The ‘Voor Sara’ Foundation was established in late 2016 by the parents of Sara Verbrugge, shortly after they learned that Sara suffers from the incurable muscle disease Lama2-MD (also known as MDC1A). Children with this muscle disease generally do not live long, and the muscle weakness brings significant limitations in daily life. Since the diagnosis, they have been wholeheartedly dedicated to supporting Sara and all other children affected by this terrible muscle disease. They also aim to raise awareness about the many lesser-known and very rare muscle diseases and the impact these conditions have on patients and their families.

The Voor Sara Foundation firmly believes that ALL muscle diseases must be eradicated, and this can only be achieved through proper medical research. Currently, it is difficult to raise funds for small patient groups, leading to less investment and research into the rarest muscle diseases. However, these diseases are not more difficult to address, and in our view, these patients also deserve a chance at a healthy life. Lama2-MD belongs to a group of muscle diseases that share a common underlying issue. If a solution can be found for this, many patients with various muscle diseases could benefit.

The parents dream that despite her muscle disease, Sara will one day be able to lead an independent and happy life. They believe that children and adults with muscle diseases can look forward to a healthier future through better diagnostics, quality care, and ultimately, a cure. We hope that all these patients can grow old without worries.

To support the fundraising events, various graphic materials have been designed.

Project:
Print, outdoor and event support.

Service:
Graphic design, Desktop Publishing and image editing.