As patients living with Asherman’s Syndrome, we know firsthand the challenges this condition brings—not only physically but also mentally. The isolation and uncertainty throughout the process of finding treatments and explanations often leads to stressful and sometimes traumatizing experiences.
Our initiative stands as a bridge between the patient community and the medical field, bringing together experience and evidence. By sharing research, experiences, questions, and outcomes, both patients and professionals help build a broader foundation of knowledge—knowledge that supports ongoing research and shapes future treatment.
Because this journey can feel isolating and overwhelming, our goal is to create a space where patients can find support and understanding in one another. At the same time, we aim to share information that goes beyond what is typically available in standard hospital settings—particularly regarding the formation of Asherman’s Syndrome and its possible connections to other syndromes or autoimmune conditions. By looking at the broader picture, we hope to encourage deeper awareness and continued research.
Our content is supported by research from respected medical institutions such as the Carlos Simon Foundation, Spaarland Gasthuis, Cleveland Clinic and Mayo Clinic which we thank for their incredible dedication to decoding this syndrome and fighting for women’s health globally.
Asherman Foundation 