Patient stories
Michael was a high-flying company director when he was diagnosed with Multiple Sclerosis earlier this year. Only shortly afterwards, amidst the economic impact of the pandemic, he lost his job. Here, he describes the devastating reality of such a double blow, and why he is determined to find the confidence to get him through.
“I was diagnosed with Multiple Sclerosis just before lockdown. Five months later, I was made redundant. The two events weren’t linked, but both have been central to the real uphill battle I feel I’m fighting at present.COVID-19 has presented many challenges for brain injury patients, with the cancellation of groups and appointments meaning a pause in their rehabilitation. Here, Paul shares his story of how his experience of the past few months has left him dreading the impending ‘second wave’.
I sustained a brain injury just over 18 months ago now. It was in circumstances many people describe as a ‘freak injury’ but I really hate that description, as I’m constantly well aware I probably now seem like a freak, thanks to my condition. I was decorating at home, something I never do, but we were trying to save some money so I thought I’d give it a go. I was standing on some ladders which were a bit wobbly, but they seemed fine for a DIY novice such as myself.Having experienced a brain haemorrhage five years ago, 52-year-old Jane Hallard from Gloucester has had to rebuild her life. Here, she details her struggle and how she has learned to look to the future with positivity.
In the five years since my brain injury, I’ve had to come to know a whole new me. While I look the same as I did, I’m far from being the same person. On that day, back in 2015, when I was helping my son to clean his car, little could I have imagined what lay ahead.







