Support those dedicated people who have set-up their own events to raise NF awareness and funds.
Listed here are fundraising and awareness-raising events created by our members to support neurofibromatosis and NF Midwest’s mission to improve the lives of children and adults with neurofibromatosis.
It takes special, dedicated people to take their valuable time and resources to raise funds and awareness. We appreciate them all for their efforts and hope that you will support them in whatever way you can.
Kalona is selling her art and plants to support NF1. Her granddaughter has neurofibromatosis and I am trying to help by creating art and selling plants.Visit Fundraiser Page
Every year in August or September Sam and his family hold an all-day music and brew festival in Carlinville, IL.Visit Fundraiser Page
Every year since 2012 Steve Reason has organized NF Midwest’s participation in John Deere’s Birdies for Charity program every year.Visit Fundraiser Page
January 30, 2016
Always looking to give back and to help others, Aydin’s family and friends put together a 9 pin bowling party to raise funds for their Chippewa Falls Great Steps 4NF team.Visit Fundraiser Page
Raised $8,600 with goal of $8,000
4 years ago, my daughter was diagnosed with Neurofibromatosis at the age of 4 months. I had never heard of it. I was given a brochure for NF Midwest from her doctor and I signed up for their symposium. Shortly thereafter, I received a call from the Director, Diana. She let me know that her husband and two children have NF as well. She asked if I had any questions, and let me know that they were there for us. I had just received shocking, frightening news about my infant child. I didn't know where to turn, and suddenly I had a place to go for answers and help. NF Midwest has been there for my family every step of the way. We are so grateful for the work they do, and proud to support it.
The resources on this site should not be used as a substitute for professional medical care or advice on Neurofibromatosis. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional.