Hi Kimberley
One of the side effects of synthroid can be ringing in your ears. I've had
it for years. And also I have muscle spasms in my back that lead to
tingling in my hands and arms. The tingling happens when a nerve gets
slightly compressed. My solution to this is more exercise and
physiotherapy.
Kate

----- Original Message -----
From: <ThyroidDisease2@yahoogroups.com>
To: <ThyroidDisease2@yahoogroups.com>
Sent: Friday, September 30, 2005 10:11 AM
Subject: [ThyroidDisease] Digest Number 651


>
> There are 2 messages in this issue.
>
> Topics in this digest:
>
> 1. Re: Please respond
> From: judith viera <jvp_k@...>
> 2. Re: Please respond
> From: kim finch <frkim2u66@...>
>
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> ________________________________________________________________________
> ________________________________________________________________________
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> Message: 1
> Date: Thu, 29 Sep 2005 09:40:27 -0700 (PDT)
> From: judith viera <jvp_k@...>
> Subject: Re: Please respond
>
> Hello Kimberly:
> I had lots of ringing in my ears and lots of sensitivity to noises, it
has been better now with armour, and I also done some ear candle and did
helped me. The other symtoms also seem to be part of thyroid problems, but
to rule out all other possibilites wait till the mri result, but my personal
opinion is that is related with thyroid problems. Love and Light.
>
Judith
>
> Kimberly <frkim2u66@...> wrote:
> I was wondering if anyone out there experieces ringing in the ears
> constantly? Along with muscle spasms, twitching, sharp pains ,
> electrical sensations that are constant, pins & needle feeling? I am
> still waiting to get my MRI to see if I have MS. A friend just told me
> that those symptoms could be from my thyroid. Has anyone experienced
> these symptoms?
>
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> Message: 2
> Date: Thu, 29 Sep 2005 21:55:43 -0700 (PDT)
> From: kim finch <frkim2u66@...>
> Subject: Re: Please respond
>
> Judith,
> Hi, thanks for responding. I had my thyroid taken out 8 or 9 years ago.
I've been on synthyroid and was fine untill last year, my thyroid went wild,
the endo could not get it regulated, this went on for about 5 months.
> Then what I thought was for sure a herniated disk ended up being muscle
spasms in my lower back, I also started with all these crazy symptoms, so my
reg doc sent me to a nerologist and he did a couple of tests and then told
me I may be experiencing early symptoms of MS. That really scared the hell
out of me. Then he did a muscle and nerve test about3 weeks later and it
came back normal. He told me come back in 6 months. Slowly I started feeling
fine( about 6 weeks) than wam oh, it came back and now my reg doc is sending
me to get a MRI on Monday. WHich most likely will come back normal to. From
what I hear from people with MS is that it could take years to get
diagnosed. The lessions don't always show up. So now I wait.
> I plan on getting my thyroid tested tommorow, I'm sure it is low, because
my hair is falling out so much. So I'll let ya now.
>
>
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