Your home for healing

Our providers will work with you and the rest of your care team to conduct a thorough evaluation and develop a personalized treatment plan that addresses your symptoms and their root cause.

We believe you deserve a dedicated care team to help you in your journey to diagnosis and healing. Most people struggle with mysterious symptoms for 10 years or more before finally getting diagnosed with Ehlers Danlos Syndrome. We are here to change that. We offer best-in-class care to you in your home via telehealth, and we are proud to be part of the Ehlers Danlos Society's Network of Excellence Program

We recognize that many people have have had their symptoms dismissed ignored by the medical system. We are different. We listen. We understand these conditions in ways that others do not because we work with Hypermobility and Ehlers-Danlos Syndrome on a daily basis. Our team has diagnosed and cared for more EDS patients than most doctors see in their entire career. Some of us even live with these conditions.

Our Mission

We are deeply committed to improving acess to EDS diagnosis and treatment for all members of our community. Ten years ago, Professor Rodney Grahame, remarked that “no other disease in the history of modern medicine has been neglected in such a way as Ehlers-Danlos syndrome.” Since then, EDS awareness has dramatically increased, but access to care still lags behind. It takes decades to change the practice of medicine, and we aren't willing to wait that long. That's why we are building a virtual center of excellence to provide care for EDS patients across the United States. We won't be able to provide accessible care for everybody today, but we are building towards a future in which every EDS patient can access quality care that is covered by insurance.