Find Support Communities
Below are third-party community resources that may be helpful to you. Please note that these third-party entities are not affiliated with, or endorsed by, Boehringer Ingelheim Pharmaceuticals, Inc.
Inspire
Inspire is an organization that partners with national advocacy groups to help connect people living with conditions like interstitial lung disease (ILD) and their caregivers. Through Inspire, users can find support from people who understand the disease and what it’s like to live with it.
PF Warriors
PF Warriors is a volunteer-based group comprised of people living with different types of pulmonary fibrosis and dedicated to helping people understand and manage life with the disease.
Pulmonary Fibrosis Foundation
The Pulmonary Fibrosis Foundation connects people living with pulmonary fibrosis to each other for support and inspiration. The organization also offers education, resources, and access to care for both people with pulmonary fibrosis and caregivers.
Support Communities for Conditions that May Cause ILD
Arthritis Foundation
A community that provides support, information, and connection for those impacted by arthritis.
Foundation for Sarcoidosis Research
An organization committed to sarcoidosis research and improving care for people with sarcoidosis.
National Organization for Rare Disorders
For over 40 years, the National Organization for Rare Disorders (NORD) has been dedicated to individuals with rare diseases and the organizations that serve them. NORD is the leading and longest-standing patient advocacy group for the more than 30 million Americans living with a rare disease. Alongside its more than 330 patient organization members, NORD is committed to improving the health and well-being of all people with rare diseases by driving advances in care, research, and policy.
National Scleroderma Foundation
A nonprofit organization dedicated to providing support, education, and research for the scleroderma community.
Sjögren’s Foundation
A community whose mission is to increase research, education, and awareness of Sjögren’s syndrome and provide support to help people face the challenges of living with the disease.
The Myositis Association
An organization committed to improving the lives of those affected by myositis through research and advocacy.