Acute Respiratory Distress Syndrome (ARDS) affects thousands annually. We fund critical research, provide patient resources, and advocate for better treatment protocols.
We are a network of patient-advocates, scientists, disease experts, and drug developers who have joined together to leverage our collective knowledge and resources to educate, influence policy makers and accelerate research to transform our understanding of ARDS and ECMO.

We host weekly support groups with the patient community.
We are working towards a comprehensive patient registry to improve research and clinical trial participation

We host and participate in educational webinars on topics affected the ARDS and ECMO communities.
We are working to expand reach of education and support through creation of educational materials.

We lend patient voices to policy issues impacting the diagnosis and treatment of ARDS

We have established a grant program that provides small grants to ARDS survivors to reduce financial burden post-ARDS.
We collaborate and extend partnerships with other nonprofits, academic institutes and industry to advance ARDS and ECMO treatments and care.







Please provide us with your first name, last name, a valid email address and your role in order to register for our support group.