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Hi and thanks so much for your kind words.
![]() Your suggestion just opened up some other possibilities for me. My MS doctor wanted me to have a doctor locally who would be able to help with steroids or what ever might come up in between my check ups with her. My PCP said he'd preferred I find someone besides him because he does not know enough about MS to feel comfortable. He only has 3 of us with MS. We are in a very small country community. But there are other PCP's and internists around here. The neurologists in this area seem to be stuck on the same page when it comes to MS. I was shocked when this doctor moved the conversation away from the reason I was there and started to add his own opinion. My MS doctor said NOTHING about our family size and I was not there for a second opinion. I was afraid another neuro would try to throw their own opinion in on my situation. So in the end, after the trauma, he said it was MS. Thank you for the link. I will go out there and post about the doctors I have seen! LA Quote:
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LA Optic neuritis May 2007 and again January2008 Diagnosed February 13 2008 Started Avonex February 22 2008 (still progressing) July 2009 started Betaseron..... "Don't argue with an idiot. People watching may not be able to tell the difference." |
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