Today, September 24th is our annual Atypical Hemolytic Uremic Syndrome Day. It’s our designated “special day,” a chance to share with the world the story of our disease and the impact that it has on our families. This year is doubly special as we are proud to bring you our new Foundation website…aHUS.org. We are proud to share with you our progress to date and ask that you check back with us to see our progress in the future. This site is dedicated to all our patients and caregivers who we know today and those yet to be diagnosed, and especially to all those who lost their battle with this disease. It is your site and we hope that you will communicate to us how we can better make it meet your needs. Please feel free to share any feedback with Alyssa at Alyssa@aHUS.org.