Lynn Coleman
Hello friends!! As you know, Cystic Fibrosis has had a huge impact on our lives! We are so very grateful that Rachel and Amy now have medicines that have greatly improved their health and allowed them to live very normal lives!!! It took many years to get that medicine! Our contributions over the years to the Cystic Fibrosis Foundation were so vital in the development of this medicine!
While our girls' lives and many others' have been changed by this medicine, there are still many CF patients who cannot use this medicine for one reason or another. There are many mutations of the CF gene and for some - this medicine does not work. So - there is still a need to fundraise!! There is a walk in Charlotte on September 20th. Amy and some friends and I walked last year and it was a really fun time!! There are always plenty of snacks. I think there were coffee and donuts beforehand and hot dogs or hamburgers afterwards! The walk starts at 9:30 so we try to get there around 8:30. I am hoping you can sign up and/or donate through this link.
We appreciate you and your consideration for joining us!!
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