My son has HSP (Hereditary Spastic Paraplegia), a type of Motor Neurone Disorder, which means he is gradually loosing the use of his legs, along with many other health issues related to this insidious, and rare disease. As his Mum, it breaks my heart to see him struggle every day to do the things that most of us take for granted. There is nothing that can help at present, so the only way I can support him, is by trying to raise funds for research into a cure. All funds raised go directly to the HSP Research Foundation, which is completely run by volunteers.
Hereditary Spastic Paraplegia (HSP) Research Foundation
The HSP Research Foundation is an Australian-based organisation formed in 2005. Our Purpose:
The HSP Research Foundation is an incorporated, registered Australian charity that facilitates and funds research to find an effective treatment. The Foundation is also the community hub for HSPers in Aust.
About Fundraiser
Chris Whitehead
EASTWOOD, SA
Fri, 15 Aug 2025
Erica Davis
$ 200
Mon, 30 Jun 2025
Yanti
$ 390
Thu, 19 Jun 2025
Roger Pope
$ 900
Sat, 14 Jun 2025
Anonymous
$ 500
Sat, 3 May 2025
Pieter
$ 45
Mon, 3 Feb 2025
Yanti
$ 1500
Mon, 30 Dec 2024
Alex Glikmann
$ 100
Let’s hope in 2025 progress will be made towards a cure.
Hereditary Spastic Paraplegia (HSP) Research Foundation
The HSP Research Foundation is an Australian-based organisation formed in 2005. Our Purpose:
The HSP Research Foundation is an incorporated, registered Australian charity that facilitates and funds research to find an effective treatment. The Foundation is also the community hub for HSPers in Aust.
Let’s hope in 2025 progress will be made towards a cure.