Welcome to The Spastic Paraplegia Foundation (SPF) Website
The Get Involved section is probably the most frequented part of the website. ‘Donate Here’ helps raise money for SPF. The primary goal of SPF is to raise money to find a cure and 93% of donations go toward funding research. There are many ways to donate: create a fundraiser, use Amazon Smile to shop online, schedule a monthly monetary gift and more.
There are in-person and virtual ways to participate under ‘Events’ which are in an Events Calendar. There are also yearly events: Annual Conference, Awareness Week, and more. In the ‘SPF Store’ there are lots of different items to choose from along with logo designs. Under ‘Ambassadors’ there is a list of people volunteering to help others with HSP or PLS. If you have a question and looking for a person in your area who knows exactly how you feel and what you are experiencing, contact a SPF Ambassador. Plus, there is information on ‘Support Groups’ and ‘How to Help’.
The section called Resources contains a great deal of useful information. Here you can 'Register/Update' with SPF for FREE. There are informational booklets on HSP & PLS which can be printed and given to family members to help them better understand your situation and a glossary of medical terms. The 'directories' have lists of Physician/Clinics and Physical Therapists. You will also find information on our 'Newsletters' (Synapse and Spastic World), 'HSP Forum', 'Self-help Guides', 'Government Aid & Charity Programs', and 'Special Offers'.
Research contains a description of SPF’s mission, 'Research Impact', 'Current Studies Seeking Participants', 'Genetic Testing and International Organizations', Patient Registry information, and submitting a research proposal.
If there is still something you'd like to find just type it in the SEARCH area on the top of all pages. Also don't forget to visit our social media pages, especially our YouTube channel. We have preserved most of the SPF's presentations from world renowned physicians. The social media icons appear at the bottom of the webpage.
You are no longer alone in this fight! Please REGISTER with our foundation.