Hereditary Angioedema Association
Delete media item?
Delete this item from the media gallery? It will also be deleted from any related story update.
Set as ?
The campaign video will appear in social media and email.
The campaign cover picture will appear in social media and email.
The will appear at the top of your campaign page and in social media and email.
Reset ?
It will be removed from the top of your campaign and won't be used as default in social media and email. The will remain in the media gallery.
Delete update
Delete this story update?
Any pictures or videos will remain in the campaign's media gallery.
Organization campaigns
Anita Shaffer in 1977 at the age of 6 was diagnosed with Hereditary Angioedema Type 1. For 35 years I've tried new drug therapies (with terrible side effects) and getting life saving intervention at my local emergency room as many as 2 times per month.
Finished June 16, 2016
The HAEA has worked for 15 years to support the development of new HAE drugs, therapies, and research. We are humbled and inspired by the community we serve and the bravery and persistence exhibited by our patients. To the Finish line, Katie and Tim!
Finished April 18, 2016
Michael Ardito is a 15 year old high school student on a mission. For the last 5 years his goal has been to raise awareness and money for research to find a cure for Hereditary Angioedema. Both his step dad, John Harrington and his sister Kati Harrington
Finished November 6, 2015
Hereditary Angioedema (HAE) is a rare, debilitating and potentially fatal genetic disease resulting from a deficiency of a key plasma protein. Patients suffer from unpredictable attacks of swelling that involves the hands, feet, abdomen, face, and airway.
Finished June 13, 2015
Profile privacy settings
Stats and activity can only be shown when the profile is public.
It might take up to 3 minutes until changes appear for visitors.