This month we have been talking about professional support and interventions.

Professional intervention plays a key part in someone's Huntington's journey and getting the right support at the right time can make a big difference. From utilising our Youth Engagement Service (HDYES) for young people in Huntington's families, Genetic Counsellors for testing and family planning or Occupational Therapists for adapting to life with Huntington's. Never feel like you can't ask for help. 

If you are unsure what professional you might need for yourself or your loved one, you can ask your local Huntington's adviser or call our helpline on 0151 3315444.

We have put together this handy factsheet for you to download. You can share it on your social media or with friends, family or employers.

Download the factsheet

How the Huntington's Disease Association can help you

Guides and resources

As Huntington's is still a relatively rare disease, people may come across a medical professional such as a GP, mental health or social worker who may have never dealt with someone at risk or affected by Huntington's.

We have created a range of guides that you or your Specialist Adviser can share with professionals if needed.

• A guide for GPs

• A guide for mental health workers

• A guide for social workers

A story from the community

Getting the right support for your loved one - Hannah's story

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Your questions answered by healthcare professionals

We asked the community what questions they would like to ask a Neuropsychiatrist and an Occupational Therapist. You can read the Q&As below.

Q&A with an Occupational Therapist - Professional perspective

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Q&A with a Neuropsychiatrist - Professional perspective

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Symptoms of Huntington's disease and who can help

Huntington's disease affects people in three main ways. It affects people's mind, movement and mood. Below you can see some of the symptoms people may experience and what healthcare professionals you may need.