Laura,
If I understand it correctly it a med for EP that they are testing.
Check it out on the Internet.
Millie
> What is this med used for? Laura
>
>
>
>
> ____________
> From: "mylmy@bnin.net" <mylmy@bnin.net>
> To: epilepsy@yahoogroup
> Sent: Wednesday, June 3, 2009 10:43:04 AM
> Subject: Re: [epilepsy] Carisbamate
>
>
>
>
>
> Hi Carolyn,
>
> No, I have never heard of Carisbamate. I just looked
> it up on the Internet and there are 3,550 website for it.
>
> Some time ago I answered a letter here in the group replying
> that I would be willing to talk to someone about EP. Some
> time later I got a phone call wanting to know if I would
> like to try an experimental drug. Some would get it and
> some wouldn't.
>
> I told her that No, I feel quite controlled since my last
> sz was 2 years ago. She couldn't understand why I didn't
> want to be in the experiment.
>
> But I do understand why it would be OK for you. Under those
> circumstances I might do that also.
>
> Millie
>
>> Millie,
>>
>> I hope you receive this, I keep thinking I mess up sending messages, but
>> thanks for hearing me. The name of the new study drug is called
>> Carisbamate. I take 1 50 mg in the morning, a 100 mg morning and night.
>> It
>> seems to be working, but I also had a VNS put in me in 2001 after I
>> crashed my car. I was able to drive for 10 years and out of no where,
>> bang! After that my neurlogist said I was a good candidate for this
>> study
>> drug. Like I said hope you get this, I miss hearing others reponses
>> about
>> their experiences. Do you know anything about this medicine?
>>
>> Thanks,
>>
>> Carolyn
>>
>>
>> >
>>
>
>
>
>
> [Non-text portions of this message have been removed]
>
>
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