‘Parkinson’s hasn’t stopped me from enjoying my life’

A Beragh man who was diagnosed with Parkinson’s almost eight years ago has said the improved treatments and supports which he has received during that time have helped him to continue living a full life.

Peter Rodgers worked as a Technical Officer with the Housing Executive in Omagh until his retirement in 2014. His diagnosis just two years later after experiencing tremors in his hands came as an immense shock. However, it’s one which he has learned to accept and move on from during the intervening decade.

He has accepted the diagnosis and learned to accept and live with Parkinson’s. He is also a member of the Parkinson’s Support Group in Omagh and says its work in helping those suffering from Parkinson’s and their families deserves immense credit.

Members of the group recently marked World Parkinson’s Day and hold a monthly series of events, including meetings, trips and other activities. Each is aimed at raising awareness of Parkinson’s and the support available.

“My view was that Parkinson’s was a complete rather than a gradual shutdown. It was around that time I spoke to a Dr McVerry who gave me reassurance about what the future held. I tried to never let the diagnosis stop me from doing things that I enjoyed,” he said.

BEFRIENDING

“For four years until the pandemic I worked taking people to hospital appointments and in a befriending service locally. I felt it was important to help people who had difficulty getting transport, or talking to people who maybe had no company.

“My Parkinson’s progressed at that time and I personally went through a period of gloom, darkness and discontent. I was at a low stage, until my doctor reviewed my medication. This led to a good improvement and helped me to realise how important it is to maintain a healthy outlook on life.”

Mr Rodgers now undergoes a six-monthly review, and has gained valuable support from the Omagh Group of Parkinson’s.

It meets regularly each month and allow people to meet others affected by Parkinson’s. There’s a chance for a chat, to socialise and relax, often with a cup of tea and a slice of cake. There are also opportunities to take part in a range of other activities, including getting active.

VITAL

“The support which I’ve received from the Parkinson’s support group has been vital. We have speakers who come regularly. For me, if there’s an issue you can contact the Area Coordinator who will then get advice or an appointment with a GP Practice Nurse,” he added.

“Over the past seven years I feel able to live with Parkinson’s and plan my life around it. My mind is very clear and I can communicate and be aware of what’s going on. My only two difficulties are with regard to walking and driving.

“I used to be a keen walker but now I have to take my time and be careful. I can still drive shorter distances while my wife drives if we have to go somewhere further away.”

Now, as he looks to the future with optimism, Peter has some sound advice for anyone facing into a new diagnosis of Parkinson’s.

He has stressed the importance of maintaining an active life, both socially and in terms of exercise.

“It’s crucial to keep in contact with people. Go to the various clubs and stay active. I believe it’s important to investigate all the different medical services and treatments which are on offer,” he added.

“For me, I’ve found music and the radio to be of a great benefit. There’s a chance to get more depth while listening to something on the radio. Ultimately, it’s vital to think positive all the time because if you dwell too much then that can have a negative effect.

“That then translates into your physical condition. I feel that if I’m not positive then this will lead to pains in my arms and legs. If you’re positive and doing things on a daily basis, then you soon forget about the ailments which can be associated with Parkinson’s.

“The help of both my own and my wife’s family has also been so important. The support and encouragement which they provide on a daily basis has been just amazing.”