'I felt like I was on trial trying to get sickness benefits - I almost lost everything'
01.10.2023 - 07:17
/ manchestereveningnews.co.uk
At the age of 25, Rob Denholm was in the prime of his life and the future was looking bright. He had a partner, a stable job and was set to embark on an exciting new career opportunity.
But his world was turned upside down when he was hit by a shock diagnosis that would change the course of his life forever.
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Rob, who was working in IT recruitment, was visiting his brother in America when he suddenly started experiencing balance issues and numbness in his hands and feet.
As his symptoms escalated, Rob, from Newton-le-Willows, decided to visit a US doctor and was diagnosed with peripheral neuropathy. The condition is a type of nerve damage that can cause pain, numbness or weakness.
The strange symptoms worsened once he returned to the UK and he was then diagnosed transverse myelitis, an inflammation of part of the spinal cord.
However, what doctors didn’t know was that Rob was actually suffering from multiple sclerosis, a lifelong and incurable condition that affects the brain and nerves.
MS has since impacted every aspect of Rob’s life – with his symptoms ranging from cognitive difficulties, fatigue and mobility issues.
Unable to work, Rob signed up for Disability Living Allowance payments which he received up until 2019.
When the benefit was replaced by PIP in 2019, Rob was automatically transferred but he needed to be reassessed.
But he claims he was mistreated through the process, had medical evidence ignored and was forced to challenge their decision after it concluded his condition wasn't that debilitating - leaving him fearing he would “lose everything” without the financial support he had come to depend on.
“It took me more than