Journey with Hereditary Angioedema

The Rare Disease Day was marked on the last day of February (29th Feb 2016) at the Gertrude’s Children’s Hospital, Muthaiga.This was the first physical meeting held to mark the day in Kenya.
Medical Media Services had a chance to talk to Patricia Karani , an advocate for Rare Diseases as well as a patient with Hereditary Angioedema.