These resources are for people with Severe or Very Severe ME, their carers, families, and advocates. They are especially useful in hospital or care settings where there is little understanding of severe ME, or where a patient’s needs may be overlooked or denied.
The resources provide guidance for talking with health and social care professionals and help ensure the challenges and needs of those affected are recognized.
Severe ME: Tools for patients, carers and advocates to navigate care settings
Disclaimer: The information in this post is for general information purposes only. While we endeavour to keep the information up to date and correct, we make no representations or warranties of any kind, express or implied, about the completeness, accuracy, reliability, suitability or availability with respect to the post or the information, products, services, etc contained in the post for any purpose. Any reliance you place on such information is therefore strictly at your own risk.The suitability of any solution is totally dependent on the individual. It is strongly recommended to seek professional advice and assistance.
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