NF Midwest, Texas NF, NF Northeast, and The Littlest Tumor Foundation present an online day of learning for the NF community. This event is designed for, and by, patients and families affected by neurofibromatosis type 1 and neurofibromatosis type 2. Look for a separate event early in 2022 for schwannomatosis.
There will also be a Friday night “social” for patients and families to meet others.
We can’t get together in person, so we’re bringing it right to you wherever you are!
Learn more at www.nf-info.org.
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.