Edwards Syndrome Association: Awareness Materials
At the Edwards’ Syndrome Association, we believe that raising awareness is one of the most powerful ways to support children and families impacted by Edwards’ Syndrome (Trisomy 18). To make it easier for our community to share accurate information, we’ve created a collection of free awareness materials that you can download, print, and distribute.
These resources are designed for families, caregivers, medical professionals, schools, and advocates who want to help educate others and spark meaningful conversations. From brochures and fact sheets to informational flyers, each item is created with compassion, clarity, and care.
We’ll continue updating this section with new tools and resources. We offer printed brochures and pamphlets that can be shipped directly to you. Donations are always appreciated to help make this possible and to keep expanding our outreach efforts.
Together, we can spread knowledge, inspire hope, and strengthen the Edwards’ Syndrome community.
Podcast Brochure
Discover the Edwards’ Syndrome Association Podcast with our beautifully designed brochure! Inside, you’ll find everything you need to know about our mission, hosts, and how to tune in. This brochure is perfect for sharing with friends, family, and medical professionals—or simply keeping as a resource for yourself.
You can view it online, download the PDF, or print and share it to help spread awareness and invite others to join the conversation. Every share brings more voices to our community and strengthens the impact of Edwards’ Syndrome awareness.
Informational Brochure
The Edwards’ Syndrome Association Informational Brochure is a resource designed to raise awareness about Edwards’ Syndrome (Trisomy 18) and share our mission of advocacy, education, and support.
This brochure can be saved, downloaded as a PDF, or printed and shared with families, medical professionals, schools, and your community. By distributing this material, you help spread knowledge, empower families, and strengthen the movement toward a more inclusive world.
Medical Professional Brochure
The Medical Professional Brochure is designed to engage and inform healthcare providers about Edwards’ Syndrome (Trisomy 18). It emphasizes the importance of advocacy, evidence-based perspectives, and collaborative care to improve outcomes for children and their families.
Our mission is to partner with medical professionals in challenging outdated perceptions and advancing a more compassionate, informed approach to care.
This brochure can be viewed online, downloaded, or printed for use in hospitals, clinics, universities, and medical conferences. By sharing and utilizing this resource, you play a vital role in ensuring families receive the support they need while strengthening the broader movement of advocacy, education, and inclusion.
Angel Brochure
The Angel Brochure honors children with Edwards’ Syndrome (Trisomy 18) whose legacies continue to inspire change. It shares our vision of creating a more inclusive world, while empowering families and raising awareness through advocacy, education, and support.
You can view, download, or print this brochure to share with loved ones, medical professionals, and your community—helping to keep every angel warrior’s story alive and fueling the mission of the Edwards’ Syndrome Association.
Infographic
The Edwards’ Syndrome Association Infographic offers essential facts about Edwards’ Syndrome (Trisomy 18), its prevalence, survival outcomes, and the importance of individualized care. It emphasizes that Trisomy 18 is not inherently lethal—interventions and access to consistent medical care can improve outcomes and change lives.
This resource is designed for families, caregivers, and medical professionals, covering:
Key statistics on Trisomy 18 survival and prevalence
The importance of fair and consistent medical care
Advocacy for equitable access to interventions, including heart surgeries
You can view, download, or print this brochure to share with medical providers, hospitals, schools, and your community. Every copy distributed helps challenge outdated assumptions, spread accurate information, and support children with Trisomy 18 and their families.
