Canadian CdLS Foundation
Empowering CdLS families for life. Advocacy, Support, Education, Awareness.
Canadian CdLS Foundation Email
Canadian CdLS Foundation Email
Canadian CdLS Foundation Facebook
Canadian CdLS Foundation Facebook
Canadian CdLS Foundation Instagram
Canadian CdLS Foundation Instagram
Canadian CdLS Foundation X
Canadian CdLS Foundation X
CdLS YouTube Channel - Brave Heart & Warrior Spirit, Emily Turner
CdLS YouTube Channel - Brave Heart & Warrior Spirit, Emily Turner
Upcoming Events
Upcoming Events
FIVE FRIENDS FUNDRAISER | CanadianCdLS
FIVE FRIENDS FUNDRAISER | CanadianCdLS
Help us find Canadian families effected by Cornelia de Lange Syndrome by increasing awareness and early diagnosis. Your donations will support the education of healthcare providers and educators to ensure each person with CdLS survives and thrives.
Email us at support@canadiancdlsfoundation.com
Email
·
support@canadiancdlsfoundation.com
Email us at support@canadiancdlsfoundation.com
Meet Madison - a thriving young woman with CdLS
Podcast
·
Podcast
Meet Madison - a thriving young woman with CdLS
Podcast Episode · CdLS Connections · May 30, 2024 · 1h 59m
Charity # 707263885 RR 0001
Canadian CdLS Foundation Website
Canadian CdLS Foundation Website
The Canadian CdLS Foundation is a non profit registered charity raising awareness, providing support, improving diagnosis and education to individuals and families impacted by Cornelia de Lange Syndrome, their healthcare providers and educators. We support Canadians with this rare disease that impacts 1:10 000 Canadians.
Canadian CdLS Foundation Facebook Page
Canadian CdLS Foundation Facebook Page
DONATE | CanadianCdLS
DONATE | CanadianCdLS
DONATE | CanadianCdLS
Help us find Canadian families effected by Cornelia de Lange Syndrome by increasing awareness and early diagnosis. Your donations will support the education of healthcare providers and educators to ensure each person with CdLS survives and thrives.
Book a Virtual Consultation
Book a Virtual Consultation
FAMILY SUPPORT | CanadianCdLS
FAMILY SUPPORT | CanadianCdLS
CdLS Connections
CdLS Connections
Navigating the challenges & triumphs of Cornelia de Lange Syndrome (CdLS) and where we explore, learn, and share everything related to CdLS. We will learn from families, clinicians, researchers & educators and those exploring new frontiers...
LinkedIn
LinkedIn
Canadian CdLS Foundation | 83 followers on LinkedIn. Supporting individuals with Cornelia de Lange Syndrome & other rare conditions, their families, clinicians & community. | We provide families and individuals with CdLS the support and resources they need to love their best lives. We support timely access to accurate diagnosis, medical care and other resources. We support families in advocacy by participating in care team meetings, IEP meetings and individual one on one family support meetings.
Shop | Canadian CdLS Awareness Foundation
Shop | Canadian CdLS Awareness Foundation
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