
Levi – A Face of NF
Levi, 8 This is our beautiful son, Levi Howard. He was diagnosed in March of 2017 with NF1 when he…
Levi, 8 This is our beautiful son, Levi Howard. He was diagnosed in March of 2017 with NF1 when he…
Check out our Spring 2018 NF Midwest Newsletter! The highlights of this issue include… Research grants are given to the…
The Fillmore Family (GSWalk4NF Wisconsin/Madison team) invite you to join them at their annual Neighbor Day. This year part of…
The Fillmore Family (GSWalk4NF Wisconsin/Madison team) invite you to join them at their annual Neighbor Nite. This year part of…
On Wednesday, June 13th there will be another Adult Game Night in Chicago hosted by Ilene and Emily Bluestein. The…
If you’re in the NF Midwest service area of Illinois, Indiana, Iowa, Kentucky, Missouri (east half), or Wisconsin and are…
Great news! A new, detailed clinical practice guideline has been made available on the care of adults with neurofibromatosis type…
Erin Carter, whose 4 year old son, Cash, was diagnosed with NF in 2015, is determined to raise awareness and…
Happiness is yelling BINGO! The last game night was such a success that the next one has already been planned….
Are you the parent/caregiver of a child with neurofibromatosis type 1 (NF1) between the ages of 3-18 years? The MIND…
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