Guest guest Posted November 25, 2004 Report Share Posted November 25, 2004 Maureen; for me any extremes in temperature is bad (the neuros will tell that is normal with MS). Here in Alberta our winters can be cold and windy and that makes me so stiff that I can barely move if out doors for more than a couple of minutes. Its the opposite with the heat; complete melt down. Those are very very typical for MS. Kathy On 25-Nov-04, at 9:40 AM, bentleyfam26 wrote: > > > > Russ said: > > >My old GP asked me regularly if hot baths made > >me limp. They didn't until some time after my > >diagnosis. Maybe that effect came later for me > >than for some, or maybe my diagnosis came earlier? > > The same thing happened to me, Russ. I am RRMS; I had my first > symptoms (numbness) about 25 years ago; subsequent symptoms (more > numbness) were mild and far apart. This year, however, I developed > L'hermittes and partial deafness; and suddenly I can't take hot > baths anymore. > > Up till this year, I NEVER had a problem with hot baths. > Loved 'em. The hotter the better. I also loved hot weather. But > now I can't get anywhere near a hot bath, and any weather above 80, > I've got the AC on. > > I wonder what this means. Russ, was there any change in your > symptoms that corresponded time-wise with the inability to take a > hot bath? Just wondering... > > -- Maureen > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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