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Huntington's Disease (HD)

About Huntington's Disease (HD)

Huntington’s disease (HD) is a complex neurological condition with symptoms that typically begin to develop between the ages of 30 and 50.

In around 5-10% of cases HD symptoms develop before the age of 20 - this is known as Juvenile Huntington’s disease.

HD is hereditary, meaning it impacts upon entire families over generations rather than on individuals alone. Each child of a person with HD has a 50% chance of inheriting the condition.

As HD progresses it can affect a person’s:

  • Movement (or motor skills): People with HD can suffer from repetitive involuntary movements resulting in mobility, balance and coordination problems as well as difficulties with speech and swallowing.
  • Thinking processes (or cognition): People with HD can develop a type of early onset dementia, which affects their ability to process information, make decisions, solve problems, plan and organise.
  • Mental health: People with HD can also experience a decline in mental health. Depression, anxiety, irritability, obsessive pre-occupations and apathy are amongst the most common mental health problems experienced. Psychosis may also occur.

Symptoms generally progress slowly over a long period time. Those impacted may experience gradual loss of independence and require increasing care and support. Most people with the condition will eventually require 24 hour care.

A well coordinated multi-disciplinary approach to the care and support of people living with Huntington's disease is essential.

The National Care Framework for Huntington’s Disease

The Scottish Huntington’s Association has published a National Care Framework which outlines the care and support that HD families should be entitled to receive throughout the country.

The National Care Framework is funded and supported by the Scottish Government and backed by all parties in the Scottish Parliament. It was developed by a multi-disciplinary expert group and has been supported and endorsed by the National Advisory Committee for Neurological Conditions, NHS Boards, Health and Social Care Partnerships, professional bodies, HD family members, academics and national and international third sector partners.

The Framework seeks to ensure that the care and support provided to individuals and their families living with Huntington’s disease takes account of their specific health & social care needs throughout their experience.

The National Care Framework for HD can be viewed at

Greater Glasgow & Clyde Contact Information 

HD Specialists (contact for all enquiries or to make a referral)

Sally Woolvine (Senior HD Specialist)
Gillian Blair (HD Specialist)
Helen Maginnis (HD Specialist)
Ann Waugh (HD Specialist)

Scottish Huntington's Association - Glasgow Services

Business First, Burnbrae Road, Paisley, PA1 2FV

0141 556 4100 
[email protected]

HD Clinical Lead
Post currently vacant. Please direct all enquiries to the HD Specialist Team (above) in the first instance

Youth Service Lead
Kirsten Walker
0141 5562136
07983 724201
[email protected]

Financial Wellbeing Officer
Melissa Higgins
Financial Wellbeing Officer
07710 391621
[email protected]

We have no record of any locations offering this service.

Last Updated: 07 September 2021