Here we go....

It seems like almost weekly I see a story on the news, an article in a magazine or a Facebook post about Cystic Fibrosis. It is slowly and surely (and sadly) becoming a disease that is well known. It doesn't affect a large number of people, so it's no wonder people aren't sure what the disease is. I sure didn't before Kendell was diagnosed, but boy do we know all about it now! I blog Kendell's appointment updates, fundraising efforts and any events we attend on my personal blog, but I decided it was time to do more, raise even more awareness and keep family and friends posted and informed on what Cystic Fibrosis is (CF for short) and what it's like to have it. Not sure why it's taken me 11 years to do this? But they're so close to finding a cure and I want to be more involved than ever in helping that happen!