Chris Plus Morgan – A Face of NF
May is NF Awareness month. This year, to grow awareness, we are going to be sharing stories of how this…
Read MoreMay is NF Awareness month. This year, to grow awareness, we are going to be sharing stories of how this…
Read MoreKatherine (or Katy) is 5 years old and was diagnosed with NF1 in October of 2018. Our first sign of…
Read MoreNoah was 7 months old when he was diagnosed with NF1. He is almost 3 years old now. Noah has cafe…
Read MoreOur daughter Janna was diagnosed with neurofibromatosis type 1 when she was five months old. Doctors tell us that it…
Read MoreMy husband and I had never heard of NF1 until May 2015 when our daughter, Ifunanya or Ify (pronounced “eff-ee”),…
Read MoreJay, 10 Mos. Our sweet baby boy Jay was diagnosed with NF Type 1 in May of 2018 at six…
Read MoreSam, 33 I was diagnosed with neurofibromatosis type 1 (NF1) while being treated for scoliosis when I was 4 years…
Read MoreLevi, 8 This is our beautiful son, Levi Howard. He was diagnosed in March of 2017 with NF1 when he…
Read MoreWe inherited NF1 from our mom, Shirley, who passed away from breast cancer at the age of 53. She fought…
Read MoreI inherited NF1 from my father. I was diagnosed shortly after my birth. The doctor noticed that I had flat,…
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