It's about time we kicked back, I have been deemed fit for work by a 'medical professional' from the ATOS team and have ESA taken away and I can't get jobseekers as I have a £400 a month occupational pension I'm expected to survive on. I also have a report from the ME specialist consultant who writes the NICE guidelines on the condition that says in black and white I should not work as it would be severely detrimental to my health. ATOS and the Prime Minister and Chris Grayling DWP...
It's about time we kicked back, I have been deemed fit for work by a 'medical professional' from the ATOS team and have ESA taken away and I can't get jobseekers as I have a £400 a month occupational pension I'm expected to survive on. I also have a report from the ME specialist consultant who writes the NICE guidelines on the condition that says in black and white I should not work as it would be severely detrimental to my health. ATOS and the Prime Minister and Chris Grayling DWP completely disregarded this. I wonder if the PM's wife had ME he would make he go out to work? NO I think not! x
That is a joke...these professionals have no idea of the real world and how any illness affects our ability to live and work without pain and stress.. They should be made to spend time with you so they see 1st hand what you suffer, not read about in a book...unfortunately Pam you need to be foreigner who has come here with no prospects...
Oh Pam, that is just awful! Hugs. Xx
What is happening with this Country?
Hope you're ok Pamela
Big hug xxx
good luck with this petition. yes we do suffer. life is impaired. I have absolutely no support from any service. it is abysmal.
It's terrible Lou on all counts!
'tis petal ! XXX
hi robert !! yep. still battling for the dla !! not succeeding as yet, but god loves a trier !! LOL !! advocacy, is just what i need. have started phoning round today funnily enough !! fingers crossed i find someone !! watch this space !!! hope you are well. XXX
Ok, lets get the balls rolling.. no not Camerons.. I'll sign.. as long as all yes ME sufferers all take a month long look at a Flouride free water month.. not too much to ask? (N.B. water filter isn't going to cut it..this toxin is too soluble).. and No I'm not 'Waterboy'..
I think if one of Camerons Relatives had M.E then maybe he would realise what a struggle our life really is!
my doughter has m e and get no supprot so please sssssupport them.
I have severe ME and I cannot function daily living tasks.
Geef ze een duwtje, is ook in ons voordeel.
I have had M.E for 14 years now and it is something I have to live for now!
hi debbie cliftonpark court off t cliftonville area its taxed 2 end feb mot is up next month, but will pass npz if u want 2 call out hve wee look at it.
done loads of work 2 my wee car hve all recipets here running like new.
we must help myelegic patients.
yes they need our sympathy and help..
There needs to be something done in the treatment of this debilitating and painful illness. Please devote more resources to research so that we can find a cause! Too many people are suffering and this needs to be prioritized.
Seriously. Cancer, disease and undiagnosed/misdiagnosed illnesses are a worldwide problem. Since the government wants to get involved in people's lives anyway, why not get involved in a way that will help people? A friend who is directly affected by this illness sent me the link and it only takes a moment of time to get involved and sign a petition.
I can understand the confusion- but actually chronic fatigue is just an offshoot, one of the many symptoms in a mix of this illness.