Since LivingwithCGD.org launched in January 2015, the Immune Deficiency Foundation has asked members of the community to share their story of Chronic Granulomatous Disease (CGD). This video features individuals, parents and families and how they are living with CGD.

Living with CGD – The IDF Resource for the Chronic Granulomatous Disease (CGD) Community from Immune Deficiency Foundation on Vimeo.

If you would like to share you story of living with CGD, want to speak with someone who understands or would like to request educational materials, click here to contact IDF.

Thank you to all those who have shared their story and continue to be a part of the CGD community!