Just this afternoon Shannon, my sister, told me she learned she can access the computer from her hospital room. HELLO? Why wasn’t this brought to our attention earlier? She’s been cooped up for over a month and they just tell her now? Ok, so she’s not an internet junkie like I am so she probably didn’t ask….but now we know. SO…..I’m thinking it might be a gas if I sent her an email tomorrow and said ‘hey, have you been to my blog lately?’ and when she gets here she’ll first roll her eyes (at me) and then she will be so touched and overwhelmed by all your messages. What do ya think? Wanna join me?
They have been doing what they can with adjusting meds and all that, but I think there are very powerful things that assist the way to wellness – things that can’t be bottled or sent via IV to battle cystic fibrosis like gestures, words, and presence. Since I can’t be there right now I thought I’d muster up, with your help, all the cheer we can manage from our keyboards.
Some years ago there was an invented saying for cystic fibrosis: sixty-five roses. I think it came from a child that mis-heard or mis-said the name of the disease (much easier to say). So my goal is get at least 65 comments. Are you with me?
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