 
                    Tori – A Face of NF
I inherited NF1 from my father. I was diagnosed shortly after my birth. The doctor noticed that I had flat,…
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                    I inherited NF1 from my father. I was diagnosed shortly after my birth. The doctor noticed that I had flat,…
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                    I was diagnosed with neurofibromatosis type 2 (NF2) at the age of 10. Six Months after I was diagnosed, I…
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                    I was diagnosed with neurofibromatosis type 1 (NF1) when I was 16 years old. As a child in school, I suffered from…
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                    Erin Carter, whose 4 year old son, Cash, was diagnosed with NF in 2015, is determined to raise awareness and…
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                    NF Midwest member, Libby, did an amazing job in her third appearance on The Doctors television show and her reveal…
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                    NF Midwest community member, Libby Huffer, will appear for the third time on The Doctors on Monday, January 15th. Check your local…
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                    Did you know that in 2017 your donations provided research grants to the University of Chicago, the University of WI-Milwaukee,…
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                    Our walk in Naperville is just two days away on Saturday, June 3rd; today is Throwback Thursday; and NF Awareness…
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                    Let’s hear it for Laura Fillmore who kicked off NF Awareness month with an amazing interview on Wisconsin’s 57 Talk of the…
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                    Heather and Cynthia gave a great interview to WQOW in Eau Claire, Wisconsin about the Great Steps 4NF Walk that…
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