United Brachial Plexus Network, Inc.

Have you seen this new site? Its for Ian's Hope Foundation. Just found it on the web. Anyone heard of this? http://www.ianshope.org/faq.htm

Yes, I know (through the net) the mom who made it. Very nice lady! Cute kid too!

Marieke (31, LOBPI)

This is the non profit organization that I created to help other children and families that suffer from Brachial Plexus Injuries. I am so thrilled that you found it! We are still a young organization and are trying to raise funds to help people. Any expertise or advice pertaining to fund raising would be welcomed! I am eager to start helping people! It is so expensive to travel to get the proper medical care, I hope that we can start assisting people very soon! Also FYI... we are a recognized 501(c)3 corporation.

luvmykidz...I have a degree in youth and human services. we did a lot with fundraising when I was in college. If you have any questions I would be more than happy to give you some advice. I've been out of the loop for a bit but some things don't change.

Kissygoose,
I would love any help that you can offer! Please feel free to email me. Thanks!

Layne,

I happened across this posting and looked up your web page. Congratulations on starting such a wonderful organization! I hope you remember me (Paige's mom), but you were the first parents we met after Paige's birth. You and your husband words and meeting Ian was very helpful in preparing us for the road ahead. Terry let us know you relocated out of AZ and I hope your family is doing well!

Laura