2017 Scholarship Recipients
Neurofibromatosis Midwest is proud to announce our eleven scholarship recipients for the 2017-2018 academic year. Now in it’s third year,…
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Neurofibromatosis Midwest is proud to announce our eleven scholarship recipients for the 2017-2018 academic year. Now in it’s third year,…
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From Jenn, mom of Audrey, a 5-year-old with NF1 I think your daughter might have a condition called neurofibromatosis. Don’t…
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Erin and Jonathan are big on raising awareness for neurofibromatosis and being advocates for NF Midwest. The two have a…
Read MoreLiving with a chronic illness can be extremely difficult. NF is no exception. The article linked in this blog post…
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Protect federal funds for neurofibromatosis by acting now. Fill out the form below to send your message in support of…
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There is an urgent and devastating threat to neurofibromatosis research, and we urge you, your friends, family and everyone you…
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Join “Happy Haddie” and the “CrazyTwins” in the campaign to spread the word! What’s the word? #TheWordIs neuro-fibroma-tosis! Take your…
Read MoreCheck out our Spring 2017 NF Midwest Newsletter! The highlights of this issue include… An announcement of research grants given…
Read MoreNeurofibromatosis Midwest is proud to announce our seventeen scholarship recipients for the 2016-2017 academic year. Now in its second year,…
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Marissa and her mom from Madison’s Great Steps team, Marissa’s Mighty Mob, did a fantastic interview on “Talk of the…
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