On Sept. 23, 2019 my life took a turn when my neurologist (I never dreamed I would ever have a neurologist) looked at me and said “Kathy, you have Parkinson’s Disease”.
That was last year. Then the pandemic hit. The BC Parkinsons Society pivoted and continued to offer services so that I was able to access the resources I needed over the last year. Having these folks at the end of the phone or email is valuable. The courses offered virtually were easy to access and definitely helpful.
Those of us with Parkinson Disease are fortunate that this group exists. So, on September 11 I will be part of a super walk in New Westminster to raise funds in support of all that the Society offers. If you have a few dollars in your donation fund please come to my site (https://tinyurl.com/b7e3dws2) and follow the prompts. If you are keen to walk with me get in touch and I'll give you the coordinates.
Thank you for caring