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 been a true blessing. My husband and my son have Neurofibromatosis . We didn't know who to talk to for doctors and support. My husband has NF 1, he is a Veteran . And goes to VA hospital. Our son has NF 1. He has had to have surgeries to remove fibros . We have run into many obstacles. As NF family we need to talk to people who have gone threw what we were, emotionally. Physical and financially . Without support of NF Midwest I don't know where we be now.
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.
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