As a rare disease family ourselves, we’re always honored to have the opportunity to support events for rare disease associations and foundations. We offer discounts for clients like these.

We did photography and video for the Koolen-de Vries Syndrome (KdVS) Foundation’s annual patient advocacy summit when it came to Orlando.

We did event photography on day 1 and returned on day 2 with our studio kit to be on hand for families and KdVS clinicians and scientists who wanted portraits taken.

Those portraits can be seen here.