In December 2024, our mother Janet Keene was diagnosed with ALS. The disease progressed incredibly quickly and within a short few months, had taken away her ability to walk, talk, eat and move her body.  Janet fought this cruel disease with incredible strength, and never lost her bright and beautiful smile. She passed away in June 2025, only 6 months after diagnosis. 

In honour of Janet's memory, we will be participating in the Walk to End ALS on June 7th. Our goal is to help raise money and build awareness for this devastating disease.  Currently there are limited treatment options and no cure for ALS, and after diagnosis, the average life expectancy is 2-5 years.

We would greatly appreciate any support to help bring hope to other families facing the harsh realities of ALS.

We miss you every day Janet.