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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 Logo


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.

Visit Inspire

PF Warriors, Logo

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.

Visit PF Warriors

Pulmonary Fibrosis Foundation Logo

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.

Find Support Groups

View PFF Educational Resources

Watch PFF Educational Videos

Support Communities for Conditions that May Cause ILD

Arthritis Foundation, Logo

Arthritis Foundation

A community that provides support, information, and connection for those impacted by arthritis.

Visit the Arthritis Foundation

Foundation for Sarcoidosis Research, Logo

Foundation for Sarcoidosis Research

An organization committed to sarcoidosis research and improving care for people with sarcoidosis.

Visit the Foundation for Sarcoidosis Research

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.

Visit the National Organization for Rare Disorders

National Scleroderma Foundation

A nonprofit organization dedicated to providing support, education, and research for the scleroderma community.

Visit the National Scleroderma Foundation

Sjogren's Syndrome Foundation, Logo

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.

Visit the Sjögren’s Foundation

The Myositis Association, Logo

The Myositis Association

An organization committed to improving the lives of those affected by myositis through research and advocacy.

Visit the Myositis Association

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