the Mellon's

the Mellon's
Happy Families

Saturday 18 February 2012

Groundhog day

G'day, G'day!
I have been a bit slack lately with my witty and hilarious blog posts (...) so thought it was about time I hit the keyboard to bring you all up to speed. I was all phsyced up to write to you all an awesome piece on the mysterious Kidney stone ordeal, which might i add, the drama was seriously down played by Dad on the blog, but his screams are still ringing in my ears.. heh heh heh! He will do anything to stop me from eating my delicious yellow thai curry, 6 hours in A&E is obviously proof!

Chemo 4 started on Tuesday 7th Feb with a session in Day Oncology and then straight up to the ward to be pumped with Cycle B drugs.
I'm sure you can remember cycle B from last time - exhausting, nausea and the big rash. This time it didn't fail to deliver yet again. Bed bound for a few days, suitcases under his eyes, vomitting and diarrhoea (yum) and the infamous rash, all making an appearence. The punishment for all of these symptoms? ISOLATION! Much to Dads dismay (and boy oh boy did he let the nurses know!) he spent the hours climbing up the walls, getting very frustrating for not being able to even leave his room. After completing his sentence of 48 hours in isolation after the symptoms has passed Dad could be heard from our house 15 minutes away negotiating with the nurses, time to go and sit in the sun!
Geoff, dads new friend, who is also suffering with the same type of Lymphoma who was in isolation at the same time as dad for the same condition, was let out of isolation after only 24 hours. Dad is still making reference to that one, days later...

Then Wednesday 15th hit and the neutropenia kicked in, the white blood cells dropped off the charts and it was back to lock down for dad. He is allowed out of his room this time, but he has to wear a mask. As he is feeling well and normal, he has been inventing new cheeky ways to pass the time. If you happen to be up on ward 31 anytime soon you will most probably notice a bald man with a series of different pictures drawn onto his face masks! (Avoid him at all costs! kidding!)

So now we sit and wait until Monday, which will be almost 2 weeks straight in hospital! Monday will see the stem cells hopefully being harvested to be frozen for future use. Once enough stem cells have been harvested he will be free to come home! The big key to harvesting enough stem cells is to avoid infection, which is why he has been kept in hospital for these couple of weeks. A small price to pay if the stem cells can be harvested correctly!

Hope this has filled you in a little bit!
Love to you all,
Hayley :)

3 comments:

  1. Thanks for the update, Hails. Glad to see your dad is hanging on to his sense of humour. lots of love to you all Aunty G, M.M&Z xxx

    ReplyDelete
  2. Well it's Wednesday now, 16 days in hospital! I'm still waiting for my blood levels to recover, which they are beginning to do (somewhat slowly). With a fair wind, the stem cell harvest will start tomorrow, else Friday and will likely be for two days. I should then get out for a while, and it is likely that chemo 5 due next Tuesday will be delayed a week to again allow blood counts to recover. I'm currently watching arvo TV and receiving a blood transfusion, so that is how exciting life really is. Take care all we'll update next wek when we know what is happening with chemo 5.

    Alan

    ReplyDelete
  3. Just had the phone call, that those wiggly Alliewobble stem cells are finaly going to be captured and frozen for future use. Just hang in ickkle bruvver, they probably wont let you stay in Hospital for that long again (if the Nursing Staff have a say). Good work on your report Hayley, see you around the 12th when I have the babysitting job, (takes me back 50 years or so when I had to babysit him then, bet he's not as well behaved lol.) Love Sissypops xxxxxx

    ReplyDelete