…We will always honor it…
“I think the biggest thing I want the (donor) family to know is how eternally grateful Jeff and I are for their gift and that we will always honor it. Everything we are doing to pay it forward with the Lung Transplant Foundation would make her really proud.” – Martha Austrich
What does it mean to celebrate my first year of breathing on my own
We asked one of our Facebook followers, Lisa, what it meant to celebrate her first year of breathing on her own after a double lung transplant on June 11, 2018. Lisa says, “I’m loving life again. I am so grateful for the donor and the donor’s family; they will forever be in my prayers.” Reflecting […]
This is a story of deep gratitude.
This is a story of deep gratitude. A story of a relationship with a donor’s family. “I am Jerry, and I received the gift of life with double lung transplant at IU Health Methodist Hospital in Indianapolis on June 2, 2015. In 2008 during a routine examination, scarring was noted on my lungs. A follow-up […]
More hope for more adventures, more tomorrows…
Laura – Transplanted 2014 Having a lung transplant allowed me to travel and see the places I love. The Lung Transplant Foundation gives me more hope for more adventures, more tomorrows. Support Lung Transplant Foundation A lung transplant transforms lives affected by diseases such as cystic fibrosis, pulmonary fibrosis, and COPD. These diseases affect more […]
I have been gifted nine years of wonderful life
“All you have to decide is what to do with the time that is given to you.” -Gandalf Because of my donor, I have been gifted nine years of wonderful life. Jess – Transplanted April 18, 2010 Support Lung Transplant Foundation A lung transplant transforms lives affected by diseases such as cystic fibrosis, pulmonary fibrosis, […]
The gift of life…
The gift of life has given me my life back. Deepest gratitude to my donor family forever & ever…. 2 years & 9 months post double lung transplant at UCLA! Maqsuda – Transplant date: 2016 Support Lung Transplant Foundation A lung transplant transforms lives affected by diseases such as cystic fibrosis, pulmonary fibrosis and COPD. […]
She will never forget when the nurse said: “It’s a go!”
Double Lung Transplant Recipient. Maria is from Caracas, Venezuela. In April 2007, Maria was diagnosed with Systemic Scleroderma. At 35 years old, Maria had already survived atypical viral pneumonia, chronic encephalitis and several days in a coma. Systemic Scleroderma is a rare autoimmune, degenerative and incurable disease that causes Pulmonary Fibrosis and Pulmonary Hypertension, among […]
Born with Cystic Fibrosis
Born with Cystic Fibrosis, I never thought I would be going through the transplant process at such a young age. Luckily, I had an unofficial mentor to help guide me through the process, someone my age who was transplanted a few years earlier than me. Hannah – Transplanted: Jan 1, 2015 Support Lung Transplant Foundation […]
Pulmonary Fibrosis Awareness Month
Cincinnati woman Tammy Robinson was young and active until idiopathic pulmonary fibrosis derailed her life. By the time she was in her 40s, she was so breathless that she struggled to walk the short distance between her car and the door to her work. But now, she is able to compete in events like the […]
I’m just a regular man…
I’m just a regular man who was given the supreme gift in life – another chance. I have no idea why I was chosen for this second chance but I intend to do whatever I can to help whomever I can in all ways possible. Lung Transplant Foundation is an organization that raises money for […]