Andy
Senior Member (Voting rights)
A blog about personal experience of PACE recommended 'treatments' published earlier this year.
https://mookpixie-chronicills.blogspot.com/2018/03/the-pace-trial-complaint.htmlThe PACE trial - a complaint.
This is a tough read - I make no apologies for that. I felt it was important to share my experiences of how the PACE trial has indirectly affected me, and so the following is an excerpt from my letter supporting Dr Sarah Myhill's campaign against those responsible for the trial. If my story moves you in any way and you wish to help, please sign the petition supporting Dr Myhill's complaint, available here.
I first became ill in August 2011, when I came down with a nasty viral infection that lasted several weeks. I was diagnosed first with a chest infection, and then a sinus infection and although both went away with antibiotics my body never really recovered. I began to suffer with aches and pains all over my body as well as swelling in my hands and feet. I tried carrying on with daily life and going to work (I was an Infant School teacher) but eventually my body gave up on me. I was signed off work at the end of September and unable to do anything except lie in bed and sleep. Since then, I have not been well enough to work at all. My doctor diagnosed Post Viral Fatigue just before Christmas 2011 and then when I was still no better by October 2012, my diagnosis was changed to ME/CFS.