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From Kitty: If Jack is on DWTS then I'm happy for him. Glad he's still able to do those kind of things. When my sx first became apparent I could still walk with no problem. Not now, though. I'm just waiting for the comments about how he can still do all these things so I must be exaggerating my own sx of MS.
I get so tired of people comparing MSers. We all have it, but we all have it different. Similar symptoms, but different ways. That saying, "you don't get MS until you get MS" is so true. I know a man who has MS and his gf has MS and he goes to the gym lifts weights rides his mountain bike and she can barely get out of bed and doesn't do a lot and all he does is yell at her because she doesn't even clean the kitchen. Now, to me that's aweful. He should know better than anyone that each MSer suffers differently.
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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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