From finding kidney-friendly recipes to accessing help with debt and housing, Rayhanneh, Emily, Glenn, Dave and Lee share how Kidney Care UK's services have supported them.

Mariann explains how a rare diagnosis of CKD and PTLD has impacted her life, from difficult chemotherapy sessions to her uncle Jeff donating a kidney to her.

From diagnosis tips to the importance of support networks, Karisse, Stuart, Sara, Michelle, Gillian, Anoushica and Berlina share the ups and downs of living with lupus and CKD.

Jade has been living with CKD since childhood. She discusses how CKD has impacted her, and, with her partner Darren, explains how and why they both fundraise for Kidney Care UK.

Mike's family has a history of CKD and he was diagnosed with a rare condition as a teenager. He has recently had his second kidney transplant and feels like he has been given his life back.

From delayed diagnoses to new medication, Katie discusses how living with LPHS and CKD has taken its toll and how she's striving to help others living with the condition.

After fears of a second transplant kept him on dialysis, Tony explains how his godson inspired him to go back on the transplant list, and how his altruistic donor is a 'real life superhero'.

After a bout of sepsis in hospital, it took months for Penny to receive a diagnosis of CKD but she maintains a positive outlook. It is always 'What's next', and never 'What if...'

After living through two kidney transplants and seven bouts of sepsis, Jon shares how sepsis has impacted him, and explains the vital importance of knowing the signs.

Diagnosed with CKD at 27, Deborah has since received a 'perfect match' kidney transplant. She discusses living with CKD, from the joys of holidaying to the frustrations of benefits.

After a diagnosis as a teenager, Sally received a kidney transplant. Now, 30 years later, she is cruising around Croatia and making kidney disease work around her.

Laura’s kidney disease diagnosis hasn’t stopped her from enjoying music festivals. She shares her story and provides tips and advice on how to party with kidney disease.

After her diagnosis of stage 3 kidney disease, Jacqueline struggled to balance life with CKD and bipolar. But neither has stopped her from travelling the world, from Greece to Tonga.

Kidney patients Sumaya and Rehana share their experience of Ramadan while living with chronic kidney disease (CKD).

Ravi's life was transformed by the gift of a kidney from his living donor, Daksha Varsani. He shares his story to highlight the live-saving power of organ donation.

Back when he was 17, Professor Andy Demaine just wanted to be normal and like other people. Now, 40 years after receiving his second kidney transplant, Andy is enjoying his retirement,

After his kidney transplant gave him a second chance at life, Marc has climbed Mount Kilimanjaro and reached Everest Base Camp to raise money for Kidney Care UK.

Alison Brown discusses her experience of the Enhanced Recovery After Surgery (ERAS) programme after her second kidney transplant.

John is the bass guitarist for the band Da Management. Grateful for the care he has received for his rare kidney condition, he's raised money for charities like Kidney Care UK for years.

It was time for Sharon to decide whether to opt for a whole-organ pancreas transplant or islet transplantation after her successful kidney transplant.

Angela had a life-saving kidney transplant back in 1970. In 2020, she celebrated 50 years of healthy active life with the same kidney.