org/kddaydonate22/): Over Half A Million Dollars Donated to Kawasaki Disease Research Thanks to YOU, we have contributed $532,000 to advancing KD research; most significantly, we provided a grant to the Kawasaki Disease Research Center at the University of California San Diego that helped grow and support a KD biorepository. The biorepository is now the largest DNA bank of KD samples
- [KDF Youth Highlights](https://kdfoundation.org/kdf-youth-highlights/): KDF Youth Highlights KDF Youth is a KD Foundation program created by youth for youth. The group was launched in September 2020 to increase Kawasaki Disease (KD) awareness among youth and teenagers. Since its inception, the group has met consistently to create KD awareness campaigns and involve other KD youth. See the group's most recent
- [Gregory Chin, founder and president of the Kawasaki Disease Foundation, retires](https://kdfoundation.org/gregory-chin-founder-and-president-of-the-kawasaki-disease-foundation-retires/): Gregory Chin, founder and president of the Kawasaki Disease Foundation, retires Under his leadership, the KD Foundation has donated over half a million dollars to KD research over the past 21 years. Gregory Chin, founder and president of the Kawasaki Disease Foundation (KDF) has stepped down from his role as president after 21 years of
- [KDF Newsletter - April 2022](https://kdfoundation.org/kdf-newsletter-april-2022/): KDF Newsletter April 2022, Volume 1, Issue 1 In this issue: 2022 Kawasaki Disease Awareness Campaign Results; KDF Founder & President; Gregory Chin’s Retirement; Union University College of Pharmacy KD Awareness Fundraiser; KDF Youth Highlights; Lisa Connelly Case Study: Sudden Cardiac Death in Adult With Prior History of KD Without Coronary Artery Involvement; 2021 UCSD
- [Heart surgery survivor shares road to recovery](https://kdfoundation.org/heart-surgery-survivor-shares-road-to-recovery/): Heart surgery survivor shares road to recovery Paige Garnica was diagnosed with Kawasaki disease before her second birthday. Since then, she and her family have been advocating for Kawasaki disease awareness and funding and have remained involved in the KD community. Recently, Paige shared her story after undergoing heart surgery due to KD. You can
- [Kate Xu, KDF Youth President "Daily Point of Light" Honoree](https://kdfoundation.org/kate-xu-kdf-youth-president-daily-point-of-light-honoree/): Kate Xu, KDF Youth President "Daily Point of Light" Honoree Kate Xu is a friendly, engaged 16-year-old who enjoys reading, photography, math and science. She has extraordinary piano skills that have led her to perform in Paris and at Carnegie Hall, the latter as a result of placing in the American Protégée competition. Recently, she’s
- [MIS-C and KD are on the same immune response continuum as COVID-19](https://kdfoundation.org/mis-c-and-kd-are-on-the-same-immune-response-continuum-as-covid-19/): MIS-C and KD are on the same immune response continuum as COVID-19 A recent study revealed that MIS-C and KD are on the same immune response continuum as COVID-19, with MIS-C being a more severe version of the response than KD. The study was published on May 16, 2022, and can be read here. The
- [Ellen Xu - KDF Youth Board President Honored as One of 25 Most Remarkable Teens in San Diego, CA](https://kdfoundation.org/ellen-xu-kdf-youth-board-president-honored-as-one-of-25-most-remarkable-teens-in-san-diego-ca/): Ellen Xu - KDF Youth Board President Honored as One of 25 Most Remarkable Teens in San Diego, CA One of our very own KDF volunteers, Ellen Xu, is definitely a 'remarkable' teen! San Diego leaders gathered together recently to recognize a group of teens for not only their talents but also their drive to
- [Formal plans needed to support teens with Kawasaki disease in transition to adult care](https://kdfoundation.org/formal-plans-needed-to-support-teens-with-kawasaki-disease-in-transition-to-adult-care/): Formal plans needed to support teens with Kawasaki disease in transition to adult care According to the American Heart Association, an increasing number of children who developed coronary artery aneurysms from Kawasaki disease are becoming adults and require transitioning to adult health care. However, a poor transition to an adult health care team could reduce
- [Kawasaki Disease Rates Dropped During COVID-19 Pandemic](https://kdfoundation.org/kawasaki-disease-rates-dropped-during-covid-19-pandemic/): Kawasaki Disease Rates Dropped During COVID-19 Pandemic A study published by the Jama Network Open Pediatrics found that cases of Kawasaki disease (KD) in the United States dropped by 28% during the Covid-19 shelter in place orders. The decrease in ambient air pollution, masking and school closures, and reduced circulation of respiratory viruses are credited
- [UCSD 2022 Kawasaki Disease Parent Symposium ](https://kdfoundation.org/2022kdparentsymposium/): What: UCSD 2022 Kawasaki Disease Parent Symposium When: Saturday, October 29, 2022, from 9 am to 12 pm PST Who: Jane C. Burns, M.D. Director, UCSD KD Research Center | Adriana Tremoulet, M.D. Associate Director, UCSD KD Research Center Why: Learn about Kawasaki Disease Hear KD experts give research updates Learn about new KD treatments
- [Pharmacy alumni and faculty work with research team to develop North America’s first test to predict Kawasaki disease](https://kdfoundation.org/pharmacy-alumni-and-faculty-work-with-research-team-to-develop-north-americas-first-test-to-predict-kawasaki-disease/): Pharmacy alumni and faculty work with research team to develop North America’s first test to predict Kawasaki disease A new tool under development by University at Buffalo researchers could one day help clinicians better predict resistance to immunoglobulin therapy among children with Kawasaki disease in the United States. The new tool – described in a
- [KDF Newsletter | October 2023](https://kdfoundation.org/kdf-newsletter-october-2023/): October 2023, Volume 1, Issue 1 In this issue: 1. KD Research Updates — KD Aneurysms & Transition of Care; 2. Dr Portman Explains How Cardiac Disease Differs Between Pediatric, Adult Patients; 3. Upcoming KD Events: 2023 UCSD KD Parent Symposium; 1st International Kawasaki Disease Registry & EUROKiDs Joint Meeting; 2024 International KD Symposium, Montreal,
- [Kawasaki Disease Foundation Quarterly Newsletter | April 2024](https://kdfoundation.org/kdf-newsletter-april-2024/): KDF Newsletter, April 2024 In This Issue: 1. 13th National Kawasaki Disease Awareness Day 2. KD Cases Increase at Rady Children's Hospital, San Diego 3. Pharmacogenomics of IVIG Response in KD 4. Watch the 2023 UCSD KD Parent Symposium 5. Paige Garnica's Heart Surgery Story 6. KDF Youth Highlights - Kate Xu, Daily Point of
- [Adult KD Study Seeking Control Participants with no History of KD](https://kdfoundation.org/akd/): Adult Kawasaki Disease Study Needs Control Participants The Kawasaki Disease Research team at the University of California, San Diego is currently looking for individuals over the age of 18 who have no previous history of Kawasaki Disease. They are seeking participants to be a part of their control group, which is required for their study
- [Announcing Dr. Tomisaku Kawasaki Memorial Scholarship Recipient: Julia Fitzgerald](https://kdfoundation.org/jfitzgerald/): Dr. Tomisaku Kawasaki Memorial Scholarship Recipient: Julia Fitzgerald Scholarship Recipient: Julia Fitzgerald Scholarship Year: Fall 2024-Spring 2025 Scholarship Type: Student currently enrolled in a university University Name: University of Illinois Urbana-Champaign Scholarship Amount: $10,000 Julia Fitzgerald was diagnosed with Kawasaki disease (KD) in 2006 at the age of two. It took a few days for the doctor to make a
- [Announcing Dr. Tomisaku Kawasaki Memorial Scholarship Recipient: Aditya Gupta](https://kdfoundation.org/agupta/): Dr. Tomisaku Kawasaki Memorial Scholarship Recipient: Aditya Gupta Scholarship Recipient: Aditya Gupta Scholarship Year: Fall 2024-Spring 2025 Scholarship Type: High school student entering a university University Name: Tufts University Scholarship Amount: $5,000 Aditya Gupta's journey into the medical field was not just a career choice, but a testament to his resilience and determination. Diagnosed with Kawasaki
- [KD Foundation is Hiring a Communications Intern (Stipend-Based Position)](https://kdfoundation.org/commsintern/): Kawasaki Disease Foundation Internship Program POSITION DESCRIPTION: The Kawasaki Disease Foundation (KDF) is accepting applications for one part-time position in communications and administration. APPLICATION DEADLINE: The recruitment for this position will begin on June 7, 2024 and may close on or before August 30, 2024. LOCATION: 100% Remote/Online, must reside in the United States. SCHEDULE/SHIFT: Flexible, 8 hours per
- [JUNE 25 | IKDS EXPERTS COMMUNITY MEETING](https://kdfoundation.org/june-25-ikds-experts-community-meeting/): Fostering Global Collaborations to Solve Kawasaki Disease Join us on June 25th at 1:30 PM ET / 10:30 AM PT for a conversation with Dr. Adriana Tremoulet and Dr. Nagib Dahdah, the Presidents of the 14th International Kawasaki Disease Symposium. Get a sneak peak of the topics that will be discussed at the symposium,
- [Dr. Kawasaki Memorial Scholarship, Application Deadline: April 30, 2024](https://kdfoundation.org/dr-kawasaki-memorial-scholarship/): Announcing the Dr. Tomisaku Kawasaki Memorial Scholarship Presented by the Kawasaki Disease Foundation Scholarship award(s): $5,000 scholarship for high school students, $10,000 scholarship for college students. Application deadline: April 30, 2024 Award date: Fall 2024 semester The Dr. Tomisaku Kawasaki Memorial Scholarship was created by the Kawasaki Disease Foundation to honor Dr. Tomisaku Kawasaki's contributions
- [Rady Children’s Hospital seeing increase in Kawasaki disease cases](https://kdfoundation.org/rady-childrens-hospital-seeing-increase-in-kawasaki-disease-cases/): Rady Children’s Hospital seeing increase in Kawasaki disease cases. Cause remains elusive. After experiencing a lull during the COVID-19 pandemic, clinicians at Rady Children’s Hospital have been somewhat surprised at the number of young children diagnosed with Kawasaki disease in the new year. In January, said Dr. Jane Burns, director of Rady’s Kawasaki Disease clinic,
- [International Kawasaki Disease Symposium (IKDS) 2024 Patient/Caregiver Survey](https://kdfoundation.org/international-kawasaki-disease-symposium-ikds-2024-patient-caregiver-survey/): International Kawasaki Disease Symposium (IKDS) 2024 Patient/Caregiver Survey The 14th International Kawasaki Disease Symposium (IKDS) will take place from August 26-29, 2024, in Montreal, Canada. The Kawasaki Disease Foundation and Kawasaki Disease Canada are proud to support the first IKDS held in Canada. As the date is approaching fast, we are seeking your assistance. KDF
- [There is still time to register for the 2023 Virtual KD Parent Symposium](https://kdfoundation.org/there-is-still-time-to-register-for-the-2023-virtual-kd-parent-symposium/): There is still time to register for the 2023 Kawasaki Disease Parent Symposium! What: UCSD 2023 Kawasaki Disease Parent Symposium When: Saturday, November 4, 2023, from 9 am to 12 pm PST Who: Jane C. Burns, M.D. Director, UCSD KD Research Center | Adriana Tremoulet, M.D. Associate Director, UCSD KD Research Center Why: Learn about Kawasaki Disease; Hear
- [1st International Kawasaki Disease Registry & EUROKiDs Joint Meeting](https://kdfoundation.org/1st-international-kawasaki-disease-registry-eurokids-joint-meeting/): 1st International Kawasaki Disease Registry & EUROKiDs Joint Meeting What: 1st International Kawasaki Disease Registry & EUROKiDs Joint Meeting When: Thursday, November 2nd to Saturday, November 4th Where: Online (100 Euros discounted virtual attendance trainees, family members or members of family associations) CLICK HERE TO REGISTER>> IKDR-EUROKiDS Joint Meeting_Italy_Flyer
- [2023 Virtual Kawasaki Disease Parent Symposium](https://kdfoundation.org/2023-virtual-kawasaki-disease-parent-symposium/)
- [2023 Conferencia Virtual Para Padres Sobre la Enfermedad de Kawasaki](https://kdfoundation.org/2023-conferencia-virtual-para-padres-sobre-la-enfermedad-de-kawasaki/)
- [Save the Date: 14th International Kawasaki Disease Symposium](https://kdfoundation.org/save-the-date-14th-international-kawasaki-disease-symposium/)
- [Kawasaki Disease Foundation 1000K Virtual Run](https://kdfoundation.org/1000kvirtualrace/): Learn More & Register>>
- [The Venice 6 (6 & 3 Mile Run Benefitting KDF)](https://kdfoundation.org/the-venice-6/): What: The Venice 6 (3 mile option available) When: Sunday, November 13, 2022 9:00 AM 3:00 PM Where: Windward Plaza 1 Windward Avenue, Los Angeles, CA, 90291 The Last 6 is back with its annual fundraiser run benefiting the Kawasaki Disease Foundation. We will run a 6 mile out and back starting at Windward Plaza
- [Virtual KD Parent Symposium | Oct 29th](https://kdfoundation.org/virtual-kd-parent-symposium-oct-29th/): You are invited to join the 2022 Kawasaki Disease Parent Symposium! What: UCSD 2022 Kawasaki Disease Parent SymposiumWhen: Saturday, October 29, 2022, from 9 am to 12 pm PSTWho: Jane C. Burns, M.D. Director, UCSD KD Research Center | Adriana Tremoulet, M.D. Associate Director, UCSD KD Research CenterWhy: Learn about Kawasaki Disease; Hear KD experts give research updates; Learn
- [Union University College of Pharmacy (UUCOP) Kawasaki Disease Awareness Fundraiser](https://kdfoundation.org/uucop/): Union University College of Pharmacy (UUCOP) Kawasaki Disease Awareness Fundraiser “Dr. Sean King is giving back by supporting the Kawasaki Disease Foundation (KDF), and he needs your help! A major aspect of his campaign includes a competition within the Union University College of Pharmacy (UUCOP). As part of this competition, Dr. King is sacrificing his
- [KD Parent Spotlight: Aubry Shackelford](https://kdfoundation.org/kd-parent-spotlight-aubry-shackelford/): KD Parent Spotlight: Aubry Shackelford At the age of five, my daughter Allison was diagnosed with Kawasaki Disease. Like many other KD parents, her mother Jean had to become relentless in her pursuit of a diagnosis when initial visits to various pediatricians came up empty. Luckily, Jean found a pediatrician who had encountered KD before
- [Treatment Intensification in Patients With KD](https://kdfoundation.org/treatment-intensification-in-patients-with-kd/): Treatment Intensification in Patients With Kawasaki Disease and Coronary Aneurysm at Diagnosis Coronary artery aneurysms (CAA) are a serious complication of Kawasaki disease. Treatment with intravenous immunoglobulin (IVIg) within 10 days of fever onset reduces the risk of CAA from 25% to
- [Fever, conjunctivitis, rash, and belly pain](https://kdfoundation.org/fever-conjunctivitis-rash-and-belly-pain/): Fever, conjunctivitis, rash, and belly pain KD case study written by two medical doctors highlights that children with KD and prominent GI (gastrointestinal (GI) symptoms of abdominal pain and diarrhea) or hepatobiliary (having to do with the liver plus the gallbladder, bile ducts, or bile) involvement appear to be at a higher risk for IVIG
- [KDF See's Candies Fundraiser](https://kdfoundation.org/sees/): KDF See’s Candies Holiday Fundraiser KD Mom, Samantha Encinas, invites you to help raise funds to support the KDF’s mission via this online Yum-Raising Event! What: See’s Candies Holiday Fundraiser When: October 9, 2021 to December 3, 2021 Where: See’s Candies – KDF Store CLICK HERE TO VIEW STOREFRONT>>
- [My son's fight with Kawasaki disease taught me to trust my instincts](https://kdfoundation.org/my-sons-fight-with-kawasaki-disease-taught-me-to-trust-my-instincts/): My son's fight with Kawasaki disease taught me to trust my instincts (CNN)The latest pandemic news has many parents on edge. If we didn't have enough to worry about already during this pandemic, parents now have another dire warning from medical experts. A rare inflammatory disease, similar to toxic shock syndrome and Kawasaki disease, is
- [KD Awareness Advocates: Donna Collins Tribute](https://kdfoundation.org/collins/): Dear KD Families, It’s with a heavy heart that we share news of the passing of Donna Collins after a long battle with cancer. For those of you who didn’t know Donna, it’s our honor to share a little about her and how she tirelessly advocated for families of children affected by Kawasaki Disease. We
- [KD Awareness Advocates: Mckenzie Graham](https://kdfoundation.org/mckenzie-graham/): KD Awareness Advocates: Mckenzie Graham In the Fall of 2019, the Foundation was approached by Mckenzie Graham and her mother who expressed interest in contributing to KD awareness. Mckenzie's younger sister, Savannah, was diagnosed with Kawasaki disease at the age of three. Savannah was misdiagnosed three times and was diagnosed and treated for KD after
- [Ask the KD Experts: Biomarkers of Inflammation and Fibrosis in KD Patients](https://kdfoundation.org/ask-the-kd-experts-biomarkers-of-inflammation-and-fibrosis-in-kd-patients/): Ask the KD Experts: Biomarkers of Inflammation and Fibrosis in Kawasaki Disease Patients Years After Initial Presentation With Low Ejection Fraction Question: Can you please explain the results of a recent study published titled "Biomarkers of Inflammation and Fibrosis in Kawasaki Disease Patients Years After Initial Presentation With Low Ejection Fraction"? Answer: The study results
- [KD Awareness Advocates: Michael Lau](https://kdfoundation.org/kd-awareness-advocates-michael-lau/): KD Awareness Advocates: Michael Lau My name is Dr. Michael Lau, and I'm a licensed pharmacist currently completing a Post-Graduate Year 1 (PGY-1) Residency at NYU Winthrop Hospital. Throughout the course of the year, residents complete rotations in various fields (cardiology, oncology, pediatrics, etc.). During the month of September, when I was training with the
- [Ask the KD Experts: Kawasaki Disease & Z Scores](https://kdfoundation.org/z-scores/): Ask the KD Experts: Kawasaki Disease and Z Scores Question: What is a Z score? Answer: A Z score normalized for body surface area represents how much larger (or smaller) a measured coronary artery internal diameter is compared to the average coronary artery diameter for a child of the same size (body surface area includes both
- [Ask the KD Experts: Autoimmune Diseases](https://kdfoundation.org/ask-the-kd-experts-autoimmune-diseases/): Ask the KD Experts: Kawasaki Disease an Autoimmune Disease? Question: Is Kawasaki disease an autoimmune disease? Answer: The term “autoimmune” disease is used to describe diseases in which the primary immune response is to “self.” That means that the body’s immune response gets confused and starts attacking itself. Once that program is set in motion,
- [Ask the KD Experts: KD & Hearing Loss](https://kdfoundation.org/ask-the-kd-experts-kd-hearing-loss/): Ask the KD Experts: Kawasaki Disease and Hearing Loss Question: Our son was diagnosed with KD January 2007, he was 2 years 9 months old. After presenting with all the symptoms was treated with IVIG on the fifth day. The test came back normal and he was sent home two days later on low dose
- [Ask the KD Experts: KD & Long Term Effects](https://kdfoundation.org/ask-the-kd-experts-kd-long-term-effects/): Ask the KD Experts: Kawasaki Disease and Long Term Effects Question: My daughter is now 12. She had Kawasaki disease when she was four years old. After treatment and the follow-up tests, they determined that she did not suffer any permanent damage to her heart. She did her follow up visit five years later and,
- [Ask the KD Experts: KD & Vaccines](https://kdfoundation.org/ask-the-kd-experts-kd-vaccines/): Ask the KD Experts: Kawasaki Disease and Vaccines Question: Hello. I was wondering if you can share any information regarding Kawasaki disease and immunizations after onset. My son is 16 years old. He had Kawasaki disease when he was 33 months old. I have been researching the HPV Virus vaccination and those who have side
- [Ask the KD Experts: KD & Calcium Testing](https://kdfoundation.org/ask-the-kd-experts-kd-calcium-testing/): Ask the KD Experts: Kawasaki Disease and Calcium Testing Question: I had KD when I was 2. I am now 22 and have had several weird heart issues that they weren't identifiable with an echo since then. I was just reading about other tests that can be done, such as the calcium test. Would that
- [Etanercept With IVIg for Acute KD](https://kdfoundation.org/etanercept-with-ivig-for-acute-kd/): Etanercept With IVIg for Acute Kawasaki Disease: A Randomized Controlled Trial Dr. Michael A. Portman and colleagues have published the results of a clinical trial showing benefits by etanercept (brand name Enbrel) for Kawasaki Disease patients. The results were published in the American Academy of Pediatrics journal Pediatrics. The manuscript abstract and publicly available video
- [Groundbreaking KD research at Seattle Children’s Hospital](https://kdfoundation.org/groundbreaking-kd-research-at-seattle-childrens-hospital/): Groundbreaking research at Seattle Children’s Hospital to help diagnose rare health condition SEATTLE – A groundbreaking researching happening right here in Washington is giving doctors new hope at better treating and diagnosing a rare health condition called Kawasaki disease. It’s a rare inflammatory condition that mostly affects children under 5. READ MORE>>
- [New study aims to better understand KD](https://kdfoundation.org/new-study-aims-to-better-understand-kd/): New study aims to better understand Kawasaki disease BALTIMORE – A new study looks to define the antibody characteristics, including clonality, of plasmablasts during Kawasaki Disease (KD). Findings from the study will be presented during the Pediatric Academic Societies (PAS) 2019 Meeting, taking place on April 24 – May 1 in Baltimore. “We still don’t

## Pages

- [Home](https://kdfoundation.org/): Kawasaki Disease Foundation is your home for Kawasaki Disease Awareness and its resources, symptoms, care, and support from the KD Foundation.
- [Thank You For Contacting Us](https://kdfoundation.org/thank-you-for-contacting-us/): Thank you for contacting us. We will be in touch with you shortly.
- [Fundraise Confirmation](https://kdfoundation.org/fundraise-confirmation/): Thanks for contacting us! We will get in touch with you shortly.
- [Donation Confirmation](https://kdfoundation.org/donation-confirmation/)
- [Make a Donation](https://kdfoundation.org/donate/): "Lights On, Hearts Strong"General DonationDonate in TributeSupport a Personal Fundraiser"Lights On, Hearts Strong" “Lights On, Hearts Strong” This January, we unite to honor the strength of children affected by Kawasaki Disease. “Lights On, Hearts Strong” is a movement to raise awareness and celebrate the courage of KD kids and their families. Your donations support the
- [KDF Youth](https://kdfoundation.org/kdfyouth/): Welcome to KDF Youth! KDF Youth is a KD Foundation program created by youth for youth. The group was launched in September 2020 to create a supportive, creative, and empowering space for KD youth survivors and supporters. Who We Are The KDF Youth Program is a supportive, empowering space for Kawasaki Disease (KD) youth survivors
- [KDF Board & Volunteers](https://kdfoundation.org/board-team-volunteers/): KDF Board of Directors – Officers Vanessa Gutierrez President San Francisco Bay Area, CA Kate Davila Vice President Richmond Hill, GA Catherine Frank Secretary Havertown, PA Gregory Chin KDF Founder/Treasurer Boston, MA KDF Board of Directors – Board Members Matt Ham Charleston, SC Cheshire, CT Julia Jayatilaka Durham, NC Sean King Jackson, TN Jennifer Lau
- [Dr. Tomisaku Kawasaki Memorial Scholarship](https://kdfoundation.org/dr-tomisaku-kawasaki-memorial-scholarship/): Dr. Tomisaku Kawasaki Memorial Scholarship – Call for Scholarship Applications Spring 2026 The deadline for applications for the 2025-2026 scholarship closed on March 7, 2025. We will reopen submissions for the Fall 2026-Spring 2027 scholarship on January 26, 2026. Statement of Purpose: The Dr. Tomisaku Kawasaki Memorial Scholarship (the “Scholarship”) was established by the Kawasaki
- [Submit Photos to Help Improve Kawasaki Disease Diagnosis with AI](https://kdfoundation.org/photo4ai/): Support Smarter Diagnosis of Kawasaki Disease Help us build a powerful AI tool that can assist doctors and families in identifying possible cases of Kawasaki Disease earlier and more accurately. By sharing photos of KD symptoms, you’ll be contributing to a research project that could improve outcomes for children everywhere. Your photo submission will help
- [Find a KDF Event](https://kdfoundation.org/find-a-kdf-event/): Upcoming KD Events Kawasaki Disease Across the Ages Symposium What: Kawasaki Disease Across the Ages: 4th Mount Sinai Adult Congenital Heart Disease Symposium When: September 12-13, 2025 Where: Leon & Norma Hess Center for Science and Medicine 2nd Floor, Davis Auditorium 1470 Madison Avenue, New York, NY 10029 Patients and their families are invited to
- [Contact KDF Youth](https://kdfoundation.org/contact-kdf-youth/): Have a question about our KDF Youth Program? Contact us using the link below! For general inquiries about KDF, please click here. Contact KDF Youth Name* First Last Email* Phone*Reason/s for contacting KDF Youth?*FileMax. file size: 5 MB. CAPTCHA Submit Δ
- [Rare Disease Day Fundraiser](https://kdfoundation.org/rarediseaseday/): Rare Disease Day Fundraiser Did you overlook Kawasaki Disease Awareness Day? No worries, you can raise awareness on Rare Disease Day – held on the last day of February every year to raise awareness of rare diseases. KD is a rare disease affecting approximately 5,000 individuals each year. By setting up a Rare Disease Day
- [Sara Millener](https://kdfoundation.org/sara/): In Loving Memory Of Sara Millener August 25, 1948 ~ June 27, 2020 (age 71) Sara Margaret Oliver Millener, 71, passed away into the arms of her Lord and Savior on the morning of June 27, 2020. Born August 25, 1948 at Ft. Sanders Hospital in Knoxville, TN, she was the daughter of the late
- [My KD Kid's Fundraiser](https://kdfoundation.org/kidsfundraise/): My KD Kid’s Fundraiser An online fundraiser in honor of your KD child is a great way to help raise Kawasaki disease awareness among your friends and family while raising funds for KD. Whether you are setting up a fundraiser for your child’s birthday, KD diagnosis anniversary, or to celebrate a rite of passage in
- [Online Fundraising](https://kdfoundation.org/virtualfundraisers/): Support KDF by joining our virtual fundraising efforts today! Online Fundraising Join us in our mission by launching your own online fundraiser! Raising funds online not only helps gather essential resources but also spreads awareness about Kawasaki disease. By sharing your personal story, you can inspire your family, friends, and colleagues to contribute towards your
- [KDF Newsletter Archive](https://kdfoundation.org/newsletter/): KDF Newsletter Archive KDF Newsletter | Spring 2025 In This Issue: 1. KD Specialist Highlight: Annette Baker; 2. CalPlasma: Saving Lives; 3. UCSD Research Study; 4. Dr. Rowley’s Breakthrough Study; 5. KD Intern Highlight: Grace Choe; 6. Dr. Tomisaku Kawasaki Scholarship; 7. My Health Planner Toolkit; 8. FAQs, Researched + Answered; 9. Becoming a KDF
- [KDF Latest News](https://kdfoundation.org/latestnews/): KDF Latest News Ask the KD ExpertsKDF NewsKDF NewsletterKD ChampionsKD EventsKD NewsKD ResearchKD Research NewsKD StoriesAsk the KD Experts 2025 KD Parent Symposium The 2025 KD Parent Symposium brought together leading clinicians, researchers, and families for a powerful day of education, research updates, and community connection. The program featured emerging AI developments, new insights into
- [KDF Bridges Volunteers](https://kdfoundation.org/kdf-bridges-volunteers/): United StatesOther CountriesUnited States KDF Bridges Volunteers Across the United States Regional Support Volunteers KDF Bridges Support volunteers have been screened and trained to provide support to families of patients recently diagnosed with the disease. Although they have offered to have their email address and telephone numbers listed, please do not contact them directly. To
- [Dr. Tomisaku Kawasaki Memorial Scholarship Recipients](https://kdfoundation.org/dr-tomisaku-kawasaki-memorial-scholarship-recipients/): Dr. Tomisaku Kawasaki Memorial Scholarship Recipients Scholarship Recipient: Kate Xu Scholarship Year: Fall 2025 – Spring 2026 Scholarship Type: High school student entering a university University Name: Massachusetts Institute of Technology (MIT) Scholarship Amount: $5,000 Kate Xu was diagnosed with Kawasaki Disease (KD) at the age of three after multiple misdiagnoses in the emergency room. It wasn’t until her third
- [KD Researchers](https://kdfoundation.org/kd-researchers/): Kawasaki Disease Nationwide Researchers Jane C. Burns, MD Professor and Director, Kawasaki Disease Research Center “So really KD came and got me. I had no choice. Here was a new disease, a mystery waiting to be solved. I was a smart, young person. This was an amazing opportunity to find the missing pieces of the
- [KD Articles & Journals](https://kdfoundation.org/articles/): Essential Reading on Kawasaki Disease: Recommended Articles to Expand Your Knowledge and Awareness Kawasaki Disease (Journal of the American College of Cardiology) Kawasaki Disease Click here to read the full article>> The article on Kawasaki Disease (KD) provides an in-depth analysis of the long-term implications and management strategies for individuals who have experienced this acute
- [KD Day Fundraiser](https://kdfoundation.org/kddayfundraiser/): Kawasaki Disease Awareness Day Fundraiser January 26th is National Kawasaki Disease Awareness Day By setting up a KD Day fundraiser, you can help raise awareness of KD among your friends, family, and colleagues. Share your KD story with them and, most importantly, tell them why knowing the symptoms of KD is crucial to a timely
- [KD & The Heart](https://kdfoundation.org/heart/): Kawasaki Disease and the Heart Kawasaki disease (KD) primarily affects the blood vessels and can cause significant damage to the heart, particularly when not diagnosed and treated early. The disease causes inflammation of the arteries, including the coronary arteries, which supply blood to the heart muscle. This inflammation can lead to several serious cardiac complications
- [Holiday Fundraiser](https://kdfoundation.org/holidaygiving/): Holiday Fundraiser This holiday season invite your friends and family to support your cause by asking them to donate to the Kawasaki Disease Foundation in lieu of gifts. Inspiring others to support your efforts during the season of giving is simple, simply: Decide to host a holiday fundraiser for KDF Complete the form below, preferably
- [Foundation FAQ's](https://kdfoundation.org/foundation-faqs/): Kawasaki Disease Foundation FAQ’S My child or loved one has symptoms of Kawasaki disease, but their doctor has not diagnosed them yet. What should I do? If your child is showing symptoms and their doctor is having trouble confirming a diagnosis of Kawasaki disease, please have them contact the Kawasaki Disease specialist team at Rady
- [Dr. Jane Newburger](https://kdfoundation.org/dr-jane-newburger/): Jane Newburger, MD Associate Cardiologist-in-Chief, Academic Affairs; Director, Cardiac Neurodevelopmental Program; Director, Kawasaki Program Commonwealth Professor of Pediatrics, Harvard Medical School My Kawasaki Disease Story I first became involved in caring for KD patients and their families in the early 80’s, before IVIG was an established therapy. At the time, I had recently completed my
- [Dr. Jane Burns](https://kdfoundation.org/dr-jane-burns/): Jane C. Burns, MD Professor and Director, Kawasaki Disease Research Center Why I Study Kawasaki Disease In 1979, I was a resident on the wards at The Children’s Hospital in Denver, Colorado. It was my first month as a “supervisory” resident, leading a team of interns and medical students and admitting children to the ward
- [Dr. Anne Rowley](https://kdfoundation.org/dr-anne-rowley/): Anne H. Rowley, MD Professor of Pediatrics (Infectious Diseases) and Microbiology-Immunology My Kawasaki Disease Story As a physician-in-training in pediatric infectious diseases more than 30 years ago, I was struck by the patients I saw with Kawasaki disease and the conversation with affected families about the condition. These families were faced with the new onset
- [Dr. Adriana Tremoulet](https://kdfoundation.org/dr-adriana-tremoulet/): Adriana Tremoulet, MD Associate Director, Kawasaki Disease Research Center How KD Chose Me as a Career Path? I came to Kawasaki disease in a rather circuitous fashion. By the time that the fascinating world of KD research found me, I had completed medical school at UCLA, pediatric residency training at Cedars Sinai Medical Center in
- [Contact Us](https://kdfoundation.org/contact-us/): Do you have a question or general inquiry? Answers to many common questions can be found on our Frequently Asked Questions page. READ THE KDF FAQ’S>> CLICK HERE FOR MEDIA REQUESTS>> If you would like to contact the Kawasaki Disease Foundation, please use the email form below or reach us by regular mail at
- [Birthday Fundraiser](https://kdfoundation.org/bdayfundraiser/): Birthday Fundraiser A birthday fundraiser lets you support your favorite charity or cause – ahem, the Kawasaki Disease Foundation – on your special day. Setting up a birthday fundraiser to support the KDF’s mission is simple. To donate your birthday: Decide to donate your birthday to the KDF Complete the form below, preferably 30-45 days
- [Become a Volunteer](https://kdfoundation.org/volunteer-2/): Become a Volunteer Why Volunteer? Funded in October 2000, the Kawasaki Disease Foundation is a by-product of a highly successful educational symposium for KD families hosted and organized by a group of volunteers. Since its inception, the KDF has been supported entirely by donations and volunteers who have contributed a significant amount of time and
- [About KD](https://kdfoundation.org/aboutkd/): Understanding the rare illness in children About Kawasaki Disease Kawasaki Disease is a rare but critical condition that deserves our immediate attention due to its potentially severe impact on children’s health. Timely diagnosis and treatment can significantly reduce the risk of serious complications, underscoring the necessity for heightened awareness among parents, caregivers, and healthcare providers.
- [Ask the KD Experts](https://kdfoundation.org/ask-the-kd-experts/): 2025 KD Parent Symposium The 2025 KD Parent Symposium brought together leading clinicians, researchers, and families for a powerful day of education, research updates, and community connection. The program featured emerging AI developments, new insights into diagnosis and treatment, research on vulnerable patient populations, and long-term care for adults who had KD in childhood. Two
- [KD Families | Their Stories](https://kdfoundation.org/kdstories/): Heart to Heart, Episode 2: What Is Kawasaki Disease? What exactly is Kawasaki disease, and why is early recognition so important? In the second episode of Heart to Heart, we review Kawasaki disease—what it is, who it affects, and why timely diagnosis and treatment matter. Whether you’re a newly diagnosed family, caregiver, or curious, this
- [Annual Educational Patient & Parent Symposium](https://kdfoundation.org/kdsymposium/): Annual Kawasaki Disease Patient and Parent Educational Symposium Since 2009, the Kawasaki Disease Foundation has proudly organized an annual educational symposium for patients and their families, featuring insights from leading medical experts. Set in esteemed locations across the United States, these symposiums have become vital resources for understanding Kawasaki Disease. Since 2014, we’ve expanded our
- [Our Impact](https://kdfoundation.org/ourimpact/): Our Impact The KDF has achieved remarkable milestones, including the establishment of the annual KD Parent Symposium, the successful designation of January 26th as National KD Awareness Day by Congress, and supporting the creation of the KD Biorepository at the KD Research Center through a $100,000 donation from KDF. These initiatives have fulfilled our mission
- [Take Action](https://kdfoundation.org/takeaction/): Help us make a difference by supporting the advancement of KD issues! Take Action There are countless ways for you to actively support our mission to advance KD issues. As an all-volunteer organization, your contributions are crucial to our success. By uniting our efforts, we can create a much stronger impact. Achieving our goals of
- [About Us](https://kdfoundation.org/aboutus/): Our mission to advance KD issues About the Kawasaki Disease Foundation The Kawasaki Disease Foundation is proud to be the first and oldest non-profit organization in the United States focused on Kawasaki disease. We unite parents, patients, community members, supporters, and medical researchers to tackle the critical issues related to this disease. Our mission—to raise
- [Become a Fundraiser](https://kdfoundation.org/fundraise/): Fundraise Become a Fundraiser By organizing an event to raise funds or asking friends and family to support the Kawasaki Disease Foundation’s mission, you can mobilize your community to help find the cause of KD and improve treatment for future patients. Host a signature KDF online event or let your creativity guide you and turn
- [Our Collaborators](https://kdfoundation.org/collaborations/): Our Collaborators The Kawasaki Disease Foundation -U.S. is proud to collaborate with worldwide organizations that share KDF’s mission and values. By sharing resources and information with our collaborators, the KDF hopes that a day will come when a cause will be determined, a diagnostic test will be developed, and every child is diagnosed and treated
- [KD Research Centers](https://kdfoundation.org/researchcenters/): Kawasaki Disease Research Centers Researchers worldwide are working to solve the Kawasaki disease puzzle. Understanding the disease can lead to improved care and treatment for KD patients. Learn about the different research studies taking place and help accelerate breakthroughs in KD treatment by participating in research. University of California San Diego Kawasaki Disease
- [Participate in Research](https://kdfoundation.org/research/): Your Role in Research Research studies need volunteers to understand Kawasaki disease. Although participating in a research study may not be possible for all KD patients, current research studies need your help. By enrolling in a study you can help accelerate breakthroughs in Kawasaki disease treatment. To get you started, the Foundation offers a list
- [Kawasaki Disease 101](https://kdfoundation.org/kd101/): ABOUT KD What is Kawasaki Disease? Kawasaki disease (KD), or Kawasaki syndrome, is a severe illness characterized by inflammation of blood vessels throughout the body that primarily affects young children and infants. LEARN MORE KD & THE HEART What are KD complications? KD is the leading cause of acquired heart disease in U.S. children, but
- [KD Resources](https://kdfoundation.org/kdeducation/): KD ARTICLES Read published articles on KD Learn more about KD. Read open-access published journal articles written by researchers and other experts on long-term outcomes of KD and other topics related to the disease. LEARN MORE KD RESEARCH CENTERS Learn about KD research studies KD researchers across the country are studying the disease to understand
- [What Is Kawasaki Disease?](https://kdfoundation.org/what-is-kawasaki-disease/): What is Kawasaki Disease? Overview Kawasaki disease (KD), also known as Kawasaki syndrome, is a severe illness characterized by inflammation of blood vessels throughout the body that primarily affects young children and infants. Kawasaki disease is the leading cause of acquired heart disease in children. Although about 80 percent of patients are under five years
- [Lights On Hearts Strong Donation](https://kdfoundation.org/lights-on-hearts-strong-donation/)
- [KD Symposium Videos](https://kdfoundation.org/videos/): KD Symposium Video Archive 2024- UCSD KD Parent Symposium (Virtual Event) Annual Kawasaki Disease Parent Symposium hosted by the University of California San Diego, Kawasaki Disease Research Center. The event was held virtually. WATCH VIDEO>> 2023- UCSD KD Parent Symposium (Virtual Event) Annual Kawasaki Disease Parent Symposium hosted by the University of California San
- [Treating Resistant Kawasaki Disease](https://kdfoundation.org/treating-resistant-kawasaki-disease/): Treating Resistant Kawasaki Disease Kawasaki disease (KD) is a rare condition that predominantly impacts children. While KD is treatable, some children experience resistant KD and do not respond to initial treatment. Thanks to funding from PCORI, a comprehensive study was conducted to compare the safety and effectiveness of two treatments for resistant KD. This study
- [KDF Funded Studies](https://kdfoundation.org/fundedstudies/): Kawasaki Disease Foundation Funded Studies Since 2000, the KDF has awarded grants to accelerate KD research, including support for a biorepository in San Diego. This biorepository is the largest DNA bank of KD in North America and has provided valuable samples for research projects. The KD DNA bank has significantly advanced KD research, with the
- [Our Programs & Initiatives](https://kdfoundation.org/ourprograms/): Our Programs & Initiatives Our programs and initiatives at KDF are strategically designed to support our core mission: raising awareness about Kawasaki disease, providing comprehensive support to those affected, and advocating for increased funding for crucial research efforts. Our efforts involve educational campaigns, patient support programs, fundraising activities, and collaborations with research institutions to advance
- [The "Tote Bag" Project](https://kdfoundation.org/totebag/): The Kawasaki Disease Foundation “Tote Bag” Project The “Tote Bag” is a new initiative launched by the Kawasaki Disease Foundation in 2019 to support newly diagnosed patients and their families. The care bags are intended for children hospitalized with KD and include several care items for the parent/guardian, information on KD, resources on the Foundation,
- [The Olowin Family's KDF Virtual Walk](https://kdfoundation.org/olowin/): The Olowin Family’s KDF Virtual Walk The Olowin Family’s KDF Virtual Walk Challenge Type: Walk Challenge Goal: 100 miles Fundraising Goal: $500.00 Why we are participating in the KDF Virtual Walk ? Tristan was diagnosed with Kawasaki’s Disease at the age of three and a half. We were fortunate to be able have him treated
- [Host a Fundraiser](https://kdfoundation.org/fundraising/): Thank you for your interest in hosting a fundraising event for the Kawasaki Disease Foundation (KDF). Funds raised for KDF will be used to directly support our three-fold mission of raising awareness, facilitating family support, and supporting KD research. The Kawasaki Disease Foundation must authorize you/your event as an official KDF fundraiser before you initiate any
- [About the KDF Bridges Program](https://kdfoundation.org/bridges/): Kawasaki Disease Foundation Bridges Program The KDF Bridges program connects families dealing with Kawasaki disease (KD) with trained Support Volunteers. These volunteers are typically parents of children who have had KD or adult patients who have recovered from KD. They undergo screening and training by experienced support professionals. The role of the Support Volunteer is
- ["30K For KD" Matching Campaign Challenge](https://kdfoundation.org/30k/): “30K For KD” Matching Campaign Challenge January 26, 2020, is National Kawasaki Disease Awareness Day, and we are kicking off our annual KD awareness campaign with a matching challenge. DONATE TODAY to see your gift DOUBLED by a generous anonymous donor who will match your contributions dollar-for-dollar up to $15,000. HELP us RAISE $30K for KD by making a donation today. Three Ways
- [Matt Nelson](https://kdfoundation.org/nelson/): Matt Ham KDF Board Member Matt Nelson is the Owner of MediaBeast Marketing Group, founded in 2012. In addition to being a Navy and Army National Guard Veteran, Matt is a media digital media expert with nearly 20 years of marketing experience. He is a Google certified partner with an extensive background in the non-profit
- [KD FAQ's](https://kdfoundation.org/faqs/): Kawasaki Disease Frequently Asked Questions The following are some of the questions most frequently asked by parents of children who have Kawasaki disease. The handout and information provided on this page were put together by the Kawasaki Disease Research Center at the University of California San Diego. To download the handout, please click here. To
- [KD Awareness Posters](https://kdfoundation.org/kdposters/): KD Awareness Poster Are you interested in raising awareness of Kawasaki disease in your local medical community? In connection with KD Awareness Day – January 26th, the Kawasaki Disease Foundation (KDF) has published a poster to be distributed to doctor’s offices, hospitals, and clinics across the country. A printable PDF version in both English and Spanish
- [Karin Wicker](https://kdfoundation.org/karin-wicker/): Karin Wicker (Right) KDF Board Member & Bridges Coordinator My daughter Stefanie (20) had Kawasaki disease in 1999 at the age of 6 months. Stefanie had most symptoms of KD but a milder version of them. She had a strawberry tongue, red blood-shot eyes, a rash, swollen lymph nodes and was running a fever that
- [Greg Chin](https://kdfoundation.org/greg-chin/): Gregory Chin – KDF Founder In 1998, our three-year-old son Taylor had Kawasaki disease. Our experience was much like that of other families. Taylor’s symptoms began with a sudden high fever on a Sunday night. The fever was unexpected because he had been on an antibiotic for the past several days for an unknown respiratory
- [KDF Media Requests](https://kdfoundation.org/media/): KDF Media Requests Form For media requests, images, or details about KDF or KD related topics, please complete the Media Requests Form below. To request permission to use images, please click here. Name* First Last Title/Role*Focus of Story*Name of Media Organization*Request of KDF*Deadline* Project Release Date* Email* Phone*FileMax. file size: 5 MB. CAPTCHA Submit Δ
- [Matthew Butler's Fundraiser for Kawasaki Disease](https://kdfoundation.org/matthewbutler/): Matthew Butler’s Fundraiser for Kawasaki Disease I am an adult living with the effects of Kawasaki Disease. I had aneurysms in my coronary arteries as a three-year-old. Recently, I was able to visit the Kawasaki Disease Center in San Diego. Dr. Burns and Dr. Bhatt helped direct my care in a new direction. A surgery
- [Raise KD Awareness](https://kdfoundation.org/raise-kd-awareness/): National Kawasaki Disease Awareness Day In 2011, the Kawasaki Disease Foundation declared January 26 the first National Kawasaki Disease Awareness Day in the United States, and they presented the resolution before the 111th Congress, 2nd Session. Click here to read the KDF Resolution, and click here to read the Library of Congress Official Designation. The
- [KD Champion](https://kdfoundation.org/kd-champion/): KD Champion KD champions work tirelessly to ensure future KD patients receive timely diagnosis and treatment and have positive outcomes. They advocate for past KD patients through research participation and fundraising to increase funds for KD research. Are you a KD Champion, or do you know someone whose dedicated work to increase KD awareness and
- [Donor Dashboard](https://kdfoundation.org/donor-dashboard-4/)
- [KD Symptoms Portfolio](https://kdfoundation.org/kd-symptoms-portfolio/): Kawasaki Disease Symptoms Portfolio In collaboration with parents of KD patients, the Kawasaki Disease Foundation compiled a portfolio of professional-quality KD symptoms photos. The photos are the sole property of the Kawasaki Disease Foundation and are available for distribution by medical professionals, media channels, partner organizations, medical students, researchers, and others. Individuals/organizations seeking to use
- [KD & COVID-19 FAQ's](https://kdfoundation.org/covid19faqs/): Kawasaki Disease & COVID-19 FAQ’s Transcription of Kawasaki Disease and COVID-19 FAQ video Recorded 07, May 2020 between Beth Avant (BA) and Adriana Tremoulet, MD (AT). Beth Avant: Hi, I’m Beth Avant. I am a Kawasaki Disease parent and also a KD Foundation volunteer. I’m here today with Dr. Adriana Tremoulet. She’s the Associate Director
- [Jayda's Birthday Fundraiser for KD](https://kdfoundation.org/jayda/): Jayda’s Birthday Fundraiser for Kawasaki Disease In August of 2018, our daughter Jayda was diagnosed with a rare childhood disease called Kawasaki Disease. Kawasaki Disease is an unusual illness characterized by inflammation of blood vessels throughout the body. The following symptoms accompany it: fever, rash, swelling of the hands and feet, bloodshot eyes, irritation and
- [Johnny’s 1st Birthday Fundraiser for Kawasaki Disease](https://kdfoundation.org/johnny/): Johnny’s 1st Birthday Fundraiser for Kawasaki Disease Johnny was diagnosed with Kawasaki Disease when he was eight months old. He was treated with IVIG within the first ten days and had an eight-day stay in the hospital. After eight days in the hospital, we took home our happy baby boy. Johnny was sent home on
- [Our Mission](https://kdfoundation.org/ourmission/): About the Kawasaki Disease Foundation Our History In October 2000, a group of parents and professionals collaborated to create the Kawasaki Disease Foundation (KDF), the first and only non-profit organization dedicated exclusively to addressing issues related to Kawasaki disease. KDF was a by-product of a highly successful event-the Kawasaki Disease Parent’s Education Symposium.
- [KDF Bridges Training](https://kdfoundation.org/kdf-bridges-training/): KDF Bridges TrainingStep 1Step 2Step 3Step 4Step 5KDF Bridges Training Dear Support Volunteer Candidate, Thank you for your interest in becoming a Support Volunteer for the Foundation’s KDF Bridges. Support Volunteers are the backbone of our program, and we’re grateful to you for considering this volunteer opportunity. By joining KDF Bridges, you can support other
- [KDF Donor Wall](https://kdfoundation.org/kdf-donor-wall/): THE KAWASAKI DISEASE FOUNDATION CELEBRATES OUR DONORS KT Kevin Trickey July 28, 2026 Amount Donated $150 Anonymous July 20, 2026 Amount Donated $150 PS Philip Stevens June 26, 2026 Amount Donated $60 AW Anna Warpe-Lillian June 8, 2026 For my son who survived KD at age 4 and is a thriving, healthy adult. Thank you
- [Share Your Story](https://kdfoundation.org/share-your-story/): Share Your Kawasaki Disease Story Name* First Last Email* KD Diagnosis Date* Child Age at Diagnosis*Child* Male Female Your KD Story*Can we post or publish your story on our site?* Yes No Are you interested in sharing your story with others? By selecting yes, you give us permission to post or publish your story on
- [Request a KDF Bridges Match](https://kdfoundation.org/support/): Request a KDF Bridges Support Volunteer Was your child recently diagnosed with Kawasaki disease? Are you looking for supportive advice from a parent or individual who has been through a similar diagnosis? The Foundation’s KDF Bridges program can link you to a trained Support Volunteer. Support Volunteers do not provide medical advice. If you
- [KD Symptoms](https://kdfoundation.org/kd-symptoms/): The Symptoms of Kawasaki Disease Bloodshot Eyes Rash Strawberry Tongue and Red, Cracked Lips Swollen Lymph Node in Neck Red Palms/Soles and Swollen Hands/Feet If your child has had a fever for at least five days, together with two or more of the symptoms listed above, ask your doctor whether he or she could have Kawasaki
- [Log In](https://kdfoundation.org/log-in/): [discussion_board_login_form] [is_logged_in]You are already logged in[/is_logged_in]
- [Cyber Fundraiser Checkout](https://kdfoundation.org/cyber-fundraiser-checkout/): [cyber_checkout]
- [Cyber Fundraiser Success Donation](https://kdfoundation.org/cyber-fundraiser-success-donation/): [cyber_success_donation]
- [Cyber Fundraiser Documentation](https://kdfoundation.org/cf-docs/): [cyber-help]
- [Share Your Story Confirmation](https://kdfoundation.org/share-your-story-confirmation/): Thanks for sharing your story! We will get in touch with you shortly.
- [Volunteer Confirmation](https://kdfoundation.org/volunteer-confirmation/): Thanks for contacting us! We will get in touch with you shortly.
- [Password Reset](https://kdfoundation.org/password-reset/): [wpum_password_recovery login_link="yes" register_link="yes"]
- [Profile](https://kdfoundation.org/profile/): [wpum_profile]
- [Submission Confirmed](https://kdfoundation.org/submission-confirmed/): [ipt_fsqm_trackback label="Track Code" submit="Submit"]
- [Donation Failed](https://kdfoundation.org/donation-failed/): We're sorry, your donation failed to process. Please try again or contact site support.
- [Donation History](https://kdfoundation.org/donation-history/)

## Donation Forms

- [Abby Helping Kawasaki!](https://kdfoundation.org/donations/abby/)
- ["Lights On, Hearts Strong"](https://kdfoundation.org/donations/lights-on-hearts-strong/)
- [Matthew Butler's Fundraiser for Kawasaki Disease](https://kdfoundation.org/donations/matthew-butlers-fundraiser-for-kawasaki-disease/)
- [2022 Union University College of Pharmacy (UUCOP) KD Fundraiser](https://kdfoundation.org/donations/union-university-college-of-pharmacy-uucop-kd-fundraiser/)
- [The Olowin Family](https://kdfoundation.org/donations/olowin/)
- [In Loving Memory Of Sara Millener](https://kdfoundation.org/donations/sarah-millener/)
- [30K FOR KD](https://kdfoundation.org/donations/30k-for-kd/)
- [Jayda's Birthday Fundraiser for Kawasaki Disease-Donor Form](https://kdfoundation.org/donations/jaydas-birthday-fundraiser-for-kawasaki-disease-donor-form/)
- [Johnny’s 1st Birthday Fundraiser for Kawasaki Disease](https://kdfoundation.org/donations/johnnys-1st-birthday-fundraiser-for-kawasaki-disease/)
- [KDF Donation](https://kdfoundation.org/donations/kd-donation/)

## Campaigns

- [Love Life And Angelica Kawasaki Disease Awareness Fundraiser](https://kdfoundation.org/campaigns/love-life-and-angelica-kawasaki-disease-awareness-fundraiser/): Angelica's Mission: To increase awareness and support for childhood Kawasaki Disease Heroes and their families. Love Life And Angelica donations will support the Tote Bag Program that provides information and essentials for families of children diagnosed with Kawasaki Disease. All donors who wish to support Kawasaki Disease Foundation
- [Kawasaki Disease Foundation 100k Virtual Run](https://kdfoundation.org/campaigns/kawasaki-disease-foundation-100k-virtual-run/): This is a national group virtual 1000k race, designed to support the efforts of the Kawasaki Disease Foundation. In fact, 90cents of every donation received supports the Foundation’s mission. We have no paid staff, and our operating costs are minimal. Your generous contributions will go directly to support programs that can make an impact on
- [Kawasaki Disease Foundation](https://kdfoundation.org/campaigns/500517/): Raising Awareness For Kawasaki Disease What Is Kawasaki Disease? Kawasaki Disease (KD), also known as Kawasaki syndrome, is a severe illness characterized by inflammation of blood vessels throughout the body that primarily affects young children and infants. Kawasaki disease is the leading cause of acquired heart disease in children. The cause of KD is unknown.

## Categories

- [KD Research](https://kdfoundation.org/category/kd-research/)
- [KD Events](https://kdfoundation.org/category/kd-events/)
- [KD News](https://kdfoundation.org/category/kd-news/)
- [KD Champions](https://kdfoundation.org/category/kd-champions/)
- [KD Stories](https://kdfoundation.org/category/kd-stories/)
- [KD Research News](https://kdfoundation.org/category/kdresearchnews/)
- [Ask the KD Experts](https://kdfoundation.org/category/ask-the-kd-experts/)
- [KDF News](https://kdfoundation.org/category/kdf-news/)
- [KDF Newsletter](https://kdfoundation.org/category/kdf-newsletter/)
- [KD Facts](https://kdfoundation.org/category/kd-facts/)

## Tags

- [Kawasaki Disease](https://kdfoundation.org/tag/kawasaki-disease/)
- [Kawasaki Disease News](https://kdfoundation.org/tag/kawasaki-disease-news/)
- [Kawasaki Disease Research](https://kdfoundation.org/tag/kawasaki-disease-research/)
- [Ask the KD Experts](https://kdfoundation.org/tag/ask-the-kd-experts/)
- [kawasaki disease effects long term](https://kdfoundation.org/tag/kawasaki-disease-effects-long-term/)
- [Kawasaki disease scholarships](https://kdfoundation.org/tag/kawasaki-disease-scholarships/)
- [Scholarships for Kawasaki disease](https://kdfoundation.org/tag/scholarships-for-kawasaki-disease/)
- [Kawasaki disease health care transition](https://kdfoundation.org/tag/kawasaki-disease-health-care-transition/)

## Campaign Categories

- [Fundraising](https://kdfoundation.org/campaign_category/fundraising/)

## Campaign Tags

- [kdrace](https://kdfoundation.org/campaign_tag/kdrace/)