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Living kidney donor Tom leaning on a walking milestone in front of a wide open grassy field, underneath a bright blue sky. He is wearing a navy bucket hat, a blue shirt, and thick-rimmed black glasses, smiling for the camera.

I have been a blood donor since I left school. I worked on a large industrial site where the collection was conveniently arranged on site, with the benefit of free biscuits and a break from work. I always carried a battered organ donation card and had registered as a bone marrow donor as well, although bone marrow donation always sounded a little worrying to me.

I knew about Kidney donation and had heard of altruistic donation, although originally I thought it was only a thing in the USA. However, after hearing a Clare Balding radio programme with an early altruistic non-directed donor, I decided to investigate living kidney donation.

The donor who spoke on the radio, who I thought was a doctor and so well informed, was clear that he considered the risks were minimal and fully recovered from the operation with no lasting effects. When I relistened to the programme recently, it turns out he was a vet and his knowledge was based on experience with horses: fortunately I did do my own additional, more relevant research!

I researched a wide range of sources about the risks from the UK and other countries. A primary objective of my work in the engineering world has been risk reduction, so I’m used to evaluating risk in a structured way, using numbers if available. Although, it was novel to be consciously doing something that does increase risk by a small amount, in crude numerical form the benefits for recipients massively outweighed short-term inconvenience and risk to me.

In practice, my decision to donate was emotional and heartfelt. My immediate family has been lucky to have excellent health; however, many close relations, friends and colleagues have been saved by excellent and miraculous modern health care in the UK. So, although I have not had immediate contact with kidney disease, the opportunity to donate just made sense. I would no doubt donate to a relation or friend, so why not another member of the community?

During my research, I had discovered the benefits of a non-directed donation, in enabling further donations where donors did not match their intended recipients, which I found both intriguing and encouraging. So I took the simple first step and contacted my local donor transplant centre.

I was very nervous visiting a hospital, as I had never visited one as a patient. From the initial administrative contact onwards through the extensive tests, Leigh the transplant nurse was very clear and helpful. I never seemed to have a long wait for the various tests. The only frustration was that I wasn’t allowed to watch the screen during tests: unlike pregnancy scans, you don’t get a picture to take home and have to wait for the results.

I was worried about telling my family, until I had passed all the tests – and then I was worried about their reaction, when I told them late in the process. Fortunately, while they were surprised, my family were all very supportive. One relation, a very experienced and wise doctor, did challenge me robustly, to test that I had really thought through my donation decision. Although an exception, one close friend who I greatly respect clearly didn’t really understand my decision and found it odd. In addition to the very thorough evaluation by the hospital as part of the formal donation process, I found these challenges understandable and useful in prompting me to reconsider and reconfirm my decision.

My donation was in early 2022 and I was part of a ‘chain’. The risk at the time of catching COVID required isolation and was slightly inconvenient. I worried that catching COVID would delay all the operations in the chain. After my initial blood testing for a match, I was called in again for more testing. I think it needed an intimidating 12 different samples, which Leigh handled like a conjuror, whilst I wondered how we could possibly match so many tests. But we did!

The operation went fine, despite my trepidation about general anaesthetic and all the warnings of discomfort. Although I found the stay in hospital okay, I was keen to leave after the second day because there was a patient in my ward who only ate ice-cream while I never got any. However, a nurse pointed out that leaving hospital would stop the strong painkillers, so waited and I went home after three days.

Living kidney donor Tom on a walking holiday, standing in front of a wide open plain beneath an overcast sky. He is smiling for the camera and wearing a black raincoat.

I started gentle short walks when I got home and enjoyed forced relaxation for a couple of weeks. Because I can work from home or an office, I was then back working after two weeks. Loose trousers with braces instead of a belt were a good idea for a few more weeks; however, now my scars are disappointingly almost invisible. Three months later I went on a walking holiday with friends in the Welsh mountains and was back playing squash again.

On the day of my operation there was a huge crash and congestion on the motorways, so I worried that my kidney would not arrive in time. However, Leigh assured me it was successfully delivered. Although I do not know the name or details of the recipient, they sent me an anonymous letter and donation anniversary cards. These letters are better than any birthday card, giving me some insight into the difference a new kidney made to my ‘special friend’ and their family, as well as their continuing enjoyment of freedom from dialysis.

One tiny detail I always remember was that my ‘special friend’ can now enjoy coffee and orange juice without concern. In addition, their relation who didn’t match them but successfully donated a kidney is also doing very well.

The short-term inconvenience of my donation has significantly improved someone’s life; rationally and emotionally, it’s one of my life’s best decisions and my easiest contribution.

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