Volunteer to join a committee, the board, work an event, create an event…we have lots of opportunities! Let us know what you like to do!
NF Midwest and the neurofibromatosis cause needs you!
Everything you do, big or small, will move the neurofibromatosis cause forward.
Thank you very much [for the packet]! My 6 year old son was diagnosed with NF last fall. My 8 month old will have his first appointment at the NF clinic in July. We are very excited about the walk. We just finished a T-shirt fundraiser. I had never even heard of NF before he was diagnosed, so NF Midwest has been a wonderful resource for us. Thank you for all that you guys do!
The resources on this site should not be used as a substitute for professional medical care or advice on Neurofibromatosis. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional.