My Summer Update!

lights, camera, action! Claire helps spread the word about fighting cystic fibrosis What have I been up to this summer?
I’ve been doing a lot this summer! We started off doing the ABC thing, so I can’t give too many details, but it’s for a program called, “Everyday Health Heroes.” Please look out for it on TV and tune in! I am still not sure who referred us, or how they heard about us, but they were interested in what we were doing. So they came to our house and filmed for three days and we did another flash mob for Read More

Flash Mob Take Two!

That’s right we are doing it again! I am so excited to do our flash mob again because it was so much fun and this time it will be filmed for National TV! Can you believe it? Our first Flash mob in May got so much… Read More

A Flash Mob dance is coming to Santa Monica! Get Ready!

Claire's Place Foundation logoEver 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

Making a Difference is a Snap

bubble wrap dress funWhat inspires you? Recently, all of us here at the NorthStar Moving® family have been inspired by one little girl’s smile. A few months ago, we had the great privilege of meeting Claire while working with the Make-A-Wish Foundation to help make Claire’s wish come true. Although she has been diagnosed with Cystic Fibrosis from birth, Claire’s positive attitude and enthusiastic spirit proves to us she is a Read More

Travel Tips by Claire

Claire & Melissa Wineland getting ready for the take offHello! 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