Stories

My name is Jacqueline McKay. I’m from Calgary, Canada but have lived in Brisbane, Australia for a year.  My dad Bill, was diagnosed with Parkinson disease 7 years ago. I still remember the moment I noticed. Dad had picked me up, and the vehicle was shaking as he was driving.  We realized his foot was tremoring, […]

Monty and Yolande came to Parkinson Association of Alberta shortly after learning of Monty’s Parkinson disease diagnosis. They shared with us the impact our programs and support have made in moving forward with hope. Their story Our neurologist suggested we contact PAA for support and information after confirming Monty’s diagnosis just over a year ago.

Carol and her family were no strangers to Parkinson disease when they received news of her diagnosis. They had witnessed first-hand the dread that accompanied such news, but they also knew where they could go to find hope. Support makes all the difference Nearly a year ago we got the diagnosis that my wife Carol

Recently my wife, who has been struggling with Parkinson’s for 13 years, underwent a procedure at the University of Alberta hospital to receive a new way of administering her medication.  It is known as “DuoDopa”; a pump method of providing Sinemet (levodopa/ carbidopa) directly to the small intestine.  A stoma (hole) is made through the stomach wall.  A tube

Colette, my wife and best friend was diagnosed with PD in 2005.  As we heard numerous time from others, the signs were there for many years before.  “Getting Old” we thought. We were fortunate in that Colette reacted well to oral medication.  Our life did not change much for the next seven years.  During those years we heard many

I first really noticed the symptoms in 2005 when I found it was difficult to walk.  My right leg had trouble working.  I went to my family doctor who sent me to a neurologist. He told me I had Parkinson disease and he would prescribe pills if I wanted them.  That was the extent of his help.  I went home