A Saskatoon woman has reason to celebrate. It was 19 years ago that Sherry Duncan Paterson underwent a double-lung heart transplant, making her a pioneer in the Canadian transplant world. 19 years ago, after the birth of her second daughter, Paterson was diagnosed with a rare disease called primary pulmonary hypertension. It's a serious condition of the lungs that forces the heart to work harder and can lead to heart failure and even death. "All of my symptoms of the disease had been masked by my pregnancy," says Paterson. "So it really hit me out of nowhere, so the news was really devastating to my whole family." At the time, doctors told Paterson her only hope was to undergo a double lung heart transplant. She was placed at the top of the wait list, and three months later received word a donor match had become available. Paterson was flown to London, Ontario, where she was given a new heart and set of lungs and was told to expect another five years out of life. "We just tried to cram so many memories and happy times into the five years," says Paterson. "I was thinking I wore myself out." But luckily for her family, five years became 10 and then 15. Now, 19 years later, Paterson is considered a pioneer in the transplant world. She's one of only a few to have done so well for so long after undergoing a multiple organ transplant - CTVThis is the blog for CARG, the Coronary Artery Rehabilitation Group, based in Saskatoon, Saskatchewan, Canada. It will contain items of interest to CARG's own members and anybody else interested in the latest news about rehabilitation and heart-related matters. Canadian charitable number: 89675 0163 RR 0001 || e-mail: carg.ca@gmail.com || website: carg.ca || Blog disclaimer
Wednesday, August 17, 2011
Saskatoon transplant pioneer celebrates 19 years of health
A Saskatoon woman has reason to celebrate. It was 19 years ago that Sherry Duncan Paterson underwent a double-lung heart transplant, making her a pioneer in the Canadian transplant world. 19 years ago, after the birth of her second daughter, Paterson was diagnosed with a rare disease called primary pulmonary hypertension. It's a serious condition of the lungs that forces the heart to work harder and can lead to heart failure and even death. "All of my symptoms of the disease had been masked by my pregnancy," says Paterson. "So it really hit me out of nowhere, so the news was really devastating to my whole family." At the time, doctors told Paterson her only hope was to undergo a double lung heart transplant. She was placed at the top of the wait list, and three months later received word a donor match had become available. Paterson was flown to London, Ontario, where she was given a new heart and set of lungs and was told to expect another five years out of life. "We just tried to cram so many memories and happy times into the five years," says Paterson. "I was thinking I wore myself out." But luckily for her family, five years became 10 and then 15. Now, 19 years later, Paterson is considered a pioneer in the transplant world. She's one of only a few to have done so well for so long after undergoing a multiple organ transplant - CTV
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