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Here is a copy of an email that I've sent to my MP. He hasn't had a chance to reply yet, but I wondered what you guys thought about it.
Dear Mr Hughes,
I appreciate you are very busy at this time (particularly with mess surrounding Brexit), but I have a serious problem that I would greatly appreciate your help with. I was diagnosed with ME (also known as CFS) and became so ill that I was unable to work. I was diagnosed in 2017, but have suffered symptoms since 2012. Myalgic Encephalomyelitis (M.E.) is a long-term and incurable neurological condition that causes symptoms affecting the nervous and immune systems. This link will explain the illness in more detail -
https://www.nhs.uk/conditions/chronic-fatigue-syndrome-cfs/
Following my ESA assessment I was placed in the support group for 12 months and declared unfit for work. I have recently been re-assessed and despite explaining to the Healthcare Professional that my condition has not improved, I have now been found completely fit for work and my money has been stopped. I do not support this decision at all and am currently challenging it. I will, if necessary be forced to take this to a tribunal hearing if my reconsideration is not successful. The HCP omitted many important facts about my condition in his report, such as widespread pain through my body, severe and constant exhaustion (where I am often unable to leave my home) and social anxiety as a result of childhood abuse.
There are several ESA descriptors that I meet (including one for the support group) but these seem to have been ignored during my assessment. They include bladder problems (incontinence), standing and sitting and social anxiety. At present, I currently have no income and very little food or money for gas, electric and water payments.
I am currently waiting for a Mandatory Reconsideration to take place and will receive no money whilst this is happening.
With the symptoms that I have I am currently unemployable and am deeply concerned that I will be left destitute in the near future. How a person with a long term and incurable illness can go from being unable to work to completely fit for work in a matter of a couple of months is beyond me, and I would be grateful if you could help me get my money reinstated before I end up with severe rent and council tax arrears, and possibly face court action or even eviction.
I understand that my need is no greater than anyone else's, but I would be grateful if you could address this in the next few working days as my situation has become quite desperate.
Thanks for your help in advance, it is very much appreciated
Best Wishes
(name and address have been removed for security reasons)
Dear Mr Hughes,
I appreciate you are very busy at this time (particularly with mess surrounding Brexit), but I have a serious problem that I would greatly appreciate your help with. I was diagnosed with ME (also known as CFS) and became so ill that I was unable to work. I was diagnosed in 2017, but have suffered symptoms since 2012. Myalgic Encephalomyelitis (M.E.) is a long-term and incurable neurological condition that causes symptoms affecting the nervous and immune systems. This link will explain the illness in more detail -
https://www.nhs.uk/conditions/chronic-fatigue-syndrome-cfs/
Following my ESA assessment I was placed in the support group for 12 months and declared unfit for work. I have recently been re-assessed and despite explaining to the Healthcare Professional that my condition has not improved, I have now been found completely fit for work and my money has been stopped. I do not support this decision at all and am currently challenging it. I will, if necessary be forced to take this to a tribunal hearing if my reconsideration is not successful. The HCP omitted many important facts about my condition in his report, such as widespread pain through my body, severe and constant exhaustion (where I am often unable to leave my home) and social anxiety as a result of childhood abuse.
There are several ESA descriptors that I meet (including one for the support group) but these seem to have been ignored during my assessment. They include bladder problems (incontinence), standing and sitting and social anxiety. At present, I currently have no income and very little food or money for gas, electric and water payments.
I am currently waiting for a Mandatory Reconsideration to take place and will receive no money whilst this is happening.
With the symptoms that I have I am currently unemployable and am deeply concerned that I will be left destitute in the near future. How a person with a long term and incurable illness can go from being unable to work to completely fit for work in a matter of a couple of months is beyond me, and I would be grateful if you could help me get my money reinstated before I end up with severe rent and council tax arrears, and possibly face court action or even eviction.
I understand that my need is no greater than anyone else's, but I would be grateful if you could address this in the next few working days as my situation has become quite desperate.
Thanks for your help in advance, it is very much appreciated
Best Wishes
(name and address have been removed for security reasons)