Camp New Friends 2018
If you have a child with neurofibromatosis, consider sending them to Camp New Friends. Now is the time to sign…
Read MoreCheck out past blogs and news!
If you have a child with neurofibromatosis, consider sending them to Camp New Friends. Now is the time to sign…
Read MoreWe are very excited to welcome Christine Christensen as NF Midwest’s new Event Coordinator! Christine started last month and has…
Read MoreEvery year NF Midwest staff and volunteers travel to Washington, DC to advocate for research dollars for neurofibromatosis and schwannomatosis through the…
Read MoreAttention, parents of children (ages 4-6) with neurofibromatosis Type 1, help researchers learn more about your child’s attention abilities! Purpose…
Read MoreAre you feeling stressed? Are your NF symptoms bothersome? The Family Center for Neurofibromatosis and the Integrated Brain Health Clinical…
Read MoreNF Midwest member, Libby, did an amazing job in her third appearance on The Doctors television show and her reveal…
Read MoreNF Midwest community member, Libby Huffer, will appear for the third time on The Doctors on Monday, January 15th. Check your local…
Read MoreNF Midwest is partnering with Prairie Farms Dairy in the Our Caps/Your Cause Campaign. This is an easy way to…
Read MoreIf you’re a post high school student with neurofibromatosis or schwannomatosis, and you live in NF Midwest’s service region of…
Read MoreIn February, NF Midwest staff and volunteers will descend on Washington DC along with other NF organizations to ask our…
Read More
© 2024 Neurofibromatosis Midwest - non profit 501(c)(t3). Site Map - Privacy Policy
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.