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EP 128: "Meeting My Kidney Sister: Sarah Green Moore’s Story of Healing and Purpose"
Title: "Meeting My Kidney Sister: Sarah Green-Moore’s Story of Healing and Purpose"
🎙️ Episode Summary
In this heartfelt episode of This Thing Called Life, we sit down with Sarah Green-Moore, a kidney transplant recipient whose story is as inspiring as it is extraordinary. Sarah shares the unforgettable moment she met her “kidney sister” — the woman receiving the other kidney from the same donor — in the hospital lobby just before their transplants. Now, thriving with a new lease on life, Sarah is paying it forward by caring for her 8-year-old daughter who needed her when she was least expecting it. This is a moving story of second chances, sisterhood, and the power of showing up when it matters most.
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✨ Episode Highlights
Sarah Green-Moore shares her story, beginning in 2015 when her primary physician referred her to a specialist for kidney issues, and a moment that would soon change her life.
Ignoring the warning signs, Sarah initially brushed off her doctor’s advice, believing she was healthy and active. But her mother’s illness with multiple myeloma in 2012 became a turning point that reminded her of the fragility of life.
Determined to face her health head-on, she decided to take responsibility for her well-being to avoid burdening her siblings, who relied on her strength and support.
When her specialist advised starting dialysis, Sarah resisted the idea, struggling to reconcile how someone who “felt fine” could be so sick.
The emotional weight of the diagnosis sank in, and she had to come to terms with the reality of living with kidney disease.
Sarah shared the difficult news with her oldest brother, whose heartbreak reflected the entire family’s shock and concern.
In seeking answers, Sarah researched her family’s health history, only to find that chronic kidney disease (CKD) didn’t run in the family — making her condition even more puzzling.
She decided to break the news to her family through a picnic, a setting filled with love yet marked by emotional reactions and tears.
Visiting dialysis centers opened Sarah’s eyes to the reality of the journey ahead, stirring both fear and uncertainty, yet also courage.
She remained steadfast in her resolve to maintain her independence and dignity, refusing to let illness define her.
With family encouragement, Sarah focused on getting healthier and being placed on the transplant waiting list.
In 2017, she received the call that changed everything — her time for a transplant had come.
In an extraordinary twist, Sarah met another patient in the hospital and soon discovered they were both receiving kidneys from the same donor, forming an unbreakable bond as the “kidney sisters.”
Eight years later, Sarah reflects on life post-transplant and her journey as a mother, a caretaker, and an advocate for others walking similar paths.
Her “kidney sister” became her accountability partner and emotional anchor, proving how shared experiences can create lasting friendships.
Sarah believes in the power of speaking openly about her experience to encourage others to face their health fears and seek help early.
She and Andi discuss the need to educate the public about organ donation, dispelling misconceptions and promoting understanding.
They highlight the benefits of the Paired Kidney Exchange Program, which helps match living donors and recipients more efficiently.
Sarah closes by encouraging everyone to consider organ donation and embrace the opportunity to give life to others.
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📝 Key Takeaways
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📢 Tweetable Quotes
“And so when I decided to listen, I went to the specialist, and the specialist was like, It's time for you to do dialysis. I'm looking at him like, ‘You're whack’, I'm not having any symptoms, and I've always dealt with being anemic from when I started my menstrual cycle, so that was nothing new to me.”
“ I had to tell him the only thing that's wrong with your sister. She needs a kidney. That's the only thing that's wrong with me.”
“I almost started wanting to fight again, especially when it was time for me to get my access, I was like. I could not fathom being connected to a machine that I knew would save my life.”
“This doesn't define me. This doesn't say who I am, but I have to be honest about going through that journey and visiting the different centers and things that scared the fool out of me.”
“To be able to have somebody where I could just be there for each other, just hold her hand, and she can hold my hand.”
Resources:
Donatelifeky.org
https://getoffthelist.org/
https://www.networkforhope.org/
https://www.networkforhope.org/about-us/
https://www.networkforhope.org/stories-of-hope/
https://www.facebook.com/NetworkForHopeOPO
https://www.youtube.com/@NetworkforHope.
https://aopo.org/
RegisterMe.org/NetworkforHope
View all episodes
By Network For Hope
4.9
1111 ratings
Title: "Meeting My Kidney Sister: Sarah Green-Moore’s Story of Healing and Purpose"
🎙️ Episode Summary
In this heartfelt episode of This Thing Called Life, we sit down with Sarah Green-Moore, a kidney transplant recipient whose story is as inspiring as it is extraordinary. Sarah shares the unforgettable moment she met her “kidney sister” — the woman receiving the other kidney from the same donor — in the hospital lobby just before their transplants. Now, thriving with a new lease on life, Sarah is paying it forward by caring for her 8-year-old daughter who needed her when she was least expecting it. This is a moving story of second chances, sisterhood, and the power of showing up when it matters most.
----more----
✨ Episode Highlights
Sarah Green-Moore shares her story, beginning in 2015 when her primary physician referred her to a specialist for kidney issues, and a moment that would soon change her life.
Ignoring the warning signs, Sarah initially brushed off her doctor’s advice, believing she was healthy and active. But her mother’s illness with multiple myeloma in 2012 became a turning point that reminded her of the fragility of life.
Determined to face her health head-on, she decided to take responsibility for her well-being to avoid burdening her siblings, who relied on her strength and support.
When her specialist advised starting dialysis, Sarah resisted the idea, struggling to reconcile how someone who “felt fine” could be so sick.
The emotional weight of the diagnosis sank in, and she had to come to terms with the reality of living with kidney disease.
Sarah shared the difficult news with her oldest brother, whose heartbreak reflected the entire family’s shock and concern.
In seeking answers, Sarah researched her family’s health history, only to find that chronic kidney disease (CKD) didn’t run in the family — making her condition even more puzzling.
She decided to break the news to her family through a picnic, a setting filled with love yet marked by emotional reactions and tears.
Visiting dialysis centers opened Sarah’s eyes to the reality of the journey ahead, stirring both fear and uncertainty, yet also courage.
She remained steadfast in her resolve to maintain her independence and dignity, refusing to let illness define her.
With family encouragement, Sarah focused on getting healthier and being placed on the transplant waiting list.
In 2017, she received the call that changed everything — her time for a transplant had come.
In an extraordinary twist, Sarah met another patient in the hospital and soon discovered they were both receiving kidneys from the same donor, forming an unbreakable bond as the “kidney sisters.”
Eight years later, Sarah reflects on life post-transplant and her journey as a mother, a caretaker, and an advocate for others walking similar paths.
Her “kidney sister” became her accountability partner and emotional anchor, proving how shared experiences can create lasting friendships.
Sarah believes in the power of speaking openly about her experience to encourage others to face their health fears and seek help early.
She and Andi discuss the need to educate the public about organ donation, dispelling misconceptions and promoting understanding.
They highlight the benefits of the Paired Kidney Exchange Program, which helps match living donors and recipients more efficiently.
Sarah closes by encouraging everyone to consider organ donation and embrace the opportunity to give life to others.
----more----
📝 Key Takeaways
----more----
📢 Tweetable Quotes
“And so when I decided to listen, I went to the specialist, and the specialist was like, It's time for you to do dialysis. I'm looking at him like, ‘You're whack’, I'm not having any symptoms, and I've always dealt with being anemic from when I started my menstrual cycle, so that was nothing new to me.”
“ I had to tell him the only thing that's wrong with your sister. She needs a kidney. That's the only thing that's wrong with me.”
“I almost started wanting to fight again, especially when it was time for me to get my access, I was like. I could not fathom being connected to a machine that I knew would save my life.”
“This doesn't define me. This doesn't say who I am, but I have to be honest about going through that journey and visiting the different centers and things that scared the fool out of me.”
“To be able to have somebody where I could just be there for each other, just hold her hand, and she can hold my hand.”
Resources:
Donatelifeky.org
https://getoffthelist.org/
https://www.networkforhope.org/
https://www.networkforhope.org/about-us/
https://www.networkforhope.org/stories-of-hope/
https://www.facebook.com/NetworkForHopeOPO
https://www.youtube.com/@NetworkforHope.
https://aopo.org/
RegisterMe.org/NetworkforHope