3 Too Many

Friday 16 November Ramble

“Friends are made by many acts and lost by only one.” – Proverb

Spent about 2 hours last night reading about my cancer – hoping in a way that something may have been developed hat will eradicate them or that.  Unfortunately no such luck.  Still the same prognosis and life expectancy. Another night down, and spent a bit of it asleep, finally.  Wake at just after 7, bugger, I was hoping to sleep in a bit as it is a holiday today.  Oh well, not to be.  Lachie makes me a cup of tea, and brings my meds box up to me as hurting a bit and he is trying to save me suffering a bit – how considerate.  Feeling on a mental high if you like, then as quick as a snap of the fingers, I’m in a deep low.  Fantastic I’m in for one of these days :-(  Sue takes the dog for a walk, and I decide to go into the garage for a bit.  Spend nearly an hour in there, but unfortunately instead of it doing it’s usual upper, it has not done that.  If anything I feel a lot worse than before.  AT least I’m not hurting too badly with pain.  Also the twitching I have had the past couple of days has seemed to stop.  See I managed to suppress that enough that no one noticed it.  Get ready then to face the day.  Really start wondering what sort of mental state I’m in as I feel so sad and low but can’t shed a tear in the shower where I normally get it out of the system.  OMG – I have gone so low I can’t even cry about how low I am, that’s sad in itself.

Start to feel better again, but nauseous.  Force some lunch down, then we head off to meet the Reid family at the Jet Ski lake in the Sawyers Arms Reserve.  Mark does well taking all the boys on rides onn the Jet Ski.  Not sure whose having more fun Mark or the boys ;-)  Spend the afternoon there and have a good catch up with Kylie and Mark.  Thank you so much for today – it was fun.  Head home then and pick up Fish & Chips on the way for tea. Lachie and Sue go with Roh and Kate to the movies to see Breaking Dawn, while Jacob stays home with me.  I do the blog and Jacob plays on the PS3. 

Thought I would share a quote that I think is quite relative to what I am going through:-

ATTITUDE

by: Charles Swindoll

The longer I live, the more I realize the impact of attitude on life.

Attitude, to me, is more important than facts. It is more important than the past, than education, than money, than circumstances, than failures, than successes, than what other people think or say or do. It is more important than appearance, giftedness or skill. It will make or break a company… a church… a home.

The remarkable thing is we have a choice every day regarding the attitude we will embrace for that day. We cannot change our past… we cannot change the fact that people will act in a certain way. We cannot change the inevitable. The only thing we can do is play on the one string we have, and that is our attitude… I am convinced that life is 10% what happens to me and 90% how I react to it.

And so it is with you… we are in charge of our attitudes.

Hope this gives something to ponder about how you live your life.  I have had to look at ways of changing my attitude.  Some days I get it wrong, others I seem to get it precisely.  I could have looked at my cancer with the wrong attitude and it would have consumed me.  Fortunately I choose to look at it as the unknown adventure and strange journey that it is.  I think Pam’s comment to me from yesterdays blog (thanks Pam), about been able to look at me and not know I have cancer, well today at the lake I was talking to a couple of guys about cars and jet skis, as you do.  We had the FPV Falcon out there and one of them said about driving, and I said I t is fun and one that I miss as I loved driving that car, and they asked the obvious why I couldn’t drive.  I said that I have cancer and can’t, and they just looked at me with that sad faced look (you start to become a good face reader btw), then one of them just asked what sort so told them 3 brain tumours.  Theirmouths did that open speechless look – not sure why.  Then they said that without knowing that they would never had guessed that I had cancer.  So that help bouy me up again.  So thanks for those that say I’m looking well.  It’s good to know that all the work of fighting it hasn’t changed me to much.  But if you could see inside my mind or spend a day in my body then you wouldn’t probably say it.  It takes a lot of sucking up of pain and things, and making sure the game face is looking right – as don’t want people fussing over me.  Enough waffle for now.

Quiet night in really, which suits me fine. Play some PS3 against Jacob, and watch some TV, M&D time, then head to bed as shattered as usual.  Hope you folk that worked didn’t have to do it too hard.  Really hope you have a great, relaxing weekend too.  Take care, have fun.

Kia Kaha.

Posted in Ramble. 6 Comments »


6 Responses to “Friday 16 November Ramble”

  1. markandkyliereid  Kylie Reid Says:

    Thanks for coming out with us, it’s always great catching up with you guys! What a fun afternoon…….the kids faces said it all !! I don’t think we will have much trouble getting you all to come out again! Hopefully next time we might get you on it for the short ride over to a beach at Brooklands………kids can then do some hotdogging and kneeboarding. Speak soon. X

    • southez  Headless Says:

      Thanks so much for having us.definitely will be up for another outing. Brooklands sounds perfect.
      Be in touch soon. Take care

  2. mark  Mark Says:

    Hey mate,was great to spend time with you and family:0)

    • southez  Headless Says:

      It was a great day out.thanks Mark for being the driver ;-) Like wise was great spending time with yours.

  3. bevan.toni  Toni Ferguson Says:

    Hi Tony, havent been in touch for ages…various reasons, but no real excuse. I am saddened reading of your pain levels, and wonder just how much the human body can endure. I do like that Attitude quote, and read something like that some time ago when I was having issues at work. It is very true, but not easy when things are rough! Your day out with the jetski sounded great! We are all fine down here, boys forever on ipods or messing round with scooters and bikes. Am enjoying that they are a bit more independant.
    On a differnt note, two weeks ago we learned that my fathers partner of 13 yrs has pancreatic cancer. she is only about 54, incredibly fit (competed at the world ironman comps in Las Vegas this year – doing the half ironman in 40 degs – grueling stuff!)…I have been doing lots of reading about it, and was hopeful she might be able to go to some specialist in the US, as the surgeon here said its inoperable…dont think its likely it will help. Currently waiting on a biopsy in Chch – incredible when someone is so sick, that they still have to sit and wait. We’re all pretty emotional about her situation, as she is already suffering intense pain in her back. Cant commence chemo until biopsy done….Not sure that you want to know about this, but you will understand all the fear and concern she will be experiencing at this point, with really not knowing what lies ahead. You express your feelings in writing so well Tony, and I admire you for your openness and honesty with this. Say a big Hi to Sue, Jacob and Lachie from me. Caleb would love to contact Lachie on his ipod (Face timing?)…do you know his username or whatever?

    • theedmonds  Headless Says:

      Hi Toni,

      It’s ok as I realise life gets busy and before you know it months have past. I really like that quote to as it is so true.sounds just like our house, with their faces glued to some device most of the time. Great though for punishment as taking of them for as day it’s like you’ve removed a limb. Great to hear all good and well in the deep South. Everything rocking on still.

      So sorry to hear about your Father’s partner. I can relate totally to what she is going through, as my biopsy results took over a week to get done, but when they explained why it made sense (due to the rarity of my cancer they needed it confirmed by another lab and retested several times). It doesn’t make it any easier to wait for. If she wants to talk about it out anything about dealing our living with it then I’m happy to share or listen. Yep they usually won’t do anything until they have the full picture then plan treatment. It is a cruel torture, as all you seem too think about is the tumors growing while nothing is been done to them. It becomes quite consuming really. Tell her to get a notepad and write notes from each appointment in it, in another part write any questions and there will be lots, in the back write your drugs down and the doses and any hospital admissions and what they give you. This is probably the one most valuable record that we have of my journey, and has been handy in getting help when I’ve ended up in the hospital as they can take a while to get your records.

      The fight she will face is hard and initially it is physiological but then becomes physical as well. The Oncology team here are brilliant. Oh and get in touch with the cancer society, as they are really helpful. I wish her the best for the fight ahead, stay strong. She already has a head start on the cancer fight with being so fit, and will also have fantastic mental strength. The one bit of advice I was given early on was make sure you define the cancer, don’t let the cancer define you.

      I can’t remember Lachies details so will find out in the morning. Take care and a huge Hi to everyone there. Still hoping to make a family trip South some time.