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Living with HSP – Management & Treatment News

New drug available on the NHS in England

For children with Duchenne muscular dystrophy

‘Gaming’ the challenge of HSP

Happier, healthier, stronger

A new era in genetic testing for HSP

What it means for HSPers

2016 survey of HSPers

Home modifications, quality-of-life

HSP gait study in children

Important findings about spasticity and weakness

Genetic Alliance wants your thoughts

Survey on gene testing

Fatigue, pain, depression and HSP

Research study establishes the link

Alleviating spasticity important for mobility

Exercises from a physio who has HSP

TEK mobility device

An HSPer shares his story of using it

New exoskeleton device to aid walking

Lighter and cheaper than earlier models

Posts pagination

Newer posts Page 1 … Page 19 … Page 36 Older posts

HSP Research Foundation

Welcome to the HSP Research Foundation - created in 2005 to find a cure for Hereditary Spastic Paraplegia - an inherited, degenerative disease affecting mainly the legs, causing muscle weakness, spasticity and severely impairing walking. Read more »

Information on this website and resources to which we have links are general knowledge about HSP. We are not medical professionals, nor do we offer medical advice. Always consult your own medical professionals regarding your particular circumstances.

Registered charity

The HSP Research Foundation Incorporated ABN 46648875912 is an Income Tax Exempt Charity endorsed by the ATO as a Deductible Gift Recipient organisation.

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