United Brachial Plexus Network, Inc.

Pat,

I'd love to meet for lunch. I e-mailed you.

Joanie

Hi, I am Solomon - Father to Isreal 14 months old, LOBPI,Horner's, Monroe, NY

I am new to this board. My name is Eva, and I am adopting a little boy from China with LOBPI. We will name him Caleb. He's 33 months old.

Eva Welcome! When will Caleb come home to you?
We have many forms here and you are Welcome to post on all of them. In fact many of us post on all of the boards.
There is a General Board where parents exchange ideas on therapy etc.
I have a niece from China and she came home to us almost 10 years ago.

I am so glad you found us this will be a great resource for you and Caleb.
Let us know when he arrives.
Kath robpi/adult

mel
20
LOBPI
no horners (idk what it is!)
F/RI, but going to school in MA

Thanks, Kath.

We anticipate traveling at the end of November to bring him home. It's nice to hear you have a niece who is also from China. I can't wait to travel. I'm also glad I found this board. I'm sure it will be a great resource for us. I will keep you posted on our travels.

Eva

HI ya'll! Nancy Ann in Texas. 39 years old. ROBPI with other complications at birth.
No Horner's. I'm a sped teacher and aquatic therpist (great for BPI).

Melinda mother of Amber 13 LOBPI, I found this site about 8yrs ago. At first I was consumed with the information then obsessed and finally overwhelmed so I stopped coming. I stopped by just because...Its always on my mind. Acworth, GA

Hi,

I'm Joe, 31 yr old Male, LOBPI, Live in Ewing, NJ I don't think i have Horner's Syn., I had The Mod Quad surgery performed by Dr. Nath in 2005 I have seen minimal improvement post-op.I have a wonderfully supportive wife and an amazing 13 mo old Daughter.

Hi
I'm Andrea.I am married 34 yrs.Have 2 kids and 2 grandkids.Have ROBI,LOBI,worse in left.No Horners.Also have severe scoliosis,syrinx,chiari 1 and just had abulging disk removed at c4-c5.I'm now fused from c2-c5.c2-c3 fused on there own.