The CF & MS Fund Foundation Inc. is a 501(c)(3) non-profit organization dedicated to raising funds and awareness in the fight against Cystic Fibrosis and Multiple Sclerosis. The commitment to these two non-affiliated diseases began many years ago from a personal family connection to each disease. Today that commitment has evolved into a successful donor based, non-profit organization. Since the CFMS Fund’s inception in 2009 we have donated almost 3 million dollars to the Cystic Fibrosis Foundation and the National Multiple Sclerosis Society. These two nationally recognized organizations, over a century old combined, are ranked among the top non-profits in the United States. The CFMS Fund is proud to support them. Together we are improving and extending the lives of those living with CF and MS.

The Cystic Fibrosis Foundation is the world’s leader in the search for a cure for cystic fibrosis, funding more CF research than any other organization. The Foundation’s drug development model has been recognized by Harvard Business School and by publications such as Forbes, The New Yorker, and Bloomberg Businessweek.

The National Multiple Sclerosis Society helps each person address the challenges of living with MS through a 50-state network of chapters. The Society helps people affected by MS by funding cutting-edge research, driving change through advocacy, facilitating professional education, and providing programs and services that help people with MS and their families move their lives forward.

The CFMS Fund raises money through unique, five-star events, retail purchase add-on campaigns, letter campaigns, and various community building events like Tip a Teen, where middle and high school students donate their time waiting tables at local restaurants, providing any tips they earn to the Foundation. Visit our schedule of events to learn more.

For all inquires, contact: dtoupin@cfmsfund.org

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