HAE Afghanistan

20/06/2025

Great news for HAE Patients in afghanistan

Clear and simple HAE information

07/05/2025

07/05/2025

Understanding HAE

21/02/2025

به HAE در افغانستان خوش آمدید ما یک گروه حمایوی برای بیماران مبتلا به آنژیودیما ارثی و همچنان خویشاوندان، داکتران و محققین آنها هستیم. ما همه با هم یکجا میشویم تا محیط ...

21/02/2025

One step ahead, I would like to share HAE Afghanistan's website, where you can now access information about HAE in our native language.

به HAE در افغانستان خوش آمدید ما یک گروه حمایوی برای بیماران مبتلا به آنژیودیما ارثی و همچنان خویشاوندان، داکتران و محققین آنها هستیم. ما همه با هم یکجا میشویم تا محیط ...

21/02/2025

❗300 million people worldwide live with a rare disease. 1 in 10,000 to 1 in 50,000 of them have HAE – hereditary angioedema – a very rare, potentially life-threatening genetic disease ❗

Though we are small in numbers, we are very active, creating awareness of HAE and making governments, physicians, and the general public aware of the disease and how it affects our lives to improve time to diagnosis and advocate for approval and reimbursement of lifesaving therapies.

With over 100 Member Organizations worldwide, we are represented in almost every corner of the world, and the number continues to rise 🙌 🌍

Read more about HAE and get contact information for all our Member Organizations on our website 👉👉 https://haei.org/

12/12/2024

25/09/2024

15/07/2024

🇹🇳 News from around the world

In this year's first edition of Global Perspectives, HAE Tunisia (ANAOH) tells us about their activities so far in 2024, including as organizing a medical caravan and training front-line doctors on HAE.

Read more about the activities in the article on our website 👉👉 https://buff.ly/4eNQLO6

Want to read more news from our member countries? Please visit our website:
Member Countries 👉👉 https://buff.ly/3snBD64
Global Perspectives 👉👉 https://buff.ly/2XeIJbO

16/05/2024

Happy HAE day