United Brachial Plexus Network, Inc.

We are moving to the Bay Area in CA. Our son Douglas (ROBPI) just turned 3. I've called CCS and will get him evaluated for their services... I'd love to connect with other OBPI families in the area. Is there anyone out there?

Jennie

There are a bunch of them !!! Good Luck with the move, it is really nice there !!!
GAYLE

Hello,
I'm from california. Kinda in the middle of it. CCS is a good thing but it takes a while to get started. But once you do it's good. So, good luck with the move and be patient with CCS (it's worth it).
Breonna, Joseph's mommy (9months,LOBPI)

I live in Southern Ca, but have seen specialists up in No. Cal. Lucille Packards Childrens hospital at Stanford has some really neat therapists. What a nice place to live, my sister lives up there too!

Jennie,
Here's wishing you a good experience in your move to CA.
Click on the UBPN Registry and you'll find 30+ members in CA.

HUGS,
Carolyn J
LOBPI/68 & count..'.g [YIKES!]