Notice: Function _load_textdomain_just_in_time was called incorrectly. Translation loading for the atahualpa domain was triggered too early. This is usually an indicator for some code in the plugin or theme running too early. Translations should be loaded at the init action or later. Please see Debugging in WordPress for more information. (This message was added in version 6.7.0.) in /home3/aboarddi/public_html/blog/wp-includes/functions.php on line 6114
Aboard Dignity (Lagoon 420) Blog

Categories

A sample text widget

Etiam pulvinar consectetur dolor sed malesuada. Ut convallis euismod dolor nec pretium. Nunc ut tristique massa.

Nam sodales mi vitae dolor ullamcorper et vulputate enim accumsan. Morbi orci magna, tincidunt vitae molestie nec, molestie at mi. Nulla nulla lorem, suscipit in posuere in, interdum non magna.

Complete Remission

Live the next 36 hours with us

My mind boggles. For a sailing blog I am gobsmacked that I now have very nearly twice as many visits a day than I did than when I was sailing across the Pacific. At least as measure by the wordpress stats which I presume are reasonably accurate. And that’s with me blogging only every few days. That’s phenomenal. It’s also very humbling.

So I invite you all to live this next day and a half with us. As mentioned in my last blog entry I spent 90 minutes in the MRI last Friday. This will form a significant input into the diagnosis I will receive next Tuesday morning.

The two words any cancer survivor wants to hear are ‘Complete Remission’ (CR). Wants is barely an adequate word. There really is no such thing as complete recovery in any literal sense but this term essentially means the cancer is no longer detectable.

The next best thing is ‘Partial Remission’ (PR). This means the cancer has been significantly reduced. I achieved this at the end of my first 5 rounds of chemo so it’s unlikely I’ll be any worse than this. So I won’t go any lower than PR.

So while I have a lot to talk to the doctor about, that’s what Tuesday is going to boil down to. Complete or Partial Remission.

It’s now a waiting game. I’ll blog what the doctor says. Good or bad. For most readers the result will be given to us while you’re tucked in your beds and you’ll be able to know the results when you wake up.

Saturday turned out to be a rough day. I had a very bad headache for most of the day. Regular painkillers struggled to make a difference.

One of the guidelines for dealing with cancer fatigue is to get some exercise each day, even if it’s gentle. We did go out for a short walk yesterday afternoon and I felt a bit better.

Then, late in the afternoon, in the space of a few seconds the headache went from being quite intense to hovering in the background in just a few seconds. I could even feel the rapid change in pain level quite distinctly. It seemed too good to be true so I held off mentioning it to Helen until I was sure. She had been understandable been very anxious as it did appear to be like some of my old symptoms returning.

Today has been all good. No need for any painkillers, just a faint uncomfortable feeling in the distance. Did a lot of planning for our Hong Kong trip and organized my music collection a little. Well, just a bit of the E’s.

Also today, Sarah, Russ, Jack and Ros returned from a trip to Sydney. We’ve been looking after the animals for a few days. We have all missed each other and it was good to see them again. It was bitter-sweet as it reminded us all the clock is now ticking down the last few days/hours of our time here. The feelings Helen and I for this prospect are so mixed. I think I’ll leave it to later to express how we feel as I’m sure this will intensify as the last few days tick by.

We went out again messing with a semi-VR game on my ‘phone’ called Ingress. It was a bit cold so we didn’t stay out too long. Being at the very beginning of the learning curve not a lot made sense but I did manage to collect 2 resonators and was attacked, virtually, by somebody nearby. I think I know who it was even. Anyway, this will make less sense to most of you and a lot of sense to some.

No more blogs planned until after the results on Tuesday. Ride the hours with us.

R&R

The last few days have been mainly R&R. In hindsight I realize I’ve really overdone it recently. I finished 6 months of brutal treatment and felt like superman. Acting like superman, so to speak, was not the best thing to do. My body eventually told me so.

After a few days of rest I’m feeling quite a bit better but not as good as I’d like. It’s all a learning experience. I must confess my mind did drift to alternate explanations for my condition. I didn’t like it.

There is a common condition called cancer fatigue. What I have been feeling seems to fit the description. It’s common and comes with a lot of guidelines. I’m following them.

This morning I had my final MRI. 90 minutes in the machine is a long time but they had a lot to scan. It’s now the evening and there’s been no calls from the hospital. That, if I may use a macabre expression, puts a nail in the coffin of my worst fears. Next Tuesday we see my senior consultant here and get to learn the full results.

More good news in that the PAs of the various Profs are now chatting about my medical records. Hopefully this will progress without complication. We also managed to pick up a digital copy of my first MRI from last June – the one that triggered my emergency input into the Australian hospital system. They all came on a DVD complete with software to view them. It’s a strange thing seeing the inside of your own head.

Connected

Huge news.  We are now connected to Prof Linch in the UK who is the top man for my type of lymphoma in the country.  We even have an appointment to see him in April and are on our way to get a 3 month MRI booked.  If things go pear shaped between now and then we have the direct line of contact and can go straight to them.  This is something we’ve been working for for sometime and is the best result possible.  We feel good.

On Saturday we allowed Sam to spend time with his nth cousins here as Chris was due to fly back to college in the US the following day. In the evening each family branch went out for a meal together. We had a delicious Sri Lankan curry.  On Sunday we had a day out in Melbourne.  We had another Dim Sum with Sam followed by some shopping, a trip up the Eureka tower, a tram ride and a visit to Federation Square. It was a fun day out.

Yesterday we had ambitious plans. We first headed to Churchill National Park where we previously saw many kangaroos. We didn’t see any this time, perhaps because we went near to midday. We did find a geocache in the bush and put in quite a hike. This time, though, I got wiped out and had to slow right down. I’m hoping it was just dehydration. So after a picnic lunch we headed back so I could sleep and rest.

Today, Sam is off to visit a friend he made during his time in Fiji. That’s really good for us as I think we’ve really overdone it recently. It’s still only just over a week since my final chemo and we’ve done a lot.

Family Time

Yesterday we picked up Sam from Melbourne Airport. He’s now staying with us for the next week. The family here now number eight. In the evening we all shared takeaway pizza, a light game of charades and an in house movie, Loopers. Sam played a little guitar for us all.

I have to make a comment about Tiger Direct. They have a bad rep here in Australia. Everyone ‘knows’ they’re often late. We’ve flown with them lots. The only delays we’ve had were due to runway closures at Brisbane which affected all planes. Yesterday, either Sam caught the wrong plane or his arrived 25 minutes early. Both hypotheses seem implausible but we can think of no others. All good.

On Wednesday Helen and I went out for a walk to Jell’s Park again. We hunted down two geocaches. The first required us to traverse long grass so we passed on it. The second we found. I took a ‘photo sphere’ of the location. Take a look. Use your mouse to drag the image around. It goes all the way around. You can even go full screen. Cool don’t you think?  (Turns out the following links hammer Chrome so for now I have put in a break and you can choose when to head on and look)

Continue reading Family Time