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I am so sorry that Gary is not doing well. Hopefully taking away that medicine will help improve his lung function.
Both of you, Gayle and Betsi, have every right to be angry and frustrated. It really isn't fair. My daughter has MS, and I also don't think it's fair. She doesn't deserve that! Neither do the children, or Steve, or me, for that matter. She isn't feeling well right now - not a bad exacerbation, but she has to just wait until it passes. She has finally found a neurologist locally who takes her insurance, and who she really likes! She's back on one medication, and has to go to physical therapy.
I have learned to just take one day at a time, and to just take it as it is. There is no other way for me to do it.
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