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HAEA app for the 2019 summit in Atlanta, GA
This app will show you all the track scheduling information and any changes which may happen during the conference. This app will allow you to receive realtime updates via push notifications from the HAEA staff. You will be privy to detailed information about each session.
The US Hereditary Angioedema Association, Inc. (HAEA) is a non-profit, patient advocacy organization dedicated to serving patients with C1 Inhibitor Deficiency or Hereditary Angioedema.
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