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.

Close up shot of micro pipette tubes in an orange holder

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.