Kawasaki Kids Foundation

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Kawasaki Kids Foundation

Dedicated to supporting children and families fighting Kawasaki Disease while growing awareness and e What is Kawasaki Disease? It is not contagious.

Someone does not have to be directly affected by Kawasaki Disease (KD) to understand the work and how their support, time, and donation/sponsorship can make a difference. KD affects over 4,200 kids every year in the US. KD, also known as Kawasaki syndrome, is a serious illness (rare disease) characterized by inflammation of blood vessels throughout the body that primarily affects young children and infants. KD is the leading cause of acquired heart disease in children. KD is more common in boys than girls, and the majority of cases are diagnosed in the winter and early spring. The disease is named after Tomisaku Kawasaki, a Japanese pediatrician who first described the illness in the medical literature in 1967. Although, it is more prevalent among children of Asian and Pacific Island descent, KD affects people of all racial and ethnic groups. Without treatment, about 25% of children develop heart disease involving the coronary arteries. Timely diagnosis (to prevent complications KD needs to be diagnosed within 10 days) and treatment (which usually includes intravenous gamma globulin) is highly effective in preventing coronary complications. Doctors continue to study the long-term outcome of children who do not appear to have coronary involvement. Other kinds of longer-term consequences (e.g., non-coronary) are extremely rare. There is no evidence that links KD with autism or a seizure disorder. A very small number of KD children might have a seizure in the early acute stage of KD when there are very high fevers, but there is no on-going or long-term seizure prone condition. FIRST PHASE SYMPTOMS:
• Fever which often is higher than 102.2 F (39 C) and lasts more than five days (Please be aware that this may be the only symptom)
• Extremely red eyes (conjunctivitis) without a thick discharge
• A rash on the main part of the body (trunk) and in the genital area
• Red, dry, cracked lips and an extremely red, swollen tongue (strawberry tongue)
• Swollen, red skin on the palms of the hands and the soles of the feet
• Swollen lymph nodes in the neck and perhaps elsewhere
• Irritability
SECOND PHASE:
• Peeling of the skin on the hands and feet, especially the tips of the fingers and toes, often in large sheets
• Joint pain
• Diarrhea
• Vomiting
• Abdominal pain
THIRD PHASE
• In the third phase of the disease, signs and symptoms slowly go away unless complications develop
• It may be as long as eight weeks before energy levels seem normal again

History of the Foundation
Kawasaki Kids Foundation was started in 2013 by the Logan family after their 3 year old son, Cooper, was diagnosed in 2012. Cooper was diagnosed at 12 ½ days which is outside the critical 10 day window. Since, the Logan family has struggled with not only the medical expenses but with the fact that everything could be different if the doctors would have been more aware of KD and its symptoms. Cooper was misdiagnosed with an appendectomy, a nasty virus, and then finally, correctly diagnosed with Kawasaki Disease. Unfortunately, it was too late and Cooper’s diagnosis resulted in a giant aneurysm in his right coronary artery. He has since been diagnosed with chronic kidney failure as a result of an adverse reaction to his heart medications. His life of anti-coagulants, heart surgeries and kidney transplant would have been avoided if he was correctly and timely diagnosed. The Logan family knew they could make a difference by starting and running a foundation to help support research, awareness, and affected families.

11/03/2026

14 years. It's hard to even wrap my head around that.

14 years ago, our world was turned upside down when Cooper was diagnosed with Kawasaki Disease. I can still remember the fear, the uncertainty, the hospital rooms, and the helpless feeling of watching your little boy go through something you never imagined he would have to face.

As a parent, you just want to protect your kids. You want to take away their pain, make everything better, and tell them it's all going to be okay. But sometimes life puts you in a place where you don't have the answers.

We learned a lot during those days. We learned how quickly life can change. We learned how strong a little boy could be. We learned the importance of family, faith, hope, and the incredible people who helped us through some of our darkest moments.

And somewhere along the way, that experience became something so much bigger than us. It became the reason Kawasaki Kids Foundation exists today.

Now here we are, 14 years later, and that little boy in the hospital bed is a SENIOR IN HIGH SCHOOL. Man, where did the time go?

Looking at his senior pictures and then looking back at those hospital photos brings up emotions that are hard to put into words. So much life has happened between those pictures. So many memories, challenges, laughs, tears, and moments I wish I could slow down.

I wouldn't wish what we went through on any family. But I can say that we came out of it stronger, with a different perspective on life and a purpose I never could have imagined.

Cooper, I'm so incredibly proud of the young man you've become. You may not realize it, but your story has touched more lives than you'll ever know. And because of you, we've had the privilege of walking alongside so many other Kawasaki families over the years.

14 years ago, I was just a scared dad praying his little boy would be okay.

Today, I'm a proud dad watching that same little boy get ready to take on the world.

And I couldn't be more grateful.

Love you, Coop. Always and forever. DJ Coop | 16 Yr. Old DJ & Entrepreneur

11/02/2026

MEET KAWASAKI KID DAMIEN

What started as a family vacation quickly turned into a parent's worst nightmare.

A rash, cracked lips, fever, and eventually, 2-year-old Damien refusing to walk.

After initially being told it was a virus, Damien's family finally received the diagnosis they never expected. Kawasaki Disease.

Thankfully, Damien received treatment and today he's a happy, healthy little boy!

Stories like Damien's are exactly why we work so hard to spread awareness. Early diagnosis matters!

Read Damien's full story here:
https://www.kawasakikids.org/post/meet-damien-a-family-vacation-that-took-an-unexpected-turn

Want to help us support more Kawasaki Kids and their families? Visit www.kawasakikids.org/donation to make a donation.

10/28/2026

❤️ **KAWASAKI KID SPOTLIGHT: MAX!**

Today, we're giving a HUGE shoutout to Kawasaki Kid Max and his incredible family!

Max recently celebrated his 14th birthday, but this year he and his family decided to do something extra special.

They turned his birthday into an opportunity to give back to Kawasaki Kids Foundation and help other children and families facing Kawasaki disease.

**And they raised OVER $600!**

Max was diagnosed with Kawasaki disease just before his 4th birthday, and his family knows firsthand the challenges that come with this disease.

Seeing our Kawasaki Kids grow up and give back to help others is something that truly fills our hearts.

Max, we couldn't be more proud of you! Thank you for turning your special day into something that will make a difference in the lives of others.

And to his amazing family and everyone who donated, THANK YOU for your generosity and support!

**Happy 14th Birthday, Max! Keep doing amazing things!**

10/24/2026

Michigan, you made our hearts full today! ❤️

Our first Kickin’ Kawasaki 5K back since 2018 reminded us just how special this community is. Seeing our Kawasaki Kids again and how much they’ve grown was one of the best parts of the day. These connections are the heart of why we do what we do.

A huge thank you to Rachel for organizing this beautiful day, and to every volunteer, sponsor and participant who helped make it possible. You showed up for our kids and families, and we are so grateful.

Want to bring this kind of hope and connection to your own community? We’re looking for event coordinators to help us reach more families and grow Kawasaki disease awareness. Comment below or send us a message. We’d love to build something meaningful with you!

10/22/2026

Michigan here we come. Hope to see you all on Saturday morning in the Grand Rapids, MI area. Find out more info and get signed up at Kawasakikids.org/michigan

10/16/2026

❤️ BIG CHANGES ARE COMING IN 2027! ❤️

Here's a little sneak peek at what's ahead for Kawasaki Kids!

We're giving our 5K events a fresh new look and feel for 2027, and we can't wait to share what's coming!

Want to bring Kawasaki Kids to YOUR community? We're looking for passionate, motivated race coordinators who want to help us create an unforgettable event, bring people together, raise awareness and make a difference for children battling Kawasaki disease.

Could your community be next?

Text, call or message us if you're interested in bringing an event to your hometown!

Stay tuned. 2027 is going to be exciting! ❤️

10/13/2026

Every child deserves a little Christmas magic. ❤️🎄
https://www.kawasakikids.org/donation

For many families, the holidays are filled with excitement, traditions, and memories being made. But for some families who have faced Kawasaki disease, this year has brought challenges they never expected. Medical bills, missed work, financial struggles, and the emotional toll of caring for a sick child can make the holiday season especially difficult.

That's where YOU can make a difference!

Through our **Kawasaki Christmas Wishes** program, we want to bring a little extra joy, hope, and Christmas magic to children and families who could really use a reason to smile this year.

We're asking our amazing community to help us make that happen. Whether it's $10, $25, $50, or whatever your heart allows, your generosity can help make Christmas morning a little brighter for a child who has already been through so much.

**Imagine being part of the reason a child wakes up on Christmas morning with a huge smile on their face.** That's what this program is all about.

You don't have to spend a fortune to make a difference. Sometimes the smallest act of kindness creates the biggest memories.

**Will you help us make some Christmas wishes come true this year?**

Donate today and help us spread a little extra Christmas cheer to some pretty incredible kids! ❤️

Because every child deserves to feel the magic of Christmas.

10/12/2026

Big news! 🎉 The Johnstown SCHEELS Giving Campaign is officially live, and we need your support! This year, they are giving away $100,000 in donations - awarding $5,000 to 20 different non-profit organizations.

Winning one of these $5,000 donations would mean the world to us and help us continue our mission. We'd be incredibly grateful if you took a moment to nominate us.

🗓️ Nominations are open NOW through October 20! Tap the link below to submit your nomination. Let’s do this! ❤️

(here's the link https://tinyurl.com/3m6y9z74)

We look forward to seeing all of the nominations come through!

10/09/2026

🚨 DON'T MISS OUT, MICHIGAN! 🚨

Want a FREE race T-shirt? Time is running out!

October 14th is your LAST CHANCE to register for the Kickin' Kawasaki 5K and score a FREE race T-shirt with your registration!

Join us on Saturday, October 24th in Walker, Michigan, for an incredible day of fun, community, and making a difference for kids and families battling Kawasaki disease. ❤️

Every step you take helps us spread awareness, support families, and give hope to kids who need it most.

❤️ Don't wait until it's too late! Get registered, secure your race shirt, and come make a difference with us!

👉 REGISTER TODAY: kawasakikids.org/michigan

Address

1298 Main Street, Unit A #4221
Windsor, CO
80550

Website

http://kawasakikidsfoundation.org/

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