An important part of Ataxia UK's work is improving treatment and healthcare for people affected by ataxia.

Due to the rarity of the ataxias, many healthcare professionals will not be familiar with them. In the Healthcare Professionals area of the website, you can find out how to refer patients to a specialist clinician or one of our Specialist Ataxia Centres; access our Ataxia Medical Guidelines and other publications to advise how to treat people with ataxia, and training opportunities.

We work closely with healthcare professionals with expertise in ataxia and are keen to engage with others and provide support where needed. Ataxia UK has a Medical Advisory Panel who provide advice to the charity.

You can also apply for a grant or search for on-going healthcare research projects.

Staying up to date

Join our Medical Professionals Registry to stay in touch with us, and access the most up-to-date advice and information.

Keep an eye on our Ataxia Training Days page to read more about our training opportunities for speech therapists, neurologists, clinicians and physiotherapists (and more) that raise awareness and understanding of ataxia through seminars from researchers and presentations from ataxia patients.

For your patients

If you have a patient with ataxia and would like to receive an information pack in the post, please contact the Helpline ([email protected]). Please do refer your patients to join Ataxia UK free of charge and access our services. We will be happy to send you joining forms, also accessible through the Helpline ([email protected]).


Improving Healthcare And Treatment

Ataxia UK works in partnership with other organisations to campaign for better healthcare services for people with ataxia. We are active members of the Neurological Alliance, the organisation that campaigns for people with neurological conditions and various Friends of Ataxia UK are involved with local branches of the Neurological Alliance. Ataxia UK is also a member and works closely with Genetic Alliance UK and Rare Disease UK, the umbrella organisations working for people with genetic conditions and rare conditions respectively.

Ataxia UK’s CEO is also actively involved in influencing NHS policies by being a member of the NHS England Commissioning Board Specialist Services Commissioning Public and Patient Engagement Steering Group. The group has overseen all of the patient and public involvement in the consultations over the design of the new structures and clinical services of the NHS. In the light of the prominence given to the Patient Voice in the ‘new’ NHS, this group has been one of the most important fora of relevance to people affected by ataxia, to which the voluntary sector has had access. This group was a transitional group and has now been replaced by Public and Patient Voices Assurance Group for Specialised Commissioning.