Another $15 Million for NF Research
This past February, NF Midwest brought volunteers to Washington DC to once again advocate for federal dollars for neurofibromatosis type…
Read More
This past February, NF Midwest brought volunteers to Washington DC to once again advocate for federal dollars for neurofibromatosis type…
Read More
Neurofibromatosis Midwest is excited to award $1,000 academic scholarships to six adults affected by neurofibromatosis or schwannomatosis. This is the fourth…
Read More
Check out our Spring 2018 NF Midwest Newsletter! The highlights of this issue include… Research grants are given to the…
Read More
If you’re in the NF Midwest service area of Illinois, Indiana, Iowa, Kentucky, Missouri (east half), or Wisconsin and are…
Read More
Erin Carter, whose 4 year old son, Cash, was diagnosed with NF in 2015, is determined to raise awareness and…
Read More
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 More
NF Midwest member, Libby, did an amazing job in her third appearance on The Doctors television show and her reveal…
Read More
NF Midwest community member, Libby Huffer, will appear for the third time on The Doctors on Monday, January 15th. Check your local…
Read More
If you’re a post high school student with neurofibromatosis or schwannomatosis, and you live in NF Midwest’s service region of…
Read More
© 2026 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.