Hi Val,

My daughter was born with the Pierre Robin sequence cleft palate and
receding chin. The important thing is to find a surgeon the parents can work
with. If you're in New York, I can give you some names.
The first month or two of dealing with this condition are the hardest -
after that, it becomes routine. Feeding is critical. It's much harder for
babies with this condition to eat, they burn more calories during the act of
eating than babies without this condition so it's important to follow your
doctors' guidelines.
Our daughter had her cleft palate repair surgery this past January at 13
monts and within a week or two, you'd never have known there had ever been
anything wrong with her. She's right on target now for 18 months speechwise
(whereas she didn't babble at all before the surgery).
It's not easy but its very very doable.

Good luck!

-Marla

-----Original Message-----
From: sticklersyndrome@yahoogroups.com
[mailto:sticklersyndrome@yahoogroups.com] On Behalf Of Valley
Sent: Tuesday, June 03, 2008 11:30 PM
To: sticklersyndrome@yahoogroups.com
Subject: [Stickler Syndrome ] new to pierre robin sequence


Hi, my name is Val, and I happen to be an RN. But.. my grandaughter was
born sunday June 1 , with Pierre Robin sequence. she has a cleft palate and
a receding chin. As far as sticklersyndrome, we have not be diagnosed with
that yet. I am just out here searching for information, support. This is
my son and his girlfriends second child. Looking for any support we can
arrange... thanks for any help or information.

Val


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