Compel the NHS to trace and contact people at risk of Huntington’s Disease

The NHS has a confused, inconsistent and arbitrary approach to HD; because the disease is not treatable, it is not seen as serious enough to require medical staff to breach their patient’s confidentiality in order to tell people who are at risk. However, the NHS will not provide genetic testing on demand, forcing people to have counselling prior to testing, even then maybe denying a test to people whom they feel are not robust enough to cope with knowing they carry they gene.