Blog

Posted Wed Apr 1st 2020 to Uncategorized

Peter Chakaya talks about the difficulties of receiving dialysis in Kenya, where it turned out to be very expensive and difficult to find a good doctor. Meanwhile,  as a result of misleading information, he struggled for many years to find a matching donor, only to finally receive a kidney from a family member. I am […]

Posted Wed Mar 18th 2020 to Uncategorized

Ruth Njeri tells the story of her son who suffered end-stage kidney disease at a very young age leading to him needing multiple organ transplantations. She shares her family’s efforts in finding matching donors and raise funds for medical bills on her son’s transplant path which started in Kenya and even let him as far India. My son, Brian Karuga, was […]

Posted Wed Mar 4th 2020 to Uncategorized

Chiara Improta suffered from a PUJ (pelvic-ureteric junction) obstruction. She chooses to share her story to raise awareness about her disease and to explain the medical steps that she had to take, including a nephrectomy,  in order to avoid further complications. I was watching TV in my room when suddenly, I felt a strong urge to […]

Posted Wed Feb 19th 2020 to Uncategorized

Joab Wako, a kidney transplant patient, is raising awareness about the reality of living with chronic conditions and the unfair way CKD patients are often treated. In particular, he describes the difficulties for a chronically ill patient to receive health insurance coverage in Kenya. As a person living with chronic kidney disease, I am always […]

Posted Wed Feb 5th 2020 to Uncategorized

Sara Ammar was diagnosed with Chronic Kidney Disease (CKD) when she was 32 years old. Ever since she has been writing a blog to spread positivity about living with CKD. She shares her experience of going through hemodialysis over the last four years and how she has learned to be grateful for what she has […]

Posted Thu Jan 16th 2020 to Uncategorized

Guillermo Garcia-Garcia is a nephrologist based in Mexico and he is sharing his experience with kidney disease. He describes the emotional story of a father struggling to get a slot in hemodialysis for his son and the difficulty for those in need to have access to treatment.  One of many days, by the morning, I’m […]

Posted Thu Dec 12th 2019 to Uncategorized

Theresa Mocek is a 38-year-old housewife living with Minimal Change Disease, IgA Nephropathy, and Nephrotic Syndrome. She shares her story with kidney disease, from sudden onset, treatment and remission at 19 years old to her relapse ten years later. Now she helps others struggling with the same problems she has faced living with CKD.   […]

Posted Sat Nov 23rd 2019 to Uncategorized

Daniella Effrim-Botchey, tells of the real-life struggles of a mother-to-be whose unborn son who was diagnosed with posterior urethral valves (PUV). She poignantly describes the emotional work of coming to terms with the diagnosis and how she adapted to caring for her son whose kidneys would ultimately fail. When faced with difficult circumstances, she found […]

Posted Fri Nov 22nd 2019 to Uncategorized

Daniella Effrim-Botchey, tells of the real-life struggles of a mother-to-be whose unborn son who was diagnosed with posterior urethral valves (PUV). She poignantly describes the emotional work of coming to terms with the diagnosis and how she adapted to caring for her son whose kidneys would ultimately fail. When faced with difficult circumstances, she found […]

Posted Thu Nov 21st 2019 to Uncategorized

Daniella Effrim-Botchey, tells of the real-life struggles of a mother-to-be whose unborn son who was diagnosed with posterior urethral valves (PUV). She poignantly describes the emotional work of coming to terms with the diagnosis and how she adapted to caring for her son whose kidneys would ultimately fail. When faced with difficult circumstances, she found […]