Swell is a documentary film that showcases the lives of people suffering from a rare, genetic disorder, Hereditary Angioedema (HAE). For more information on HAE, visit the U.S. HAE Association’s website at: www.haea.org

Where can I find the documentary "Swell"?

Is there anyone in this group who has been diagnosed with Acquired Angioedema?

I'm HAE III, subtyped as post menopause exacerbated. UGH. It got so much worse after menopause. I now have weekly abdominal attacks, have gone through millions of dollars worth of special medications, ER visits, diagnostics, etc. Am currently using icatibant/Firazyr when the attacks start. It's helping a lot. No more pain meds. Fingers crossed that it keeps working. Also have Kalbitor/Ecallentide as a rescuer med too, but it cannot be self-administered, and so far the Firazyr, a Bradykinin inhibitor seems to be working better. No side effects of being really tired after dosing. Thank God I have a pretty good insurance plan.

http://www.swellmovie.com/

How did you all go about getting a diagnosis? My doctors just don't seem interested