Skip to main content

Dialysis & The Human Tissue Authority

As expected the week just gone was an interesting one!  It started with my dialysis training at Treliske on Tuesday.  As I'm sure you can imagine, I was apprehensive about being dialysed for the first time!

When I arrived at the hospital, the dialysis nurse put me at ease straight away.  She slowly went through the procedure for setting up the dialysis equipment then "plugged me in" so I would experience how it feels.

It was a funny sensation, as you felt your insides filling up.  The very first bit of solution is cold but then the rest has been warmed by the machine.  Once the fluid is inside it is left there for a period of time, where, via osmosis and diffusion , impurities and toxins are taken out of your system.  Then the fluid is removed before the process is repeated.  Now that is the bit which I wasn't so keen on.  When almost all of the fluid is removed you can sometimes feel a little pinch inside.  The best way I can describe it is like when you drink the last bit in a glass with a straw or if you put a hoover on your skin!!  Not painful, just a bit uncomfortable!!

On Wednesday Mum and I went up to Derriford where we met with the surgeon and we were quizzed by a Chaplin on behalf of the Human Tissue Authority.  The surgeon and the live donor nurse went through all of the risks of the operations mostly for mum as she only has risks in having the operation as she is not ill (the reward being seeing her lovely daughter better of course!!).  They also went through in detail what would happen on the actual day of the operations and in the following days and weeks. 

Next mum and I were interviewed together and individually by the Chaplin.  His job is to write a report to the Human Tissue Authority advising whether he feels there has been any pressure applied onto mum or money involved in the process and that we both know what we are letting ourselves in for!  I have to say I was surprised at the detail he went into.  He really wanted to know that we were both aware of the risks we were facing as a result of the operation.  At the end he said that he was happy and that he didn't think there would be any problem getting the go ahead!

On Thursday the dialysis nurse came out to my home so I could have some more dialysis training.  I set up the equipment in my bedroom myself whilst the nurse observed.  When both of us was happy we left the machine set up ready for that evening where I would be plugged in for the night for the first time.

My first night of dialysis resulted in very little sleep, but I think that is to be expected, since then, I have still not had a full nights sleep but it is getting better!  In the end exhaustion will set in and you won't see me for days!!

Finally I had my last blood results pre-dialysis yesterday and my creatinine level hit 999!!  I have to say I am disappointed not to have hit 1,000!! 

Comments

Popular posts from this blog

Time Flys When You're Having Fun!!

Well here I am again letting you know that another year has passed since I had my transplant FOUR years ago! The difference this transplant has made to my life is enormous. Whilst on dialysis, although I carried on with my life, the fatigue meant I spent the majority of my free time in bed or with my feet up wrapped in loads of blankets with the heating on full as I could never warm up. Now life is unbelievable! In my last blog in August I was telling you the story about my success at the British Transplant Games.  Since then I have had the honor of being asked to represent Team GB in the World Transplant Games in Argentina which will take place in August this year!! I entered the British Transplant Games initially for two reasons, firstly to raise awareness of organ donation and that is still extremely important to me, so if you haven't done so already please sign up here  but don't forget to discuss your wishes with your loved ones. Secondly to get fit and healt

Six Year! WOW!

Another year has passed with the gift of life which I received from mum six years ago! It has been a year of ups and downs, with actually way too many downs. The Pirate FM Awards In April last year I had the honour of receiving the "Sporting Achievement Award" at the Pirate FM Local Hero Awards.  Trev had put my name forward unknowingly to me and I won!  You can read more in my blog HERE .   At the awards ceremony Poorly Mum At the Pirate FM awards ceremony, mum wasn't very well.  In fact she wasn't well for a very long time with several long stays in hospital and two operations.  Mum was not actually beginning to feel better until late August.  I'm pleased to report that mum is back to her normal self again now. Mum & I at Christmas The British Transplant Games The British Transplant Games were in Liverpool last year at the end of July.  As is always the case, the Plymouth Team was small but mighty!  Winning 25 medals between jus

Goodbye Dad

It  is with great sadness that I am writing this blog. My Dad, Terry Carroll, passed away on the 31st August following a cardiac arrest on Helston Bowling Green on the 24th August. We take great comfort in the fact that he was doing what he loved. Dad was taken to hospital by air ambulance and had his heart restarted, however, his brain was without oxygen for too long and we were told by the doctors that he was very unlikely to survive.   After three days with no response from dad, the doctor introduced us to the donor nurse. As you know, all of my family are advocates for organ donation, but we never thought for a minute that we would be on the other side of that conversation. Dad had been on the donor register for many years, long before I was unwell, and had made his wishes very clear, therefore we said yes.   The fact that dad wished to donate his organs meant that there was a delay before the doctors took dad off his ventilator, 12 hours or so.  We discovered that dad