Our Mission
TRPM3 Foundation is dedicated to increasing awareness of TRPM3-related disorders and improving the lives of individuals affected by these conditions. Through education, advocacy, and research, we aim to promote a better understanding of these disorders and improve access to diagnosis, treatment, and support for those affected.
Focus Areas
Raise awareness about TRPM3-related disorders among healthcare professionals, policymakers, and the general public.
Support individuals and families affected by TRPM3-related disorders by providing access to information, resources, and peer support.
Advocate for increased research funding and development of new treatments for TRPM3-related disorders.
Foster collaboration among researchers, healthcare professionals, and patient communities to advance knowledge and improve outcomes for those affected by TRPM3-related disorders.
Empower individuals with TRPM3-related disorders to lead full and meaningful lives by promoting access to healthcare, education, employment, and other opportunities.
Image courtesy of Francisco J. Enguita, B.Pharm, Ph.D
Our Values
Empowerment: We believe in empowering individuals and families affected by TRPM3-related genetic disorders through education, advocacy, and support. We strive to provide resources and tools that enable individuals to take control of their health and well-being.
Collaboration: We recognize the importance of collaboration among researchers, healthcare professionals, patients, and their families in advancing research, improving treatments, and enhancing the quality of life for individuals affected by TRPM3-related genetic disorders. We are committed to fostering collaboration and building partnerships that drive progress towards our shared goals.
Innovation: We embrace innovation and are dedicated to promoting cutting-edge research and technology to improve the diagnosis, treatment, and management of TRPM3-related genetic disorders. We support novel approaches and the development of new therapies that hold promise for individuals with these conditions.
Advocacy: We are passionate advocates for individuals affected by TRPM3-related genetic disorders. We advocate for increased funding for research, improved access to healthcare, and the development of policies that support the needs of the rare disease community.
Inclusivity: We are committed to creating an inclusive and diverse community that values and respects the unique experiences and perspectives of all individuals affected by TRPM3-related genetic disorders. We strive to create a safe and welcoming space where individuals and their families can connect, share their stories, and find support.