Paul Tierney

Paul Tierney shares his story with us as part of the #IaMSomeone campaign to mark World MS Day.

One challenge I have faced is having to adapt my sporting life. I miss playing and competing in rugby and GAA however, I have found alternatives like volunteering at Parkruns and coaching yoga -something I never would have done before.

“I was diagnosed with MS in 2013, at the age of 21. I live on a farm with my family in Tipperary. My story is a bit different to most or all. I began experiencing groin/hip problems and was referred by my GP to Whitfield where I underwent surgery. Soon after, I underwent a balance test the surgeon wasn’t satisfied with my balance and coordination. They referred me to a Neurologist in Dublin. Between the two appointments, I had blurred vision and developed a limp. I was referred for and MRI scan and lumbar puncture. Soon after, I was given the news I had MS. I remember being asked if I had heard of MS before. I said no. After receiving the news I remember feeling numb. I was unaccepting of the diagnosis and hid it from friends for some time.  Once I did accept it and shared news of my diagnosis with friends it weirdly felt like a massive relief. It removed the strain and energy I was using up hiding the diagnosis.

One challenge I have faced is having to adapt my sporting life. I miss playing and competing in rugby and GAA however, I have found alternatives like volunteering at Parkruns and coaching yoga -something I never would have done before. When I think back, I realise the inner strength I had.  My advice to those diagnosed is not to dwell and to try stay as positive as possible. I have found the family support and new people I have met due to MS a bonus. From those I have met in South Tipperary to those I have met in the National MS Care Centre in Bushy Park and further afield, I have enjoyed getting to know new people and that has been a benefit in my view.” – Paul Tierney

#IaMSomeone

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