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Helping sarcoidosis patients live well.

Educate, Empower, Support

Upcoming Events

Take a Breath for Sarcoidosis Awareness

Dejon Vinyard, Hydes MD

Sunday, April 14, 2024

Virtual Option Available

Join Life & Breath, Sarcoidosis Patients, and supportive friends for this walk/run to spread sarcoidosis awareness.


Topic:
Neurosarcoidosis 101

March 20th (Wednesday), 8 pm EST

Dr. Paula Barreras is a board-certified neurologist with expertise in neuroimmunology. She is an assistant professor of neurology and part of the neuroimmunology center at Cedars-Sinai Medical Center. Dr. Barreras specializes in immune-mediated conditions affecting the brain and spinal cord including neurosarcoidosis and other rare neuroimmunological disorders.


Sarcoidosis Support Group

With Dick and Patt Hewitt

2nd and 4th Thursday, 8 pm EST

Jan 11 & 25, Feb 8 & 22, March 14, 28

Our mission for this support group is to provide support, empowerment, and hope to individuals and families affected by sarcoidosis. Through a compassionate and understanding community, we strive to create a safe space where members can share their experiences, find valuable resources, and gain knowledge about this complex condition.


Josh is Racing 70.3 miles in 8.5 hours!!! With Sarcoidosis! Follow and support his journey here….

Sarcoidosis Awareness Swag

My Life & Breath

A Sarcoidosis Planner

We have built this planner as a pathway for a sarcoidosis patient to follow with guideposts along the way of best practices in living with this disease.

Sarcoidosis Speaker Series

The Life & Breath hosts monthly webinars with leading doctors and specialists. These sessions provide an opportunity to educate patients and caregivers, while also allowing them to gain advice from experts.

Want to register for the next upcoming live webinar? Learn more.

Find a Sarcoidosis Doctor in the USA

Life & Breath has been working to put together a list of Sarcoidosis physicians in the USA (the international list is next). These doctors are not endorsed by Life & Breath in any way. If you have an update to this list please email us.

Coming soon…

The Sarcoid Summit

Join Life & Breath for a week of educational webinars and learning about Sarcoidosis.

Monday- Personal Wellness

Tuesday- Mental Health

Wednesday- Understanding Sarcoidosis

Thursday- Being a Patient

Friday- Ask the Experts

Our Story

Sean Hull unexpectedly lost his mother in 1996. She had been struggling for more than 13 years with Sarcoidosis. She was a strong and courageous woman who never let the pain of Sarcoidosis affect her spirit or touch her soul. The way she lived her life helped create the building blocks for the Life & Breath Foundation. Read Ida Hull’s story.

Founded in 1998, the Life & Breath Foundation’s mission is to provide the Sarcoidosis community with the vital resources needed to manage their medical care and to offer a supportive environment where they can be empowered. Since its inception, it has raised over $500,000 for Sarcoidosis awareness and research studies. 

Patient Stories