Sunday, July 27, 2008

Some basic site stats (WARNING - NERD ALERT)

Some really cool stuff comes with blogging (cool in a VERY uncool, nerdy way I mean). Take the following for instance:

  • People from five countries have read this blog - Australia (duh!), United Kingdom, United States, Malaysia and Spain
  • In Australia we've hit Canberra, Sydney, Brisbane, Perth and Melbourne (I think only capitals are reported, sorry to you country/regional folks)
  • In Malaysia we hit Kuching - I put that in because I thought the name of the city sounded pretty cool
  • We've had over 100 unique visitors over the past week
  • It looks like most of you have returned to check for updates as there have been over 250 visits in total
Thanks to everyone who has left a comment or two. Ali has read them all and appreciates the thoughts (and laughs) that they offer.

If we don't respond to your comments, please don't feel offended. It's not email and we cannot simply hit 'reply' to get back to you (the blog comments don't automatically include your email addresses).

For all of you that are not too familiar with blogging or computers (you know who you are - CP), don't forget, you can catch up or re-read old posts by clicking on the triangles under the heading "Blog Archive" to the right of these posts. The number in brackets tells you how many posts there are under the relevant date. Simply click on a heading and the blog will take you there.

Signing off, from your advertising-free blogspot (I tried to convince Ali to let me put some advertising here but it's still under negotiation, as are the MySpace and FaceBook franchises).

Chemo 1: Day 7

Things are going fairly well and life seems to be settling back into a rhythm, although I wouldn't quite call it normal at this stage.

Ali is doing quite well, most of the nausea has gone but she still has to put up with being tired and feeling drained of energy most of the time. Certainly she is looking better than she did earlier in the week and she seems to be laughing more at the crazy stuff that the kids & I get up to. I reckon she's being a bit harsh when she says she has three kids, not just the two - it's just laughter medicine that we're trying to offer.

If you're interested in what we've been up to for the past couple of days, read on...

Saturday was spent at soccer for the boys while the girls stayed home. Harry's team didn't do so well after the long school holiday break and were slow to start their game. They played much better in the second half and scored more goals than the other team but it wasn't enough to catch up and the other team ended the game with 6 goals to 4.

Annelise has been carrying a cough around for the last couple of days and missed out on netball on Saturday as it was simply too cold to send her out. Still, she was feeling well enough to go to jazz ballet later in the day so she wasn't too bad.

The big highlight of the day for the kids was a trip to the go-kart track. This was their first go at driving and they loved it. Annelise is an absolute maniac and raced like a madwoman, nearly bumping me off the track and almost smashing through the tire barriers at one stage when she forgot how to brake. Harrison's approach is a bit more analytical and he's plotting how he can approach and exit corners faster so that he can get around the track in the quickest time. He's hoping for a professional karting career later in life.

To finish off a big day, Harry & I sat up and watched the Wallabies run over the All Blacks (Ali & Annelise went to bed just after the national anthems). Not something that happens very often and apparently we were pretty noisy as they lost the lead and then regained to finish in front when the final whistle went. WALLABIES 34 - ALL BLACKS 19 !!!!

Sunday started with taking Harrison out to watch Gererd (one of his best friends) play rugby league. Harry is a huge sports fan but just loves rugby league, despite many attempts to convince him that rugby union is superior. During the game when Gererd had a break on the sideline, Harry got the chance to sit with him on the bench and watch the game. For a kid on warfarin, being so close to being on the field was a great buzz and one of the best parts of the morning. After the game, he took off with Gererd's family for the day and ended up indoor rock climbing. All up, one very tired boy came home.

Annelise had a much more sedate day, initially spending some time with Ali to start and then a couple of movies snuggled up under a blanket (it was a very cold day).

Ali took some time to head off to Koko Black to catch up with some friends in the afternoon and had a good old chat. This was with a group of mums that she first met when Harrison was born and they've managed to stay in touch over the past 7-8 years.

Well, that's about it for this long post. So long for now.

Thursday, July 24, 2008

Some pics of the kids

Hi there

Because we're getting a lot of people coming through and looking at the blog here, including many people that we haven't caught up with for quite a while, I thought some of you may like to see a few pics of the kids.

Here's a couple I had handy but as time goes by, I'm sure I'll be able to track down a few more to post.


Harrison -Annelise -
Take care all.

Wednesday, July 23, 2008

Chemo 1: Day 2

Just a brief update to fill you all in. So far the reaction to the chemo is pretty close to as good as we could hope for.

Ali says it feels a bit like morning sickness (or like a hangover for the blokes and those who haven't had the pleasure of morning sickness). She is getting tired fairly quickly and by the time night comes, very much looks forwards to getting into bed for a big snooze.

Last night was one of the best night's sleep she's had for a while so that was good.

That's it for now, thanks.

Monday, July 21, 2008

Chemo 1: Day 0


Alison had her first session of chemo today and here she is with the canula in her arm. The whole deal went from 10:00am this morning through to 2:30pm. The people at the Zita Mary were very good and made the whole thing go as well as it can.

So far (five hours after it finished) it's only making her feel a bit drowsy, a bit off colour and giving her a headache starting at her sinus.

We have a bag full of drugs to help treat her if she does start to feel sick, as well as some more serious stuff that needs to be injected. (We have a mobile number to call a professional for this 24/7. Once again, they will not let me use the needles!)

Kids are back at school again so there'll be a bit more peace and quiet around the house, at least during the daytime. This should be good for Ali as it is likely that she'll just want to rest up and snooze for the next few days.

I'll post another update later in the week.

Friday, July 18, 2008

Details on the chemotherapy

I thought that some of you may be interested in the more technical details of Ali's treatment - but then again many of you may not.

I know I didn't know much at all about chemotherapy right up until last week. I still don't know much but I know a lot more than I did then. It seemed to be one of those things that would be interesting to learn more about if I had the time or could find the right person to ask. Anyway, here goes my version of how it all fits together.

How it works
Chemotherapy is considered a body-wide (systemic) treatment, it travels through the whole body. In Ali's case, this means the chemo drugs will work on the cancer in the breast and the liver.

The chemo targets cells that rapidly divide, such as cancer cells. Part of the problem here is that there are three other main areas in our bodies where there are rapidly dividing cells. The chemo can damage or kill cells in each of these areas resulting in side effects.

Blood
This is where the immuno-deficiencies may come into play. White blood cells have a life span of 13-20 days (red cells can go up to 120 days). By switching off production through chemo, the body can experience low counts of white blood cells which reduces our ability to fight infection. Any signs of infection will get us a fast ticket through the emergency room.

Hair
For Ali, her hair will fall out. I mentioned in an earlier post that she's looking at wigs already. She reckons they only cost about 2-3 hair cuts and argues that I'm getting a good deal as the wig should last much longer than that. She also tells me that she tried a blonde one on but it just didn't suit her complexion (there goes that idea!).

The hair should grow back once treatment stops.

Gastrointestinal tract
This can play games all through from the mouth right down to the other end. Rather than dig into the details on this, if you're interested, it's probably best you look this up yourself.

The Drugs
The two operative drugs that will be prescribed to Alison are:
  • Doxorubicin
  • Cyclophosphamide

Duxorubicin
This drug works to stop the process of duplication through affecting the DNA. We're told that the liquid that is injected is red in colour so it will be quite interesting to see. Also, I read somewhere that it costs nearly $1.1m per kg to make (not sure how true or recent this bit is).

See below for the chemical structure (just a little something I threw together).

Cyclophosphamide
This one scared me at first, I thought the doctor and nurse both said psychophosphamide. I didn't think Ali needed any 'psycho' drugs and in my mind there where all sorts of images of Ali on the rampage. Luckily, this is not the case and I'm OK with them using cyclophosphamide.

This drug works to slow the growth of the cancer and interestingly, is carcinogenic itself. It is manually injected rather than relying on a gravity fed drip feed or automated pump. The reason for this is that if the canula slips out of the vein, the drug can cause necrosis of the surrounding tissue (the nurse we were speaking to assured us that he had seen this only twice in well over 20 years of experience).

See below for the chemical structure.


The Process
Ali will turn up in the morning and been seen by her medical oncologist who will check her general health and the blood test results (most likely taken the Friday before), with a particular eye on white blood cell count. If all's good, the chemo proceeds.

This will begin by the nurse inserting a canula into her arm which will be used for administering all the drugs. First off the rank will be anti-nausea drugs. Two types of anti-nausea are provided through the drip feed. I'm not so sure on which ones are used but I think it is Ondansetron and Palonosetron. These work in various ways to trick the mind and body into believing that the chemo drugs are not harmful. This part takes about 30 min.

Next, the chemo drugs above will be administered. These will take probably another hour and a half to work through. So all up, Ali should be at the clinic for probably three hours.

When released, Ali will be sent home with a small cocktail kit of pills to help manage any further headaches or nausea.

It was interesting to hear that they use different types of anti-nausea drugs after 1-2 days as it will be different reactions causing the nausea once this period has passed.

Post treatment
Ali is most likely to be feeling nauseas and tired during that first week. Her white cell blood counts will probably be low during the latter part of the second week to the middle of the third week, and thus be most susceptible to infections during that stage.

Hair will probably go close to the time when she is due to go back for her second treatment.

After three weeks, we start all over again. It does sound like we're in for the full six-cycle treatment.


Hopefully this has been interesting, educational and useful to you all. At the very least, it should give you some idea of what will happen with the chemo and a very basic, but hopefully correct, understanding of what goes on.

How it all actually affects Alison, given that every person has their own tolerances and different reactions, is yet to be seen.

Some photos


Aha! At last I found a photo.

Ali is very sly and usually hides whenever a camera is around or if I do manage to catch her, she's got her eyes closed or a nasty scowl on her face (if you've ever been on the end of one of Ali's scowls, you'll understand why I won't be posting any of those shots).


She has promised that she'll smile for some new pics before the hair goes so keep an eye out.

In fact, while I'm at it, here is another of her with the kids, busy at one of her favourite activities, hehe. (She'll probably tear a limb off me for this but I don't think she knows how to edit the posts)