We are a nonprofit organization founded in 2018 by Tim and Kasie Evans. Kasie was diagnosed with Achalasia in 2012 after 2 years of being told it was all in her head. We are currently awaiting approval for our 501(c)(3) nonprofit status. We are committed to finding a cure for Achalasia through research, education of those afflicted, and education of medical professionals. We aim to be a resource for those who might not yet be diagnosed with Achalasia but are experiencing symptoms. We want to help those people get diagnosed sooner. For those who have a diagnosis we are a support system, community of ideas, and an ever growing force with one common goal...To make Achalasia a thing of the past and go on to live normal lives.
Have you or someone you love been diagnosed with Esophageal Achalasia? Do you think you might have it? Maybe you're a medical professional who would like to learn more and find out how you can help. We are always looking for people to get involved and help on any level. Contact us today and we'll be happy to help answer any questions. Only together can we overcome this horrible disease.
Our mission to find a cure for Achalasia is not possible without your generous donations. Whether you prefer a one time gift or a monthly donation, you can be sure that we are hard at work doing everything we can to make this dream a reality. I, (Tim) watch my beautiful wife Kasie suffer daily, and we will not rest until her pain is a distant memory. Click on donate now at the bottom of this page to join our fight.
Your generous gift will help us fund our mission to save lives through education, research and ultimately curing Achalasia.