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...For information about HSP and PLS

The Spastic Paraplegia Foundation is proud to be THE source for information regarding Primary Lateral Sclerosis and Hereditary Spastic Paraplegia. Please note that content is based on expert opinion, professional advice and published experience, but does not represent therapeutic recommendation or prescription.

There is a wealth of information at this site and it’s highly likely your questions will be answered here. If you are having trouble, try our Search.

Please consult your personal physician regarding individual medical questions.  If you need help finding a neurologist, click here, or, join our email support group and ask if others in your area have suggestions.

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To make a donation to support research now, click Donate! Or, visit our Giving Guide to read about other ways to support research. For information about the SPF Research Grant program or participating in research, please contact info@sp-foundation.org.

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The SPF is volunteer-driven. Our biggest need is help with fundraising, outreach and organizing local meetings and conferences. Please see How to Help or contact volunteer@sp-foundation.org.

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SPF receives no funding for its website. It is maintained by volunteers and under review by the SPF Medical Advisor and Scientific Advisory Board.

If you have a comment about the content of this site or would like to contribute something for the Patient Forum section, please contact community@sp-foundation.org.

For technical concerns, please contact webmaster@sp-foundation.org.

You can call us at 978-256-2673 or write to us at our national headquarters:

Spastic Paraplegia Foundation, Inc.
209 Park Rd.
Chelmsford, MA 01824

 

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