It’s a small thing - probably something that most of you have done already this year. Certainly the lawn needed a good trim. However, for me it is a sign of a return to normality. Since last summer I really have not had the energy to contemplate much in the way of housework let alone … Continue reading Cutting The Lawn
I have settled into the routine. Each Monday, Wednesday and Friday evening I get dropped off at 6pm for a 4 hour session of dialysis. At a time which varies but is usually between 10:30pm and 11:30pm I get picked up and go home to sleep. Those of you who are mathematically minded will notice … Continue reading Matter of Routine
I was released from the Churchill Hospital at 4pm on Thursday with a large bag of medication, This included a two week dose of cefazolin, an antibiotic. This needed to be handed over to the dialysis nurses in the renal unit at MKUH where it would be used for intravenous application at the end of … Continue reading Back Home
I’ve been unwell for a few days now. This first manifested at dialysis last Wednesday and again on Friday when I had uncontrollable shivers. Bloods were taken and cultured, I was admitted to MKUH, where I stayed until yesterday. At the weekend the bloods taken from my line, and from my arm were grown to … Continue reading Churchill Transfer and Tesio Lines
I have been admitted to MKUH following a bout of gastroenteritis which left me feeling very unwell. It possibly started on Monday when my Tesier Line became very sore. The first symptoms came Wednesday when during dialysis I suddenly became extremely cold and started shivering uncontrollably. This lasted quite a while and led to body … Continue reading Infection
I have got into a routine. Every Monday, Wednesday and Friday I head off to MKUH at about 5:30pm for dialysis. Generally I am on from about 6:30pm until 10:30pm. The exception is Monday where generally I am on fom 7:00pm to 11:00pm. During my 4 hours dialysis I will listen to music or watch … Continue reading It was all going so smoothly and then…
Following a phone call this morning and in view of my health Dialysis is starting today! A two hour session from 2:30pm to get me started. Then we go from there!
The phrase “it never rains but it pours” describes the current situation in my family at the moment. This blog post is a bit different as it concerns not just me but many of those in my family. It would be true to say we are under attack. For those of you who share my … Continue reading Under Attack!
It’s 4:30am. The usual sleep pattern has been followed. An initial hour or two of sleep which is broke at 1am or thereabouts with a trip to the loo and then hours of wakefulness. If I am lucky I might fall asleep again about 6am for an hour or so - but it’s not guaranteed. … Continue reading D-Day
As my kidney condition has moved towards its ultimate destination (End Stage Kidney Disease -ESKD) the range of medications needed to replace kidney function has both changed and grown. My morning pot of meds has now become quite a mouthful. In addition there are meds to take with each meal and meds to take at … Continue reading Medication
It’s just before 4am as I write this. The middle of yet another sleepless night. I have seen each hour of the night so far and it’s been like this for days now. The sleeping tablets (Amitriptyline) had limited effect and I have stopped taking them. Basically they made me drowsy but did not result … Continue reading Wide Awake
Yesterday I travelled to Oxfordshire to the town of Banbury. The purpose of the journey was to undergo an operation on my arm to create a Fistula. The first stage of a process which will lead to Dialysis. The past couple of weeks have been challenging as I have come to terms with the magnitude … Continue reading Fistula
It’s virtually continuous and can strike anywhere on the body. It is often much worse at night, and has made it difficult to sleep. Imagine itching all over, the urge to scratch at the skin but with limited relief. This is one of the many effects of Chronic Kidney Disease. There are no obvious rashes … Continue reading It’s rather irritating!
When I started this blog in 2017. The principle manifestation of the Myeloma seemed to be orthopaedic ie related to my bones - I had developed lesions in various bones indicative of the actions of the Myeloma over the previous months. Hence, the title of the Blog was Battling the Bone Breaker. In truth, the … Continue reading Combatting the Kidney Crusher!
Today is the last day of Covid isolation. I return to work tomorrow morning. Thankfully I’m feeling a lot better. For me Covid has been similar to a heavy cold as far a symptoms. I am left with a heavy cough and blocked nose but little else. During the past 10 days the biggest issue … Continue reading Day 10