The E.WE Foundation

Global healthcare advocacy network for families affected by Trisomy 18 (Edwards Syndrome) and other rare and complex medical conditions.

[The E.WE Foundation @EveryoneIsWe]

Understanding co-occurring conditions and available treatments are essential to supporting whole-person care. Join The E.WE Foundation, in partnership with Pfizer, for a two-part learning series exploring alopecia areata and shared decisions. Register: https://t.co/ROEjfB5CAH

[DR. Ashley the Charlatan 💚✊🏳️‍🌈🏳️‍⚧️✊💚 @BecauseIMatter]

Today, one of the questions we were asked was what we thought needed to happen to cause change in the medical field…

I jokingly said “burn it down” while being partially honest about it but my answer was simple, we have to stop the respectability politics in medicine.

[The E.WE Foundation @EveryoneIsWe]

The LEAP into Advocacy Summit is bringing more than education and advocacy—we're bringing the energy too! We're excited to welcome John B. Kimber Jr., musical artist and guitarist from Birmingham, AL, as our featured live entertainment! Register today: https://t.co/7rdcZBgsf8

[The E.WE Foundation @EveryoneIsWe]

⏰ The countdown is on! Only 23 Days Until LEAP Summit 2026! Join participants from around the world for the 2026 LEAP into Advocacy Summit. LEAP offers a unique opportunity to learn, connect, and drive meaningful change.

🔗 Register today: https://t.co/7tS2QioNBB

[The E.WE Foundation @EveryoneIsWe]

New Learning Module Available! Mental health is an essential part of every care journey. As we wrap up mental health month, we're proud to share our latest self-guided learning module: Mental Health in the Rare Disease Community. Access the module here: https://t.co/CY63nPUGRY

[The E.WE Foundation @EveryoneIsWe]

The E.WE Foundation had the opportunity to participate in the Annual North Alabama Health & Wellness Fair at Calhoun Community College! Thank you to the organizers, sponsors, volunteers, and everyone who stopped by our table to learn more about the work we do!

[The E.WE Foundation @EveryoneIsWe]

Mental health support shouldn’t be a privilege but for many families living with rare and complex conditions, access to care remains out of reach. We believe in creating spaces, resources, and conversations because mental health matters for every diagnosis, caregiver, and family.

[The E.WE Foundation @EveryoneIsWe]

Mental wellness starts with small actions that create meaningful impact. We invite you to take simple steps to support mental health.
✔ Learn
✔ Share
✔ Start a conversation
✔ Check on a caregiver
Mental health matters at every stage of the journey. https://t.co/jNowfGi9kA

[The E.WE Foundation @EveryoneIsWe]

Living with a rare or medically complex diagnosis can impact the entire family emotionally, mentally, and physically. Too often, those struggles go unseen. That’s why we created our Mental Health Resource Center. Visit https://t.co/jNowfGi9kA to learn more.

#MentalHealthMatters

[The E.WE Foundation @EveryoneIsWe]

Caregivers carry more than schedules and medications. And often… they carry it silently. If you’re a caregiver—your mental health matters too. You deserve support, space to breathe, and care that includes you. Explore our efforts: https://t.co/fvjALLnh8D
#CaregiverSupport

[The E.WE Foundation @EveryoneIsWe]

Mental health matters. For individuals and families with rare or medically complex conditions, the emotional impact is real, and often invisible. This May, we’re raising awareness, sharing resources, and holding space for the rare community. Learn more https://t.co/jNowfGi9kA

[The E.WE Foundation @EveryoneIsWe]

Join us for the 2026 LEAP into Advocacy Summit! This year’s theme: Transforming Knowledge and Innovation Into Real-World Impact. This event is approved for 6 CEs.
📅 June 25, 2026
📍 In-person at the University of Alabama in Huntsville + Virtual

Register: https://t.co/yIzR6iqyrk

[The E.WE Foundation @EveryoneIsWe]

Every child deserves to feel safe. But each year, at least 1 in 7 children experience abuse or neglect—and some are at even greater risk. In just 6 minutes, you can become part of the solution. Access our short, self-paced learning module here: https://t.co/2DsieMwvBB

[The E.WE Foundation @EveryoneIsWe]

Child abuse and neglect are more common than many realize—but prevention starts with awareness. Every child deserves to feel safe, seen, and supported. Learn the signs. Share the message. Be part of prevention.
https://t.co/9ejrDzH0bl

[The E.WE Foundation @EveryoneIsWe]

Save the Date! Our annual LEAP into Advocacy Summit is happening June 25 at the University of Alabama Huntsville and virtually! Join us in-person, June 24 for a networking meet and greet! Enjoy food, music, and conversation! Registration opens in April! We hope to see you there!

[The E.WE Foundation @EveryoneIsWe]

Trisomy 18 Awareness Day. Trisomy 18 is often defined by clinical language that tells families what won’t happen. We exist because families deserve more. Our work is rooted in advocacy, equity, and changing systems. Today we honor every child and family impacted by Trisomy 18.

[The E.WE Foundation @EveryoneIsWe]

What is Trisomy? Trisomy means an extra chromosome. Trisomy 18 happens when there’s an extra copy of chromosome 18. This alters development and medical needs, and life expectancy, but it doesn’t erase joy, growth, or connection. Learn more at https://t.co/OV37CYRd4x!
Image: WebMD

[The E.WE Foundation @EveryoneIsWe]

March is #TrisomyAwarenessMonth — a time to honor families, raise awareness, and shine a light on trisomy conditions. This month, we’ll share stories, resources, and moments that matter. Join us as we celebrate families and push for equitable care.
Happy Trisomy Awareness Month!

[The E.WE Foundation @EveryoneIsWe]

Behind every diagnosis is a family seeking answers, a researcher pushing boundaries, and an advocate driving change. That’s why LEAP into Advocacy Summit 2026 matters. Join us June 25, at the University of Alabama in Huntsville and virtually.

Save the date. Join the movement.

[The E.WE Foundation @EveryoneIsWe]

We spent Rare Disease Week in Washington, DC. We’re proud to stand alongside advocates, clinicians, researchers, and organizations from across the country, united by a shared commitment to improving care, access, and outcomes for people living with a rare disease. @SaritaEdwards