Hae International

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HAEi is the global umbrella organization for the world’s Hereditary Angioedema (HAE) patient groups. We are dedicated to improving the lives of people with HAE. A global not-for-profit network of patient associations dedicated to improving the lives of people with hereditary angioedema (HAE) by raising awareness of HAE, improving diagnosis time and providing advocacy for approval and reimbursement for lifesaving therapies.

Founded

2018

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Address: 10560 Main St Ste Ps40, FairfaxWeb: Sign in to see organisation websiteX (Twitter): HAEDAYVolunteers: 20Revenue: 6004421ICO: 832498576

HAE International - HAE International (HAEi) LIVING WITH HAE. YOURE NOT ALONE Traveling on holiday. Plan a safe trip 102 MEMBER COUNTRIES AROUND THE WORLD united we are stronger. Who we are Welcome to HAE International HAE International is a global nonprofit network of member organizations dedicated to raising awareness of hereditary angioedema and improving the lives of people with HAE.

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Laura

Amazing work being done by HAE International! Every effort counts in improving the lives of HAE patients. Keep shining your light! 🌟 #HAE #PatientAdvocacy

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Mark

So proud to support HAE International and their mission! Together, we can make a difference for those living with hereditary angioedema. 💙 #StrongerTogether #HAEAwareness

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Louis

- How can we better support HAE patients and caregivers in navigating the challenges of travel while managing their condition?

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Christine

- What strategies can HAE International implement to enhance awareness of Hereditary Angioedema in countries with limited resources and healthcare access?

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