Subject: | |
From: | |
Reply To: | St. John's University Cerebral Palsy List |
Date: | Mon, 23 Dec 2002 09:22:42 -0500 |
Content-Type: | text/plain |
Parts/Attachments: |
|
|
That's just it. I honestly couldn't see myself going through it all (even for
a pump) if I'd already improved some, and then had it done, and had to go back
several times a year for infusions of the botox into the disc attached to the
pump. Too time-consuming and too nebulous for me to seriously consider. And
as my neuro said, it doesn't work in a lot of cases anyway.
If it works for people, great! But it's not for me at this time.
Kat
On Mon, 23 Dec 2002 09:13:09 -0500 "Cleveland, Kyle E."
<[log in to unmask]> wrote:
> That's what all my research turned up--Botox is
> not a panacea and the
> effects don't last long. I was hoping that
> Ken's neuro had some news about
> Botox that I hadn't heard. Ken, are you having
> a single injection, a series
> of injections, or are you having a pump
> implanted?
>
> -Kyle
>
> -----Original Message-----
> From: Kathy Salkin
> [mailto:[log in to unmask]]
> Sent: Monday, December 23, 2002 9:10 AM
> To: [log in to unmask]
> Subject: Re: Ken's procedure; was RE: holiday
> greetings
>
>
> Thought you were already investigating the
> possibility of botox? If not,
> then
> you should. It's not in the books for me (yet)
> because my surgery eased up
> the spasticity and it's not so bad. It'll
> never go away completely, my
> neuro
> says, not even with botox.
>
> Kat
>
|
|
|