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Welcome to the A.L.S. Family Charitable Foundation

on Cape Cod

The A.L.S. Family Charitable Foundation began in 2001 in hopes of creating a brighter future for those living with A.L.S. in New England and honors all of the courageous individuals and families touched by this disease.

For those we love, for those we lost, we walk.

MARY ANN SCIABA SINGERSEN, president & co-founder
PATIENT PROGRAMS

To provide A.L.S. patients and their families with the best possible financial and emotional support through their unique A.L.S. journey.

GET INVOLVED

Find out how you can get involved in the A.L.S. Family Charitable Foundation...

  • Volunteer
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A.L.S. is a progressive, fatal neuromuscular disease characterized by a degeneration of motor nerve cells in the brain and spinal cord.

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