ME IS PHYSICAL in the body it's there through an infection a complicated infection of course it effects the mental but that's after , after the devastating effect on the physical body.
C
Catherine Murney
10 years ago
Had M.E CFS for over 30yrs can't do house work or most daily tasks, cooking, showering etc?? Family, friends and mostly doctors don't understand this awful illness. This is not a life its just existing. Please help
M
Martina marks
10 years ago
It's about time something was done about this issue
A
Alison
10 years ago
Invisible illnesses need looking into to!!
K
Kerryn Groves
10 years ago
It really is about time this very complex illness is taken far more seriously and money is spent on biological research to find a treatment or cure.
A
Adele Hirst
10 years ago
I'm sure we would all like some help on this, sick of being sick :(
D
Dawn
10 years ago
We need more understanding!
M
Melvyn Readman
10 years ago
I support campaign.
A
Amanda mann
10 years ago
I am a M.E sufferer
A
ann hayes
10 years ago
When is the medical profession going to get it through their head that. M.E.is real. Love to see a doctor get this, who does not believe it is real. Wonder what his reaction would be
M
Mike lingard
10 years ago
My wife Pat is now in her 7th year suffering this debilitating disease, she is virtually bed ridden, we need help.
B
Bethanie Warren
10 years ago
My I know a lot of people with ME including my mum and a lot more research needs to be done. So many people are uneducated.
R
ROSEMARIE JONES
10 years ago
DISS
GUSTING
DISGUSTING
T
Theresa mcmullan
10 years ago
We all need help please help us. I am fighting a loosing battle every day. Pain everywhere and severe fatigue. I just want a normal life like I used to have.
P
Paul Dacre
10 years ago
Psychiatry, in relation to this most serious disease, must be investigated.
C
Claire Taylor-Jones
10 years ago
I am an ME sufferer and believe more research should go into this cruel illness.
F
fiona
10 years ago
ME/CFS patients & their families need much more research & support.
M
Michelle walsh
10 years ago
Help us become visible by our doctors and recognised as physically sick.
K
keith sutcliffe
10 years ago
Knowing people with this who have to miss weddings and going out at times this does need proper research by doctors.
A
Audrey Skilton
10 years ago
This is a genuine debilitating disease and should be treated as such.
ME IS PHYSICAL in the body it's there through an infection a complicated infection of course it effects the mental but that's after , after the devastating effect on the physical body.
Had M.E CFS for over 30yrs can't do house work or most daily tasks, cooking, showering etc?? Family, friends and mostly doctors don't understand this awful illness. This is not a life its just existing. Please help
It's about time something was done about this issue
Invisible illnesses need looking into to!!
It really is about time this very complex illness is taken far more seriously and money is spent on biological research to find a treatment or cure.
I'm sure we would all like some help on this, sick of being sick :(
We need more understanding!
I support campaign.
I am a M.E sufferer
When is the medical profession going to get it through their head that. M.E.is real. Love to see a doctor get this, who does not believe it is real. Wonder what his reaction would be
My wife Pat is now in her 7th year suffering this debilitating disease, she is virtually bed ridden, we need help.
My I know a lot of people with ME including my mum and a lot more research needs to be done. So many people are uneducated.
DISS GUSTING DISGUSTING
We all need help please help us. I am fighting a loosing battle every day. Pain everywhere and severe fatigue. I just want a normal life like I used to have.
Psychiatry, in relation to this most serious disease, must be investigated.
I am an ME sufferer and believe more research should go into this cruel illness.
ME/CFS patients & their families need much more research & support.
Help us become visible by our doctors and recognised as physically sick.
Knowing people with this who have to miss weddings and going out at times this does need proper research by doctors.
This is a genuine debilitating disease and should be treated as such.