
Eric & Kai – A Face of NF
I have NF type 1. For the most part, my symptoms have been mild, but the most significant challenges I’ve…
Read MoreI have NF type 1. For the most part, my symptoms have been mild, but the most significant challenges I’ve…
Read MoreAna is 10 years old. She was diagnosed with neurofibromatosis type 2 when she was seven. Her genetic disorder was…
Read MoreMaverick is the first in his family to be diagnosed with NF1. He started showing symptoms at 2 months old….
Read MoreHi I’m Karissa, I’m 27 and I have NF1. My story may be a little long, but sometimes that’s the…
Read MoreMy little guy’s name is Conor and he is 1 year-old and has been diagnosed with NF Type 1. Conor’s…
Read MoreAurorah (Rory), now age 9, was diagnosed with neurofibromatosis type 1 shortly after her sixth birthday. She was born with…
Read MoreOur three-year-old son, Benjamin, was diagnosed with Neurofibromatosis Type 1 one year ago due to multiple cafe-au-lait spots (birthmarks) and…
Read MoreThis is my son Joel. He was born with neurofibromatosis type 1. Neurofibromatosis (NF) is a genetic disorder of the…
Read MoreHi! My name is Jackson and I’m 10 years old!! I was diagnosed with NF1 at 18 months old. It’s…
Read MoreWhen Eli was three years old, he was diagnosed with neurofibromatosis type 1, something we had never heard of before….
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