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Re: MS and anhidosis

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I am experiencing similar symptoms and don't know why. I used to sweat from the

head a lot - more than most (before MS). Now I hardly ever sweat at all. I

went through chelation therapy (60 min IV for 10 weeks) about 6 months after

being diagnosed. I do not know if it helped. I anxiously await responses to

your question.

Tim - Diagnosed PPMS 2/1/08

>

> anyone else experiencing a reduced ability to sweat? mine has been diminishing

over the years and now is to the point where i just am not sweating at all, no

matter how hot the temp. on the contrary, am always cold. and yes, i've had my

thyroid checked, many times. it's fine. be interested in your feedback.

>

> janet--have you tried NAC? that helps me chelate, and i can't tolerate much

else.

>

> oh, btw, i don't seem to be able to post answers to anyone from the forum, i

keep getting an error message. any ideas?

>

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I feel like I don't sweat much.  I over heat when walking in 40 degree

weather. 

Its so weird. 

________________________________

To: mscured

Sent: Tue, December 21, 2010 2:52:47 AM

Subject: MS and anhidosis

 

anyone else experiencing a reduced ability to sweat? mine has been diminishing

over the years and now is to the point where i just am not sweating at all, no

matter how hot the temp. on the contrary, am always cold. and yes, i've had my

thyroid checked, many times. it's fine. be interested in your feedback.

janet--have you tried NAC? that helps me chelate, and i can't tolerate much

else.

oh, btw, i don't seem to be able to post answers to anyone from the forum, i

keep getting an error message. any ideas?

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