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Living with HSP – Management & Treatment News

Victorian HSPer takes up rowing

Encourages others to try it

Survival tips for caregivers

Ask for help, take time for yourself

Daily duration stretching pays off

Improved mobility and range of motion

Lack of movement has negative impacts

Brain and nerves affected

Botox effects on kids and adults with HSP

The findings of two studies

Is muscle growth impaired in HSP kids?

Earliest age of onset are most affected

Living with a rare disease

New thinking, new ideas

Comparing intrathecal vs oral baclofen

Evaluating intrathecal delivery system

‘Living with the Enemy’

Coping with the stress of a chronic condition

New genotype – phenotype correlations found in paediatric HSP

Warning on imitations of current methodologies

Posts pagination

Newer posts Page 1 … Page 14 … 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.

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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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