Eli – A Face of NF
When Eli was three years old, he was diagnosed with neurofibromatosis type 1, something we had never heard of before….
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Check out past blogs and news!
When Eli was three years old, he was diagnosed with neurofibromatosis type 1, something we had never heard of before….
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Wyatt was diagnosed with NF type 1 when he was 2 years old. He will be turning 13 years old…
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May is NF Awareness month. This year, to grow awareness, we are going to be sharing stories of how this…
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Katherine (or Katy) is 5 years old and was diagnosed with NF1 in October of 2018. Our first sign of…
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Noah was 7 months old when he was diagnosed with NF1. He is almost 3 years old now. Noah has cafe…
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Check out our Spring 2019 NF Midwest Newsletter! The highlights of this issue include… Page 1 Information on the new…
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Here’s an event you can participate in from your couch and possibly win a two year lease on a 2019…
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The American Academy of Pediatrics has published an updated clinical guideline on the Health Supervision for Children With Neurofibromatosis Type…
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Amazing volunteers in Fort Wayne are doing it 4NF and have put together a special family night for people in…
Read MoreJoin the Panozzo Family for a Day at the Ball field to benefit the Ann and Robert H Lurie Children’s…
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