Our Branches

Scottish Huntington’s Association currently has Branches in Tayside, Fife and Moray. The Branches are run by volunteer members who have personal experience of Huntington’s disease, and are headed up by a Branch Committee made up of a minimum of a Branch Chair, a Branch Secretary and a Branch Treasurer.

Branches play an important role in providing help and support at a local level and offer a significant source of interaction for a person with Huntington’s disease, their families, carers, and friends. They also form a vital link with the national organisation.

Branch activities can include:

Holding meetings on a regular basis for information sharing and mutual support

Organising social occasions such as a Christmas meal or a summer outing

Providing information on Huntington’s disease

Liaising between families, local HD Specialists and Scottish Huntington’s Association services as necessary to improve health and lifestyle options for members

Fundraising to support both local and national activities (such as HD Specialist Service, Youth Service, Financial Wellbeing Service etc)

Disbursing local funds as necessary to support member families through Welfare Grants and assistance in purchase of equipment to assist those with Huntington’s disease

Individual Branches

Each branch is run by its own members and is accountable to the Board of Trustees, who work together to ensure branches operate within the law and in line with the strategic direction of the charity.

To find out more about our Branches, or to join your local group, please contact sha-admin@hdscotland.org

Membership of Scottish Huntington’s Association

Scottish Huntington’s Association was formed in 1989 by families to support individuals and families at risk of, or living with, Huntington’s disease.

In addition to being a charity registered with the Office of the Scottish Charity Regulator (charity number SC010985) and a company limited by guarantee, it is also a membership organisation.

Our membership is made up people who have accessed, or continue to access, Scottish Huntington’s Association services; those who have joined in a professional capacity; and people who have chosen to support our charity, for example through partnership working or fundraising.

This community of likeminded individuals is helping to engage with, and further, our mission on behalf of all Huntington’s families, while also supporting vital work to ensure the sustainability and good governance of the charity.

Membership benefits

  1. Shaping the work of the charity
    Members have voting rights at the charity’s Annual General Meeting (subject to eligibility, see categories of membership below).
  2. Increased transparency
    You will help to uphold the accountability of the organisation, ensuring effective governance is maintained.
  3. Eligibility
    As a member of Scottish Huntington’s Association you are eligible to become an office bearer (Chair, Treasurer or Secretary) or committee member in a local branch of the society if there is one in your area.
  4. Access to membership content
    You will receive regular email bulletins with important updates, including the appointment of Trustees and other activities of the Board; announcements; and opportunities to increase your involvement in the work of the charity.
  5. Advocacy and representation
    You may choose to help raise the voice of the Huntington’s community to increase public awareness and funding, including by sharing your own experiences with the wider public.
  6. Creating opportunities
    As an active member of our membership community, you will also be supported to deepen your involvement, for example as a volunteer fundraiser or an advocate for our work to your professional and personal networks.

Membership of Scottish Huntington’s Association is free.* Once registered as a member, your membership will continue until you notify us that you wish to cancel. To keep our records up to date, we may also contact you from time to time to ascertain whether you wish to remain a member.

Categories and qualifications of membership

Principal Member

Any person who is over 18 years of age, resides in Scotland, and has an interest in Huntington’s disease, shall be eligible to become a Principal Member of the Association with voting rights at our Annual General Meeting.

Representative Member

Any person who is over 18 years of age, resides in Scotland and represents a local authority or statutory body invited by the Board to nominate one or more representatives, shall be eligible to become a member of Scottish Huntington’s Association with voting rights for as long as they remain the representative of the body to which they are affiliated AND that body retains access to membership at the invitation of the Board (see Article 6 of the Articles of Association).

Associate Member

Any person who is:

  1. under 18 years of age, and/or
  2. not resident in Scotland, and/or
  3. a staff member of the Scottish Huntington’s Association,

shall be eligible to become an Associate Member of the Association with no voting rights.

In recognition of the considerable financial burdens that living with Huntington’s disease can bring, we are happy to provide membership of the Association free of charge. We also provide free membership to professionals and other supporters in recognition of their contribution to meeting the needs of the Huntington’s community.

However, if you wish to donate or set up a regular gift to help sustain our services then this will be gratefully received. Please contact our Income Generation team at fundraising@hdscotland.org for further information.

*Please note that because Scottish Huntington’s Association is a company limited by guarantee, in the very unlikely event that it should ever be wound up members would be legally liable to contribute no more than £1 each towards the costs of winding up. Details are contained in Article 6 of the Scottish Huntington’s Association Memorandum of Association.

Support Groups

Local support groups are open to everyone whose life is impacted by Huntington’s disease, including carers. They operate in Greater Glasgow and Clyde, Lothian, Tayside, Fife, Highland and Grampian.

Find out more by contacting your HD Specialist or emailing sha-admin@hdscotland.org

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