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Join Mikala and the millions of people like her who are impacted by any type of neurofibromatosis, or NF, or schwannomatosis. If NF affects your life or someone you know, we welcome you to submit your Make NF Visible video today and help the world to see you, and see NF. Click here to submit your video: https://form.jotform.com/210418014183... After we have reviewed and captioned your video, it will be included here, on the Make NF Visible YouTube channel within about 48 hours. Please subscribe so you don't miss it! Click the CC button for Closed Captions. Donate today to end us end NF: https://join.ctf.org/campaign/make-nf... Learn more: https://www.ctf.org/get-involved/nf-a... Note: The experiences, opinions, or information expressed in each of the self-submitted Make NF Visible videos is unique to each participant and does not necessarily reflect that of the Children’s Tumor Foundation, nor is meant to serve as diagnostic information or medical advice.