Personal Stories of ME Sufferers
 

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Now, nearly eight years later, going from a student at the top of my class with an unlimited future to a dependent, rather helpless person with no real hope for healing is something that only others in this situation can understand.....................     .... read more


So now it looks like I will have this illness forever. It has taken some of my personality away but I fight each day to preserve the bit of me I still have....................     .... read more


I would say that the M.E started off quite moderately. I suffered with feeling as I had with the Glandular Fever, only with worsening symptoms! Now at 35 I'm 99% bedridden, I am paralysed down the right hand side and in both legs. I am incontinent and have a supapubic catheter fitted through my stomach into my bladder...................     .... read more


It's a continuous FIGHT with the disease, with the doctors (lack of interest or knowledge), with relatives (lack of understanding) and life itself. .......... .... read more


All that is available for me in the way of 'treatment' is CBT and GET. Even though, I relapsed very badly on an aggressive GET programme. In spite of WHO classification of ME as physical condition - it's a neurological illness not a psychiatric condition - and despite the excellent Canadian Guidelines published last year, it is impossible to find a consultant within the NHS with a biomedical approach to this illness. .............. .... read more


I was interviewed by this supervisor every Monday and every Friday from then on. I felt like I was a criminal. She took me into a small office and every time asked how I was doing and how long would it be before I worked full time again because I was straining the section as they had to cover for my absence..................     .... read more


After the examination he said that my MRI scan was clear, therefore there was nothing he could find wrong with me. He said that I should go back to work! I mentioned the possibility of it being M.E. but he said that he knew nothing about it. That was the end of the consultation, and I was discharged from his care. .      .... . read more


A nurse friend told me it was very like something called Royal Free disease she had witnessed when she worked there. So I started to look into it and determined to rest now instead of "getting fit" as the doctors had been advising.      .... . read more


It would help if you had a supportive family who understood it but mine are not that kind of family. It is not a nice illness to have.     ..... read more


I am still waiting for a proper diagnosis as well as my doctor believes that I have ME and I have had lots and lots of blood tests, etc, but he has referred me to a specialist and I am still waiting for the appointment.     ..... read more


At work I have been asked to go to see the company doctor as no-one believes I'm unwell yet they see me struggling to walk on occasions!     ..... read more


M 

An experience of Graded Exercise Treatment for a person with ME.     ..... read more

After hearing my story, viewing my countless blood tests, x-rays, internal examinations and MRI results and a thorough examination, the neurologist immediately suspected that I was suffering from ME. He asked me to look up the internet and check if all my symptoms were recorded on an ME patient's list of complaints. Suddenly everything started to make sense and the relief was priceless. A visit to a sensitive and patient physician, confirmed the neurologist's diagnosis.     ..... read more

Jan 

We arrived at the doctors and the female doctor refused to see me, saying I was not her patient, and she wasn't prepared to see me. I was just in a state of shock and my partner was furious. The Doctor in question didn't come out to the waiting room to see me, instead wrote a prescription for three months of anti-depressants     .... . read more

Who am I?      ..... read more

My family called the doctor to the house on one occasion after I had become too weak to walk or talk and couldn't make the bathroom without assistance.

The GP advised me to go out for a jog in the sunshine.     ..... read more

Despite strenuous efforts on my part to keep well and fulfil my duties to the best of my capabilities, I suffered a complete collapse in September, 2003 and was almost bed-bound for many months.
I have been unable to work full-time since then and even very small, part-time jobs cause the flu-symptoms, severe headaches, blackouts, loss of balance, nausea, weak limbs, IBS, brain-fog and exhaustion  to start up again.     I'm one of the lucky ones.    ..... read more

The months passed still unwell, unable to work and I was made redundant from my job, I took them to court for unfair dismissal and won my case. The stress set me back and combined with battling doctors for more tests and trying to convince them I was not depressed but ill was even more distressing.
You desperately want to get better, get back to work, to the life you had before, to socialise, to be able to read and cook and have conversations without your words getting all mixed up. To get through the day without collapsing on the sofa exhausted..... read more

I was subjected to a regime of the threat of physical torture, bullying, intimidation, scorn, derision, lies, deception, malice, and above all hatred. The stress and emotional torment induced in my mind was extreme beyond description...... read more

Just one disaster on top of another!  But it all started with the stupid TMJ..... read more

I felt humiliated and ridiculed by someone who was clearly a psychiatrist of some description....... read more

I remember asking my doctor one day when I would stop feeling so tired!!! ...... She said give it time,....... read more

How do I deal with family that say things like "stop researching that...don't you think your just wallowing in it just the more?" How do you stop looking for answers? When is it time to give up? Why don't people that have known you all their lives...know you and what your suffering is REAL?? Why do doctors still say this doesn't exist and yet look at many of us ...completely destroyed by this disease....... read more

When I try to get medical care, the strain of trying to convince someone I am ill and the hurtful things they say to me practically make me crack up. Just the physical demands of leaving the house, even in the wheelchair, are enough to make me sicker for weeks. I can't describe how ill it makes me. ...... read more

My GP thought I had ME but kept saying, work through it, do lots of exercise you'll get over it. They sent me to a sports centre to do a fitness course but I went once and never again. It was about this time I saw the psych and he said there was nothing mentally wrong that feeling well again wouldn't fix. ...... read more

Blaze  

At this time last year i was able to still care for my own needs butt as the summer progressed so did my illness...... read more

Gary  

I was assessed for one ME clinic but they said I was too disabled and that there were other issues that needed to be worked on. They also said that because I was confined to a wheelchair they thought that would be too upsetting for the other members of their group...... read more

Alice  

In 2004 when I was 24 I became acutely ill with the Epstein Barr virus and was admitted to hospital with severe anaemia and jaundice. I had become so ill but did not seek advice from my doctor because my fears of being disbelieved are still with me to this day. ...... read more

Angela  

I was a happy normal child. I was 14, had friends, a happy home and a LIFE.
This, as I was about to find out, was all going to change...... read more

Wendy  

I fell ill with the flu the same time as Antony, my then boyfriend/fiancé. He got over it, I didn't.....

It was a struggle to get the illness recognised.... read more

Di  

Diagnosed with "very severe Myalgic Encephalomyelitis (ME) 80% disabled" after becoming profoundly ill in 1984, with what followed a "sever bout of flu".

Unable to move my legs, arms and hands.......... read more

Judith  

Originally written for ME Awareness 2003 Judith's story tells of her experiences.

Since suffering with this illness I have reached an all time low in my life.
At 36, I was a happy-go-lucky Mum who was mad enough to try anything, go anywhere...
.... read more


Lauren  

I had just turned 12 when I first started to feel ill. For months I assumed it was a succession of bug and viruses, Glandular fever was brought up as a possibility. It was only on looking back that I realised I wasn't "shaking this off"..... read more


Joan 

Up until 1999 I had been a fit, active person. I enjoyed long distance cycling, hill walking, sailing, and skiing. I enjoyed a very active social life and a challenging job managing an oil refinery. I got a buzz out of living a full life and I did not prescribe to the notion that stress is bad for you; for me, a challenge was a good thing.... read more


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