Friday, January 15, 2016

Day 33 to Day 57

Luckily on Christmas Day I was allowed out on pass from hospital, so got to spend a very relaxing day at home, and then was finally discharged from hospital completely on Boxing Day. So overall I had a lovely festive period at home, and surprise surprise, I even managed to stay awake for the bells on New Years Eve!

However, I was still having some problems with nausea and my temperature still wasn't really settling, which was making life a little difficult for me. So finally, when I visited Glasgow for a hospital appointment last Thursday, it was decided I should be readmitted to hospital again, only this time it would be in the Beatson, so we could hopefully find out what was really going on, as they specialise in post bone-marrow transplant care.

It was quickly assumed that I had GvHD. This is Graft vs. Host Disease, where basically the new cells that I have been given begin to attack the tissue in my organs. It sounds scary on the face of it, but a small dose of GvHD is actually a good thing, with it often being shown that those that have GvHD have less chance of redeveloping the initial disease, i.e. hopefully I now have less chance of my leukemia coming back - which can only be a good thing, as it is shown that those with a little GvHD have a better chance of recovery. This is because, as well as attacking my own tissue, the new cells will also attack any remaining leukemia in my body.

Luckily, the GvHD is also pretty easy to treat as I only have to take steroids. Although, I am a bit wary of this. If you have been following my story from the beginning, you will know that I had problems with steroids when I was originally put on them, as they caused a blood flow problem in my hips. The doctors have tried to help this time by giving me another drug to support my bone health, so hopefully it will do the trick. I will be sure to keep a close eye on any change in feeling in my hips, as it was very painful last time and not something that I wish to repeat. Despite this though, the steroids seem to be doing the trick - and I don't feel nauseous for the first time in weeks!

I was only in hospital until Tuesday, so have had a couple of nice days of home since I returned. I even managed to get out for a walk in a bit of the Aberdeen sunshine, so overall I am feeling much more positive - onwards and upwards I think.



8 comments:

  1. Aberdeen sunshine in January ..... I don't believe it.

    xxx

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  2. Really good to hear your on the mend. Best wishes from Berwick. X

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  3. You haven't missed much weather wise over the last couple of months - hope there's lots of sunshine for you now you're home. Pxxx

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  4. Hope things are still improving little by little. No nausea sounds like a real plus.

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  5. Hello Laura - I read about your Blog in The Daily Record (Sat 10 November). Your story is indeed inspirational.
    However, my reason for commenting is that your story is almost a mirror image of mine. I was diagnosed with ALL on 10 November 1986 - BMT 28 March 1987. It will be 30 Years next year since my transplant.
    Your story echoes so much of the thoughts and feelings I experienced at that time.
    I do not wish to say too much in a comment on your blog page, but feel free to contact me directly via my email address (rooshappell@hotmail.com), or get one of your family to do this if you are unable at present.
    I understand exactly the thoughts and feelings you are having at the moment.
    Good luck and kind regards,

    Ross Happell

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    Replies
    1. Hi Ross - Thank you so much for reading my blog and getting in touch. It's absolutely incredible that you went through such a similar experience, and it gives me great hope that you are coming up to 30 years since it happened!
      I tried to send you an e-mail, but unfortunately it came bouncing back. It would be great to hear about your story in more detail, so if you fancy getting in touch just send me an e-mail at: Laura-e-regan@hotmail.co.uk
      I hope to hear from you soon.
      Best Wishes,
      Laura

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