Hereditary Angioedema Patient School

With the aim of defending the rights of patients with Hereditary Angioedema (HAE), disseminating accurate information about this disease to the society, promoting early diagnosis and access to treatment, our association organized the "HAE Patient School" event in Izmir on May 12 in cooperation with the Hereditary Angioedema Patients Solidarity and Assistance Association (HAÖDER). The event, held at the Doubletree By Hilton Hotel Alsancak, was attended by approximately 50 patients and was broadcast live on the internet to a wide audience.