From the Network
A Consumer’s Perspective: “Headed in the Right Direction…”
My name is Kim Bischoff. I’m the Executive Director of the Neurofibromatosis Network. But most importantly, I’m the mother of Jennifer, who is 34 years old, and she has neurofibromatosis type one.
Las Vegas’ 8th Annual NF Hope® Concert
Las Vegas’ most notable headliners will come together under one roof for Las Vegas’ eighth annual NF Hope® Concert.
New to Our Team
Join us in welcoming Breanna to the NF Network!
Send us your personal NF story, we'll deliver to Congress
On February 12 and 13, NF advocates will be storming the halls of Congress to educate its 535 members about neurofibromatosis and ask for their support to fund vital NF research.
Newman's Own Holiday Challenge
The NF Network has teamed up with the Newman's Own Foundation for a $500,000 holiday challenge.
Join us at Las Vegas’ 7th Annual NF Hope® Concert!
In less than a month, neurofibromatosis families and friends from across the country will gather for the 7th annual NF Hope Concert, Sunday, October 22 at The Palazzo in Las Vegas, Nevada.
NF Network Supports the UW-Madison NF1 Swine Project
We are optimistic that this research will speed up the development of NF 1 therapies.
The word is neurofibromatosis
May is Neurofibromatosis Awareness Month! Spread awareness by joining the #TheWordIs campaign.
2017 NF research funding secured
Congratulations to all in the NF community for this achievement!
My NF compass: Aunt Flora
Cheri Stewart, president of the Neurofibromatosis Network, shares inspirational comments.
2017 NF Advocacy Program
The NF Network Advocacy Program stomped the halls of congress February 5 through 7.