We set this site up with a goal to help Pete and his family, and the thousands of other people impacted by Amyotrophic lateral sclerosis (ALS), Lou Gehrig’s or Motor Neuron Disease, the various names by which it is commonly known around the world.
“Like Lou Gehrig who was a determined, committed and a focused athlete who played 2130 consecutive baseball games before being diagnosed with ALS, I’d like to be the Lou Gehrig of life and continue to play as many consecutive games as is possible.”
– Pete Wood 2015
A touching explanation as described by his 8 yr old son Zac…
Please help us give HOPE to people suffering from ALS by supporting the advancement of Stem-Cell research in Canada. For those suffering from this disease, time matters most.
Help us spread the word and donate to this incredible research being done by University of Toronto, the University Health Network (UHN), and Sunnybrook Hospital.
Video by ALScanuck.org
Learn more from the latest ALS Fact Sheets to upcoming clinical trials…
Let’s hit it out of the ballpark and raise money for Pete and ALS by supporting clinical trials for Non-Invasive Stem Cell Research!
Please consider signing this petition.. PETITION TO THE GOVERNMENT OF CANADA Whereas: On April 5, 2017, motion M-105 was passed, which calls upon the government to increase funding for amyotrophic lateral sclerosis (ALS) research and to substantially increase national efforts to develop and launch a comprehensive strategy to assist with the eradication of ALS at […]
I recall Siena learning the months of the year. One month on the calendar always caused us trouble. She said November, but I said Movember. It’s the month when men grow mustaches to raise money and increase awareness for prostate cancer. A worthwhile cause and something I’ve been keenly aware of for many years. Why? […]
In mid September, we participated in the first ALS Walk held in the Toronto Beach. The weather was perfect and the support fantastic. There was an opening ceremony with speeches and a ribbon cutting. The walk circled Woodbine Park once then stretched along Lakeshore Blvd to Leslie and back to the park. They had a […]
One of my early cultural influences were television shows of the 70’s and 80’s. Mary Tyler Moore, King of Kensington, Love Boat, Happy Days, All In The Family and MASH, to name a few. I could go on. Welcome Back Kotter, WKRP, Three’s Company, Barney Miller, Good Times and The Brady Bunch. Once I start […]
I’m a little late in posting this, but I want to share something Siena made me for Father’s Day. No, it’s not a tie or socks. Something slightly more unique. It’s the product of five year old’s imagination and unbridled feelings. This was made at school. A game of tic tac toe, with decorated rocks […]
Hey stranger. It’s been too long. What’s been going on? I know, I know. I intended to communicate more often. I don’t know what happened. My time management scheme never quite got off the ground. To be honest, I enjoy eating too much. As a result, my meals are in the tradition of the Slow […]
Happy New Year! Wishing you a peaceful and healthy 2017. I’m sure we have all tried to get more efficient with our time. At work we enrolled in time management courses. They emphasized being organized with tasks, prioritize them, and dedicate specific time to the most important. A key success factor is to avoid distractions. […]
Siena declared this Halloween the “Best Ever!!” Stop right there. The title of best Halloween ever is up for debate. I would counter with the Halloween of 1972, as unforgettable. If I remember correctly, I was dressed as Oscar the Grouch and brought home an epic haul. A run of candy that included a toothbrush […]
I sent this out recently to folks who supported our Pitch4Pete event. The sentiment of the post applies to everyone reading my blog. I love writing. It means so much to me that you take the time to read my work. With feedback or not you keep me going. Thank you. If you know me […]
The mice have joined the club. No, not the Mickey Mouse Club. A club with exclusive membership. There are only 3,000 members in Canada and 30,000 in the United States. So really, not extremely exclusive. I’m talking about the same club that I hold a membership card to. The Amyotrophic Lateral Sclerosis (ALS) club. The […]
Let’s Help Pete Wood and defeat Lou Gehrig's Disease, By donating to the research!
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