Re: Re: Scared, joan u are not alone

July 14, 2000

Dear Weak Muscles (sorry, I don't know your name),

I had that also. It felt like my legs were encased in cement and they ached

so. My

LLMD attributed some of it to a chronic magnesium deficiency and I was on IV MG

1000 mg

three times a week for almost 1 year. (Along with IV AB's). My legs are much

better now.

I hope you get adequate treatment and feel better, too.

Eileen, USA, NJ

July 15, 2000

Hi ALKA SELTZER (?!),

Thanks for trying to make me feel better all the way from merry ol'

England.

I have heard from a # of Lyme friends who have experienced the

non-responsive muscle thing...all say to increase Magnesium...so I went

from 500mg a day to 1000. It seems to be helping the severe muscle

twitching and some of the other muscle problems :-). I have experienced

the lead-like legs before, but they always moved on command...until

yesterday. I'm wondering if this is happening because I am now being

treated for Babesia as well...

As far as extended herxes go...who knows. I feel as if I have been

herxing for the past month, which is a long time for

me.

It was nice hearing from you, and I hope you improve with further

treatment.

Thanks,

Joan LI NY

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