Building Community in Columbia: Kristi’s Leadership with NF Midwest
In Columbia, Missouri, the Walk for NF did not appear overnight. It grew because someone decided that people in her…
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In Columbia, Missouri, the Walk for NF did not appear overnight. It grew because someone decided that people in her…
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When Audrey was born, there were no signs of neurofibromatosis. She was healthy and adorable. It wasn’t until she was about two months…
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They gave 10 AMAZING YEARS to the cause and raised a lot of funds. Thank you to the Oswald family…
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I was diagnosed at age 2. I have cafe au laits, bilateral optic gliomas, a few cutaneous neurofibromas, innumerable internal…
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In 2020, NF Midwest awarded $1,000 academic scholarships to six adults affected by neurofibromatosis or schwannomatosis. This is the seventh…
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In 2017, I became involved in a clinical research trial through Medical College of Wisconsin for benign cutaneous neurofibromas. Being…
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Sera has a tumor that runs the length of her arm, all the way from her hand up to her…
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My name is Evita Ali and I have NF1. I was diagnosed with neurofibromatosis when I was 30 years of…
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I joined the Army at 19 years old. I did all the training and arrived at my duty station. In…
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My sixteen-year-old son began getting café au lait spots at two months old. Our pediatrician at the time gave us…
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