The ThinkGenetic Foundation is committed to positively impacting the rare disease community by offering education, awareness, and patient advocacy. Our mission is rooted in the belief that collaboration and support are crucial to advancing the well-being of patients and healthcare providers in this unique space. As such, we have established a no-cost Advocacy Organization Network Membership for support groups and non-profits focused on these shared beliefs.
We take great pride in fostering an environment where like-minded organizations join forces to amplify their efforts and work together for the greater good. As part of our advocacy network, our members have the opportunity to share valuable information and raise public awareness about the challenges faced by those with rare diseases.
Are you part of a non-profit or support organization in the rare or genetic disease space? We invite you to participate in this initiative by submitting a membership application form below. If you would like to chat with us to learn more before filling out an application please contact us and a Foundation team member will get back to you with more information.
