Yes, the weekend of October 9, saw the Hereditary Angioedema Association (HAEA) a mile high and happy–but not the way you’re thinking! What’s wrong with you?
The HAEA hosted the 2015 National Patient Summit in Denver, Colorado that weekend, boasting brand new opportunities for involvement and innovation.
Participants came to play their part in “shaping the future” for people suffering from HAE by…
Giving their bodies up for science. You didn’t need those kidneys anyway, right?
Source: Quickmeme.com
Becoming a politician for the day and enacting laws that do nothing but bring HAE to the forefront of public awareness
Learning about treatment options and how to harness their combined power to extinguish HAE for good
Source: Giphy
Meet the folks behind the label and tell them how you really feel about the price of their drugs
Develop a cure for HAE at the Cure-Finding Discovery Table
Source: Cloudfront.com
Click here to learn more about the HAEA National Summit and how most of the information in this article is greatly exaggerated.
In actuality, the Summit was a great and wholesome time to learn about HAE, play a part in making a difference, and meet others on a similar hereditary angioedema journey.
