
Evita – A Face of NF
My name is Evita Ali and I have NF1. I was diagnosed with neurofibromatosis when I was 30 years of…
My name is Evita Ali and I have NF1. I was diagnosed with neurofibromatosis when I was 30 years of…
NF Collective Launches New Website to Connect NF Patients with Doctors The NF Collective, a group of organizations dedicated to…
I have been running competitively for almost 2 years and love it. It helps me relax, great stress reliever gave…
My name is Rick. I wasn’t diagnosed with NF Type 1 until I was 32 years old. I had no…
I am 64 years old with no prior neurofibromatosis family history and none of my 6 siblings have NF, making…
Ana is 10 years old. She was diagnosed with neurofibromatosis type 2 when she was seven. Her genetic disorder was…
Aurorah (Rory), now age 9, was diagnosed with neurofibromatosis type 1 shortly after her sixth birthday. She was born with…
Amazing volunteers in Fort Wayne are doing it 4NF and have put together a special family night for people in…
Protect federal funds for neurofibromatosis by acting now! Fill out the form below to Raise your Voice for NF Research….
Because the neurofibromatosis cause needs New Fighters and young iNFluencers! See photos This January I had the extreme privilege of…
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