When I wake up with post-exertional malaise, there is an elephant sitting on the mattress. “I feel like I wake up with a mattress on me most mornings. It is like being on a carousel: you have ups and downs but you can never get off.” The way you would feel at the end of that is how it feels to have M.E. “It’s like having glandular fever, taking your glandular fever on an all-night drinking binge, then taking your glandular fever and your hangover and doing a 30km forced march over the Brecon Beacons. Our booklet, Newly diagnosed with M.E., has advice for you and your GP, facts about M.E., guidance to help you be an active partner in your own care, suggestions for questions for you to ask your GP and information about existing guidelines. This section gives you more information about M.E., including possible causes and sub-groups within the disease. This is similar to many other chronic illnesses. Some people find that they don’t go back completely to the way they felt before they became ill, but they do recover sufficiently to lead happy and fulfilling lives. Some make good progress and may recover, while others can remain ill for a number of years and may not get better. can vary enormously in their experience of the illness, and also how long their symptoms last. Not everyone will experience the same symptoms so it's important not to compare someone who has M.E. experience debilitating pain, fatigue and a range of other symptoms associated with post-exertional malaise, the body and brain’s inability to recover after expending even small amounts of energy. affects an estimated 250,000 people in the UK, and around 17 million people worldwide. Myalgic Encephalomyelitis (M.E.) is a long-term (chronic), fluctuating, neurological disease that causes symptoms affecting many body systems, more commonly the nervous and immune systems.
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |