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Mom has ‘very emotional’ meeting with woman who received ...
SWNS · 2026-05-08 · via New York Post

A mom has met the transplant recipient who received her daughter’s hand, saying she would be “over the moon” to know she’s made such a difference.

Jackie Kirwan, 65, lost her daughter, Georgie Peterson, following complications from a congenital brain malformation, which led to debilitating seizures.

Georgie, 33, from Liverpool, died on August 25 last year and had been on the organ donation registry since she was 17 years old.

Jackie Kirwan and Georgie Peterson smiling at the camera.

Jackie Kirwan, 65, lost her daughter, Georgie Peterson, following complications from a congenital brain malformation, which led to debilitating seizures. Jackie Kirwan / SWNS

Georgie Peterson in a hospital bed with a nasal cannula.

Georgie, 33, from Liverpool, died on August 25 last year and had been on the organ donation registry since she was 17 years old. Jackie Kirwan / SWNS

Georgie Peterson as a child on playground equipment.

Georgie pictured as a child.  Jackie Kirwan / SWNS

Her mom, Jackie, decided to donate Georgie’s limbs — with her left hand going to Kim Smith, who lost her hands and feet as a result of sepsis in 2017.

The women decided to meet earlier this year and said the experience was “very emotional.”

Speaking at their second reunion, Jackie said, “We referred to Georgie as our ‘human sunshine.’

Jackie Kirwan (left) and Kim Smith (right) holding hands and smiling.

Georgie’s mom, Jackie, decided to donate Georgie’s limbs — with her left hand going to Kim Smith, who lost her hands and feet as a result of sepsis in 2017. William Lailey / SWNS

Two women smile at the camera, holding hands.

The women decided to meet earlier this year and said the experience was “very emotional.” William Lailey / SWNS

“Her opinion was that the body is what you live in and it’s the soul that’s important.

“I’d decided that if Georgie’s donor recipient got in touch, I would meet them.

“Meeting Kim was unreal. We were both crying and she told me she was forever grateful and she would look after her hand forever.”

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Georgie had been diagnosed with a rare brain disorder called peri-ventricular nodular heterotopia (PVNH) — which is where neurons fail to migrate properly during development and form clumps.

The condition causes focal and often drug-resistant epilepsy and was diagnosed in Georgie after she completed her A-Levels.

Her mom, Jackie, a cleaner, said, “Everybody thought Georgie was great but she believed she was a burden.

Georgie Peterson, a young woman with blonde hair and blue eyes.

Georgie had been diagnosed with a rare brain disorder called peri-ventricular nodular heterotopia (PVNH) — which is where neurons fail to migrate properly during development and form clumps. Jackie Kirwan / SWNS

“She struggled with eczema, asthma and depression, while her only symptoms of PVNH were seizures and being hypermobile.

“Growing up, she used to bite her tongue, randomly wet herself and suffered from a lot of headaches.

“A week before her A-Levels she had a massive seizure which we thought was exam stress.

Georgie Peterson, a young woman who was an organ donor, smiling at the camera.

“She struggled with eczema, asthma and depression, while her only symptoms of PVNH were seizures and being hypermobile,” Jackie said of Georgie. Jackie Kirwan / SWNS

“But three months later, she had another one and was referred to tests. Those childhood symptoms were actually seizures all along.”

Georgie, who was close to her sisters Steph and Sammi, went to university and got a degree in English, and loved dancing, the gym and swimming.

But her epilepsy was so severe, she was unable to drive, work or take public transport on her own.

Jackie Kirwan smiling in front of a wall of photos of her daughter.

“We referred to Georgie as our ‘human sunshine,'” Jackie said. William Lailey / SWNS

Doctors implanted electrodes in her brain so they could determine which part of her brain was causing the seizures in 2023, and she underwent a further surgery last year.

But in May 2025, Georgie’s seizures increased, and just a few months later, Jackie found her collapsed in the bathroom.

She said, “I thought she was asleep at first.

Kim Smith in her wheelchair, smiling, with a Christmas tree and decorations in the background.

Kim Smith, from Milton Keynes, suffered a quadruple amputation and celebrated her first Christmas with her new hand following a transplant. Emma Trimble / SWNS

“But her brain had been starved of oxygen and from the way she was positioned, we think she’d got up and had a seizure.

“Despite everything, her theory was always: ‘I’d rather it was me than have anybody else suffer from this.'”

Georgie passed away on August 25, 2025, after three days in the hospital.

Jackie Kirwan, mother of hand donor Georgie Peterson, touching the arm of Kim Smith, the recipient of her daughter’s hand.

“Despite everything, her theory was always: ‘I’d rather it was me than have anybody else suffer from this,'” Jackie said of Georgie. William Lailey / SWNS

But when a donation nurse came to speak with Jackie, she was surprised to hear that limbs were an option.

She said, “It was the easiest decision to agree to the organ donation.

“Georgie had joined the register when she was 17, but I never realized families still had to sign on their behalf.

Close-up of a hand with a bracelet touching a transplant recipient's arm.

When a donation nurse came to speak with Jackie, she was surprised to hear that limbs were an option. William Lailey / SWNS

“The nurse asked me about Georgie’s limbs and I stopped for a moment.

“But Georgie had said it was the soul that was important and I agreed. You don’t get to know where the donations go due to patient confidentiality.

“But, I later received a letter from Kim, thanking me and asking to meet. My first thought was that I could meet her and hold Georgie’s hand.

Kim Smith, the recipient of a hand transplant, waves to the camera.

“But Georgie had said it was the soul that was important and I agreed. You don’t get to know where the donations go due to patient confidentiality,” Jackie said. William Lailey / SWNS

The arm of a hand transplant recipient, featuring surgical scars and a tattoo that reads "all times."

“But, I later received a letter from Kim, thanking me and asking to meet. My first thought was that I could meet her and hold Georgie’s hand,” Jackie said. William Lailey / SWNS

“But then I realized that was wrong as it is Kim’s hand now — not Georgie’s.

“I think Georgie would be over the moon if she knew what it had done for Kim.”

Kim Smith, 64, lost all her limbs after contracting a UTI and then suffering from sepsis while on holiday in Alicante, Spain, in 2017.

A woman in a pink jacket and yellow pants sits in a boat on a river.

Kim Smith, 64, lost all her limbs after contracting a UTI and then suffering from sepsis while on holiday in Alicante, Spain, in 2017. Courtesy Kim Smith / SWNS

She was later put on a UK waiting list for a double hand transplant and received a new, working left hand in August last year.

The former hairdresser had initially undergone a 14-hour-long double-hand transplant operation, but sadly, the right hand was not successful.

She has now become naturally left-handed — despite her right being her dominant before.

Jackie Kirwan, the mother who donated her daughter's hand for transplant, smiles while wearing a brown polka-dotted shirt.

Kim was later put on a UK waiting list for a double hand transplant and received a new, working left hand in August last year. William Lailey / SWNS

The ambassador for Sepsis Research enjoyed her first Christmas with her new limb last year and said Georgie had given her a “wonderful gift.”

She said, “It is extremely rare for a donor’s family and the recipient to meet.

“I wrote a letter of thanks six weeks after my surgery but a thank you never seems quite enough.

Kim Smith, a hand transplant recipient, holding hands with Jackie Kirwan, the mother of her hand donor Georgie Peterson.

“I wrote a letter of thanks six weeks after my surgery but a thank you never seems quite enough,” Kim said. William Lailey / SWNS

“In the letter, I had said I’d love to meet my donor’s family and in February, I had a reply from Jackie.

“We met for the first time at the end of March and it was very emotional.

“I didn’t think I was nervous until she walked through the door and I then was shaking like a leaf!

“But we chatted like we’d known each other for years. It was lovely.

“It’s so nice that we’re still in touch.”

The pair are now keen to continue to raise awareness of both sepsis and epilepsy — and keep Georgie’s name alive.