It was about 5 years later I started to really notice some changes, some challenges even. I was still doing pretty good, some good days, some bad days, but it was still more good than bad. I knew this disease was sticking around, so I needed to learn more about it; what to expect, how to prepare and where to find support.
I found Parkinson Association of Alberta – and found my community!
I started attending their regular support groups, to both learn more about PD, but to also (hopefully), meet others living a similar life, walking the same path. I love my support groups, and my support group family. As someone who lives alone, finding others to share my concerns with, to talk about my challenges with, to ask question, was very important, and very much needed. Learning ways to manage my Parkinson’s was valuable, but so was the social aspect of these groups.
How would I describe Parkinson’s Association of Alberta, and their wonderful and knowledgeable team; I’d say they are like a big brother, or mother, in that they are always there for me, always have my back, always concerned for me and helping me do better, move forward, with patience and understanding. I know I can call anyone on the PAA team with any issue, and they will cheerfully help, and make me feel supported. I feel like I am part of their family, and that means the world to me.
My Parkinson’s is not going away, it’s here to stay, it is part of my life now, I am so glad PAA is also part of my life, helping me along my journey.
Ron Davidson