The main purpose of our non-profit organization is to support both domestic and international scientific research projects and the access of these projects and genetic researches to the clinical trial phase in order to find possible treatments for congenital muscle diseases. Basically; We focus on finding treatment and research.
It is very important to determine the diagnosis of the patients and to know which disease is caused by the mutation in which gene. It is incredibly valuable to bring patients to the diagnosis and to provide patient families with the necessary information about patient care. Unfortunately, there are many patients in our country and in the world who have not yet been diagnosed and do not know the name of the disease and what should be considered. Our association aims to provide support in this regard.
In addition, we aim to create unity by bringing families together for social awareness and information exchange. We believe that the more we are together, the more we can make our voices heard.