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Re: lyme/husband/als????

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The twitching and muscle loss are late stage lyme things. Four months ago

my arms and legs were almost totally useless. My meds have really made a

difference. I am now back to about 60%. I will so be praying for you all.

Remember that the Western Blot must be done. If you are like me you most

likely feel like there is nothing to lose. I was at the point where I had

lost all hope and the Lyme dx in a way scared me even more. It had been

three years, and I had finally accepted that I had MS and that my life was

no longer in my control. I was afraid to hope for a recovery when I was told

it was Lyme. I thought the very idea of " bacteria infection " destroying my

mind and body was nuts. Now my memory is better, my speech is clearer and I

enough wits about me that I can actually recognize my own progress. That

alone is a miracle. Hang in there. This Lyme thing is a crazy emotional

ride, but there are others who have survived the worst of it and actually

recovered a decent life for themselves. Keep on.

davy thomas

-- [ ] lyme/husband/als????

Hi again...for those of you that have written directly to me I so

appreciate your support...We go to a Lyme dr on Oct 14th so pray for

us that this ALS Diagnosis is wrong....

I just want to know if anyone suffering from late stage lyme has the

severe muscle twitching, loss of muscle or the weakness of the hands?

These night sweats he is having are awfull...hes been floating

between below normal temp and a slight fever(100.9)and this waiting

game i guess is what is so hard...the not knowing which to deal with

and sad as it is praying to GOD that IT IS LYME!!!!! Im so thankful

to have found this site...God Bless you all! Laurie

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Hi, I also have the muscle twitching, sometimes it is annoying and sometimes it

hurts.My arms actually jerk at my fiance while i am sleeping. I am taking

calcium and zinc supplements....eve

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  • 2 weeks later...

Your message has been edited.

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Lyme Aid Owner

==========

eve...he was dx with ALS which is Lou Gehrigs disease although i still think its

neurological lyme and we went to a specialist yesterday so hopefully we will be

on the road to recovery....he started him on anitibiots so we can get an

accurate lyme test from Igenex....

eve <eveandal@...> wrote:

Hi, I have a question, if you don't mind my asking how the doc came

to the conclusion of aids?? I have a lot of the same symptoms and I

was diagnosed with lyme,...eve

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eric...his fever come and goes at night with the sweats...sometimes his body

temp is below normal sometimes elevated

eric schulman <eric_s11050@...> wrote:did your husband have a fever first!

eric

very important!

--- Laurie <laurie362004@...> wrote:

>

>

> eve...he was dx with ALS which is Lou Gehrigs

> disease although i still think its neurological lyme

> and we went to a specialist yesterday so hopefully

> we will be on the road to recovery....he started him

> on anitibiots so we can get an accurate lyme test

> from Igenex....

>

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