Please visit Jess' blog at Jess' CF Journey and watch her video! She is waiting to see if the surgery is a-go, so keep her and the other families in your thoughts !
Update on CFSteph- She is doing well, off the vent, up and moving, allowed to eat and wrote, "I can't believe how fast this is going!" on her facebook!
The daily ponderings of Beth Peters as she writes about Cystic Fibrosis and lung trasnplant.
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Yo Old Friends! It's me, Beth Peters / CysticGal / the artist actually known as Mary ElizaBeth Peters . I am moving on from this bl...
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I don't have the energy to post all the update but just wanted to say hello. Things are progressing every day. A little better and a lit...
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Dear CG Readers, I was having such difficulty deciding how to communicate with you again as everything unfolded over the past week and a hal...
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This'll be yet another quick post to hopefully launch me into posting more often. I finally arrived home on Thursday late afternoon, and...
Go Steph! Go Jess! Go CG! Gooooooooooooo LUNGS!
ReplyDeleteThat's my peppy little cheer way of saying "you gals are awesome, I'm totally impressed, and our time is coming, CG!"
Much much love!
these things come in three's, right?? :)
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