Check out this incredible video courtesy of Leggat Auto Group about this year's ride.

Click the image below to watch a documentary about the 2015 ride by our awesome friends at Steeltown Chick Productions.

Yesterday was a bittersweet day. It was sweet because Max was very happy to get a new stroller - for him it means more freedom as he can save energy on outings for the things that interest him. Max tends to get tired when he's on his feet for too long and his new stroller allows him to save his legs for the important stuff - like climbing, playing tag and flossing. It was also sweet because the staff at Ron Joyce Children's Health Centre are really awesome and have been since day one. Yesterday was bitter because his stroller isn't really a stroller. Eight year old boys don't have strollers. If I am honest, his stroller is a wheelchair, and a wheelchair isn't something any parent dreams about getting for their child. I love the freedom it gives Max and how happy he is to have it - but I can't help but wish we spent yesterday picking up a new bike, a pair of hockey skates or a skateboard. Today was bitter because for 4 years I have been talking to the press about Duchenne and how most boys end up in a wheelchair by age 12-13 with a life expectancy in their 20's or 30's. I always say how if we could keep Max how he is now, running as fast as you or I can walk and just barely getting off the ground when he jumps, if we could just keep him like he is now, things would be okay. I always say the future is what scares us. Today, a glimpse of the future arrived. Help us rewrite it. For Max. #duchenne #DMD #MuscularDystrophy #nevergiveup #ppmd
Today Max went to school in his @cureduchennemd t-shirt. Today is also World Duchenne Day – which seems a very good time to share the news that Dr. Gunning’s lab here at @uoftmississauga recently sent off 4 of their chemical compounds for testing to a lab in Ottawa. These compounds will undergo a series of studies - and there should be some initial results in the next month or so. The big hope is that these compounds will inhibit STAT3 and help to grow muscle cells. We are very proud and lucky to be partnered with Dr. Gunning, Yasir Raouf and the rest of the team in the Gunning Lab – and everyone here has their fingers crossed for what might be around the corner. 🤞 #duchenne #duchenne #DMD #musculardystrophy #maxsbigride #nevergiveup #research #cure #raredisease
First day of Grade 3: done! Max had a great day, but the first day back is always a little stressful for the parents of kids with special needs. Getting through each year is a real team effort, and thankfully we've always been extremely lucky in that regard. Here's wishing our boy a great year ahead! #duchenne #DMD #musculardystrophy #cargobike #maxsbigride #nevergiveup #father #son #family #research #cure #raredisease
Saturday night jam - rocking out to Heima by @sigurros with the xylophone and drum. Drumsticks courtesy of @arkellsmusic + @timoxford 👍 Two very awesome bands that have supported us along the way. ❤️ #duchenne #longweekend