ARDS has a 40% mortality rate
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.
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 Community.
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 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.