It’s time to trade those dancing shoes for running shoes!!! I had so much fun at our Flash Mob Dance in Santa Monica. I was so excited to see so many friends showing off their dance moves and showing their support for Claire’s Place Foundation.… Read More
Ever been a part of a flash mob? I am going to be and you are all invited! Hope you’re all well, because exciting things are happening all around! We’ve started Claire’s Place Foundation dedicated to helping people with Cystic Fibrosis and their families.
I’m super excited about Claire’s Place Foundation’s first big event. What is it? Well, it has to do with dance, music, people coming together, fun, and a surprise. What’s not to be excited about? We have Read More
Hello! Claire here…just back from an amazing adventure to Sitka, Alaska. We had a great time and learned so much. I had an idea that it might be helpful to share some traveling tips with those of you who have special medical needs and issues. I was a little nervous to go because I have Cystic Fibrosis and I have tons of medications and equipment and oxygen to travel with. I have Read More
So who is Claire?
That’s an interesting question. To start off I’m 13 years old, my name is Claire, and I have an illness called Cystic Fibrosis, which I was diagnosed with at Birth. It’s interesting because for a lot of people it’s totally different, it’s like, “oh my gosh! She has a disease, take pity on her!” But it’s interesting when you have lived with Read More