
‘I lived, Maeve died’: ME patient who got help writes to coroner
https://www.thetimes.com/article/36f4961d-b02f-476d-ba4f-3dea1bff8f72?shareToken=5a8a2ad15fb4ba78e17552760e0f399f
by cuzbrushtruewood

‘I lived, Maeve died’: ME patient who got help writes to coroner
https://www.thetimes.com/article/36f4961d-b02f-476d-ba4f-3dea1bff8f72?shareToken=5a8a2ad15fb4ba78e17552760e0f399f
by cuzbrushtruewood
5 comments
This is truly moving it’s crucial to highlight these stories to improve awareness and support for ME patients. My heart goes out to Maeve’s family and all affected by this condition 😔
They aren’t even from the UK, this isn’t the me support sub, it’s a sad condition but I don’t get why this has been posted
I read this story. It’s saddening and disgusting at the same time. I have family with ME. All symptoms are different. I have symptoms but my GP says not.
At this point, we are going to need an ME mega thread.
All this me spam is kind of bringing it full circle. I felt bad for sufferers but an article everyday, making them seem a bit whiney.