43 Years of Care and Ensuring No One Fights Alone!

NF Midwest News

Check out past blogs and news!

NF Midwest News/Blog

Janna – A Face of NF

Our daughter Janna was diagnosed with neurofibromatosis type 1 when she was five months old. Doctors tell us that it…

Read More

Ify – A Face of NF

My husband and I had never heard of NF1 until May 2015 when our daughter, Ifunanya or Ify (pronounced “eff-ee”),…

Read More

Jay – A Face of NF

Jay, 10 Mos. Our sweet baby boy Jay was diagnosed with NF Type 1 in May of 2018 at six…

Read More

Sam – A Face of NF

Sam, 33 I was diagnosed with neurofibromatosis type 1 (NF1) while being treated for scoliosis when I was 4 years…

Read More

Get the Latest NF News & Updates

Sign up to be notified of new posts to our website.

Sign Up for Updates

Visit Us
Follow Me
Tweet
Share