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Home » Mum holds late daughter’s hand again as she hugs woman who received it in transplant
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Mum holds late daughter’s hand again as she hugs woman who received it in transplant

thebusinesstimes.co.ukBy thebusinesstimes.co.uk7 May 20263 Views
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Mum holds late daughter’s hand again as she hugs woman who received it in transplant
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Jackie Kirwan said daughter Georgie Peterson would be “over the moon” to know she had made such a difference to Kim Smith’s life after Kim received Georgie’s left hand after a sepsis battle

Mum meets transplant recipient who received her daughter’s hand

A mum has been able to hold her late daughter’s hand once more – after meeting the woman who received it in a limb transplant.

Jackie Kirwan, 65, said her daughter Georgie Peterson would be “over the moon” to know she had made such a difference to someone’s life.Georgie, 33, from Liverpool, sadly died last August following a long term serious illness which led to debilitating seizures.

She had been on the organ donation registry since she was 17 years old, and after she died Jackie agreed to donate her limbs.

READ MORE: Organs donated by boy, 8, save four lives as mum makes heartbreaking appealREAD MORE: Two teens’ lives saved by transplant heroes are on the road to full recovery

Her left hand went to Kim Smith who lost her hands and feet as a result of sepsis in 2017. The women decided to meet earlier this year after Kim wrote to her donor’s family – with the pair saying the experience was “very emotional”.

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

Kim, 64, 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. 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.”

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.

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

Doctors implanted electrodes in her brain so they could determine which part of it was causing the seizures in 2023 and she underwent a further surgery last year. But in May 2025, her seizures increased and just a few months later, Jackie found her collapsed in the bathroom.

She said: “I thought she was asleep at first. 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 hospital. 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 realised families still had to sign on their behalf.

“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. But then I realised 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. 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.

Now an ambassador for Sepsis Research she enjoyed her first Christmas with her new limb last year and said Georgie had given her a “wonderful gift”. Jackie and Kim are now keen to continue to raise awareness of both sepsis and epilepsy – and keep Georgie’s name alive.

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