The Sweet Melissa Fund provides financial assistance to lung transplant recipients and their families, founded in January of 2005 in memory of Melissa Alexander, a vibrant young woman who lost her battle with cystic fibrosis during her lung transplant surgery. http://www.sweetmelissafund.org/
Transplant Success is proud to now offer CarePages for the transplant community. CarePages are private, personalized Web pages that allow a transplant candidate and his or her family to stay in touch before and even after their transplant. CarePages are free and comply with all patient privacy regulations. CarePages give patient families greater control over communication and provide an easy way for friends and loved ones to respond with messages of support. Learn more about CarePages >
Notice
Transplant Success Inc. has begun the process of dissolving and will cease all operations as of November 4, 2008. The website will remain online at least until December 31, 2008 but will no longer be updated.
Thank you to all who visit this website, to those that have financially supported Transplant Success, and to those that have participated by providing stories, profiles and quotes.
The need to promote organ donation is greater today than it was even 6 months ago. More life saving organs, are needed than are currently available. Please consider sharing your transplant success stories and profiles at www.transplantcafe.com.
Please direct all comments to bruce@transplantsuccess.org
QuotesSimple expressions of gratitude from recipients to their donors and donor families. Anyone whose life has been touched by organ donation may add a quote.You have the ability to enhance and even save the lives of countless transplant recipients by becoming an organ and tissue donor. Please register and inform your family about this important decision.
Nick's New Heart - Heart transplants are high drama. They make national headlines and are subjects for TV shows. People are interested in reading about someone who has the odds stacked against them, especially if it is a twenty-three month old child. Our nation as a whole is interested in medical advances, particularly when children are involved. Nick’s New Heart is about that drama. It is the story of my youngest son’s heart transplant. Nick was born with a heart defect, had three open heart surgeries, and a heart transplant before the age of two.
In Nick’s New Heart I share how my husband and I had to plan for the eventuality of a funeral and how we struggled to explain Nick’s situation to our other three children. I tell what it was like to wait for a heart as well as what life was like after the transplant. Included is how our family lived as normally as possible even with a chronically ill child. Today, sixteen years later and despite the fact that the shadow of death is always over us, life is good. Nick is a normal, well adjusted teenager. (As normal as a teenager can be.) Our family found that life can be wonderful among the unknown and uncontrollable. Learn more about Nick's New Heart >
In the book, "Heroes of my Transplant," you will find my stories of some remarkable people who have given me, over the past several years, many of the tools I now reflect upon as essential to the journey involving my liver transplant. See Allen's Profile >>>
Fundraising and Financial Assistance. These organizations provide financial assistance, medication grants, and/or fundraising expertise to qualifying transplant candidates and patients. Learn more about C.L.A.S.S. >
The Climb of My Life: Scaling Mountains with a Borrowed Heart This inspirational tale of hope and accomplishment is something everyone can find personal meaning in. The Climb of My Life tells the story of Kelly's transplant, recovery, and ascents up such mountains as Mt. Kilimanjaro-all on a borrowed heart. Learn more about The Climb of My Life >
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