Helping Children & Adults with Cystic Fibrosis

Our Mission

The Lagnese family established the Muriel’s Breath of Life Foundation in 2010 to help close the financial gaps of care for people in the tri-state area of Pittsburgh affected by Cystic Fibrosis.

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Ease a family's burden by giving to the foundation to meet today's needs or to the endowment to protect the mission of Muriel's Breath of Life in perpetuity.

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Muriel’s Breath of Life is a non-profit initiative created by Muriel’s family and friends to honor the life and memory of Muriel Lagnese by helping Cystic Fibrosis patients and their families cover medical expenses and associated costs that are not covered by health insurance.

Funds raised by Muriel’s Breath of Life are administered by the Children’s Hospital of Pittsburgh Foundation and are intended for CF patients with special financial needs who are undergoing treatment at the Adult Cystic Fibrosis Care Program at UPMC’s Comprehensive Lung Center or the Antonio J. and Janet Palumbo Cystic Fibrosis Center at Children’s Hospital of Pittsburgh.

2019 Annual MBOL Picnic

The ninth MBOL picnic was held on September 2, 2019 at the Rose Barn in North […]

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MBOL 2019 Golf Raffle

Muriel’s Breath of Life Golf Raffle 2019 The seventh edition of the Muriel’s Breath of Life […]

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MBOL Sports Night at Wildwood Golf Club

On October 19, 2018 Wildwood Golf Club hosted a Sports Night to benefit Muriel’s Breath of […]

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“Eddie is a 13-year-old CF patient who lives in Pennsylvania with his parents and two siblings. His father was recently laid off from his manufacturing job, but due to periodic call backs, Eddie’s family is not eligible for unemployment compensation. Muriel’s Fund was critical in providing Eddie’s family with heating oil as well as groceries since his family only qualified for a very small amount of food stamps.
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