Almost normal

2 minute read time.

I'm so far out of transplant now I've given up putting day +??? in front of the title because its getting more and difficult to work out! Needless to say its been nearly 7 months now since my transplant and I'm finally starting to glance at what its like to be normal again (not that I want to ginx it).

There have been a few problems, I developed this rash a few weeks ago and was itching like mad. The Doctors were worried it was going to be another bout of Graft vs. Host Disease, though it didn't seem similar to the rash I had the first time, but it did coincide with my weening off the Cyclosporin (goodbye immune suppression drugs). So needless to say I was pretty worried they were going to get me back on steroids again which would probably have pretty much destroyed my chances of finishing University this year. Luckily, after a few trips to the Dermatologist and skin biopsies later, a Dermatologist Consultant took one look at me and said I had eczema. Apparently its pretty common to pick up a suceptability to it from your donor after a transplant, especially if there was some suceptability to it in your family already (both my sisters have suffered from it when they were kids).

So after a couple of weeks of itching and having the most incredibly dry and flakey skin all over my body I was finally given a couple of steroid creams to help. They've worked really well, although I do have these little chicken-pox-like spots on my face now but hopefully they'll be gone fairly soon.

I had been feeling a bit down about the constant barrage of crap I seemed to be getting. I mean with between the burst blood vessel in my eye, the steroid effects, the IBS, the throat infection and now this skin thing it felt like it was just going to be one thing after another. I know it sounds ridiculous to complain about stuff like this when you've been through so much horrendous Chemo and treatment but I always managed to put a positive slant on that stuff because I knew it was what had to be done to make me better. Now it just feels like, having been through all that crap, it isn't really fair to keep on getting these little set backs. I suppose its partly because I expected to be right as rain a couple of months after my transplant, I wasn't really prepared for the long slog of recovery.

Still, like I said, I'm really starting to feel normal again now. I'm getting Uni work done, going to the gym to get my strength back and only going in to the hospital once a week. Now if I could just stop itching and get some more sleep...

Anonymous
  • FormerMember
    FormerMember

    Good to see you blogging Will and that things are finally looking up.  Yours was most definately a marathon of treatment but look at you crossing the finishing line.

    Long may it continue.

    Debs xx

  • FormerMember
    FormerMember

    great to see u feelin normal

    uni and gym ........... fantastic news!

    methinks you'll be havin a very merry crimbo!

    xNx

  • FormerMember
    FormerMember

    Great to see you are feeling well & all the best for a busy 2010 at Uni

    Dave

  • FormerMember
    FormerMember

    great to see your latest news. You're doing so well to be coping with Uni work on top of dealing with treatment and all the other 'niggles' - you've certainly been tested and are heading in the right direction which is great for me to read - I'm wondering if I'll ever do 'brainwork' again:D

    onwards and upwards!

    karen x

  • FormerMember
    FormerMember

    Hi Will, I am so pleased to see an update from you, and actually undernealth the niggles a positive one, so good for you, well done and for sure you have so nearly come out the other side of the tunnel. Delighted the Uni work is back on course, be a busy year for you.

    Take care Will and keep us posted!

    With love

    Debbie xx