I read that the UBPN would help offset the cost of transportation to camp. Can someone explain this to me.

I was going to ask the same "daft question"! We live in Louisiana and did not know what to expect. You all have answered my question!

I will be there with Zavian(lobpi) and my sister. It's our first time up north(we live in Louisiana)...so wish us luck!

<t>How any one been treated at the Cincinnati Children's Hospital Brachial Plexus Clinic? My contacted them about seeing my daughter, Zavian who has a lbpi, but would like to know a little about their doctors and clinic before we go. We are scheduled to be seen on June 7, 2005. Any input is greatly ...

HELP!!! I am in desperate need of info. My daughter(lbpi) is scheduled to have botox on her triceps muscles next month. I curious as to the outcome of this. Has anyone else had this on themselves or their children for bpi? Anything you can tell me would be greatly appreciated.

Please keep us posted on Tyler's progress! We're all glad to know everything went great.

<t>I am also in the process of suing the doctor for my daughter's injuries. I think the settlement that the family above recieved was fair and for a legitimate reason. No child should have to suffer from the negligence imposed by a doctor, someone who we trust to do their job to the best of their ab...

<t>I had the same feeling some time ago. The first therapist my daughter was seeing ended moving to Texas. I was mortified as to how my daughter would react to a new therapist. Well, Christy is sweet and she makes my daughter sessions fun for her. Zavian, my daughter, seems to enjoy working with Chr...