Mariana et al.,

apologies for the slightly incorrect wording, I do not yet have any
contact with adults with CP, so I need yet to learn how to phrase
things.

Please let me know if there is anything else in the verbage of my future
mails, that could be changed to be more appropiate.

Thanks & regards, OG


Mariana Ruybalid wrote:
>
> Dear Oliver,
>         Great to meet you!  I have heard good things about "Peto" therapy in
> Hungary but I have not experienced it myself.  I do a lot of Yoga and
> Feldencrais.  I was born with cerebral palsy 49 years ago, I am challenged
> by it, but I don't say that I "suffer from it" because then I would be a
> victim.  I am an active participant, not a sufferer or a victim.  But then,
> English may not be your first language.
> Regards, Mariana
>
> Oliver.Gernand wrote:
>
> > Hi all,
> >
> > my name is Oliver Gernand and I am a new member to this list server. I
> > have a 17 months old son, who unfortunately suffers from CP. His name is
> > Can Taylan (which is Turkish, first word meaning for "life") and he has
> > been getting Bobath therapy for the past 9 months or so. We will be
> > going to Budapest, Hungary during April for a 3-week look at the
> > so-called "Petö" therapy.
> >
> > If anyone has any experiences with this kind of therapy then your
> > feedback would be highly appreciated.
> >
> > Thanks a lot in advance and best regards, OG
> >
> > P.S.: Apologies if this is an inappropiate way of contact the list, but
> > I did not find any reference to a FAQ section anywhere. If there is one,
> > then please provide this as well.