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#1 | |||
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Elder
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Sit with them MD and remind him that YOUR out of pocket expenses for such tests are considerable. Is there a change from one to another? Can he gain information from the new one that he couldnt from the old? Is there a way to limit your out of pocket expenses such as 2x a year vs free wheeling it? Ask him to explain the process as its lost on you and now you are worried about money on top of disease.
Good luck. ![]()
__________________
RRMS 3/26/07 . Betaseron 5/18/07 . Elevated LFTs Beta DC 7/07 Copaxone 8/7/07 . . |
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#2 | |||
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Member
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Quote:
__________________
It isn't a quest; it's the unknown reaction to the unaswered question. If you don't ask it, you'll never know. The journey, needs answers. . |
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"Thanks for this!" says: | SallyC (04-13-2012) |
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#3 | |||
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Member
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I'm on neuro # 4 since 2006.
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"Thanks for this!" says: | new2net98 (04-13-2012) |
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#4 | |||
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In Remembrance
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I stuck with my Neuro from 1992 until she retired, in 2002. She was the Partner of the Neuro who DXed me, 17 yrs prior. For those 17 yrs of remission, I didn't see a Neuro.
I saw the Neuro who took her patients, until about 2008, when I dropped him, because I had become SPMS and he couldn't help me. I may have stayed, if he would have written my LDN script, but he scoffed at me. ![]() ![]() I only see my PCP once a year now. I love him. ![]() ![]()
__________________
~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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"Thanks for this!" says: | new2net98 (04-13-2012) |
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#5 | |||
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Magnate
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I have had the same neuro for 26 years, he is the one who diagnosed me.
I am really going to hate it when he finally decides to retire ![]() I tried a neuro (3 visits) who was closer but I was not happy with him freaking out over my c-spine MRI and telling I should NOt even be able to walk. I AM still walking ![]()
__________________
Dx RRMS 1984 |
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#6 | |||
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Member
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I'm on neuro #4 which doesn't include the jerkwad (just learned this new word from Dejibo--it's so apropos for terrible doctors/nurses!) at the Mayo Clinic who told me my brain looked like Swiss cheese.
But.....I LOVE my current neuro! I went through all of them in the space of about 2.5 years. If you don't like the treatment or the doc please go find someone else. There is a doc out there that is perfect for you . You deserve it!! You just have to keep pushing on until you find him/her. ![]()
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On Tysabri and love it. . |
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#7 | |||
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Member
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I have been with the same neuro who diagnosed me since 2001. He has been pretty good (apart from the fact he waited for six months to tell me that I had an unruptured brain aneurysm).
I have never caused him any hassle though - quick and easy textbook diagnosis and not too many dramas since.
__________________
Lyn . Multiple Sclerosis Dx 2001 Craniotomy to clip brain aneurysm 2004. ITP 1993. |
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