Discovering that you or a loved one have Huntingtons Disease can be frightening and overwhelming but there is help at hand to provide support and information every step of the way.
At HDANI we have a small but dedicated team of staff and volunteers and while we cannot be there 24 hours a day 7 days a week we do our very best to provide as much help and support as we can.
We are not medically trained and cannot be experts at everything so we work closely with all kinds of health care professionals and other organisations to provide the tailored support and information you need.
As HD is a rare disease some health and social care professionals won't have heard of it or had any direct experience so we can provide information,resources and training to help improve their understanding and ultimately get the best outcomes for patients and carers. We can speak with your GP, social worker, occupational, speech and launguage or physio therapist, pharmacist, care workers, counsellors or even your employers and help them understand the needs of you or your loved ones.
We are fortunate to be part of a global network of HD support associations who share vital information and resources. You will find lots of information on our website about HD as well as practical tips and advice about caring and planning for the future. We also have a range of resource aimed at various health and social care professionals to help guide them in their treatment and support of patients and families.
It is important to stress that Association members are not qualified to dispense medical advice, however, many members of the Association are ‘experts’ in the daily realities of living with HD. HDANI can offer years of knowledge and experience to help you through any emotional and practical difficulties you may encounter.
Access to our services is free.