-end of line- an answer to the BBc relating to the removal of Disability Living Allowance.
By alphadog1
- 898 reads
I have temporal lobe epilepsy. There are many reasons why I have this condition. It is partly my fault, as in my youth I chose self medication over mental health treatment for the sexual and physical abuse I experienced at school. Also I have in my youth used my condition to skive off of work. I am ashamed of this, but I was a lot younger and far less stable than I am now.
At the moment this condition is controlled by medication. The medication I take is called Keppra. It is vital as without it, I will have generalized seizures of the temporal lope.
A generalized seizure is defined as when the body becomes fixed and ridged; the individual loses consciousness and -in my case- there is a loss of bodily functions. It can last for a minute or longer, I have had a seizure that lasted nearly half an hour and this nearly killed me. Usually it also means a short stay in an accident and emergency ward and or time for bed rest.
It also means I suffer from anxiety, short term memory loss, -due to the seizures I suffered prior to medication- panic attacks, as the world I seem to be in seems at times fluid and unreal, depression, as I feel unable to cope in environments I don't feel secure in, and -more importantly- it relates to indirect discrimination of employers whom will not employ a disabled individual over an able bodied individual.
Over ten years ago, I was assessed for D.L.A in Brighton.
Both my father and I were introduced to four Doctors: two men and two women, who asked a lot of very painful questions relating to my disability, how it affected my life and the effect it had on those around me. During this interview I stated that I could catch a bus, catch a train, understand a timetable, walk well and communicate my needs accurately. It was also during this interview that I got the impression that the doctors were prepared to offer me more money if I was dishonest and over-emphasized part of my condition. However I was honest. This honesty led me to be awarded what is now £20 pounds a week, or £80 P.C.M for transport for life.
There is no "cure" for my condition, it can only be controlled and that means medication forever. It also means discrimination against certain forms of work (prior to my condition I was a factory worker, and then a nursing auxiliary but both jobs were unsuitable.) Since becoming unemployed, and unemployable, I have matured as an individual. I found a lovely wife, and I have helped to bring into the world three beautiful girls. I have chosen to spend my time in improving my job prospects by getting an education denied me by the state through the Open University.
Since this Government have been in office, I have faced abuse from people locally, because they define me as "lazy and workshy";I have lost all benefit payments, apart from D.L.A and now live in fear of losing this, because if I do, I will not be able to have the money I need, to catch the bus, to get to Worthing to sign on to the Job program, that will never pay enough. Moreover it will remove the entitlement for being able to receive a free bus pass, so if I ever managed to get employment I couldn't get to the job that does not pay enough to feed our children.
I am one year away from finishing a BAhons degree in English, so I can attempt to do a masters in Screenwriting. (my dream career.)
The changes this government have made are wrong and unsustainable, because no employer will hire a disabled individual over an able bodied person. In doing so they have sentenced people to death. Until they can see the damage they are doing, I pray constantly that they are held accountable for their actions.
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Comments
A poignant and punchy piece.
Linda
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I to am furious that those
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Thank you for sharing your
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This government is picking
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