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Foundation News

NDIS update December 2019

Government announces plan to improve the NDIS

International Meeting on HSP and Ataxia

Leading researchers presenting

Synapse (USA) and HSP Group Newslink (UK)

News from other HSP groups

HSP clinical trial program update September 2019

Progress in preclinical studies and clinical trial preparation

SPF Annual Conference, June 2019, presentations

And research funding allocations SPF (USA)

HSP community socials in NSW & WA

Fundraising in SA & Facebook birthdays

SPF Synapse (USA)

Newsletter of the USA group

Gene testing for all seriously ill children

No national strategy on rare diseases

NDIS update September 2019

Parliamentary committee wants your comments

HSP clinical trial program update June 2019

Progress in preclinical studies and clinical trial preparation

Posts pagination

Newer posts Page 1 … Page 11 … Page 37 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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