A Special Letter from an NF Mom
From Jenn, mom of Audrey, a 5-year-old with NF1 I think your daughter might have a condition called neurofibromatosis. Don’t…
Read MoreCheck out past blogs and news!
From Jenn, mom of Audrey, a 5-year-old with NF1 I think your daughter might have a condition called neurofibromatosis. Don’t…
Read MoreThe Kentucky NF Midwest group is holding an NF support group meeting this Saturday, September 16th, 2017, from 10 am…
Read MoreErin and Jonathan are big on raising awareness for neurofibromatosis and being advocates for NF Midwest. The two have a…
Read MoreThis FREE seminar in Notre Dame, Indiana provides an opportunity to raise awareness about Neurofibromatosis and share resources, experiences, & expertise to…
Read Morebe iNFormed! Join us for an exciting day in which you will learn from the experts and share experiences about…
Read MoreLiving with a chronic illness can be extremely difficult. NF is no exception. The article linked in this blog post…
Read More12 hours of music, six bands, 10 varieties of Schlafly Beer, great food, tub auction, Carribbean cruise raffle, all benefitting…
Read MoreThe Kentucky NF Midwest group is holding an NF support group meeting this Saturday, August 12th, 2017, from 10 am…
Read MorePlease join us for an afternoon of food, fun, and competition! Whether you’re an experienced golfer or new to the…
Read MoreWe have a new be iNFormed article for our NF Midwest community. be iNFormed articles are written on various subjects of interest…
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