Angioedema Fundraiser

Hey, my name is Charis.

I have a real condition called Hereditary Angioedema Type 3. Please take time to read about this condition. Only 1 and 50,000 people get it, and most of them don’t have the type that I have. I’ve been struggling with this condition since I was 13, and I am 19 now. This real condition makes my lips and face swell so I can’t breathe. I’ve been in and out of the hospital. I’m going to see a specialist on September 23. Although it’s very rare, there is medicine for it. I will have to take shots for the rest of my life. The medicine is very expensive. Even though I have this condition I have learned that life is a gift so I will be thankful for it. Thank you for taking time out of your day to read this. All money will go to HAEA. Thank you so much for anyone who gives!!!

Want to join me in making a difference? I'm raising money to benefit Hereditary Angioedema Association Inc, and any donation will help make an impact. Thanks in advance for your contribution to this cause that means so much to me.

More information about Hereditary Angioedema Association Inc: The US HAEA is a non-profit patient advocacy and research organization serving Hereditary Angioedema patients. We provide the HAE community with a personalized support network and a wide range of services to help them lead a normal life and are committed to actively engaging our community through grassroots activities that promote disease education and awareness.