Mark Mitchell

“I was diagnosed with Primary Progressive MS (PPMS) in 2000. I pretty much knew at the time as I had researched my symptoms. However, I was initially devastated to be told I had PPMS. But It is not the end of the world to have MS. It presents an alternative and wonderful lifestyle to embrace. There is nothing I cannot do from going to concerts, football matches, playing bridge online and at the bridge club.

"I had to retire from my recruitment business as between fatigue and losing my voice, the decision made itself. It takes a while to adjust to having MS. Like everybody else, I asked, why me?

"Each person has their own timeline adjusting and coping with MS. I found that by meeting other people living with MS and sharing their stories helped me greatly and I have met so many wonderful people this way. 

"I learned how to play bridge and now play 3/4 times a week and it is simply a wonderful game. I collect Irish stamps and have every First Day Cover since the foundation of the state in 1922 to date. I have several hundred CD's and love going to concerts. My next gig is Mary Black at the Pavilion in Dun Laoghaire.

"I am a diehard Everton supporter and have been to Goodison Park several dozen times. I have a very wide circle of friends whom I keep in contact with regularly. I do a lot of fundraising for my local branch - East Wicklow Branch.

"I attend Open Door in Bray twice a week for physio and I attend a mosaic class there which I absolutely love to do and have received several commissions.” – Mark Mitchell