I was diagnosed in November...My boyfriend has been amazing and very supportive-but if you don't have CD there's no way to fully understand what its like to live with it. Have any of you had to answer questions like "are you ever going to get better"? or why dont you go to another specialist...I dont feel more doctors is the answer..its just taking my body longer to heal..i dont know is this coming up for anyone else?
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Hi all! This is for those of you that have or have had the same neurologist for 4 years or more. I have been with mine now since 2009. He is one of the best movement disorder secialists in the midwest. I know he is extremely busy on the lecture circuit now and in fact not taking new patients there is a huge waiting list for him. BUT.... I feel like my visits are not what they use to be. He...
I gave my 2 week notice last Friday 13th. Now to join you fine people in a life of leisure and nothing else to do but to look out for myself....is it just me or does that sound pretty boring? My goal was to live to retire and I guess having to take early retirement because of health reasons wasn't exactly the way I had planned things. I just can't stay in that building that is reeking mildew...