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[QUOTE=Sparky10;914186]This is one conversation. Just as MS can change from day to day, maybe another conversation on another day is in order./QUOTE]
[QUOTE=Kitty;914190] Like others have said, I wouldn't base how I felt on this one conversation./QUOTE] Sparky and Kitty, I wish this was the only conversation my dh and I have had like this. This was just the one that really got me so upset. He is always saying that if I dont take the dmd's that Im not trying hard enough to get better. Get better? Really? This isnt cureable. Im not going to wake up one day and be all better! Ive had this for 20yrs, and dh and I have been together for 10yrs. He thinks the old fashioned way that what the man says the wife has to do. Well, Im an 80s girl and we dont roll that way! I didnt speak to him at all for the rest of the night until he went to work. We spoke briefly on his break, but this morning he acts like everything is ok, well its not ok with me. I just dont want to talk to him about it just yet.
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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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"Thanks for this!" says: | Kitty (09-13-2012) |
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