We have loved ones with NF. Every dollar is a precious to us as it is to you!
NF Midwest is dedicated to improving the lives of people with NF through C.A.R.E.
To fulfill this mission, NF Midwest supports regional Clinics, raises Awareness, funds Research and provides Education and Support. NF Midwest provides programs and services designed to help people with NF and their families live their best lives while coping with neurofibromatosis.
We meet or exceed the standards set by all groups that monitor the nonprofit sector and are proud of how we ensure donor funds are put to the best possible use in achieving our mission. Currently we are a Guidestar Exchange Silver Participant.
Our EIN is 22-2580173.
As a nonprofit organization, Neurofibromatosis Midwest relies on charitable donations to fund our research programs and patient services. Your support is invested wisely.
NF Midwest is a nonprofit organization under section 501(c)(3) of the Internal Revenue Code. Donations are tax deductible. Books and records are audited annually in accordance with generally accepted accounting standards. Click to see NF Midwest’s most recent three 990’s and Financial Statements.
There are a lot of big corporate charities out there that talk about how much they help people, but when we were looking for answers we did not get the help from them. It was NF Midwest that helped us. So it is important to me to get the word out about NF and NF MIdwest so that no other family has to feel as alone as we were when we were searching for answers. WHY SHOULD YOU DONATE TO NF MIDWEST INSTEAD OF THE OTHER GUYS???? To me the answer is simple. They care! Sometimes in life companies or charities get so big that they forget about why they are doing anything to begin with, they forget about the people they are suppose to help. Nf Midwest is NOT this way. They are there for those affected by NF and for their families. Sometimes in life bigger is not better. Our family likes to say that "NF Midwest is Small enough to care...Big enough to make a difference" And I am telling you that my family and others I know in my area that means a lot more then we could say. So please consider helping us in our NF cause and donate to this walk and NF Midwest!
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.