Top Tweets for #DMDAwarenessMonth
#September is DMD Awareness Month. Itโs a call to raise awareness on DMD and express compassion through
1. Early Identification
2. Linkage to care.
The above actions coupled with support and inclusion for patients and their families, We build resilient communities. 1/2

Thank YOU for rising to the challenge throughout #DMDAwarenessMonth and helping reach monumental levels of awareness for #Duchenne #musculardystrophy across Canada. Let's continue to use the power of social media to connect, educate, and take action to #DefeatDuchenne.
"What advice would you give to other young adults living with Duchenne muscular dystrophy?" ๐ฝ๏ธ Watch the FINAL #TestimonialThursday podcast as the four #Duchenne ambassadors share their inspirational answers as part of #DMDAwarenessMonth: https://t.co/lcbAeQXTSq.

#DMDAwarenessMonth: Today is the LAST #WearRedWednesday! Whether it's a shirt, scarf, or hat - take a picture of you wearing red today and tag @Jesses_Journey in support of #Duchenne #musculardystrophy.

๐ฝ๏ธ #DMDAwarenessMonth: Watch and retweet the final #InternationalTuesday podcast as we talk to Duchenne Patient Representative Dimitrios Athanasiou from @mdahellas in Greece: https://t.co/QgqcHikW7U.

Families living with #Duchenne #musculardystrophy know the power, resilience, and strength it takes to face this progressive disease day after day.
Like and RT this final #MotivationalMonday to help raise awareness for our #DMDAwarenessMonth.

#DMDAwarenessMonth - #SharingSunday: Are you a parent or caregiver of a child or children with #Duchenne #musculardystrophy? Connect with other families across Canada at our monthly social, Canadians Talk Duchenne. The next social is THIS Wed, Sept 29: https://t.co/fS74lyzGPM.

#DMDAwarenessMonth - #SquadSaturday ๐ฎ Today is our annual Squad Up Community Day! See the full schedule and tune in to support our gamers (like @FortNerdDotCom & #Questforthecure cast) as they play and raise funds for #Duchenne #musculardystrophy: https://t.co/PwxktfTw6J.

#DMDAwarenessMonth - #WearRedWednesday: Though #Duchenne #musculardystrophy is categorized as a โrareโ disease, there is a huge national and international community fighting to defeat Duchenne every day. Didn't wear red today? Comment with a โค๏ธ below to show your support.

#DMDAwarenessMonth - #MotivationalMonday: In our community, the heroes are the boys and young men living with #Duchenne #musculardystrophy, who don't let their diagnosis define who they are and find strength from within to achieve the amazing.
๐ Who is your hero? Comment below!

๐ฌ #DMDAwarenessMonth - #SharingSunday: Research is the road to hope for those living with #Duchenne #musculardystrophy and through the support of our donors, we invest in the most promising #science. Learn more about this year's research funding: https://t.co/ijt7mFHcXm.

#DuchenneMuscularDystrophy is a rare, incurable disease that affects hundreds of thousands of boys and men worldwide. Find out more about rare disease in our 2021 Prescription Drug Trend Report. #DMDAwarenessMonth https://t.co/Ms9akVDYEU

#DMDAwarenessMonth - #FactFriday: Duchenne muscular dystrophy progresses differently for every person living with this #raredisease. Read the consensus guideline for adult Duchenne care recently published by the Journal of Neuromuscular Diseases: https://t.co/6qFQCekeZv

We're halfway through #DMDAwarenessMonth ๐จ๐ฆ! Help us raise awareness of #Duchenne #musculardystrophy with the click of a button. ๐ฝ๏ธ Watch and RT this week's podcast featuring Riley, 21 years old from Pitt Meadows, British Columbia: https://t.co/OWCipQxuk7.

Awesome job, Thundercats - A sea of red at school today! Every Wednesday during the month of September, our school community is encouraged to wear RED to bring awareness to Duchenne Muscular Dystrophy (DMD) and support Jaxson. #dmdawarenessmonth #WearRedWednesday

#DMDAwarenessMonth - #WearRedWednesday: As a part of our 30-day #Duchenne #musculardystrophy challenge, we're asking YOU to wear red every Wednesday and tag @Jesses_Journey. โค๏ธ Thank you @jeffpreston, Chair of our Board of Directors for showing your support!

#DMDAwarenessMonth - #MotivationalMonday: The Davidson family refused to give up when their middle son, Jesse, was diagnosed with #Duchenne #musculardystrophy. Learn more about how you can make a difference in the fight to #defeatduchenne: https://t.co/tVaNg8NKo4.

#DMDAwarenessMonth - #FactFriday: Did you know that the dystrophin gene is the largest gene in the body? Because of this, it can have thousands of mutations (changes) that result in #Duchenne or #Becker #musculardystrophy.

#DMDAwarenessMonth - #InternationalTuesday: Patient organizations around the world are working together to #DefeatDuchenne. Watch our interview with Elizabeth Vroom, Chair of @worldduchenne: https://t.co/c5UGZczUQ7 #WDAD2021 @DuchenneDay

#DMDAwarenessMonth - #MotivationalMonday: Do you know of another family living with #Duchenne #musculardystrophy? They're not alone - share this post and encourage them to join our monthly social, Canadians Talk Duchenne: https://t.co/fS74lyzGPM.

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