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TINGLY FINGERS

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Hello...

I noticed that you both were talking about tingly fingers. I wanted to

give you some relief. I took Topamax for what they now are giving out by

our doctors for weight loss. I took the opportunity to see what exactly my

daughter is feeling for at least one of the meds. I did take this for a

weight loss option under a doctors care, but had more of an interest when I

heard Topamax was and option. I know it sounds strange, but knowing what

she was feeling, was important to us. With all these meds, we just

wondered how much was her control or the meds???? I took it VERY slowly

like directed. The tingly fingers were the first side effect I felt. It

was also very hard to keep a thought and I couldn't remember simple words

and answers. It was a bit like you're drunk. You stumble for words and

it's extremely frustrating. I am almost 40 years old and never have been

sick in ways to need medicine. It did get better after a while, but the

tingly fingers (4 months that I was on it) was almost the worst. It was

also in my feet. I wanted to let you know that I don't have seizures and

the tingly fingers and toes are a side effect that I decided was too much

to continue the drug. It was more that I couldn't hold a thought. Now I

understand that my daughter (6) can't tell me things sometimes

quickly. She has to think and then she gets frustrated. It was a very

spacey feeling that I didn't like at all. The sooner I get her off these

drugs the better!

I hope I helped you guys understand that I don't think the tingly fingers

was a sign of an onset of a seizure. I'm only speaking for us, of course,

but if you knew the feeling...I hope I helped.

Take care.... - Sheridan's Mom

At 05:29 AM 8/1/2004, you wrote:

>Thanks - I was nosily reading your post to and was relieved

>to hear

>the bit about tingly hands. Ben gets tingly fingers quite often (only

>since we started

>withdrawal), and these odd feelings are part of the reason he is doing a

>lot of

>panicking. So this morning I was able to tell him about , to try to

>make him

>understand that it doesn't necessarily signal the onset of a seizure.

>

>Take care

>Rose Toms

>

>

>

> " The Ketogenic Diet....a realistic treatment option, NOT just a last

> resort! "

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> List is for parent to parent support only.

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Thankyou - once again you guys have been extremely helpful. The easiest

thing to do actually is to worry that the drugs or the epilepsy have screwed up

the

nervous system but I am now much more calm inside about it. I never ever let Ben

see

me panic about anything but little does he know what agony goes on in my heart

sometimes.

Lots of love

Rose

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