A message of hope to all ME Sufferers
For many months now there has been a raging debate between myself and members of the ME community.
I invertedly upset the lazy bastards, sorry ME sufferers of the world by stating they should not get blue badges.
Here’s my message of hope for every ME sufferer - You one day could be as awesome as paralysed people and overcome adversity!
Oh no, I forgot, this will never happen, because you have no energy. How many other people do you think would love to stay at home all day and bury their head in the sand? Millions would, but millions don’t because they have pride and a sense of determination.
ME is all in the head - simple as that. If ME is an actual illness then Gordon Brown’s a great Prime Minister.
For those of you that have not read the original post, feel free to see what I wrote on Fake Parking Badges which caused such controversy.
Not bothered about reading it? Well to cut a long story short I stated that ME sufferers should not get blue parking badges - this kicked off a complete stink, and the bitter twisted lazy bastards, (sorry, I’ve done it again) ME sufferers lashed out with comments they thought would offend me.
Well to all the lazy bastard ME sufferers, get this, your pathetic attempts to offend me did not work. I still stand (sit) by what I wrote/said.
As far as I am concerned ME is the disease of lazy sods and for people who cannot face life - GET OVER IT.
And before you all start, no I am not medically qualified, but I am entitled to my opinion, and just because my opinion is not PC and does not agree with yours , ou all suddenly found the energy to have a go.
I will reiterate my point - if you can sit at a computer and surf the net then you can bloody well work. It’s funny how you have the energy to surf the net!
So for all the shirkers who use ME as a front because you are weak, lazy and downright pathetic, keep wishing me bad luck in your comments as it does nothing more than make me laugh and highlight the truth actually hurts!
Written by MrCrip on July 10th, 2008 with
2 comments.
Do you agree with
MrCrip? Do you hate the diatribe on MrCrip? Who cares? Read more
Disability Views.
#1. August 21st, 2008, at 9:28 AM.
Sophia Mirza got ME when she was 26. She was severely ill, in pain, housebound. Her doctor believed M.E. was in the mind. Sophia was sectioned. Her conditioned worsened, After two weeks she was released, but did not recover. She died aged 32.
Her body was examined by two neurologists. They found that 80% of her spinal cord was inflamed, similar to the inflammation seen in virus infection. Sophia was not examined by a neurologist until she was dead.
Casey Fero got CFS when he was 9. He was not as severely ill as Sophia, and managed to continue at school, although he had to endure doctors and teachers who did not believe he was really ill. Casey died when he was 23. The autopsy said “Casey died of myocarditis, that is, his heart was infected with disease. There was inflammation, and the tissue was full of viral infection. Casey also had old fibrosis, indicating that the viral infection was not of a new onset.”
Alison Hunter also became ill while at primary school. “Alison did not want to withdraw from school. “She was so desperate to participate,” says Christine Hunter, who at her daughter’s insistence bought her school uniform gym kit even though she could not use it. After a remission in the first bout of illness, at age 10, Alison went back to school swimming lessons but taking it easy was against her nature; she swam laps until she collapsed.”
Alison died when she was 19. “In the end, heart damage, massive ulceration to her throat, failure of her gut and bowel and horrendous neurological symptoms, conspired to defeat her.”