Welcome to Spastic Paraplegia Foundation, Inc.
HSP and PLS are neurological disorders affecting the voluntary muscles. The disorders are progressive and may lead to patients being unable to walk, and more. The Spastic Paraplegia Foundation is dedicated to advancing research and finding the cures for two groups of closely related, progressive neurological disorders: Primary Lateral Sclerosis (PLS) and Hereditary Spastic Paraplegia (HSP).
The day when all individuals with HSP or PLS are diagnosed, treated and cured.
HAPPY NEW YEAR - HOT PEPPER CHALLENGE
Tour SPF Website and Join our SPF Registry!
SPF thrives to accomplish our vision of seeing the day when all individuals with HSP or PLS are diagnosed, treated, and cured.
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Join SPF Events, Fundraisers & Connections to help raise awareness, funds, and crucial resources to serve our community.
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Spastic Paraplegia Foundation - 1605 Goularte Place - Fremont CA 94539-7241 Ph: (877) 773-4483
We are a non-profit corporation under section 501(c)(3) of the U.S. Internal Revenue Code, EINTax ID#: 04-3594491
I've been dealing with Hereditary Spastic Paraplegia affecting my SPG7 for a very (very) long time and I was doing very well for myself. Then, recently, I joined a few support groups here in Ottawa and I found the Spastic Paraplegia Foundation and met a bunch of like-minded people. I put myself out there as an ambassador for Canada. Hopefully I can spread awareness, get other Canadians to join the Foundation and share my story with others.