I had a roommate with the disease M.E and he was forced to take heavy anti-psychotic drugs everyday which made him worse and they kept forcing him to take it. I was in a mental hospital with him in 2009 and they forced the same drugs on me also which made me throw up for 3 months which in the end gave me M.E destroyed my immune system. I haven't heard from my friend since 2009 when was was forced to take drugs as he was sectioned for having M.E, horrendous what I witnessed him go through, MY GOD
Linda I had a roommate with horribleM.E in 2009 and he was forced to take heavy anti-psychotic drugs against his will as he was sectioned. The psychiatrists were horrendous as to what they were doing to him they were making him worse not better. It is Mark here and I have mild M.E and have had it for 1 year 1 month now as I was given a medication that I also had to take which made me throw up for 3 months and destroyed my immune system etc thus giving me M.E and I can't do anything about it now.
I was put on a medication that made me throw up for 3 months and I am off of it now but it destroyed my immune system and now I have M.E from the result of taking the drug which I had to take.
Does any1 here believe that our bodies have the ability to heal themselves? I do. I have had ME/CFS for 5 years now and have used these 5 years 2 study presonal development, health & nutrition. I have learnt a lot from books such as The China Study (the most comprehensive study of nutrition ever conducted), Dangerous Grains, Sick & Tired & many more. The work that Dr R Young is doing on the cause of ANY disease is amazing. I am on day 12 of a 200 day challenge to heal my ME. And I will do it :-)
When will psychiatrists leave this illness alone? I don't want a psychiatrists opinion, because I do not have a mental illness. Me and millions of others would do anything to be free of our M.E.. I'm not continuing this because I am lazy, I am living with it because it's not leaving me.
I have a great psychiatrist who has helped me just the opposite way. He believes in me. He marvels at my SURVIVAL and the plight of 'us', all in a virtual medical school whether you like it or not because : 1. Invented it for info and fun; 2.some patients know more than their doctors, especially about dysautonomia.
We are SURVIVORS.
If you find me on FB, you can read some of Dr J's comments about life, forgiveness, peace, and ..... fighting when you know you are right. Stay with us. Dr M
And remember the shrinks will say having a 'supportive' GP is bad for us. That we have somehow managed to make them believe we are ill when we are actually 'hysterical' and suffering form somatoform disorders....
And being articulate is likely to make this more likely....
When will normal people located everywhere come to their senses? The unbelievable conduct reigns and everyone is under the illusion "it could never happen to me"
What a naive and very wrong approach!
Chronic and very serious illnesses are at an all time high! And the private "insurance" policies or "co-pays" won't help.
Why is the huge amount of money paid to "Pathways to Work" not actually spent on finding real medical cures for ME & MS?
I'm in the US, too. I have a horrible doctor. Both she and her partner don't believe in the illness. So every time I go, they ask me stupid questions, like can't it just be panic attacks. I don't feel I'm getting any treatment. And I'm mostly housebound. All the doctors ever do is make me worse. So I rarely go anymore. I feel very much left on my own.
I'm very chemical sensitive. I'm also weather sensitive. The list just goes on and on. I've got a million symptoms and no treatments.
I had a roommate with the disease M.E and he was forced to take heavy anti-psychotic drugs everyday which made him worse and they kept forcing him to take it. I was in a mental hospital with him in 2009 and they forced the same drugs on me also which made me throw up for 3 months which in the end gave me M.E destroyed my immune system. I haven't heard from my friend since 2009 when was was forced to take drugs as he was sectioned for having M.E, horrendous what I witnessed him go through, MY GOD
835283 1 year ago
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Linda I had a roommate with horribleM.E in 2009 and he was forced to take heavy anti-psychotic drugs against his will as he was sectioned. The psychiatrists were horrendous as to what they were doing to him they were making him worse not better. It is Mark here and I have mild M.E and have had it for 1 year 1 month now as I was given a medication that I also had to take which made me throw up for 3 months and destroyed my immune system etc thus giving me M.E and I can't do anything about it now.
835283 1 year ago
I was put on a medication that made me throw up for 3 months and I am off of it now but it destroyed my immune system and now I have M.E from the result of taking the drug which I had to take.
future273 1 year ago
My friend was sectioned for having M.E
future273 1 year ago
Does any1 here believe that our bodies have the ability to heal themselves? I do. I have had ME/CFS for 5 years now and have used these 5 years 2 study presonal development, health & nutrition. I have learnt a lot from books such as The China Study (the most comprehensive study of nutrition ever conducted), Dangerous Grains, Sick & Tired & many more. The work that Dr R Young is doing on the cause of ANY disease is amazing. I am on day 12 of a 200 day challenge to heal my ME. And I will do it :-)
alexsantoro 1 year ago
I love the name of this video! Keep it up! We will raise awareness & find a cure together! I appreciate all you do!
ironbith 2 years ago
greetings from Germany!
let´s fight our common enemy:
CFS/CFIDS/ME
!
FallaciesDetective 2 years ago
Thank you for speaking out.
MaverickMiracle 3 years ago 6
Im sensitve to so many things aswell! Mold paint fumes alcohol cold weather.
essy111 3 years ago 2
i get worse like anything around those things too. others tell me the same.
pilomaya2012 2 years ago 2
Well said, guys :)
When will psychiatrists leave this illness alone? I don't want a psychiatrists opinion, because I do not have a mental illness. Me and millions of others would do anything to be free of our M.E.. I'm not continuing this because I am lazy, I am living with it because it's not leaving me.
M.E sufferers do not relish in their inabilities.
theinnerlight87 3 years ago 9
I have a great psychiatrist who has helped me just the opposite way. He believes in me. He marvels at my SURVIVAL and the plight of 'us', all in a virtual medical school whether you like it or not because : 1. Invented it for info and fun; 2.some patients know more than their doctors, especially about dysautonomia.
We are SURVIVORS.
If you find me on FB, you can read some of Dr J's comments about life, forgiveness, peace, and ..... fighting when you know you are right. Stay with us. Dr M
DysautonomiaMD 2 years ago
And remember the shrinks will say having a 'supportive' GP is bad for us. That we have somehow managed to make them believe we are ill when we are actually 'hysterical' and suffering form somatoform disorders....
And being articulate is likely to make this more likely....
deadgirldreaming 3 years ago 8
Thank you again Greg and Linda.
I am constantly amazed by the government's ill disguised abuse of those with chronic illnesses and disabilities.
I lay in bed and listen to e.g. the Today Programme and every few days there is yet another unchallenged report about IB numbers etc.
I did notice there was a challenge to this view on the BBC site yesterday.
And with ME the problem is worse due to the shrinks view.
You are both so inspiring.
deadgirldreaming 3 years ago 7
We all appreciate your wise words, that you speak on behalf of the severe ME community - who remain ignored by the medical profession in the UK.
The fact that Greg and Linda are prepared here to make a video response, yet the medical profession remain silent - sums the situation up nicely!
Remember: The guilty shirk away and deny all responsibility, whilst the oppressed scream in pain.
We all feel your pain, and offer you both our support and good will - as always.
Thank you.
luminescentfeeling 3 years ago 6
Thank you Greg and Linda!
When will normal people located everywhere come to their senses? The unbelievable conduct reigns and everyone is under the illusion "it could never happen to me"
What a naive and very wrong approach!
Chronic and very serious illnesses are at an all time high! And the private "insurance" policies or "co-pays" won't help.
Why is the huge amount of money paid to "Pathways to Work" not actually spent on finding real medical cures for ME & MS?
So many have been misled!
StopUnumNow 3 years ago 6
I'm in the US, too. I have a horrible doctor. Both she and her partner don't believe in the illness. So every time I go, they ask me stupid questions, like can't it just be panic attacks. I don't feel I'm getting any treatment. And I'm mostly housebound. All the doctors ever do is make me worse. So I rarely go anymore. I feel very much left on my own.
I'm very chemical sensitive. I'm also weather sensitive. The list just goes on and on. I've got a million symptoms and no treatments.
Carrigon 3 years ago 6