Well, we do have parents of CP kids on this list, so I suppose this guy thinks
they 'd be interested although I'm not sure how much of a response he gets.

Mr. Freels posts here occasionally about HBOT treatment, which in my opinion
is an unscientifically tested treatment that is not standard for CP patients.
The information I've found on the net is mostly ancedotal and not scientific,
carefully controlled studies. Obviously I'm skeptical.

Kat

On Wednesday 09 February 2005 6:19 am, Brent Edwards wrote:
> Who ARE you people and why are you hijacking our list?
>
> Sorry, Kat is much more polite, but once and (hopefully?) for all: this is
> primarily a list for ADULTS who have cp, not for PARENTS of CHILDREN who
> have cp.
>
> There are some parents of kids with cp here, and there are some therapeutic
> professionals here as well. They are most welcome. But this is NOT the
> proper place to announce parental surveys, pediatric clinical trials, or
> DEFINITELY NOT the place for flame wars about wacko therapies that
> evidently are spilling over from some other freakin' list.
>
> I feel better now.  Talk amongst yourselves.
>
> Brent