From Sandy Chan, HAE HK: HAE HK was formed in August 2019 by patients in Hong Kong with HAE and incorporated as a limited company in Hong Kong on 7 November 2019. Tax exemption will be applied. HAE HK aims to achieve optimal standards of care and treatment for all people affected by HAE living in Hong Kong so that [...]
4 August 2019, the very first HAE patient meeting – with 44 patients participating –took place in Hong Kong. The meeting led to the founding of HAE Hong Kong and thus the addition of member number 76 to the HAE International family. HAE Hong Kong already has a Facebook group – you can find it at www.facebook.com/haehongkong. More good news [...]
From Chief Regional Patient Advocate Fiona Wardman: Now that the date and venue for the first patient meeting in Hong Kong have been finalized, HAE International is very excited to meet with patients, carers, doctors, industry partners and the Hong Kong Alliance of Rare Disease for this special meeting in August.
HAE International is a global non-profit network of member organizations dedicated to raising awareness of hereditary angioedema and improving the lives of people with HAE.
HAE International (HAEi)
10560 Main Street, Ste PS40
Fairfax City, VA 22030
United States of America
gro.ieah@ofni
HAE International (HAEi)
Vejlevej 16, 1.
8700 Horsens
Denmark
gro.ieah@ofni
