"I am thankful for my struggle because, without it, I wouldn’t have stumbled across my strength." - Alex Elle
Thank you to all women fighting with us to defeat #Duchenne#musculardystrophy. There is hope because of your passion and determination 💙 #InternationalWomensDay
The last couple of weeks we’ve recognized and celebrated these very deserving recipients of the Titan Character Award. Each of these students has made a positive impact on our school community in their own way! @OttCatholicSB#TitanProud#BeCommunity
Limited time only: the Mike Weir Foundation will match ALL GIFTS received on Giving Tuesday – THIS Tuesday, November 29!
Save this link and get ready to make a difference in the lives of children and young adults living with #Duchenne: https://t.co/aKKVdehqn1
📆 TOMORROW is #GivingTuesday, where all donations will be matched up to $5,000, thanks to The Mike Weir Foundation.
Join the Chip in Challenge and help us raise vital funds for #Duchenne research, care and education. Please give generously: https://t.co/aKKVdez1LB
For 27 years, Jesse's Journey has been raising funds and awareness for Duchenne Muscular Dystrophy. Jesse's Journey is now @defeatduchenne, but it's purpose remains the same: a world where those born with Duchenne can live long and healthy lives!
Families of Ontario, would you rather receive $200 per child or have your child's school get $200 per student? Imagine what $100,000 could do for a school with 500 students. #onted
Today is World Duchenne Awareness Day!
We encourage you to share your own video or join in on the conversation by using #WhatIWantYouToKnow. If you could tell the world one thing about Duchenne - what would it be?
#WDAD2022
Don't miss the upcoming #Duchenne#musculardystrophy webinar on ‘Adrenal Insufficiency and Emergency Care Procedures’ - Tuesday, April 5, 2022, from 7-8:30 pm ET with Dr. Laura McAdam @HBKidsHospital and Dr. Leanne Ward @CHEO: https://t.co/EVt3QVOUzz
U18 NGHA Champs! Being on the ice with this crazy crew has been an honour. You are the kindest, hardest working, fun bunch one could ever ask for. Keira, Chloe, Kalia, Sequoia, Shanna, Dena, Maddy, Laura, Rosie, Joelle, Sanika, Jade (and Eulalie), you are all amazing! Thank U!
"Living with Duchenne is a life-changing experience. But, it is another way to find the strength you wouldn’t know you have without the disease." - Samuel from Quebec
Today is @rarediseaseday - RT and help raise awareness of #Duchenne#musculardystrophy: https://t.co/k47CplK7qK.
The Sens Nation Podcast has a new holiday contest this week. We're giving away a classic https://t.co/CBmVMDt0si Pioneer Gift Box (with your choice of spirits). It's super easy and free to enter the draw – just retweet this post and follow @DunrobinDistill. Draw date: Dec 22nd!
🚨 Its #TicketTuesday - RT for your chance to win 2 FRONT ROW tickets to see the Senators host the Canucks tomorrow night - Presented by @BrewRevOtt 🏒🏒 #GoSensGo
Congratulations to Ken Cheeseman and his U18H2 team for bringing home gold from the Central York House League tournament this past weekend!
#GoWildcats
What does Duchenne mean to you?
#ASpaceInTimeFilm is now available on demand on Amazon, iTunes, BFI Player and Sky Store!
Release supported by #BFI#NationalLottery