Right to Know campaign - diagnosis and support
Everyone with dementia has a Right to Know
Imagine feeling ill but being told your new symptoms and behaviour were just a natural part of ageing. Imagine having a condition but no treatment, information, or support to help you manage it. Imagine if your doctor knew about your condition but chose not to tell you, as they thought nothing could be done to help.
For many people with dementia, this is the reality. Denied a diagnosis, denied treatment, and denied the chance to plan for the future while still able to do so.
At Alzheimer's Society we think this is wrong. We think everyone with dementia has a Right to Know. A Right to Know about their condition in order to tackle it head on. A Right to Know about the information and advice available to them. A right to be fully supported after their diagnosis. This is not a lot to ask, and only what people deserve.
Sign up to our campaign for change email - a quick and easy way to add your voice to this campaign and others that will improve the lives of people living with dementia.
With your help, we can ensure everyone with dementia receives the certainty of a diagnosis and the right information and support to come to terms with, and manage their condition.
What happens currently?
- Over a third of people with dementia in the UK do not receive a formal diagnosis.
- The length of time you have to wait to receive a diagnosis varies hugely depending on where you live, from two weeks to over six months.
- Once diagnosed, many people are not given adequate support to come to terms with and manage their condition. A recent Alzheimer's Society poll found that 90 per cent of people felt unsupported after their diagnosis.
What is Alzheimer's Society calling for?
We want the Government and the NHS to do more to support people with dementia as they receive their diagnosis and immediately afterwards.