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07-11-2012, 04:30 PM | #11 | |||
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Senior Member
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Hi Yeti and welcome to the group! Your history sounds familiar with all the various symptoms, etc. My GP always said I was a challenge. After finally getting the "official" diagnosis of MS, it all seemed to make sense....of course I had to have Fibromyalgia thrown in there too.
Good luck with your neuro appointment Friday. I hope you get some answers. Please keep us in the "loop", take care.
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_____________________________________________ .....Judy SPMS -- FIBROMYALGIA -- Ouch! and Ouch! . |
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07-11-2012, 04:59 PM | #12 | ||
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Junior Member
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This latest episode, with at least some mri evidence, has kind of connected a lot of weird dots. We'll see. Thanks for all the support and advice.
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07-11-2012, 07:21 PM | #13 | |||
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In Remembrance
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The idea is, that most Neuros/Docs are proud little Gods, who like to think they are the ones who come up with the DX. If you come in with it all mapped out for them, it's messes up their day.
Be gentle..lol
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~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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07-11-2012, 07:36 PM | #14 | |||
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Wisest Elder Ever
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LOL, Sally! They hate it when we know more than they do!!
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These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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07-12-2012, 12:05 AM | #15 | |||
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Member
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OMG Sally, some of the things that come from you just make me laugh!!!!!
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Dx RRMS April 1992 Yearly flares from 92 to 11 MS induced seizures 2002 Flare Oct 2011 Flare Dec 2011 Left disabled after 2 previous flares Betaseron '02, Copaxone '12, Tecfidera '13 (allergic reaction to all) No longer taking any MS therapy meds |
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07-12-2012, 06:05 AM | #16 | ||
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Junior Member
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lol Sally. I can't say my experience with doctors in general has been very good at all in my lifetime. I was hoping the neuro would be different, but I don't have any good reason to believe that.
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07-13-2012, 01:28 AM | #17 | |||
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Member
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Yeti, I was the same way for maaaaany years. Then this year I was referred to yet another neuro, and to my surprise, he was great and I really like him. First time in 20yrs I dont mind giong to the neuro Now, if he could get his billing lady to get things straight, it'd be perfect!!!!
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Dx RRMS April 1992 Yearly flares from 92 to 11 MS induced seizures 2002 Flare Oct 2011 Flare Dec 2011 Left disabled after 2 previous flares Betaseron '02, Copaxone '12, Tecfidera '13 (allergic reaction to all) No longer taking any MS therapy meds |
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