United Brachial Plexus Network

I have posted a few times and would like to hear some feedback. My son has had his surgeries but they were 2 years ago. The results were phenomenal. We were partially covered (30%) by our insurance and have been left with a bill that we could never pay off in 30 years. Has anyone found a charity or ...

Hey there and welcome to the boards. My son was seen by Dr. Grossman but I didn't care for him or his staff. We did, however, find Dr. Nath and loved him and his staff. We have had 2 surgeries with him and my son has had amazing results. The first surgery wasin WPB when he was 13 months and then aga...

Hi families of BPI's. I have been reading this site for a couple of years but haven't posted until now. I would love to know how to a support group or start a support group in my area for BPI. My son has a OBPI but we can do a support group of either. Please help me in my search or endeavor. Side no...

I am very interested too. I have gone to several lawyers and they say we have no case but my son still has limited use of his arm, can't feel the extremity of his arm and is deformed due to the OBPI. I have filed an extension in his case as he is approaching 3 years old. Any help would be greatly ap...