Transplant begins - it;s day minus 7!

3 minute read time.

Apparently it is now Thursday. I'll come back to that.

Had a nice weekend with the kiddies, and with my friends.
Friday evening Deri stayed with granny and I went to Jo's with a few other mums from the area for a rather nice gathering, lots of wine and scrummy nibbles! The mums from Deri's school clubbed together snd bought me a trollbead! Wow that was lovely. Jo then presented me with one I was saving for - a silver one called 3 siblings ... very sweet, nearly cried! Saturday, Deri started riding lessons. She has had sporadic sessions of horse riding, and been nagging me for them to be regular, and her friends aunt owns a stables, and I am friends with that aunts sister,,,, so we are paying but going in on her friends lesson which ususally is just them and  their cousin :) Deri LOVES horses and will be a happy womble every fortnight now haha! Then we came home, ate chocolate and watched movies. Her big sisters babysat that night as I was invited to my friends for another Pre Admission Knees-Up, where we drank far too much vodka (or just the right amount, depending on one's viewpoint!) and pink bubbly haha! On both evenings I had SUCH a good laugh, and just soaked up all the love and support ready to take into hospital with me... just as I have soaked up the love and support I have from everyone, at home, on Macland, everywhere! On Sunday, I sat down with Deri and her calendar, explained how the doctor wanted me back in hospital, it would be for longer but then I wouldn't need to come in again (thats my plan anyway!) and we marked off the days and gave her a poacket of stickers to stick on one night at a time. She said ''only 2 more days with you before you are away for a LONG time" ... big gulp, no tears, smile bravely and convince her it's all good! Which, it will be...
 
So, Monday is spent packing. And told to call at 9am Tuesday... wheich I did, and was told to come in for 3pm. Then called at 1 pm and said no bed free til 8pm, but I couldn't get  alift at 7pm (coz of kids) so I arrived at 3.30 and sat in the relatives room until 8.30pm, watching tv and reading and had my patient's dinner served in there too!! This seems to be a trend with me and my admissions haha!

Put on a 4 bed ward - 1 woman has HL and has a 12 day old baby born at 31 weeks via C-section in neonatal and she's in coz of temperature after chemo!! The other 2 women have leukemia. Next morning, HL lady can go home. I am given bloods etc but no treatment. Then last night about 11pm, an elderly lady was wheeled in. Qucikly established she also has advanced dementia. They inserted a catheter and she dozed off.So did we. Then at 2.30am I was woken by her at the foot of my bed, the catheter trailing behind her. "Hello? Can you help me get this thing out, I don't know what it is?"
WHOA! 'Oh no', says I, 'we can't take it out, wait there and I'll get a nurse'...
Well this happened at various intervals during the night so not much sleep had by anyone, poor old dab, she's a real sweetie.

So then it's today and there are bloods being taken and charts drawn up and protocols to read and chemo days to absorb........and then taken to the transplant ward across the corridor and through big double doors into my single room. It has an ok view, it has a flat screen tv and remote, it has my laptop and DVDs and books etc.... and I can keep the door open as much as I want until stem cells go in and then it's door closed at all times. The food is better than at Nevill Hall so far, huzzah!

Today is day minus 7... 3 hours of fluids, 2 hours of chemo, now on 11 hours of potassium/saline. days -6 through to -3 I have a different chemo, then day -2 another one again, then -1 is a rest day with no chemo, and then day Zero is stem cell day.

I have managed to SKype my kiddies each evening :D Yay!

So, here we go, da da ddaaaaaaaaa.......................

Anonymous
  • FormerMember
    FormerMember
    You are one strong brave lady xxxxx
  • FormerMember
    FormerMember

    Thank goodness for mobiles, laptops etc and skype, they will help you get through the next few weeks keeping you in touch with all you love and who love you.......

    Even having all of the above, you have to be a very brave lass to go through it all!!

    Good Luck.

    Hugs

    Respect

    xxxx

     

  • FormerMember
    FormerMember

    Oooooh hello! Gadget girl. Hoorah for gadgets so we can text and email and all that stuff and glad you got laptop willy sorted for mini laptop so you can skype your girls!

    Tomorrow the missions begin hahaaaaa.

    PFs and WB and maybe the TB one too?

    Oh and you will have to sing really loud once the door is shut for anyone to hear you!! hehe

    You are fab and brave and lovely and can't wait till you are out and able to play again cos we've got lots of fun friend stuff to play....

    Oh and oooooh shiny things trollbeads. I just took my bracelet off thinking I won't take it in tomorrow (no jewellery, thieves etc) but then felt weird and not right without it so put it back on again!

    Love you Welsh sis

    Little My xxxxx

  • FormerMember
    FormerMember

    Have been thinking about you Ems, and pleased all is going to plan. How things have moved on since I had my SCT 3 years ago.......Wi-fi, laptops and Skype! I had a mobile phone which I could send texts....and that was it 'cos i can't hear very well on mobile due to hearing loss ....Just got a new home phone that i can turn the sound up :-)

    Some things are the same though....like spending the weekend before in a alcoholic haze! Yay to that!

    You can still pull faces and hammer on the door (usually for more meds...haha) even when in solitary. Set visitors daft things to do ....like setting spider traps. Fun still to be had.

    Take care lovely lady, and hugs for your family, as they will need them too.

    Hope all goes well

    Louise xxxx

    PS Good luck to you also LM, and hope that all goes to plan for your op and that Max is being looked after and has managed the change in routine ok

  • FormerMember
    FormerMember
    Thank you everyone!! And I had a wonderful gift from Megz n Ben: an early mothers day pressie - a silver troll bead called hugging hearts... I got dust in my eye again!! Yes to missions and hugs and no baggy's. Love you all! Xxx