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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2018 Muriel’s Breath of Life Golf Raffle

The sixth Muriel’s Breath of Life Golf Raffle included three wonderful golf courses, Sunnehanna Country Club, […]

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Dinner at Casbah

On April 26th fifty guests enjoyed a fabulous dinner at Casbah Mediterranean Kitchen and Wine Bar. […]

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2018 Muriel’s Breath of Life Picnic

August 26th, 2018 at the Lodge in North Park.  More information coming soon!

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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.

Muriel's Story

Muriel’s Story

Before she lost her battle with cystic fibrosis (CF) at the early age of 56, Muriel […]

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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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