The Kawasaki Disease Foundation Gala - Can you help?
Thursday, October 18, 2012 at 12:13PM Just going to be upfront on this - I'm going to tell you a little story that may pull at your heart, then I'm going to ask you for a favor…
My baby boy was 9 months old.
Sweet, little Lucas had just celebrated his first Thanksgiving, was starting to pull himself to a standing position and was about to celebrate his first Christmas. One evening, Jason and I took him to Balboa Park, to what used to be called "Christmas on the Prado" to see the lights. He was all bundled up and tucked in tight to his stroller when our friend looked down at him and said "Wow, I never realize how red his cute little lips were!" Jason and I stared at each other, both of us wondering why we had never noticed either.
We were only 9 months into this parenting thing. Maybe the baby was cold? Maybe he ate something he shouldn't have? Thoughts raced through our minds. The next day our sweet boy had his very first fever. We called the nurse line and doled out the proper dosage of infant Motrin and gave him a lukewarm bath. Our normally happy baby was crying and sleeping and visibly uncomfortable. The next day the fever continued on. His lips grew redder and his eyes were a little bloodshot. Monday came with an early visit to our pediatrician. She made note that this looks "something like Kawasaki Disease" - but told us not to worry.. that was a very rare illness. She told me not to Google it and freak myself out. She put him on antibiotics and sent him in for a chest Xray to rule out pneumonia.
This was before smartphones - with my day spent at doctors and caring for my little one, I didn't Google Kawasaki Disease...but when he was admitted to Rady Children's Hospital the next day, I wish I had.
Kawasaki Disease is the NUMBER ONE CAUSE OF ACQUIRED HEART DISEASE IN CHILDREN. And going on 8 years later, doctors and scientists STILL don't know exactly what causes it.
We were lucky.
At the time, many pediatricians weren't trained to recognize and treat KD, and far too many parents were losing their kids to this disease. Our doctors diagnosed the disease in time for a successful treatment. Thus far Lucas has had no lasting heart damage. But as the research continues to grow and mature along with the little hearts affected by KD in the past, we are learning that things can always change.
That's why Jason and I are standing together to not only raise awareness for the disease, but help raise funds for the continued research of this disease.
BUT WE NEED A LITTLE HELP
This is going to be an amazing culinary evening at La Costa Resort in Carlsbad, celebrating all we know and raising money to keep on answering the millions of questions still unanswered.
At this event, 18 celebrity chefs will cook table side for intimate groups of 8 people. Some of the top chefs from around the country and coming in and donating their time for this cause. I'm proud to be on the committee helping with the gala. I'm happy that I can do anything to give back the community that was there for us when we needed them 8 years ago.
If you are interested in attending the event, you can find more information on the chefs at www.KDFGala.org.
But even if you can't be there - I would still love your help.
To help raise money at the event, we are looking for donations for the silent auction portion of the evening.
Anything from gift certificates to restaurants, bottles of wine, work-out memberships or a basket of products would be greatly appreciated.
I'm going to be collecting items over the next few weeks. If you can help in anyway, please let me know.
Yes, I'm begging. Because I'm still scarred from the experience and learning all we can about this disease is the only way I can help other parents not have to go through what we went through.
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