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
Thank YOU for all that you do for people with NF and their families! It brings tears to my eyes to see how much was raised for this cause. My brother had NF which turned cancerous and he passed away February 10, 2011 after a not-so-easy life with NF. My sister and father also struggled with this disease, then cancer and passed away in 1991 and 2008 respectively. This was our first NF Walk and we look forward to next year's. We were impressed with the organization of the walk, the DJ, the food, the prize baskets, the facilities and of course all of the care that went into it.My remaining sister and I, and our families, are determined to help out in any way to help cure this disease or assist other families who have NF in their lives. We look forward to raising more funds next year and dressing up our team! Our goal as a team is to raise a lot more money next year!
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.