Thursday – a week after the transplant

One week on from the transplant and feeling OK! There are some side effects from the chemo kicking in, a couple of mouth ulcers and sore gums, and my throat feels a bit irritated, but I can still swallow OK, and eat normally – although this morning’s breakfast plumbed new depths – cold and overcooked! However, last night I didn’t get any dinner at all (maybe the catering staff have been reading this!) So one of the nurses heated up some chicken soup – very nice – thank you Debbie!

It is a cold but bright morning here in London, no snow though!

The night was uneventful – punctuated as usual with the observations and the early morning blood collection. Nothing from the vein this morning though, all from the Hickman line. That was followed by breakfast, already described, the junior doctors’ ward round, and the IV Itraconazole, girth measurement (stop laughing over there!!) and weight. That has all finished, so I must go and use the exercise bike and shower.

Yesterday afternoon passed reasonably uneventfully, although I did need a platelet transfusion. I suspected as much after a large bruise formed on the area where blood was taken from the vein yesterday morning (for the cyclosporin levels). This was confirmed when a reading of 5 came back. Normal range is 150-400! I also had a visit from Viki, the Haematology Nurse Specialist, and Liz, who is another transplant specialist late of the Royal Marsden Hospital.

Felicity came up to see me yesterday and stayed for about 5 hours so I could catch up on all that is happening at home, as well as bringing some clean clothes. I also had some cyclosporin after the blood test confirmed that the levels were correct.

You may have had some problems getting the blog in the last 18 hours. Mark had a problem with his phone line, and lost broadband. Fortunately he has another BB connection, so after a bit of reconfiguring, got this back on line. However it takes up to 24 hours for all the Domain Name Servers (the servers that your browser uses convert human memorable names such as dellmar.net into a computer readable address like 21.123.200.94) to update across the internet so that your browser can find them! End of networking lesson!

3 Responses to “Thursday – a week after the transplant”

  1. Mary Morfill on 26 Jan 2006 at 11:46 pm #

    Hi Peter

    Marian sent me the link to your blog so I thought I’d see how you are getting along on this extended journey! We met at Healing Prayers last night and, of course, we remembered you and the family in our prayers. You are often in our thoughts.
    Glad to read that things seem to be going reasonably to plan even if the hospital food leaves something to be desired. Thank goodness for gifts of wine and chocolate!

    Felicity keeps us in touch with your progress, but for you I thought that any contact with the outside world might be welcome at the moment, so thought I would ‘submit a comment’? This blog must be another real life-line for you – excuse the pun.

    Anyway, Peter, our love and prayers are with you all the time and we wish you all the very best as your treatment progresses.

    Hope you get a hot breakfast in the morning!
    God bless you, Mary

  2. Faith on 27 Jan 2006 at 12:01 am #

    Hi Pete, Joyce told me about your blog. What is a blog? Will it hurt? Am I on it now? With perseverance (clever chap) I accessed this. Took me a while to work out what to do. Sorry – still technophobic! Are you in for visiting by possible bug strewn people or should one wait a while?
    Will visit blog regularly now – no escape I’m afraid – even if not in person.
    Anyway I shall await the next instalment with great excitement. Especially the weather. Its much better than here. Its just dull, dull, dull in Oxon.
    Lots of love Faith

  3. Peter on 27 Jan 2006 at 9:58 am #

    Thnk you Mary – I have sent you an e mail in reply!

    Faith – be delighted to see you – have emailed you. (Faith is another friend from University days!)

    Peter