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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1. To the guy that broke up with me right after I got out of the hospital: You are cowardly, and selfish, and also bald*. 2. To the neighbor...
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Tonight I got calls from CysticDad and CysticMommy saying that they are moving CysticGal to the ICU. She's just not breathing very well...
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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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