I had a roommate in the mental hospital I was in 2009. He had the disease M.E and the psychiatrists forced heavy anti-psychotic drugs on him without his consent and he had no choice but to take them. They made him so much worse it was HORRENDOUS watching him suffer from what the psychiatrists were doing to him, I am only 22 and have witnessed the worst of the worst, they gave me a medication which I had to take and it made me throw up for 3 months giving me M.E as it destroyed my immune system.
I can so relate to what you are experience. I didn't have the jerking, but I felt frozen in pain many days. It was awful & so frightening. My right arm would tremor & the pain was excruitiating. I couldn't move to get any meds, water or the phone. Thank god that has subsided, but I am in bed in chronic pain 95% of the day. My late 20's kids haven't talked to me in a few years. The one told me to see a psychiatrist or he would get a restraining order. The R.O. was up 2 days ago!
My best wishes for you both, and for all ME/CFS sufferers and their loved ones. Thank you for what you are doing. I believe it will have a positive impact. Thank you for sharing your insights and this part of your lives in this way. Your courage, love, and hope are beyond inspiring.
Linda you are so brave to have done this and speak so well. This should be required viewing for them all at the Gibson Enquiry, all at the Nice review and all doctors in training.
You're right Jas, The Gibson enquiry should be viewing this. So I hope you don't mind, Greg and Linda, but I have e-mailed Dr Gibson about your videos in the hope that at least he may be influenced by this powerful testimony.
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lightpeaceloveify 8 months ago
I had a roommate in the mental hospital I was in 2009. He had the disease M.E and the psychiatrists forced heavy anti-psychotic drugs on him without his consent and he had no choice but to take them. They made him so much worse it was HORRENDOUS watching him suffer from what the psychiatrists were doing to him, I am only 22 and have witnessed the worst of the worst, they gave me a medication which I had to take and it made me throw up for 3 months giving me M.E as it destroyed my immune system.
835283 11 months ago
I can so relate to what you are experience. I didn't have the jerking, but I felt frozen in pain many days. It was awful & so frightening. My right arm would tremor & the pain was excruitiating. I couldn't move to get any meds, water or the phone. Thank god that has subsided, but I am in bed in chronic pain 95% of the day. My late 20's kids haven't talked to me in a few years. The one told me to see a psychiatrist or he would get a restraining order. The R.O. was up 2 days ago!
kozmoproduction 2 years ago
My best wishes for you both, and for all ME/CFS sufferers and their loved ones. Thank you for what you are doing. I believe it will have a positive impact. Thank you for sharing your insights and this part of your lives in this way. Your courage, love, and hope are beyond inspiring.
discordis 5 years ago
Thank you for your bravery. Maybe through the internet we can get people aware of this horrible illness.
smiller693 5 years ago
Linda you are so brave to have done this and speak so well. This should be required viewing for them all at the Gibson Enquiry, all at the Nice review and all doctors in training.
Thank you for doing this on our behalf.
Jas
devongirlme 5 years ago
Thank you and bless you.
thank you for all your supportive comments.
love Linda
gregcrowhurst 5 years ago
You're right Jas, The Gibson enquiry should be viewing this. So I hope you don't mind, Greg and Linda, but I have e-mailed Dr Gibson about your videos in the hope that at least he may be influenced by this powerful testimony.
ivortick 5 years ago