Subject: | |
From: | |
Reply To: | St. John's University Cerebral Palsy List |
Date: | Thu, 7 Jul 2005 14:24:30 EDT |
Content-Type: | text/plain |
Parts/Attachments: |
|
|
Kendall,
I agree with less invasive first, also. Didn't mean to sound like I
advocated the pump. It would probably take an act of congress to get me to agree to a
pump for my son. I prefer natural methods, if available, and am very
skeptical of doctors and drugs in general. It's good that you have a good neurologist
who listens and whom you trust.
I'm just a frustrated Mom who wants it all for my boy with no side effects
;-) You are getting a taste of that yourself, I think. Spasticity is very
frustrating, but it is a part of cp. We always have to be careful that the
treatment isn't worse than the disease, don't you think? Beware of that CPPARENT
list! They are a "cure 'em" bunch! I only suggest it because there is so much
medical discussion there.
Best,
Wanda
"It has become appallingly clear that our technology has exceeded our
humanity."
Albert Einstein
|
|
|