
Cash’s Crew Raises Awareness!
Erin Carter, whose 4 year old son, Cash, was diagnosed with NF in 2015, is determined to raise awareness and…
Read MoreCheck out past blogs and news!
Erin Carter, whose 4 year old son, Cash, was diagnosed with NF in 2015, is determined to raise awareness and…
Read MoreHappiness is yelling BINGO! The last game night was such a success that the next one has already been planned….
Read MoreThe Evansville Indiana group will be holding an informal Meet4NF gathering to provide support, share resources and meet others with…
Read MoreThis month the Kentucky NF Support group meeting will be held Saturday, April 21st, from 1-5pm in Mount Sterling. One of…
Read MoreAre you the parent/caregiver of a child with neurofibromatosis type 1 (NF1) between the ages of 3-18 years? The MIND…
Read MoreThe efforts of our community, our donors, and the advocacy of NF Midwest (and other NF organizations) all worked together…
Read MoreNF Midwest is excited to add a new piece about Brainstem Tumors in NF1 to our be iNFormed series. This is…
Read MoreThe Education and Brain Sciences Research lab at Vanderbilt University is seeking participants for a new research study! The purpose…
Read MoreJOIN US FOR A NIGHT OF FAMILY FUN AND HELP SUPPORT NEUROFIBROMATOSIS WHEN: May 18, 2018 WHERE: PARKVIEW FIELD Fort…
Read MoreNF Midwest, in collaboration with NF Northeast, has awarded Dr. Vijaya Ramesh from Massachusetts General Hospital, a grant for research in neurofibromatosis…
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