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The Parkinson’s Disease Society was established in
1969.
We fund research that is focused on
transforming lives. We have invested more than £35m since the
charity was founded. This research has led to advances in the
search for the cause of Parkinson’s, improved medical and surgical
treatments, better therapies and equipment, and towards finding a
cure.
Our nurses and specialist advisors on the
Helpline offer support and advice, giving people the confidence to
manage the condition and plan ahead.
Our wide range of information sheets,
booklets, and DVDs, answer questions on all aspects of the
condition, helping people with Parkinson’s, their families and
carers, and professionals involved in the management of the
condition.
Our network of over 330 branches and support
groups located across the UK offer support and services, enabling
everyone affected by Parkinson’s and their families to meet others
in similar situations.
We work hard to campaign and influence
Government policy and the development of high-quality services at a
local and national level, including the education of professionals
working with people with Parkinson’s.
We believe all people with Parkinson’s should
have access to high quality and integrated health and social care
services delivered by professionals with a good understanding of
the condition wherever they live across the UK.
Our work is almost entirely funded by
charitable donations, and we are heavily reliant on legacies.
No one should have to face Parkinson’s on
their own and if you are affected by the condition we are here to
support you.
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