Panorama ME Investigation Campaign

All this should be properly looked into and sorted!

I want rid of this illness, more help

10 years ago Featured

Suffered 15 years and I'm bedridden now! My doctor told me the other day to go for a walk and get some sun! I'm photosensitive so can't and I also have spondylitis so can't walk! They took my pain pills and have left me to rot!

Pls help ud

Let the truth be revealed so people can be treated with respect as they battle this life changing illness.

I have m.e and Fibromailagia and would love people to no more about it and get cures etc it's horrible life changing illnesses

here you go guys, I have followed and supported many of you religiously on varies petitions, Please can you return the favour and sign this for me sue x

My life is a living hell since CFS (ME)/fibromyalgia! Can't work, can't relax, can't do anything and i'm really suffering. In Belgium most of the doctors act as if you're a mental patient and you're not sick at all! :/ I would like that researchers really put some effort into solving ME/fibrmyalgia! Antwerp, Belgium.

My life has been destroyed by this illness. My partner has suffered for last 27 years also and has lost his whole adult life to a devastating illness.

Please

I'm an ME sufferer as is my sister...we need answers like all other illnesses get!

Long term ME sufferer! Tired of watching other illnesses and diseases getting funding and research and positive media coverage and ME sufferers treated like whinging malingering leeches forgotten by medicine, society and government!

Please sign everyone

Defiantly needs to be investigated.

I have had ME 24 years and despite a growing amount of evidence that shows it is a neuro-immune disorder in the UK we are still treated as if we have a false illness belief. We are a mistreated community that has been neglected by the UK government despite the extremely severe suffering that some ME patients endure every hour. Why have secret files been locked away for so long? Why does there NHS continue to only offer GET and CBT when it has been shown that over exertion causes damage and many patients are made worse for years following this treatment?

Mod to severe ME for 13 years.

I currently receive disability forME/CFS Before I could get disability I had to undergo a psych evaluation as part of the processAlong with numerous other physical examination from many many -"ologists" I can assure you the psychologist found out that my IQ is above average.And certainly this illness is not psychiatric by nature in any way shape or form.I could go on forever and ever but I won'tJust remember the old adage never judge a book by its cover and there's always more to the story than what you seeI don't look sick on the outside But if I didn't take 11 prescription medications dailyI wouldn't be typing this messageMuch less get out of bed or even be able to walk to the bathroomAnd that's just the fact of life for me for the past 25 years

this senseless tyranny will come to an end one day-why not sooner than let any more suffer without hope.