About ten years ago I was running 5K on a regular basis. I had started as part of a plan to reduce my weight and lost over 5 stone over a nine month period. I was regularly running Park Run and my fastest run was just over 27 mins. By early 2013 I was running … Continue reading Getting Off Of The Couch
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 have just returned to my room having had my first four hour dialysis in my new fistula. This fistula fitted on the 13th Jan performed really well for 9 weeks. The whole process was very smooth. The annoying thing is that for almost five hours (I’ll explain the extra hour later) I had To … Continue reading ‘Done and Dusted‘
So today I have been back in the Foscote Hospital Banbury. I am here for a second Fistula operation. The first fistula unfortunately failed after a few dialysis sessions. There was an attempt to repair the fistula on Christmas Eve but this was unsuccessful. So on New Years Eve I had another operation to fit … Continue reading Another Day Another Op
I am beginning to see the benefits of regular dialysis. With the Tesier Line Fitted and the pain subsiding the dialysis sessions have gone well. I have yet to do a 4 hour session- yesterday’s session was shorter as they had had issues with other patients which meant I started an hour later. It wasn’t … Continue reading Reaping the Benefits
Up at 6am this morning ready to leave the house by 7am for the hours journey to the Churchill. I am back here today to undergo a procedure. This morning I am being fitted with a Tesier Line. This will enable dialysis in the medium term whilst they create a new Fistula and allow it … Continue reading New Year’s Eve
I was sent home from Churchill hospital at 8:30pm on Christmas Eve. I had completed another 3 and a half hours of dialysis to follow the previous two and a half hours on 23rd December. Finally I was feeling normal. Better than I had in months. I could feel the energy. We got home about … Continue reading Christmas
I am in the Churchill Hospital in Oxford. I was admitted yesterday following the failure of my Fistula. Last night a temporary line was fitted to my groin so I could undertake dialysis. They did two and a half hours dialysis. Today they plan to do four more hours dialysis. Also today they plan to … Continue reading Christmas Eve
Today is the winter solstice. The shortest day of the year in terms of daylight. So conversely the longest period of night. My insomnia continues to be an issue and so for all but 18 minutes of last night I lay awake. You can imagine this ongoing sleep deprivation is shattering. I have three dialysis … Continue reading The Longest Night
Dialysis came early! A phone call yesterday morning following an email to my nurse invited me in for immediate dialysis. My health had definitely deteriorated in the last couple of days and the vomiting was the ‘straw which broke the camel’s back’ I was asked to come in at 2:30pm - problem no car! Our … Continue reading Dialysis
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!
Kidney Disease is so insidious. There are so many different symptoms which combine to make life difficult. The incessant itching and insomnia are bad enough. Now as my kidney approaches the end of its function (remember I only have one kidney!) not only has my appetite dropped through the floor but I am having trouble … Continue reading Bottom of a Bucket
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!