The daily ponderings of Beth Peters as she writes about Cystic Fibrosis and lung trasnplant.
Saturday, June 13, 2009
The First Day of the Rest of Your Blog
Dear World,
I am the Cystic Gal, and I will be spending my summer sharing my thoughts on CF and life with you. Like a lot of CF patients, I have always had a dream of people understanding my story - so here is the place where I will tell it.
I thank you in advance for reading it! Please feel free to comment or share this blog with other patients, friends, or any interested reader.
Thanks! CG (Cystic Gal)
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