The CLOVES Syndrome Community Board of Directors is a passionate and dedicated group of individuals who work tirelessly and persistently to create a better life for those living with CLOVES and PIK3CA Related Conditions. It includes individuals with a diverse range of professional and personal backgrounds to support the needs of the organization. Members of the Board have achieved leadership stature in business, community involvement, healthcare, philanthropy, the rare disease space, or the nonprofit sector and are willing to support and assist with the mission, goals, objectives and values of CLOVES Syndrome Community.
Meet our Board of Directors here.
The Board of Directors is currently seeking new members to help us fulfill and expand CSC’s mission. If the description above resonates with you and your experience professionally, personally, or both, please consider applying to join the Board today.
Email [email protected] with questions.