Things need Changing

Less than one minute read time.

Today I recieved a letter from the DWP informing I was no longer entitled to the ESA I have been claiming since I was diagnosed last may. There is a generalised assessment in which you have to score 15, i score 0  the fact that i could touch my toes on that day and can string together a coherent sentence qualifies me to go back to work.

Things have to change, although i was asked about my illness in great detail, and what challenges it brings to everyday life this apparently has no bearing on my ability to work.

I would like to know why a goverment department who will see you for 20 minutes to assess you cannot take the word of the highly skilled professionals who, assess and monitor your treatment and condition on a regular basis.

I am going to see my local MP as this seems such an unfair system of assessing your physical and emotional well being.

 

Anonymous
  • FormerMember
    FormerMember

    Tell me about it...

    Make sure you appeal the recent decision, whilst you appeal awaiting the tribunal they will reinstate basic money which i guess you were on?

    They take no notice of any letters from GP's or Consultants & even tell the GP to stop issuing sicknotes!!

    After my assessment in February i scored 6 points for my Crohns but i also stated i had Leukaemia & with both i am Chronicly Fatigued.

    The assessor said in his statement "I didn't look tired", also much of what i said was twisted, innacurate or assumed when i read the report i received on Friday.

    My GP is livid, i have my Haemo appointment 6th April & will mention the fact he doesn't even exist in the eyes of the DWP.

    I gave permission for them to contact all the Consultants but they didn't bother.

    These assesors are a shame to the medical profession & have caused me much heartache & stress.

    All the best for your appeal.

  • FormerMember
    FormerMember

    the first question the assesor asked was where did you park the car? we told him in the car park at the rear, on this basis it was stated PATIENT HAS NO DIFFICULTY WALKING MORE THAN ONE HUNDRED METERS. Final score was 0 we are appealling .

  • FormerMember
    FormerMember

    This makes me SO ANGRY! There is proof from the docs what you have been through and emotionally and physically still are and yet there are people claiming and given every benefit under the sun and may not have even paid into the system all their lives and this is genuine circumstances. I wish you well on your fight but none of us need this added stress in our lives at this time.

    (getting off the soapbox)

    Good luck x

  • FormerMember
    FormerMember

    I went for a medical on 10 Dec 09....on 15 Jan 10 i was informed my ESA was stopped on the 1st Jan 10..so for 15days i had no money going into my bank...i appealed against the decision and and i was given the basic £64 ...£30 less than i was on previously..mine is now going to a tribunal...last week i recieved the report that will be looked at by the tribunal....40 pages...these were some of the comments " the patient walk 60 yards to my office unaided....he scratch his head twice while seated without difficulty ...he stood up and down twice without difficulty...he spoke without difficulty"...this report was from a doctor who did,nt know what treatment BCG was....these doctors have not a clue cancer patients go through. or what some of the treatments they are on...i have recently applied for seven part time jobs(all i can do with 1 hand behind my back and blindfolded)  knowing that i will be refused ESA..i.v had 2 interviews...but have been turned down for both..this i think is because i have had to put down that i have cancer..be it inremission and requiring checks every 3months and treatment every 6 months....it now seems government policy to kick as many cancer patients off ESA as possible...the doctors they use have not a clue..many are semi retired and are getting paid alot more than my £60 pounds a week....once again cancer patients are getting  another raw deal and its about time we all got together and told this government what we think of the way we are treated...