Today is 11 April. For many, it’s just an ordinary day. For others it marks a special day, perhaps a birthday, or an anniversary – a day to remember someone special who is sadly no longer here. It is also World Parkinson’s Day. For those of us in the Parkinson’s community, it’s an opportunity to…
Tag: deep brain stimulation
Hopefully ever after (whatever the weather)
Her Deep Brain Stimulation surgery was successful, the sun shone brightly every day, and she lived happily every after… Not quite. Yes, my Deep Brain Stimulation (DBS) surgery (18 months ago) was successful and I am so very grateful for that. The sun has definitely shone brightly on some days since my DBS surgery. As…
Living with Parkinson’s… 9 nine years and counting
When I was diagnosed with Parkinson’s nearly nine years ago, I had no idea what my future would look like. I consider myself lucky to have access to brilliant NHS services for Parkinson’s and also great support from friends and family. Without both of these, my Parkinson’s journey would have been a much more difficult…
Lost and found
I have recently returned from a wonderful week’s holiday in the Lake District. I am so grateful for the opportunity to have a break, enjoy several walks and spend the week with an amazing group of people – friends old and new on this year’s Thinking Faith retreat at Boarbank Hall in Cumbria… I last…
Things are not always as they seem
“I can wave!” I can wave my hand! I remember feeling excited about being able to wave again, shortly after I was diagnosed with Parkinson’s and started taking medication. It may seem like a little thing, but for me it was a really big deal. I had that excited feeling again, eight years later, last…
My new normal: Recharging my battery, being reunited with my orange frog and playing Scrabble with a missing tile
Being diagnosed with Parkinson’s changed me in lots of ways. At the time, I never thought I would feel ‘normal’ again, but it’s surprising how quickly we can adapt sometimes. What’s ‘normal’ anyway? I guess in this context, it’s what feels normal to each of us as individuals. Prior to my Deep Brain Stimulation (DBS)…
Rolling back the tears
After I was diagnosed with Parkinson’s, it was several months before I could say “I have Parkinson’s” without fighting back the tears. Three years after my diagnosis, I shared my first blog about living with Parkinson’s and I was overwhelmed (teary even) at the positive response and support that I received from friends, family, colleagues…
My DBS journey: Feeling afraid, holding onto hope and practising patience
For me, one of the worst things about living with Parkinson’s is knowing that it’s not going to get better. But the prospect of Deep Brain Stimulation (DBS) surgery gave me hope that my symptoms could be eased and my quality of life could be improved. This summer after struggling for so long with the…
My DBS journey continues… Alongside England’s Euro 2020 journey
The last time that England reached the semi finals in the European Cup was in 1996. That was the first time I watched an entire football match. It was also the year I had brain surgery to remove a growth in my pituitary gland. Coincidentally, England reached the semi finals again this summer 2021, and…
Living with Parkinson’s: Memorable Moments
The theme of this year’s Parkinson’s Awareness Week (11-17 April 2021) is mental health in Parkinson’s. So I thought I would share a few memorable moments which have impacted on my mental health… The letter – I was diagnosed with Parkinson’s in October 2013. I remember the day, a few months later, when I received…
Living with Parkinson's 