Request NF Research Support From Your Senators
Protect federal funds for neurofibromatosis by acting now. Fill out the form below to send your message in support of…
Read More
Check out past blogs and news!
Protect federal funds for neurofibromatosis by acting now. Fill out the form below to send your message in support of…
Read More
There is an urgent and devastating threat to neurofibromatosis research, and we urge you, your friends, family and everyone you…
Read More
The following is a blog by Dr. Luiz Rodrigues . Originally posted in Portuguese on July 3 2017. Additions and…
Read More
On Saturday, June 24, 2017, Kentucky residents had a fun filled day, courtesy of Freddy and Camillia Thomas, Jr., of…
Read More
The following is a blog by Dr. Luiz Rodrigues . Originally posted in Portuguese on May 7, 2017. Additions and…
Read More
The following is a blog by Dr. Luiz Rodrigues . Originally posted in Portuguese on September 15, 2015. Additions and translation…
Read More
Join “Happy Haddie” and the “CrazyTwins” in the campaign to spread the word! What’s the word? #TheWordIs neuro-fibroma-tosis! Take your…
Read More
The following is a blog post by Dr. Luiz Rodrigues . Originally posted in Portuguese on March 1, 2017. Additions and…
Read More
Let’s hear it for Laura Fillmore who kicked off NF Awareness month with an amazing interview on Wisconsin’s 57 Talk of the…
Read MoreCheck out our Spring 2017 NF Midwest Newsletter! The highlights of this issue include… An announcement of research grants given…
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.