Wishing for a future CURE and better CARE now.
We’re wishing for a cure, but in the meantime there is so much that is needed now and so much that we need to get there!
Paint the office
New books or small toys/prizes for our young fighters
Gift cards for our fighting adults
A Bigger Refrigerator with a Freezer (Apartment Size)
Paper for the Office
A BIG Truck To Borrow For Events
Donated Event Tickets – Sports, Concerts, Plays
A Local (or National) Celebrity to Bring Recognition to NF
Paint and Someone to Paint the Office and Bring Some Color and Inspiration In!
A Vacuum Cleaner that Doesn’t Suck…or Actually Does Suck.
Better Care For All Our Loved Ones With NF
Informed Primary Care Doctors
Items for Raffles
NF Midwest has truly been a beacon through our journey with NF. They sponsor wonderful symposiums with the top NF researchers that share their latest findings. In fact, we found Silas's neurologist through one of their symposiums. They have even hosted educational conferences to help general practitioners better understand NF.
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.