Together we can.

 Join us in our mission to make a profound impact at the KCNMA1 Foundation. We hold a steadfast belief that through unity, compassion, and unwavering determination, we can overcome the challenges associated with KCNMA1 gene mutation. Whether you are a researcher seeking collaboration, an individual affected by KCNMA1, or a compassionate soul eager to make a meaningful contribution, we deeply appreciate your interest and extend a warm invitation to you to join us on this remarkable journey. At the KCNMA1 Foundation. addressing the complexities of KCNMA1 Together, we can end KCNMA1. 

 In 2022, the establishment of the KCNMA1 Foundation marked the beginning of a noble journey, driven by an unwavering commitment to discover a cure for KCNMA1 through pioneering research in gene therapy and gene replacement strategies. Simultaneously, the foundation passionately undertakes the task of elevating awareness and imparting knowledge to the general public concerning KCNMA1-related disorders. The commitment ending KCNMA1 is etched into the very fabric of our organization. We promise to persist unwaveringly until a cure for KCNMA1 is unveiled, making it an enduring legacy within the foundation’s history.

Our mission at the KCNMA1 Foundation is to pave the way toward a cure for KCNMA1 gene mutation through cutting-edge gene therapy and gene replacement strategies. We are firmly dedicated to spearheading scientific research collaborations, educating the public, and raising awareness about KCNMA1. Our commitment remains unwavering as we tirelessly work towards finding a cure. We will persist in advancing research, promoting awareness, educating the public, and fighting the good fight until a cure is found.