Shaping Future Leaders in Rare Disease Advocacy and Education
Thank you for your interest in the E.WE Foundation Internship Program. At this time, we are not accepting internship applications. Please check back for future opportunities or contact us to learn more about the program.
Program Overview
The E.WE Foundation Internship Program is a mission-driven opportunity designed to cultivate the next generation of rare disease advocates and leaders.
Interns gain meaningful, real-world experience across key focus areas, including:
- Healthcare Advocacy
- Genetic Counseling
- Maternal Health & Infant Mortality
- Mental Health
- Community-Based Research
By working alongside professionals, researchers, and patient leaders, interns actively contribute to education, research, and awareness initiatives centered on Trisomy 18 and other rare conditions.
Internship Summary
Our internship program welcomes:
- Full-time and part-time students
- College and graduate students
- Non-degree-seeking students and recent graduates
We strongly encourage applications from individuals representing underrepresented or underserved communities.
Interns are:
- Selected through an online or in-person interview process
- Paired with a dedicated mentor
- Engaged in a 16-week internship term
- Expected to complete and present a final project
Time commitment varies depending on mentor assignment and project scope. When applicable, academic advisors are welcome to attend final presentations.
Stipend Availability
We recognize the value of our interns’ time and contributions. The E.WE Foundation strives to offer stipends whenever possible to promote equitable access to internship opportunities.
Please note: Stipends are contingent upon funding availability and are not guaranteed for every term.
Internship Activities & Learning Experience
Interns may:
- Complete meaningful, mission-aligned projects
- Participate in a virtual orientation and professional development sessions
- Attend collaborative meetings and learning opportunities
- Engage in mentorship and community-based learning experiences
Internship Focus Areas
Healthcare Advocacy
Support advocacy campaigns, public policy efforts, and initiatives that elevate patient and caregiver voices.
Genetic Counseling
Collaborate with genetics professionals to assist with patient engagement, case review support, and ethical considerations.
Maternal Health & Infant Mortality
Contribute to research, education, and advocacy addressing disparities in maternal health outcomes and infant survival, particularly within rare disease communities.
Mental Health
Explore trauma-informed care approaches and help develop mental health resources for patients and caregivers.
Community-Based Research
Assist with literature reviews, data collection, and analysis to strengthen community-informed rare disease and health equity research.
Final Project & Presentation
At the conclusion of the internship term, interns present a capstone project to E.WE Foundation leadership, gaining hands-on experience in professional communication, evaluation, and presentation.
Contact Us
Interested in learning more about the internship program or sponsoring an intern? Email us at: admin@theewefoundation.org