Searching for Hereditary Angioedema Support information? Find all needed info by using official links provided below.
US HAEA The US HAEA is a non-profit patient advocacy organization serving Hereditary Angioedema patients. Our Association was founded and staffed by HAE patients and caregivers. We provide the HAE community with a personalized support network and a wide range of services to help them lead a …
https://www.webmd.com/skin-problems-and-treatments/qa/where-can-you-get-support-for-hereditary-angioedema-hae
Feb 01, 2019 · Where can you get support for hereditary angioedema (HAE)? ANSWER To learn more about hereditary angioedema (HAE) and to find the support of others who have it, …
https://www.onepath.com/hae
US Hereditary Angioedema Association (HAEA) This non-profit patient advocacy organization, founded and staffed by HAE patients and caregivers, provides a wide range of HAE resources and personalized patient support.
https://www.drugs.com/answers/support-group/angioedema/
Oct 11, 2019 · Ask questions and get answers about Angioedema. Our support group helps people share their own experience. 32 questions, 44 members, 6 news articles.
https://www.webmd.com/skin-problems-and-treatments/hereditary-angioedema
Hereditary angioedema is a rare genetic condition that causes swelling under the skin and lining of the gut and lungs. It can happen in different parts of your body. You are born with hereditary angioedema (HAE). Although you’ll always have it, treatment helps you manage it.Author: Annie Stuart
https://haeaustralasia.org.au/
Welcome to HAE Australasia. HAE Australasia is a not for profit patient advocacy organisation, dedicated to providing support to Australian and New Zealand HAE patients and their families, as well as raising awareness of hereditary angioedema resulting from C1-inhibitor deficiency.
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