United Brachial Plexus Network, Inc.

Check out the New Brachial Plexus Palsy Foundation Site.

http://www.brachialplexuspalsyfoundation.org/
FYI

bump

Pretty good site. We need to continue to be recognized and this helps alot.

Thank you

I was gonna sign up for the message board, but, why do they need your telephone number? :/ Do you know?

Yes, phone numbers are needed so the caretakers can contact folks to make sure they are who they are. This is a private message board. There will be no doctors, lawyers, or guests allowed.

I was contacted yesterday....and had a really wonderful conversation with the caretaker. They just want to verify you are who you say you are.

Wouldnt it be great if we didnt have so many guest posters around here????

Sorry let me continue with this.... not allowing guest posters ONLY makes the individual 150% responsible for what they post. UBPN offers guest posting for those in litigation but people abuse it and post as guest to start trouble or who knows why.... just my two cents.

COurt xx

I understand about the thing with the no doctors, etc.. but if a person has been around the bpi community for a while, I don't see the need. I don't feel comfortable putting my telelephone # on the internet for a stranger, so I will just stick to this place. No biggie, I was just wondering.

Thanks Allison!

Mandie

I was contacted this morning by the caretaker-also a great conversation (with another BPI mom). I think it will be a great site.