I have just read a post from May this year and ironically have just won the war with my doctor over their lack of treatment and duty of care. The same thing had happened to this lady, albeit across the pond in the USA. I also have been gaslit, ignored, told me it was meds making sleep for up to 36 hoots every week for the past five years. I’ve gone from working with children in a school setting and had done so for twenty years. To now living in my bedroom as more comfortable for me with my chronic back pain.
I have come to the stage of writing pre legal action against the practice and complained to the Quality Care team as this should not be happening to anyone who is suffering in this way. To read this great post about the sane treatment in America fills me with dread, how long shall we sing this song. Help please doctors, that’s what you became a doctor for, or is because my disability is unseen you do not see or hear me anymore. I have at last been referred to a ME:Chronic Fatigue Syndrik clinic, be my doctor but the waiting list is horrendous. Mind you isn’t that proof there are so many people begging for help out there. It’s very scary and should not be happening. I’m just glad I opened up this post and realised I am not alone.