Josh Polito shares about his journey with sarcoidosis and how Life & Breath Foundation has impacted his life. Listen to his amazing story and support his Triathlon journey

Elena Russo speaks with Sean Hull, the Founder and President of the Life and Breath Foundation, about what Sarcoidosis is, the issue of the lack of awareness surrounding the disease, the impact they’ve had on the community, and their upcoming 11th Annual Flip Flop Festivus.

Sean Hull and Toni Robinson share about the 2018 Flip Flop Festivas in with WJZ news.

One of the first videos published for the Life & Breath Foundation in 2008 featuring Toni Robinson and Carl Robins.

Tracey Dubree, a Life & Breath Foundation Board Member and Sarcoidosis patient, shares her story with WNST.

As a Practice Liaison with Dankmeyer, Toni Robinson enjoys helping others live the fullest lives they can through using the right prosthetics and orthotics. And, through her work with the Life and Breath Foundation, she helps many others who live with sarcoidosis, a complex inflammatory disease that commonly affects the lungs and lymph nodes, but can also attack the brain, eyes, kidneys and more.

What does the Life and Breath Foundation do?

The Life and Breath Foundation has been striving to find a cure for sarcoidosis, which is a disease that causes clusters of abnormal tissue called “granulomas” to form in the body. If many granulomas form in an organ, they can keep the organ from working normally.