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August is Spinal Muscular Atrophy Awareness Month, and on this occasion, we'll be sharing voices from the SMA community. Danielle shares her family’s journey - from her own late diagnosis to raising two young children also living with SMA. Her story is one of resilience, progress, and hope for a better future. #SMAAwarenessMonth #BreakingDownBarriers Août est le Mois de sensibilisation à l'amyotrophie spinale et à cette occasion, nous donnerons la parole à des membres de la communauté de l'AS. Danielle raconte le parcours de sa famille, depuis son propre diagnostic tardif à son rôle de parent de deux jeunes enfants également atteints d'AS. Son expérience est marquée par la résilience, le progrès et l'espoir d'un avenir meilleur. #AS #MoisDeSensibilisation #FaireTomberLesBarrières - Are you or someone you know living with a neuromuscular disorder? We’re here to help. Muscular Dystrophy Canada has a wide range of programs and services designed to meet you where you are. Whether it is information about a disorder, helping you with accommodation needs at work or school, navigating the healthcare system, housing or financial issues, or helping you secure equipment – we’re here to help. Register today and our Service Specialists will be happy to work alongside you, ensuring you have the information and support you need. For more information: • Visit us online at: https://muscle.ca/access-help/ • Call us a: 1-800-567-2873 • Or, email [email protected] You can also: • Check out our educational webinars: https://muscle.ca/discover-md/webinars/ • Register for one of our fundraising events: https://muscle.ca/events/ • Ask our Research team questions by emailing [email protected] • Make a donation at muscle.ca/donate Follow us on: • Twitter: / md_canada • Facebook: / musculardystrophyca • Instagram: / md_canada • LinkedIn: / muscular-dystrophy-canada