Diary of a Kidney Warrior Podcast | Kidney Health Podcast

Can you safely lose weight when you are living with chronic kidney disease (CKD)? And what medical weight management options may be available when diet and exercise alone are not enough?

In this episode of Diary of a Kidney Warrior Podcast, Dee Moore is joined by Dr Sam, Consultant in Diabetes and Weight Management, for an informative conversation about obesity, weight loss and the particular challenges of managing weight while living with kidney disease.

For people living with CKD, weight management can be complicated. Reduced mobility, fatigue, fluid retention, dietary restrictions and certain medications can all affect weight and appetite. For some kidney patients, losing weight may also become particularly important when preparing for kidney transplantation.

Dee and Dr Sam discuss the stigma surrounding obesity and challenge the assumption that being overweight is simply the result of laziness or lack of willpower. Dr Sam explains why weight management is complex and why people seeking support should be treated with dignity rather than judgement.

They explore:

• Obesity and the stigma surrounding weight

Dr Sam also explains how GLP-1 receptor agonists work by mimicking a naturally occurring hormone involved in appetite and feelings of fullness, and discusses the considerations healthcare professionals make when assessing whether these treatments may be appropriate for someone living with kidney disease.

The conversation also looks beyond medication to bariatric surgery, specialist dietetic support and lifestyle changes, emphasising that there is no single approach that is right for everybody.

Most importantly, this episode offers a message of hope. If weight management has become difficult while living with CKD, there may be options and professional support available.

🎧 Listen now and share this episode with someone who may benefit from this conversation.

Medical disclaimer: This episode is for educational and informational purposes only and does not provide personalised medical advice. Weight loss medications and their indications, licensing and suitability can change over time. Do not start, stop or change any medication without speaking to your doctor, kidney team or another appropriately qualified healthcare professional.

Follow Diary of a Kidney Warrior Podcast for real-life kidney patient stories and expert conversations designed to educate, empower and inspire people living with kidney disease and those who support them.

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Follow Dr Sam

Instagram: https://instagram.com/running_man15

Kidney Care UK

💻 Website: www.kidneycareuk.org

📧 [email protected]

📞Tel: 01420 541 424

📘Facebook: www.facebook.com/kidneycareuk.org

📷Instagram: @kidneycareuk

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📺YouTube: https://www.youtube.com/channel/UCeqQTdAsEzXphqjHVtcTD-A

📩 To sign up to receive the Kidney Matters Quarterly Magazine Email: [email protected]

Obesity Uk

https://www.obesityuk.org.uk/

Disclaimer:

The information shared in this episode is for educational and informational purposes only and does not constitute medical advice. Always consult your doctor, consultant, or qualified healthcare professional regarding your individual health needs and before making any medical decisions. The views expressed by guests are their own and do not necessarily reflect those of the host, the Diary of a Kidney Warrior Podcast, or Kidney Care UK and are not intended to malign any religion, ethnic group, club, organisation, company, individual or anyone or anything.

#DiaryOfAKidneyWarriorPodcast #KidneyDisease #KidneyHealth #CKD #ChronicKidneyDisease #WeightLoss #WeightManagement #Obesity #GLP1 #Semaglutide #Liraglutide #BariatricSurgery #KidneyPatient #RenalHealth #KidneyTransplant #HealthyWeight

What happens when kidney failure arrives with almost no warning?

In this episode of Diary of a Kidney Warrior Podcast, Dee Moore speaks with kidney patient Laura, whose life changed dramatically after seemingly unrelated symptoms eventually led to the discovery that her kidney function had fallen to less than 5%.

Laura had been experiencing extreme tiredness, feeling unusually cold, breathlessness, a persistent cough and other symptoms, but like many people, she found explanations for each one. She was busy, she was a mom, she was working and she didn’t want to bother her doctor.

But when her health continued to deteriorate, Laura went to A&E. Blood tests revealed severe kidney failure and dangerously high potassium levels.

A kidney biopsy eventually identified the cause: vasculitis, an autoimmune condition that had attacked her kidneys.

Laura spent a month in hospital and became critically ill. She experienced a haemorrhage in her lungs, difficulty breathing and was admitted to intensive care, where she was placed in an induced coma. Her treatment included dialysis and plasma exchange.

Remarkably, Laura’s kidney function improved from around 2% to above 15%, allowing her to leave hospital without continuing dialysis.

In this powerful conversation, Dee and Laura discuss:

• The symptoms Laura experienced before her kidney failure diagnosis

Laura’s experience is also an important reminder to listen to your body. Kidney disease can sometimes present through symptoms that are easily attributed to everyday life or other conditions. Persistent or unexplained changes in your health deserve medical attention.

For anyone newly diagnosed with kidney disease, Laura offers a powerful message: you are not alone. Your health journey may not be linear, and difficult days may come, but how you feel today does not necessarily determine how you will feel in the future.

🎧 Listen now and share this episode to help raise awareness of kidney disease, vasculitis and the importance of recognising changes in your health.

Content warning: The beginning of this episode includes a discussion about miscarriage. Listeners who may find this subject difficult can skip ahead to approximately 07:07.

Medical disclaimer: This podcast shares lived experience for information and awareness and should not replace personalised medical advice. Symptoms and treatment experiences vary from person to person. If you are concerned about changes in your health, seek advice from an appropriately qualified healthcare professional.

If you were affected by any of the issues raised in this episode contact:

Miscarriage Association

Website: https://www.miscarriageassociation.org.uk/

Helpline: 01924 200 799

Email: [email protected]

Follow Diary of a Kidney Warrior Podcast for real kidney patient stories and expert conversations designed to educate, empower and inspire people living with kidney disease and those who support them.

📸Instagram: www.instagram.com/diaryofakidneywarrior 

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Kidney Care UK

💻 Website: www.kidneycareuk.org

📧 [email protected]

📞Tel: 01420 541 424

📘Facebook: www.facebook.com/kidneycareuk.org

📷Instagram: @kidneycareuk

🔵Blue Sky: https://bsky.app/profile/kidneycareuk.bsky.social

📺YouTube: https://www.youtube.com/channel/UCeqQTdAsEzXphqjHVtcTD-A

📩 To sign up to receive the Kidney Matters Quarterly Magazine Email: [email protected]

Disclaimer:

The information shared in this episode is for educational and informational purposes only and does not constitute medical advice. Always consult your doctor, consultant, or qualified healthcare professional regarding your individual health needs and before making any medical decisions. The views expressed by guests are their own and do not necessarily reflect those of the host, the Diary of a Kidney Warrior Podcast, or Kidney Care UK and are not intended to malign any religion, ethnic group, club, organisation, company, individual or anyone or anything.

#DiaryOfAKidneyWarriorPodcast #KidneyDisease #KidneyHealth #CKD #KidneyFailure #Vasculitis #Dialysis #Haemodialysis #PlasmaExchange #KidneyDiseaseSymptoms #KidneyPatient #KidneyAwareness #RenalHealth #AutoimmuneDisease #ChronicKidneyDisease #KidneySupport

Could your body be showing signs of kidney disease without you realising it?

Chronic kidney disease (CKD) can develop with few obvious symptoms, and some of the signs that do appear can easily be mistaken for everyday health problems.

In this episode of Diary of a Kidney Warrior Podcast, Dee Moore is joined by the much-loved “Aunty of the podcast”, Pat Simoyi BEM, Advanced Practitioner of Kidney Disease, to explore 10 signs that may be associated with kidney disease and why persistent or unexplained symptoms should not simply be ignored.

Aunty Pat explains the possible kidney connection behind:

• Blood in your urine

Dee and Aunty Pat discuss why blood may appear in the urine, including blood that cannot necessarily be seen with the naked eye, and why unexplained blood in your urine needs medical investigation.

They explore how damaged kidneys can allow protein to leak into the urine, potentially causing foamy urine, and why problems with fluid balance can contribute to puffiness around the eyes and swelling of the ankles and feet.

The conversation also looks at symptoms that are particularly easy to dismiss.

Tired all the time? Struggling to concentrate? Not feeling hungry? Experiencing nausea, itching, cramps or difficulty sleeping?

There can be many causes for these symptoms, and experiencing them does not automatically mean that you have kidney disease. However, Aunty Pat explains why persistent or unexplained changes deserve attention, particularly if you have risk factors for CKD.

The episode also explores why someone with declining kidney function may actually begin urinating more frequently, despite the common assumption that kidney failure must always mean producing less urine.

Aunty Pat’s message is simple but powerful:

“The kidneys don’t shout.”

Kidney problems can progress quietly, with the body giving subtle clues along the way. Recognising those clues, understanding your personal risk and seeking appropriate medical advice can help kidney disease to be identified and managed earlier.

This conversation is particularly important if you:

• Have a family history of kidney disease

Knowing the symptoms is not about self-diagnosing. It is about being informed enough to ask questions about your health.

🎧 Listen now and share this episode with someone who needs to know the signs.

Medical disclaimer: The symptoms discussed in this episode can have many different causes and do not necessarily mean that someone has kidney disease. This podcast is for education and awareness and does not replace personalised medical advice, diagnosis or treatment. If you have unexplained or persistent symptoms or are concerned about your kidney health, speak to an appropriately qualified healthcare professional.

Follow Diary of a Kidney Warrior Podcast for real kidney patient stories and expert conversations designed to educate, empower and inspire people living with kidney disease and those who support them.

📸Instagram: www.instagram.com/diaryofakidneywarrior 

📘Facebook: www.facebook.com/diaryofakidneywarrior 

🐦Twitter (X): www.twitter.com/diaryofakidneyw 

🎵Tik Tok: @diaryofakidneywarrior 

📺Youtube: https://www.youtube.com/channel/UChGUfib7lu9eKENlLJ6lafw

🔵 BlueSky: @diaryofakidneyw.bsky.social

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Stay updated with new episodes and exclusive content!

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Follow Aunty Pat Simoyi

Instagram: @simoyipat

10 Signs You May Have Kidney Disease Article by Kidney Care Uk

https://www.kidneycareuk.org/about-kidney-health/10-signs-you-may-have-kidney-disease/

For further information about Kidney Disease & support contact:

Kidney Care UK

💻 Website: www.kidneycareuk.org

📧 [email protected]

📞Tel: 01420 541 424

📘Facebook: www.facebook.com/kidneycareuk.org

📷Instagram: @kidneycareuk

🔵Blue Sky: https://bsky.app/profile/kidneycareuk.bsky.social

📺YouTube: https://www.youtube.com/channel/UCeqQTdAsEzXphqjHVtcTD-A

📩 To sign up to receive the Kidney Matters Quarterly Magazine Email: [email protected]

Disclaimer: The views and opinions expressed by Guests on this podcast are those of the Guest and do not necessarily reflect the official policy or position of Dee Moore or Kidney Care UK. Any content provided by our Guests are of their opinion, and are not intended to malign any religion, ethnic group, club, organisation, company, individual or anyone or anything.

#DiaryOfAKidneyWarriorPodcast #KidneyDisease #KidneyHealth #CKD #ChronicKidneyDisease #KidneyDiseaseSymptoms #KidneyDiseaseAwareness #KidneyFailure #KidneyHealthAwareness #KidneyPatient #EarlyDetection #BloodInUrine #FoamyUrine #SwollenAnkles #Fatigue #HighBloodPressure #Diabetes

If you are living with kidney disease, protecting your veins today could make an important difference to your future dialysis treatment.

In this episode of Diary of a Kidney Warrior Podcast, Dee Moore is joined by Dr Jeremy Crane, Consultant Transplant and Vascular Surgeon, to discuss vein preservation, vascular access, fistulas and the Save Your Vein campaign.

Why does it matter where blood is taken from? What happens to veins after repeated blood tests? And why might the veins in your arms one day become your lifeline?

Dr Crane explains how an arteriovenous fistula (AV fistula) is created for haemodialysis and why healthy veins are so important when planning vascular access. He describes a fistula as a “super vein” – a vein strengthened by increased blood flow so that it can withstand the repeated needling required for haemodialysis.

The conversation explores why people living with kidney disease may be advised to protect the veins around the elbow crease and, where appropriate, ask healthcare professionals to consider taking blood from the back of the hand instead.

Dee and Dr Crane also discuss:

• Why vein preservation matters for people living with kidney disease

One of the key messages from this conversation is that vein preservation is not simply about what you need today. It is about future-proofing your vascular access.

As Dr Crane explains, treatment pathways can change. Someone may have peritoneal dialysis, receive a kidney transplant and later require haemodialysis. Preserving suitable veins now may therefore help keep future treatment options open.

For someone receiving haemodialysis, a functioning fistula can become a lifeline. Protecting your veins before you need them matters.

🎧 Listen to the full conversation to learn more about vein preservation and the practical steps people living with kidney disease can discuss with their kidney care team.

Important: The information shared in Diary of a Kidney Warrior Podcast is for general education and awareness and should not replace personalised medical advice. Decisions about blood tests, vascular access and vein preservation should be discussed with your healthcare team, taking your individual circumstances into account.

If you found this episode helpful, share it with another kidney patient, family member, carer or healthcare professional who could benefit from understanding the importance of vein preservation.

Follow Diary of a Kidney Warrior Podcast for more real-life kidney patient stories and expert conversations designed to educate, empower and inspire people living with kidney disease and those who support them.

📸Instagram: www.instagram.com/diaryofakidneywarrior 

📘Facebook: www.facebook.com/diaryofakidneywarrior 

🐦Twitter (X): www.twitter.com/diaryofakidneyw 

🎵Tik Tok: @diaryofakidneywarrior 

📺Youtube: https://www.youtube.com/channel/UChGUfib7lu9eKENlLJ6lafw

🔵 BlueSky: @diaryofakidneyw.bsky.social

💌 Join the Diary of a Kidney Warrior Family Mailing List

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Stay updated with new episodes and exclusive content!

👉🏽👉 Join here: https://whatsapp.com/channel/0029VaO3ms71iUxipp1eeh2r

Follow Dr Jeremy Crane

Twitter: @JeremyCraneMD

Website: https://www.saveyourvein.org/

Kidney Care UK

💻 Website: www.kidneycareuk.org

📧 [email protected]

📞Tel: 01420 541 424

📘Facebook: www.facebook.com/kidneycareuk.org

📷Instagram: @kidneycareuk

🔵Blue Sky: https://bsky.app/profile/kidneycareuk.bsky.social

📺YouTube: https://www.youtube.com/channel/UCeqQTdAsEzXphqjHVtcTD-A

📩 To sign up to receive the Kidney Matters Quarterly Magazine Email: [email protected]

Disclaimer:

The information shared in this episode is for educational and informational purposes only and does not constitute medical advice. Always consult your doctor, consultant, or qualified healthcare professional regarding your individual health needs and before making any medical decisions. The views expressed by guests are their own and do not necessarily reflect those of the host, the Diary of a Kidney Warrior Podcast, or Kidney Care UK and are not intended to malign any religion, ethnic group, club, organisation, company, individual or anyone or anything.

#DiaryOfAKidneyWarriorPodcast #KidneyDisease #KidneyHealth #VeinPreservation #SaveYourVein #Dialysis #Haemodialysis #Hemodialysis #AVFistula #Fistula #VascularAccess #KidneyFailure #CKD #ChronicKidneyDisease #KidneyPatient #RenalCare #BloodTests #KidneyTransplant #PeritonealDialysis

For people receiving dialysis at home, rising household bills can mean much more than worrying about the cost of heating or electricity. Energy and water are essential to their medical treatment.

In this episode of Diary of a Kidney Warrior Podcast, Dee Moore is joined by kidney patient and campaigner Phoenix Halliwell to discuss the financial realities of home dialysis and the Priced Out of Existence campaign.

Phoenix shares how concerns about reimbursement for the electricity used to run home haemodialysis equipment led him to investigate the actual cost of his treatment. After discovering that the reimbursement he received did not cover his costs, he began campaigning alongside Kidney Care UK to raise awareness of the financial pressures facing people who dialyse at home.

The conversation explores:

• The hidden electricity and water costs of home dialysis

Phoenix also explains why the issue goes beyond household finances. For someone whose dialysis equipment must run for many hours each week, electricity is not simply another household expense. It enables life-sustaining treatment.

The possibility of being unable to afford home dialysis can affect independence, family life, mental wellbeing and potentially the way someone receives their treatment.

This powerful conversation highlights why people living with kidney failure should not be left personally funding the additional utility costs of essential dialysis treatment at home.

Phoenix’s final message to people living with disabilities and long-term health conditions is one of advocacy and solidarity: keep speaking up, make your voices heard and continue fighting for change.

🎧 Listen to the full episode and share it with someone who may benefit from this conversation.

If you receive dialysis at home and have concerns about reimbursement or the costs associated with your treatment, speak with your kidney care team or renal unit about the support available in your individual circumstances.

Diary of a Kidney Warrior Podcast shares real stories and expert conversations to educate, empower and inspire people living with kidney disease and those who support them.

Please follow the Diary of a Kidney Warrior Podcast leave a review and share this episode to help raise awareness.

📸Instagram: www.instagram.com/diaryofakidneywarrior 

📘Facebook: www.facebook.com/diaryofakidneywarrior 

🐦Twitter (X): www.twitter.com/diaryofakidneyw 

🎵Tik Tok: @diaryofakidneywarrior 

📺Youtube: https://www.youtube.com/channel/UChGUfib7lu9eKENlLJ6lafw

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💌 Join the Diary of a Kidney Warrior Family Mailing List

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👉🏽👉 Sign up here: https://diaryofakidneywarrior.getform.com/rjv47

📲 Follow Diary of a Kidney Warrior on WhatsApp

Stay updated with new episodes and exclusive content!

👉🏽👉 Join here: https://whatsapp.com/channel/0029VaO3ms71iUxipp1eeh2r

Kidney Care UK

💻 Website: www.kidneycareuk.org

📧 [email protected]

📞Tel: 01420 541 424

📘Facebook: www.facebook.com/kidneycareuk.org

📷Instagram: @kidneycareuk

🔵Blue Sky: https://bsky.app/profile/kidneycareuk.bsky.social

📺YouTube: https://www.youtube.com/channel/UCeqQTdAsEzXphqjHVtcTD-A

📩 To sign up to receive the Kidney Matters Quarterly Magazine Email: [email protected]

Priced Out of Existence Article

https://www.kidneycareuk.org/news-and-campaigns/news/priced-out-of-existence-the-true-cost-of-living-for-people-with-kidney-disease/

Kidney Care UK’s latest report summarises the campaign for home dialysis patients to receive appropriate reimbursement for their utility costs: https://www.kidneycareuk.org/news-and-campaigns/news/lack-reimbursement-leaves-home-haemodialysis-patients-left-out-cold/

Disclaimer:

The information shared in this episode is for educational and informational purposes only and does not constitute medical advice. Always consult your doctor, consultant, or qualified healthcare professional regarding your individual health needs and before making any medical decisions. The views expressed by guests are their own and do not necessarily reflect those of the host, the Diary of a Kidney Warrior Podcast, or Kidney Care UK and are not intended to malign any religion, ethnic group, club, organisation, company, individual or anyone or anything.

#DiaryOfAKidneyWarriorPodcast #KidneyDisease #KidneyHealth #KidneyFailure #Dialysis #HomeDialysis #HomeHaemodialysis #Haemodialysis #Hemodialysis #CostOfLiving #EnergyBills #KidneyPatient #CKD #ChronicKidneyDisease #RenalCare #KidneyCareUK #PatientAdvocacy #Disability

What role does primary care play in detecting and managing chronic kidney disease? What does your eGFR mean? Why is a urine ACR test important? And when should someone with CKD be referred to a kidney specialist?

In this episode of Diary of a Kidney Warrior Podcast, Dee Moore is joined by Dr Javeria Peracha, Renal Registrar and Clinical Research Fellow, to explore chronic kidney disease (CKD) in primary care and the vital role that GPs and primary care teams can play in early detection, monitoring and management.

Dr Javeria explains the tests used to assess kidney health, including eGFR and urine ACR (albumin-to-creatinine ratio), and why looking at both blood and urine results can provide important information about kidney function and kidney damage.

This conversation explores:

• The role of primary care in kidney health

A key message from this episode is the importance of knowing your numbers.

Rather than simply being told that your kidney results are “fine”, understanding your eGFR, urine ACR and how your results are changing over time can help you have more informed conversations with your GP, primary care team and kidney specialists.

Dr Javeria also discusses why identifying CKD early matters. Primary care can play a crucial role in recognising people at risk, arranging appropriate kidney tests, monitoring kidney function, managing risk factors and identifying when specialist renal input may be needed.

Chronic kidney disease can sometimes progress without obvious symptoms. That makes early detection, appropriate testing and ongoing monitoring in primary care particularly important.

🎧 Listen to the full episode to learn more about CKD in primary care, kidney function tests, eGFR, urine ACR, KFRE, CKD risk factors and protecting kidney health.

If you have concerns about your kidney health or test results, speak with your GP, kidney team or another appropriate healthcare professional for advice based on your individual circumstances.

Diary of a Kidney Warrior Podcast shares real stories and expert conversations to educate, empower and inspire people living with kidney disease and those who support them.

If you found this episode helpful, follow the podcast, leave a review and share it with someone who could benefit from understanding more about chronic kidney disease and primary care.

Follow Diary of a Kidney Warrior:

📸Instagram: www.instagram.com/diaryofakidneywarrior 

📘Facebook: www.facebook.com/diaryofakidneywarrior 

🐦Twitter (X): www.twitter.com/diaryofakidneyw 

🎵Tik Tok: @diaryofakidneywarrior 

📺Youtube: https://www.youtube.com/channel/UChGUfib7lu9eKENlLJ6lafw

🔵 BlueSky: @diaryofakidneyw.bsky.social

💌 Join the Diary of a Kidney Warrior Family Mailing List

Get updates on new episodes, vlogs, newsletters, and more!

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Stay updated with new episodes and exclusive content!

👉🏽👉 Join here: https://whatsapp.com/channel/0029VaO3ms71iUxipp1eeh2r

Follow Dr Javeria Peracha 

Twitter: 

@Javeria_Xx

Kidney Care UK

💻 Website: www.kidneycareuk.org

📧 [email protected]

📞Tel: 01420 541 424

📘Facebook: www.facebook.com/kidneycareuk.org

📷Instagram: @kidneycareuk

🔵Blue Sky: https://bsky.app/profile/kidneycareuk.bsky.social

📺YouTube: https://www.youtube.com/channel/UCeqQTdAsEzXphqjHVtcTD-A

📩 To sign up to receive the Kidney Matters Quarterly Magazine Email: [email protected]

Disclaimer:

The information shared in this episode is for educational and informational purposes only and does not constitute medical advice. Always consult your doctor, consultant, or qualified healthcare professional regarding your individual health needs and before making any medical decisions. The views expressed by guests are their own and do not necessarily reflect those of the host, the Diary of a Kidney Warrior Podcast, or Kidney Care UK and are not intended to malign any religion, ethnic group, club, organisation, company, individual or anyone or anything.

#DiaryOfAKidneyWarriorPodcast #CKD #ChronicKidneyDisease #PrimaryCare #KidneyDisease #KidneyHealth #eGFR #UrineACR #Proteinuria #KidneyFunction #KidneyTests #KidneyFailure #KFRE #Diabetes #HighBloodPressure #Hypertension #KidneyPatient #RenalCare #KidneyAwareness

Professional Actor & Teacher, Ruban Nathan, joins Dee Moore to share his inspirational Kidney Warrior story.

Ruban shares about:

• Being born with Chronic Kidney Disease (CKD)

and more!

For updates & more, follow Dee Moore on:

Instagram: www.instagram.com/diaryofakidneywarrior 

Facebook: www.facebook.com/diaryofakidneywarrior 

Twitter: www.twitter.com/diaryofakidneyw 

Tik Tok: @diaryofakidneywarrior 

Youtube: https://www.youtube.com/channel/UChGUfib7lu9eKENlLJ6lafw

Pinterest: https://www.pinterest.co.uk/diaryofakidneywarrior/

Follow Ruban Nathan

Instagram: @professionalpatients

Twitter: @roundruban

The Professional Patients Podcast is available on all Podcast Platforms

If you were affected by any of the issues raised in this episode contact:

Kidney Care UK

• Website: www.kidneycarekuk.org

To sign up to receive the Kidney Matters Quarterly Magazine Email: [email protected]

Young Adult’s Kidney Group (YAKG)

https://www.kidneycareuk.org/get-support/young-adult-kidney-group-yakg/ 

Disclaimer: The views and opinions expressed by Guests on this podcast are those of the Guest and do not necessarily reflect the official policy or position of Dee Moore or Kidney Care UK. Any content provided by our Guests are of their opinion, and are not intended to malign any religion, ethnic group, club, organisation, company, individual or anyone or anything.

How does Sickle Cell Disease (SCD) affect the kidneys? Why are people with sickle cell more likely to develop Chronic Kidney Disease (CKD)? And what can be done to improve quality of life if you’re living with both conditions?

In this episode of Diary of a Kidney Warrior Podcast, host Dee Moore is joined by Professor Ibi Erekosima, Consultant Renal Physician and Professor of Medicine. Together, they explore the hidden connections between sickle cell and CKD, the challenges around treatment, and the everyday steps that make a difference.

Expect clear explanations, expert insights, and real encouragement for anyone navigating these conditions—whether personally or as a caregiver, healthcare professional, or supporter.

🎧 Tune in to learn:

The basics of sickle cell disease and how it impacts the body

Why kidney complications are a recognised part of living with SCD

Treatment options including dialysis and transplant—and the unique challenges for people with sickle cell

Practical ways to support your health and live well day to day

This is the first-ever Diary of a Kidney Warrior episode focused on sickle cell, making it an unmissable conversation for the kidney community and beyond.

👉🏽👉 Listen now to uncover the answers and gain the knowledge you need to feel informed, empowered, and encouraged.

For updates and more, follow Dee Moore on:

Instagram: www.instagram.com/diaryofakidneywarrior 

Facebook: www.facebook.com/diaryofakidneywarrior 

Twitter: www.twitter.com/diaryofakidneyw 

Tik Tok: @diaryofakidneywarrior 

Youtube: https://www.youtube.com/channel/UChGUfib7lu9eKENlLJ6lafw

Pinterest: https://www.pinterest.co.uk/diaryofakidneywarrior/

If you were affected by any of the issues raised in this episode contact:

Kidney Care UK

•           Website: www.kidneycarekuk.org

•           Email: [email protected]

•           Tel: 01420 541 424

•           Facebook: www.facebook.com/kidneycareuk.org

•           Instagram: @kidneycareuk

•           YouTube: https://www.youtube.com/channel/UCeqQTdAsEzXphqjHVtcTD-A

To sign up to receive the Kidney Matters Quarterly Magazine Email: [email protected]

NHS Sickle Cell Information

https://www.nhs.uk/conditions/sickle-cell-disease/ 

Sickle Cell Society

https://www.sicklecellsociety.org/

CAHN: Caribbean & African Health Network

Website: https://www.cahn.org.uk/

Telephone: 07853 556 591

Helpline: 07710 022 382

Email: [email protected]

Facebook: https://www.facebook.com/cahnuk

Twitter: @cahn_uk

YouTube: https://www.youtube.com/channel/UCpTHOGbhlEV0wZA5jvnOJEA

LinkedIn: https://www.linkedin.com/company/caribbean-and-african-health-network-cahn/

Instagram: @cahn_uk

Disclaimer: The views and opinions expressed by Guests on this podcast are those of the Guest and do not necessarily reflect the official policy or position of Dee Moore or Kidney Care UK. Any content provided by our Guests are of their opinion, and are not intended to malign any religion, ethnic group, club, organisation, company, individual or anyone or anything.

University Administrator, Esra Celik joins Dee Moore to share her inspirational Kidney Warrior story.

Esra shares about:

• Being diagnosed with Chronic Kidney Disease (CKD) at 25 years old

and more!

For updates and more, follow Dee Moore on:

Instagram: www.instagram.com/diaryofakidneywarrior 

Facebook: www.facebook.com/diaryofakidneywarrior 

Twitter: www.twitter.com/diaryofakidneyw 

Tik Tok: @diaryofakidneywarrior 

Youtube: https://www.youtube.com/channel/UChGUfib7lu9eKENlLJ6lafw

Pinterest: https://www.pinterest.co.uk/diaryofakidneywarrior/

If you were affected by any of the issues raised in this episode contact:

 Kidney Care UK

•           Website: www.kidneycarekuk.org

•           Email: [email protected]

•           Tel: 01420 541 424

•           Facebook: www.facebook.com/kidneycareuk.org

•           Instagram: @kidneycareuk

•           YouTube: https://www.youtube.com/channel/UCeqQTdAsEzXphqjHVtcTD-A

To sign up to receive the Kidney Matters Quarterly Magazine Email: [email protected]

Young Adult’s Kidney Group (YAKG)

https://www.kidneycareuk.org/get-support/young-adult-kidney-group-yakg/

Disclaimer: The views and opinions expressed by Guests on this podcast are those of the Guest and do not necessarily reflect the official policy or position of Dee Moore or Kidney Care UK. Any content provided by our Guests are of their opinion, and are not intended to malign any religion, ethnic group, club, organisation, company, individual or anyone or anything.

Dating is hard enough, but what happens when you’re navigating relationships while living with Chronic Kidney Disease?

In Episode 80 of Diary of a Kidney Warrior Podcast, host Dee Moore, continues the Love, Relationships & CKD series with an honest, compassionate conversation about dating with CKD.

Dee is joined by Rob Sieradzki, who previously shared his kidney journey in Episode 78. In this episode, Rob opens up about the real-life highs, lows, fears and hopes of dating while living with kidney disease. Together, they explore the emotional, physical, and social challenges that often come with CKD, including confidence, disclosure, fatigue, comorbid conditions, and the fear of rejection, while also highlighting resilience, connection and the possibility of love.

This episode is Part 2 of a two-part interview, focusing specifically on dating with CKD. In Part 2 the conversation continues with Rob’s work supporting others through the CKD Dating UK community.

✨ In this episode, we discuss:

This episode is for anyone living with kidney disease, those dating someone with CKD, loved ones, and health professionals who want deeper insight into the lived experience beyond the clinic.

💚 You are not alone — and your diagnosis does not define your worth.

👉🏽👉 Call to Action:

If this episode resonates with you, please follow, subscribe, rate, and review the podcast. Share it with someone who may need to hear this conversation today and help us break the silence around relationships and chronic illness.

Follow Diary of a Kidney Warrior:

📸Instagram: www.instagram.com/diaryofakidneywarrior 

📘Facebook: www.facebook.com/diaryofakidneywarrior 

🐦Twitter (X): www.twitter.com/diaryofakidneyw 

🎵Tik Tok: @diaryofakidneywarrior 

📺Youtube: https://www.youtube.com/channel/UChGUfib7lu9eKENlLJ6lafw

🔵 BlueSky: @diaryofakidneyw.bsky.social

💌 Join the Diary of a Kidney Warrior Family Mailing List

Get updates on new episodes, vlogs, newsletters, and more!

👉🏽👉 Sign up here: https://diaryofakidneywarrior.getform.com/rjv47

📲 Follow Diary of a Kidney Warrior on WhatsApp

Stay updated with new episodes and exclusive content!

👉🏽👉 Join here: https://whatsapp.com/channel/0029VaO3ms71iUxipp1eeh2r

Follow Rob Sieradzki

 Instagram: @robsieradzki

Facebook: www.facebook.com/rob.sieradzki

CKD Dating UK Facebook group

https://www.facebook.com/groups/490695541426372/?ref=share_group_link

Kidney Care UK

To sign up to receive the Kidney Matters Quarterly Magazine Email: [email protected]

Disclaimer:

The information shared in this episode is for educational and informational purposes only and does not constitute medical advice. Always consult your doctor, consultant, or qualified healthcare professional regarding your individual health needs and before making any medical decisions. The views expressed by guests are their own and do not necessarily reflect those of the host, the Diary of a Kidney Warrior Podcast, or Kidney Care UK and are not intended to malign any religion, ethnic group, club, organisation, company, individual or anyone or anything.

#KidneyDisease #CKD #DatingWithCKD #ChronicIllness #KidneyWarrior #RelationshipsAndCKD #LoveAndChronicIllness #ChronicIllnessDating #PatientVoices #KidneyHealth #HealthPodcast #UKKidneyCommunity