Happily sharing the whole @CTVNews segment from last night. So proud of Emery.
@AirCanada will we hear from you today?
Advocate questions whether Air Canada has 'cultural problem' after issue with teen's wheelchair https://t.co/WNM7LQdJhH
@realColinMac@farwell_WR In Ontario vehicles travelling 40km/hr over the limit in any zones that are below 80km/hr will have their vehicle impounded for 14 days and their license suspended for 30 days. This changed last year and was previously 50km/h over posted limit to receive a stunt driving charge.
Today I’ve been dealing with more pain and circulation issues in my legs because @AirCanada broke my wheelchair.
Mobility devices are an extension of a disabled person’s body.
#NotLuggage
37 buildings across eight provinces in #Canada will light up red today to recognize World Duchenne Awareness Day #WDAD2022 🎈 https://t.co/USxI2D3x4F
Take action: Snap a pic at the location nearest you or share a selfie wearing red, tagging @defeatduchenne@worldduchenne
@JoelHardenONDP @JoelHardenONDP check out @MaxsBigRide for route options, yearly fundraiser bike ride between Hamilton and Ottawa to raise funds to find a cure for Duchenne Muscular Dystrophy (a progressive and fatal genetic disorder that weakens muscles) https://t.co/LUalPoMb9K
🎉BIG NEWS: 400 participants joined the #WalktoDefeatDuchenne across Canada on Sunday, surpassing our goal and raising $220,608 (and counting!) for research, education and care. Thank you for taking action to end #Duchenne#musculardystrophy - we can't do it without YOU 💙
🗓️ TODAY ONLY #GivingTuesdayCA: The Mike Weir Foundation - @mweirsy, will match all donations (up to $5,000) so that more boys with #Duchenne#musculardystrophy can thrive by living fuller, better, and longer lives. Donate now: https://t.co/1TlXXxoBdi.
Duchenne can be passed from parent to child, but approximately 35% of cases occur because of a random spontaneous mutation. In other words, it can affect anyone. Currently there is some great research but no approved treatment for all. There is no cure for Duchenne. #WDAD2021
Today, September 7 is #WorldDuchenneAwarenessDay. The 7th day of the 9th month representing the 79 exons of the dystrophin gene. Mutations of the dystrophin gene are responsible for #Duchenne Muscular Dystrophy, a progressive muscle wasting disease.
The genetic mutation prevents the body from producing dystrophin, a protein that is needed for muscles to work properly. Muscles cells become damaged and weaken without this protein.