Support

RARE Impact Grant Opportunities

In the past, Global Genes has provided grants to rare disease patient advocacy organizations to make specific, tangible differences for the communities they serve.

In 2024, grants were awarded to Global Advocacy Alliance member organizations to further work and to develop programs to address health and wellbeing of the rare community and research readiness.

2024 Rare Disease Grant Awardees

2023 RARE Impact Grant Program

Over the past decade, Global Genes’ RARE Impact Grant Program has provided grants to rare disease patient advocacy organizations that are part of the Global Advocacy Alliance to make specific, tangible differences for the communities they serve. In 2023, these funds:

Stewarded initiatives to develop educational tools and resources to improve health equity in underserved and underrepresented populations
Supported in-person meetings and community building opportunities to foster collaboration, social support, education, and awareness
Improved the health and mental well-being of the rare disease community, including children, siblings, caregivers/care partners and those who are grieving.

View the Global Genes 2023 Grant Report

2023 Impact Grants Were Awarded To:

Words From Previous Winners

“Thanks to the support of grant funding, we were able to focus our efforts on providing the necessary care to patients, on finding drugs and arranging their delivery, to provide psychological assistance, to interact with volunteer, state and local services to more effectively solve the problems that patients had after the start of the war in Ukraine. It is important to feel the support of friends from all over the world, it really helps a lot not to give up and keep fighting! We are very grateful to you!!! Thanks!!!”
-PHA Ukraine, Oksana

“These meetings help in so many ways! It is emotional and affirming to meet with other children and families with the same wonderful kids. The presentations are focussed and almost 100% relevant and useful – the information keeps coming thick and fast.
And the networking with other families builds bonds of support and also gives lots of useful day-to-day Tips.”
-Caregiver, Meet-ups Grant

“Thank you for your recent gift to the Global Foundation for Peroxisomal Disorders. Your generous contribution will help us support families from 39 countries around the world impacted by peroxisomal disorders, while also funding groundbreaking research initiatives to improve quality of life for patients impacted by this devastating childhood disease. Thank you for choosing to support GFP and opening your heart to our families.”
– Melissa Bryce, ED and Co-Founder of Global Foundation for Peroxisomal Disorders