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The Independent View: Coerced, bullied and fighting back: living with Multiple Sclerosis and Welfare Reform

I am a 54 year old woman who has had Primary Progressive Multiple Sclerosis for around 6 years. It involves increasing pain and loss of mobility and, as there is no remission, only progression, it takes me all of my energies to manage.

After the legion of neurological symptoms forced me to give up work I have had to endure the trauma of an Employment and Support Allowance “medical assessment” by ATOS Healthcare (a French private contractor), I have struggled to attend the mandatory Work Related Activity Group, which was not a safe place in my worsening condition.

I waited months for an appeal and won, but live in fear of the brown Department of Work & Pensions envelope that indicates that the whole sorry process will start again, as appears to be the case for many who win their appeals.

If the Welfare Reform Bill is agreed this week, I face the same stress and anxiety in yet another assessment, to test for an already proven condition, in order to retain high rate mobility Disability Living Allowance (DLA) in its new guise as Personal Independence Payment (PIP).

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