Welcome to KCNQ2 e.V.
We are delighted that you have found your way to us! Our association is passionately committed to raising awareness of the rare genetic defect KCNQ2. We are a dedicated team of affected parents, supporters, and sponsors of the association who work together on a voluntary basis to gather information, share experiences, and offer support to families facing the challenges of this genetic defect.
Our goal is to use the knowledge gained from research on the KCNQ2 gene to better understand the underlying causes of epilepsy. We firmly believe that knowledge is key—not only for greater understanding, but also for advances in the treatment and support of affected children and their families.
It is our hope that deeper insights into the KCNQ2 gene will help shed light on the condition and open up new perspectives. Together with scientists, doctors, and other organizations, we strive to improve the quality of life for those affected and pave new paths in research. Together, we can tackle the challenges of the KCNQ2 gene defect and bring about positive change. Your support is important to us—whether through membership, donations, or simply by sharing our message. We look forward to getting to know you!
Become a supporting member
Please fill out this membership form carefully so that we can welcome you as a new sponsor soon.
