NF Network Annual Appeal

With two weeks left until the end of the year, the NF Network wants to thank all those who have shared, supported, and donated to our year-end appeal. Your contributions have brought us halfway to our goal, and we still need your help to change thousands of lives!

Kim Bischoff, Executive Director of NF Network, is a #TCFGoalGetter

#TCFGoalGetters don't just dream big, but take the leap to pursue their passion. Check out Kim's story and her inspiration behind her work at the NF Network.

New Research Study at UMN and UWM for Children and Adolescents with NF1

Researchers at University of Minnesota, Twin Cities and University of Wisconsin, Madison are combining efforts to better understand the strengths and difficulties of children and adolescents with NF1.

Neurofibromatosis: The People , an Exhibit by Rachel Mindrup

As an accomplished painter and a mother of a son with NF1, Rachel Mindrup and her subjects are bringing neurofibromatosis into the light, one painting at a time.

Remembering Sam

We are forever fortunate, and the world is a better place, for the bright mind and beautiful spirit of Sam Leary who left us so young. In memory of Sam, the NF Network is proud to announce the Sam Leary Advocacy Scholarship Fund to assist our NF Advocates and to continue the critical work that has been Karen and Sam's passion.

Upcoming Events
The mission of the NF Network  "is   to find treatments and a cure for neurofibromatosis by promoting scientific research, improving clinical care, and providing outreach through education and awareness while offering hope and support to those who affected by NF."
Will you join with us?