Ana – A Face of NF

Ana is 10 years old. She was diagnosed with neurofibromatosis type 2 when she was seven. Her genetic disorder was a result of a spontaneous mutation. It has been a long road for Ana, as she has had 34 tumors between her brain and spine and multiple surgeries. She has learning disabilities, right foot drop, right sided deafness, and right sided facial paralysis.  Ana has tried a clinical trial, but it didn’t have the results we hoped for. She loves to swim, ride horses, and play with her siblings.

– Alesia (mom)

See More Faces of NF/Read Their Stories

Recent Posts

  • Nothing to Fear: A Children’s Book on NF

    For young children with neurofibromatosis, medical appointments can feel big, unfamiliar, and sometimes scary. An eye exam, an MRI, a doctor’s visit, or even the mention of a needle can bring up questions that are hard for a small child to understand — especially between the ages of 3 and 7, when imagination is strong... Read More
  • NF Awareness Month Reached Across Our Six-State Region 

    Thank you to everyone who helped raise awareness for neurofibromatosis (NF) during May!  This year, NF Midwest families and advocates helped bring NF Awareness Month into communities across our six-state region. Through state and local proclamations, more people had the opportunity to learn about neurofibromatosis and recognize the families who live with NF every day. ... Read More

Responses

Respond

Your email address will not be published. Required fields are marked *