Read THIS blog if you are interested in knowing some of the things in a cg's mind when she's feeling down about how people react to her illness.
I couldn't, or shall I say, didn't, put it better myself.
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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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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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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Hello CGers!!! It's me. Boldly, bravely, I let my Dad bring me my laptop for tonight. I have been enjoying a computer hiadus, but wanted...
aww, thanks for the shoutout, CG! Perky things to follow - especially since I have been floating on a cloud of wonderful caringfulness (nope, not a word) in the lead-up and wake of my surgery; funny how God/The Universe/HPOA (Higher Power of your Attention, not to be confused with Healthcare Power of Attorney) works sometimes - but I swear my blog won't always be a cheap and lacking substitute for therapy. Thanks for the bloggy-love, and stay tuned :o)
ReplyDeleteBS (tehehe!)