Our negative assumptions about people with Down syndrome can lead us to treat them in such a way that these assumptions become reality. In sociology, this is called a 'self-fulfilling prophecy.' Why not reverse our perspectives? If we have positive assumptions about people with Down syndrome, they will have more opportunities at school, at work, in relationships, and other activities. And maybe these positive assumptions will become reality. #AssumeThatICan Learn more about how to support World Down Syndrome Day in Canada: https://lnkd.in/gKmVttAQ #WorldDownSyndromeDay #EndTheStereotypes CoorDown
Canadian Down Syndrome Society
Non-profit Organizations
Calgary , Alberta 2,453 followers
Focused upon human rights, health, social participation, inclusive education and employment for those with Down syndrome
About us
The Canadian Down Syndrome Society (CDSS) provides reliable information to people with Down syndrome and those who support them, while positively shaping the social and policy contexts in which they live. For information about Down syndrome contact us directly at info@cdss.ca. #SeeTheAbility
- Website
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https://cdss.ca/
External link for Canadian Down Syndrome Society
- Industry
- Non-profit Organizations
- Company size
- 2-10 employees
- Headquarters
- Calgary , Alberta
- Type
- Nonprofit
- Founded
- 1987
- Specialties
- Down syndrome and Disabilities
Locations
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Primary
Get directions
1001 1st Street
Suite 202
Calgary , Alberta T2G 5G3, CA
Employees at Canadian Down Syndrome Society
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Dan Purdham
Medical Director | Board Member
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Elizabeth Kennedy
Inclusion-oriented leader that is passionate about operational effectiveness
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Samar Qureshi
President @ Human Integrity HR | Specializing in Diagnostic Imaging Recruitment | Experienced Board Member
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Courtney Cassel
Owner of Cassel Consulting, Marketing Manager of Canadian Down Syndrome Society, Full Stack Digital Marketer, Content Creator, Public Speaker, and…
Updates
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A great opportunity to learn more about the intersection of disability advocacy and climate change!
On August 1, DSRF’s Director of Communications + Sustainability Glen Hoos will be the featured speaker at a free Climate Connections Lunch 'n Learn. People with disabilities and other pre-existing health conditions have increased vulnerability to climate-related extreme weather events. Learn why climate change is a crucial issue for people with disabilities, and hear how DSRF is working to ensure the voices of those with disabilities are centred amidst the climate crisis - and how your organization can do the same. Registration: https://bit.ly/3xy4bx2
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Dedication to advocating for the rights of adults living with disabilities continues to make impact. Along with People First of Canada, Inclusion Action In Ontario, and Community Living Ontario, our organization acted as intervenor on this appeal. Thanks to all for insights and assistance.
I am pleased to share our decision that my colleague, Stephanie Timerman, and I successfully argued at the Court of Appeal affirming the rights of adults living with disabilities to procedural fairness and natural justice in litigation between their parents. I am seeing this issue more and more in my practice and the Court of Appeal has now provided the family law bar with much needed clarity in process when parents seek parenting orders under the definition of “child of the marriage” in the Divorce Act to appropriately address the intersection of disability rights and capacity for decision-making. We are very grateful for the support and assistance of the intervenors on this appeal, People First of Canada, Canadian Down Syndrome Society, Inclusion Action in Ontario, and Community Living Ontario.
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"A society is judged by how it treats its most vulnerable population. $6.66 per day is a slap in the face of these lovely humans and their families [...] I feel like we treat our communities with exceptionalities with so little care and this announcement is a manifestation of that." - Karl Nieva Read the full article on the community's response to Canada Disability Benefit in the Advocacy edition of 3.21 Magazine: https://buff.ly/4bBv80p
🗓️ It has been one full year since the Canada Disability Benefit (CDB) was passed in the Parliament. Today also marks the official day of the law coming into force and counting down to a year from now when the government must have the disability benefit fully in place. Sadly, while we have waited this past year not much has changed and many people with disabilities and their families continue to struggle in a life of poverty. This wait will continue for another year while the government works on designing the benefit and building the rules. We know a $200 per month, maximum benefit is not enough to make a difference in the lives of people with disabilities. We asked some of our current and past Board members to describe what a $200/month (or less than $7/day benefit) would mean to them. Watch Carlos, Yvonne, and Michael tell us their thoughts and reactions to the federal government’s proposed plan. We need to build a better benefit. There is still time to get this right. See Inclusion Canada’s policy brief on how the Canada Disability benefit can be better and make a significant difference: https://lnkd.in/g_DhXvr8 #BuildABetterBenefit
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"The shortest distance between strangers is a story. So I would encourage anyone to find stories of people who are not like you. Because that will serve to establish a proximity which is necessary for you to understand them, to know how much closer they are to you as a human being than you might have previously assumed." - Filmmaker, storyteller, and caregiver Moses Latigo Odida speaking on how organizations and individuals can support the Black disability community. In the most recent Advocacy issue of 3.21 Magazine, we spoke to Moses about his experience as a Black caregiver, his work on his documentary series DOWN, and his personal advice as an advocate in the disability community. We must acknowledge that although we are connected through our passion and advocacy goals, the lived experiences of people with Down syndrome and their caregivers looks very different for each family. Continue exploring this topic in the article "Finding a Village" in 3.21 Magazine: https://buff.ly/3X2mm82 #RepresentationMatters #CaregiverSupport #DownSyndromeAdvocacy 3.21 Magazine is co-published with the @DownSyndromeResourceFoundation
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Last night, not only did Assume That I Can win a Gold Lion at the Cannes Lions International Festival of Creativity, but in this amazing moment, the entire audience gave Madison Tevlin a standing ovation for her performance. We are very proud as we watch Madison represent our community and smash stereotypes on the world stage. It was a privilege to work on a campaign that resonated with millions and shifted perspectives for so many. #AssumeThatICan #SeeTheAbility
About last night at the Cannes Festival of Creativity... A gold lion, but above all the entire industry present paid tribute to Madison Tevlin with a standing ovation. An epic moment that we will never forget! #AssumeThatICan #LionsCannes SMALL | Indiana Production | Stabbiolo Music | Rich Lee Canadian Down Syndrome Society | Down's Syndrome Association | Down Syndrome Australia | National Down Syndrome Society | Global Down Syndrome Foundation | New Zealand Down Syndrome Association (NZDSA) | Down Syndrome International Fondazione Cariplo | Fondazione Compagnia di San Paolo
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Happy Father's Day to all the amazing dads in our community! Thank you for all that you do to support and advocate for your children everyday. We hope you feel loved and celebrated today. #DownSyndromeDad #DownRightAwesome #HappyFathersDay #DadLife
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The Down Syndrome Walk is TOMORROW! Can't make it out to an event? You can still show your support with a donation. The Walk ensures that life-changing projects like Inployable, Mindsets, and 3.21 Magazine reach thousands of Canadians. Donate at DownSyndromeWalk.ca ID: Team Paul Sawka gathered together in a driveway. Paul and his father hold a Down Syndrome Walk banner. #DownSyndromeWalk #EndTheStereotypes
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Over a million people in Canada with disabilities currently survive on less than $20,000 per year. In order to lift these individuals out of poverty, it is critical that provincial and territorial governments pledge that the Canada Disability Benefit will not be clawed back by their disability income support programs. We join disability organizations across the country in calling for provincial and territorial governments in prioritize the CDB; it must be implemented without delay and with no claw backs. Read the full letter: https://buff.ly/3VIGdbD ID: White text on a black background reads: Over 1 million Canadians with disabilities Under $20,000 per year to survive. A thin horizontal red line is underneath the text and a small red and white CDSS asterisk #CDB
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Very proud to have been part of this powerful campaign and grateful for the support it has received from the community.
V O T E F O R U S! "Assume That I Can" is among the Campaigns nominated by @ACTResponsible in the Education section! 🧡Just click on the heart on this page🧡: https://lnkd.in/dr2EiWEY THANK YOU!!! SMALL | Indiana Production Canadian Down Syndrome Society | Down Syndrome Australia | Down's Syndrome Association | National Down Syndrome Society | Global Down Syndrome Foundation | New Zealand Down Syndrome Association (NZDSA) | Down Syndrome International