One to Cancer, time to regroup and fight back

I went back to see Dr K on my regular 3 week cycle. We did speak last time about alternitives if my cancer cell count was to keep increasing. Well they have spiked to 145 so immediate action required. I will be going back onto full blown  fortnightly treatment as of January. Hopefully the new drugs will stop the increasing cell counts and if all goes well start reducing again. It does mean I will be back on the rollercoaster of feeling very sick and emotional when I have the treatment. Dr K has told me to slow down again and mentioned I now have no choice as the treatment will make me need more rest. I have started to get some pain in the liver region so back onto the pain killers, which has helped. Although it is a set back, in some ways a am relieved as it was starting to worry me with the increase in cancer cell counts and taking no action. At least we are getting back into the ring to fight again. Well its nearly Xmas and will be spending it with my Family and friends for the first time in many years and then catchup with Meghan's family as well. Merry Xmas and Happy New Year to all.

CT results in and just treading water

I had my appointment with Dr K yesterday. I was not expecting any good results. Meghan came with me, and for her to come with me means she was thinking the same as I was. The outcome could have been worst but now have more to play on my mind. The tumors on my liver are stable and are about the same size as previous scan, so reasonably happy with that. My tumor markers are still rising and are over 100 now. Not good. This scan also showed 3 spots in my lungs which at this stage can not be identified as they are small in size. Dr K played down the fact they maybe tumors, but it is really hard to get it out of your head when my tumor markers are rising and no growth in the liver. Seems a big coincidence!! We have decided to continue the same treatment for now, but had a lengthy discussion on what treatments are available when we feel the current treatment is no longer working. We still have one more protocol left to try before I need to call on my last resort down in Melbourne. So looks like I will be around for a while yet which is positive, but am preparing myself for some tough times over the next year. Still working full time and loving my job, but Dr K keeps telling me to slow down. I think I will have no choice soon, as even now I get to 3 o'clock in the afternoon and I hit a brick wall. I must admit I have been lucky thus far to be able to continue a normal life, well as normal as you can when you have the weight of cancer on you. I am about to embark on some pet therapy. Yes we are getting a dog. My dream of having a Boxer is about to come true. Ralph (that is his name) will be joining the family after Christmas. I will attach a picture on my next blog.
If nothing else, I have learnt to enjoy everyday and not get bogged down in the minor speed bumps we encounter. I hope everyone can take something from this as life is too short for negativity.

No good news but remain positive

Hi All, it’s been a while since my last blog, mainly because i have not had any good news to share. My cancer cell counts continue to rise, they delayed my Chemo by a week as my blood tests were no good, and generally I have not been feeling the best. I am back on Chemo again and had a CT scan a couple of days ago. Hopefully this will give us some insight into why my cancer cell counts have been increasing. So not expecting very good results from my next appointment with Dr K.  At the end of the day I just want to know so I can plan my next attack strategy to beat this terrible disease. I have a feeling the cancer is getting the better of my current chemo. It maybe I will be seeing my secret weapon down in Melbourne quicker than expected. Mentally I admit I have been struggling but managing to keep on top of it. Meghan has been my rock, and has had to console me at times when I have just needed to let it all out. I am not scared of dying, but I am enjoying my life (apart from the obvious). Work is great and achieving most of what I set out to do here in Darwin. Family life is fantastic and that is why I worry so much. I don’t want to leave Meghan and Sam for a long time yet.

I will update everyone after my next Doctor’s appointment on the 30th of November.

Wish me luck.

Is this the beginning of the end

Sounds a bit dramatic but I cannot get this thought out of my head. Last visit to see Dr K was not so good. The tumor markers which stabilized, have risen from 60 to 83. I was given the same reasoning as previous, a new tumor or overactive current tumors. Either way it tells me the cancer is getting the better of the chemo. It was always going to be a race to see who would win, and it looks like the devil is winning. This just gives me more reason to stick to my plan after my next CT scan now booked for the 16th of November. I will definitely be contacting the Specialist in Melbourne as per my last blog.  Ready to hit it hard before the cancer takes control. Other blood counts are not so good either, Hemoglobin and platelets are well down on recommended levels but the good news is my white blood cells are just within the normal range which is helping fight off any other diseases try to get in on the act. Just about to go on a 9 day holiday with my two best friends, my wife Meghan and little boy Sam. Off to Bali, and yes will need to be very careful of what I do and eat, but can't live in a cocoon. So I think the rest will do me the world of good and come back ready to keep the fight going.
Cancer but positive? the positive at this stage is I will keep fighting to the very end.

Tumor markers have stabilized

I have just had my latest results come through from my 3 weekly blood tests and my tumor markers have not increased from my last test, still sitting at 60. This is good but still a concern. Dr K thinks it could be another tumor growing but not big enough to show up on the CT scan as yet, or its just the tumors in my liver being overactive, let’s hope for the latter. The chemo has hit me fairly hard this past cycle and I am just about to go back in tomorrow for another round. I suppose after 12 months of continuously being feed lethal noxious drugs which would kill an elephant you have to expect not to be doing cartwheels around the house. I will continue with the 24 tablets a day and hopefully find a cure to this dreadful disease before the chemo takes me. I have been researching and contacting various clinics to see if I could be suitable for a liver transplant and after exhausting all avenues the answer is no. main issue I have now been on chemo for so long the doctors tell me I am too higher risk due to my low immune system to operate and my body actually accepting the transplant. So my focus has now turned to how we can go about killing the tumors in my liver before they take over. I am going to pull out the wild card and contact the specialist in Melbourne and discuss options after my next CT scan in November, and there are some options of which some are still in trail stages but never the less seem to have good results so far.

Well fingers crossed I continue to see good results and hopefully in November have a plan in place to wipe out the enemy.

Sometimes I surprise myself with my positivity!!!!!!! This is one of my good days. I don’t blog on the bad ones. Bye for now.

12 months to the day since diagnosed with this life changing disease.

I find it hard to believe myself it was 12 months ago since I sat in the Dr Michael Ryan’s office on the Sunshine Coast after a routine check up to be told I had Cancer and had between 6 to 24 months to live.

So what did I do????? Firstly I did not accept the fact I was going to die. Yes the statistics tell me otherwise, but all research seems to be on older patients and less fit than I was. Life needed to go on and not just “go home and get my affairs in order” as it was so nicely put to me. So you would think I would have just gone back to my regular way of life and set about beating this disease. No, we as a family transferred to Darwin and I took on a huge task of getting 2 of the largest Hotels in the group back on track. Now when I look back on this period it was really intense. Meghan had to leave a job she loved, Sam had to move out of an Early learning Centre he was very happy at and we had to pack everything up and move to a city we virtually knew nothing about. Twelve months later and I feel it was the right decision. It has been the toughest period of my life and obviously for Meghan as well. She didn’t count on marrying a cancer patient! So diagnosed with stage 4a cancer. Bowel tumor and a liver riddled with lesions. Not much hope given from the medical profession. Now I have beaten the bowel tumor and the liver lesions have been reducing on a slow but steady basis. Overall I have coped well I think and have had good results. I’m still here and that has to be a good thing. In medical terms I am “stable”, which means I can expect to live for a while yet. I can now focus on not just surviving but actually beating the cancer. I am a realist and know I will have to live with this for the rest of my life even if I go into remission there will always be the chance of it returning. The upside to all this, if there can be one is I have a whole different perspective on life and if it wasn’t life threatening I would recommend it to everyone. I won’t go through my new take on life, just to say I enjoy every day, and day to day issues are no longer relevant. How’s this for a crazy statement. I am now more relaxed in my day to day life than I have ever been!!!!

So enough for now as you will all get bored and continue surfing the net. Just a quick update from my previous blog. CT scans came back showing more lesions than the PET scan but they have reduced from the last CT scan so still heading the right direction.  Biggest worry at present is my tumor blood markers have increased again to 60 and no one can tell me why. Again I thank everyone who has supported me over the last 12 months as it keeps me focused on beating this disease.

Nervous about CT scan results coming up

I had my CT scan this week and waiting to go back to see Dr K on Monday. I really haven’t been feeling so great over this past chemo cycle. Physically I have been drained and haven’t felt this bad for about six months ago when I was on the full blown chemo. I have had a big couple of weeks at work which I know hasn’t helped, which my Beautiful Wife Meghan has reminded me of. She understands I need to work too keep my mind active but yes I need to get the right balance. Mentally the CT results have been playing on my mind. What if the PET scan is wrong and I haven’t seen any reduction in the tumors which would account for the higher CEA blood counts??? Or it could be the scan will prove the PET scans correct which would be fantastic. The only reason I have doubts is the high CEA result and the way I have been feeling and just yesterday I found a lump in my armpit. I will raise this with Dr K and hopefully it is nothing, but when you are not 100% these things weigh on your mind. All will be revealed in 2 days at the appointment.
Wish me luck and will update again after my Doctors appointment.

Lastest results have left me in Limbo

I am now back from Brisbane and had my PET scan. Went back to see Dr K and the PET scan results told us they could only find signs of a tumor in the right lobe of my liver. Fantastic news, BUT Dr K bought me straight back down to earth. He suggested the results may be floored and for various reasons may not be showing all the cancer spots in my liver. Looking at the big picture the results are still good, as one of the reasons they may not be showing up on the scan is they have reduced enough in size not to show up. If I compare to my last PET scan nearly 12 months ago where they could see two large tumors and a multitude of splattering throughout my liver to now only showing one tumor is a great result. So I will keep again keep positive and look at this as a good improvement. I also had my regular blood tests. The results of this are not so good. My tumor markers have increased again to 43. So in one hand we are saying the cancer is reducing in my liver but the tumor markers are telling us an increase in activity, hence my state of limbo. We have decided to do CT scans and have another close look at the liver and hopefully they will support the PET scan and show a reduction. So a CT scan and back to see DR K before the end of the month. Wish me luck. I am still on the chemo cycle and managing the side effects day by day. Working fulltime keeps my mind occupied pushes me to get out of bed everyday although some days are a struggle. Not sure how I am feeling emotionally at the moment. Maybe I am just too impatient, but I just want to know my exact situation so I can plan an attack on the cancer. Now nearly 12 months since I was diagnosed and funny enough although it has turned my world upside down it is now just a part of my life and take it in my stride and push forward every day. I have made fantastic progress from last year so I am very lucky considering the Doctors told me to go home and get my “affairs” in order. In other words prepare to die within the next 6 to 24 months!! I think the prognosis is much better now and my goal is to be able to go into remission in this year.
Thanks to everyone who has supported me over the last year, I would not be where I am now without this support. I will update again once I have the CT scan results.

Back on the Chemo Rollercoaster again

First cycle of my 3 week cycle completed since my short break. I started cycle 6 of the Avistin and Xeloda treatment toady. Intravenous dose this morning and two weeks of tablets with a week’s break after that. This will bring me up to ten months since I started Chemo. I have learnt a lot over this time and too much to mention in this blog, but the two main things have been, I would not wish cancer on my worst enemy, it’s not just the physical aspect but also the emotional roller coaster you take. The second is you really find out who your friends are and how much they really mean, and I need to mention my Family who are by my side through all of this feeling every emotion I feel. I still have a long way to go but remain positive I will see little Sammy grow up into a man. Blood tests this cycle are not so good. My CEA count, (cancer cell count in blood stream) has risen slightly from 20 to 28, and my white cell count is down. No cause for panic but will need to keep an eye on this and hope they do not get any worse. Off to Brisbane next week for my PET scan which I am looking forward to receiving the results from. I can then sit down with Dr K and discuss the best options to destroy this cancer.  I will be also sending the results to my secret weapon down in Melbourne. I have been keeping a specialist up to date with my progress and using him as my second opinion. He is at the cutting edge of research for cancer at a large hospital and has all the right connections. Just keeping Dr K honest. He has a couple of treatments up his sleeve which we may need to call on if the Chemo treatments start to go pear shaped. Hopefully I will not need to draw this card but always good to have a plan B.
The next blog will hopefully have some good news after the scan results, so wish me luck and thanks to all who continue to support me.

FIRST ROUND KNOCKOUT AND BACK INTO THE RING TO FIGHT AGAIN

I am sitting back in the oncology unit t as I post this blog, hooked up to bags of poisonous drugs which not only kill the cancer but every other cell it comes into contact with. That’s the way it works, but believe it or not I am happy just to be back in the ring fighting the killer disease which has turned my life upside down. I had a great meeting with my Oncology Doctor who I call Dr K. I explained in no uncertain terms that I am not willing to sit back and be diagnosed as “stable” after each scan I have. I want to do everything in my power to beat this and if he was not willing help I would have to look elsewhere. He sat back in his seat and I could tell he does not get this type of reaction very often. I am sure most people just take his word for it and prepare themselves to die. Not Me!!! So straight into action goes DrK, we decide to put me back onto Chemo the next day and up the dosage. We also organized to have a PET scan (this is the ultimate scan which shows every last cancerous cell in my liver), which I have to travel down to Brisbane for at the end of July as they do not have a machine in Darwin. Once we have the results of this we will discuss next steps, and it looks like we have a few options, which I will not go into as yet until we are better equipped to make a decision. So now I am back in the ring and ready to go for another Knockout. This time it may take more than one round to beat this hefty opponent, as the big C has a pretty big strangle hold on my liver, but I know if I can keep on top of it I will eventually take it down. The bell rings and into the ring I step yet again,
WISH ME LUCK.

The Good the Bad and the Ugly

I have now had my colonoscopy (not a pleasant experience I tell you) and went back to the Doctor to get the results, not really knowing what to expect so was very apprehensive. Was he going to tell me the Tumor was still growing and needs to be removed or was everything just Ok and life goes on??? He sat me down in his nice big office and put his glasses on and proceeded to review my results. It felt like 1/2 an hour had passed but in reality was most probably 1 to 2 minutes. He then looked up at me and said quote “I could not find the Tumor". My first thought was he a doctor or a quack, why couldn't he find it? I made out I didn't hear him and asked him to repeat himself. He then proceeded to tell me he could see where it was but now gone. Just some scaring which he took samples of and came back with no problems. How Good is that!!!! I was facing an operation to remove the tumor which would have had me on my back for 6 weeks and a colostomy bag for at least 3 months. So at this stage this will not be the case. That’s the good news.
The Bad & Ugly is this will not make any difference to my ultimate life expectancy. I still have the liver to contend with which what has control of my life span. Now 4 weeks off from Chemo whilst we have got the good news means now I am 4 weeks behind the battle with my liver. The Cancer has had a chance to regroup and build up some strength. I am meeting with my Oncology Doctor next Monday and discuss next steps and I will raise the option of going back onto full chemo treatment rather than the maintenance treatment which has not been successful in reducing the cancer in my liver. I am over the side effect now which is the reason why they changed my treatment in the first place. Yes it will be tough, but no glory sitting on the bench watching the team get beaten, (old football term). So maybe I might be jumping back onto the rollercoaster, which I don’t mind as I cannot sit here "Stable" and watch my life go by without doing everything possible to beat this. It is really hard when you don't know how long you have and what to do in this time. I now just take every day as it comes and enjoy the time with my fantastic family. Every time I see little Sammy smile and laugh makes it all worthwhile fighting the fight. This is the one thing this dreaded disease has done for me. Enjoy life and not worry about the small things. Remember this everyone, and not wait until something like this happens to wake us up.

First step backwards

I went for chemo today and the Oncology Doctor would not let me have the treatment. This is the first time I have not been able to be treated. This is an emotional step backwards for me as I feel it is the first sign of my acceptance that I am not going as well as think. I now have to have another colonoscopy before they will allow me to have chemo again if they find no issues. If there is a problem it may mean surgery to remove the tumor. The complication is my liver is riddled with cancer and to stop chemo may mean growth of the cancer which I have worked so hard to bring under control.
I still have a positive frame of mind, but finding it hard to maintain. I will keep fighting on and realize it will only get harder from now on.

Stable, what does it mean?

I have had my latest scan and follow up Doctors appointment, which Meghan came along to give support as she does everyday. In a nutshell, I came out of his office feeling like a just played in a sports game which ended up in a draw. The Doctor said there was minimal change in my results compared to the last scan, which is good that there has been no cancer growth, but on the other hand no reduction. The Doctor seemed happy with this result and expected it. When I probed deeper he said if my condition remained stable he would be happy until the current treatment stopped working and then we would have to look at changing again. Eventually the chemo will not be effective, so I hope we can beat it before getting to this stage. We asked the big question on life expectancy as you do! The answer. Same as I have been told before, 6 to 24 months from diagnosis. This is the standard spiel from every Doctor I have spoken to. Quote "research tells us this is the average time frame". Blah Blah!!! Looks like I will need to improve these statistics. As I write this blog I have just spent the last 8 hours in the ED at the Darwin Hospital. The tumor in my bowel bled today, which scared the hell out of me, but after multiple tests I got the all clear, but not really knowing why it happened. It could not have been due to a growth in the tumor as the scan showed no growth. We are hoping it was due to the tumor breaking down, but no proof of this. So just another trip to the Emergency Department, another day in my life now. Meghan and Sammy came out to see me with Sam also accepting it is now a part of Daddy's life and takes it for granted. I hope one day this will be just a memory for him and we never see the inside of that dreaded Hospital. Back to have my 17th round of chemo tomorrow and continue the fight against the big C.
Life goes on

Ramblings of a cancer patient

Not sure what I am going to write here but feel compelled to let my thoughts out, as this is why I started this blog in the first place, so here I go.

 I went to the oncology unit on Wednesday for Chemo treatment only to find out another patient I have gotten to know passed away. She was a lovely woman who always had a smile on her face and her husband was by her side for each visit. They have young children who now have no mother. Cancer is an evil disease which can turn your world upside down and is so unfair. This is now 2 wonderful people I have got to know whilst in Darwin who have had their lives taken far too early. It makes me realise I am not invincible and need to look after myself. It is not the cancer in some cases which delivers the final blow but other complications due to a low immune system. As you know from my blogs I am very positive but it still leaves a thought in the back of my mind it can happen to me without warning. It may sound dramatic but it is like having a hit man looking for me, as  I could suffer the same fate as the friends I made and then had taken away. Don’t get me wrong I am doing very well and have my CEA results down to 20, which is fantastic, considering they were at 5,500 last October. I expect this won’t change much now until I have surgery to remove the tumour from my bowel. The doctors are happy to leave it there until we have my liver under control, so could be near the end of the year or even early next year if no complications in the meantime. Good news is I have feeling back in my hands and feet which is great, but ironically I broke 2 toes a fortnight ago and I definitely have the feeling back!!! I have my next lot of scans at the end of this month which will give us a better indication of how I am going, so will blog again once I get the results. So fingers crossed everyone and wish me luck.

9 weeks into the new treatment

So now 3 cycles into the new drug Xeloda, and as per the doctor’s comments on the side effects, my feet and hands are giving me hell. I have managed to keep the blistering at bay and have had minimal peeling by using hemp oil every day. The main problem is the pain and tenderness in my fingertips and feet to the point I have to get Meghan to button up my shirt each morning ready for work. I also have really bad skin itches all over my body, which drives me crazy but am taking antihistamine tablets to help. Yes another tablet to the menu of 25 pills. My last visit to the doctor was positive with my CEA blood markers reducing further to 25 from a previous 40, so still dropping although at a slower rate now that they are getting lower. I suspect they will not change much now until I have an operation to remove the tumor in my bowel. The Doctors still think we can wait for this operation until the end of the year or early next year if I have no problems in the meantime and concentrate on the liver. Strange to think the root of all my sickness is still sitting in my body and we are happy to leave it there for now!!!! Scans have been booked in for the end of May and this will be the real test to see how I am progressing, especially with the tumors in my liver. Fingers crossed they have reduced further from my last scan back in January. I have gained 2 kilos in weight over the past 3 weeks and am back to my original weight before being diagnosed. I still get very tired and the drugs have affected my short term memory which is very annoying. I have managed to maintain my normal work routine, but at times struggle and wonder for how much longer I can do this at this level. It is one of the things which keeps me going so I will keep pushing myself within my limits and hopefully will be able to keep going. I just don't want to be one of the many sufferers who cannot work and stay at home and have their life ruled by this dreadful disease. It is my little boy, Sam’s third birthday soon (May 25^th) and I am thankful for everyday we spend together and intend to celebrate many more birthdays in the years to come.

For now all the results are pointing in the right direction and I remain as positive as ever.

early days but so far OK

I just had my first cycle of the new treatment and whilst I realise it is only early days, it seemed to be better than the previous, as far as how it affects me. Rather than a full-blown hit in one day and taking up to 10 days to start to feel half normal, it is spread out over 2 weeks. So just feels like waking up with a very large hangover every day and it not going away, would be the best description I can give. The side effects with this treatment are mainly peeling and blistering of the feet and hands. This is already prevalent and am using Hemp oil to combat it getting too bad. I have my first check up with the doctor next Wednesday and am hoping to get another scan done, as the last was back in January. Hoping to see positive results again, fingers crossed.
As my results since starting Chemo have been so good, I now face the demons in the back of my mind telling me this can't continue forever and a relapse may occur, as the doctor so kindly told me last visit (thanks doctor). I fight this thinking and remain strong in my thought process, and hoping the next lot of results will kill these unwanted thoughts. My Beautiful Wife and Son are by my side everyday giving me all the support they can, and i have family and friends from all over the country calling me to let me know they are here for me. Thank you to everyone without this support I would be curled up in the corner somewhere letting this terrible disease beat me.

Next steps after 6 months of my Rollercoaster ride

Had my Doctor’s appointment yesterday to determine my next steps as far as treatment goes. The current treatment has shown great results so in a way a will be disappointed to change but on the flip side the side effects and rollercoaster ride I will not miss.

The doctor has put me on a tablet form of Chemo now. This will involve about taking about 8 tablets a day on top of the 14 I currently take. Yes I will rattle as I walk!!! I will need to go into the Clinic every 3 weeks to have 1 drug still administered intravenously and then 2 weeks of tablets and one week off. I am hoping this will reduce my current side effects and stop the rollercoaster I am currently experiencing as it will be daily treatment. Obviously the new drugs still have side effects as well but will deal with these as they arise. The only negative to the appointment was the Doctor thinks at some stage my cancer cell count will increase as the cells become resistant to the drugs. We have other options once this happens, so not all that bad. Would be great to get to a remission stage before this happens, but I might be aiming too high, but that will be my target. Let’s hope the new drugs are as effective as the old ones.

No-one really knows

the pain associated with Chemo treatments. As per my last post the side effects are really kicking in, and I now know how other cancer suffers feel. I am the lucky one as it hasn't really hit me until now. I am not going to describe how it feels as to be honest I cannot. It is a whole different feeling and is just with you 24/7. I think besides the physical side effects such as mouth ulcers, skin irritations, numbness in my feet and hands etc., it is the constant tiredness which gets to you. Just getting through the day is a chore, and no one wants to spend their life just trying to get through the day without enjoying it.

I realise this may seems a bit left field for me as I am always positive. This has not changed and I am still really happy with my progress. The Specialist in Melbourne has got back to me and is very happy with my results to date, which is great to hear. As far as the removal of my bowel tumour, he recommends to just leave it for now and most probably the rest of the year unless it starts to create any problems. I am OK with this as now I can plan a nice holiday with my Family who deserve it more than I do.

One more full treatment next Wednesday then a Doctor’s appointment to discuss the Maintenance program I will be going on. I will update once I have had the Doctor’s appointment.

Thank you All again for the support I am receiving.

Scan results back and looking good!!!!!!!

So had my Doctors appointment on Wednesday and the scan results were very good again with the two main lesions in my liver reducing by approx 7mm. It may not sound much but in my world it is a good effort.  The Doctors told me I might only have 2 more treatments on the current dosage levels of Chemo and then go onto a maintenance style Chemo. This sounds much better as it is just taking tablets each day instead of having a drip attached for 2 and  a half days.  I am getting to a stage after 10 treatments were the side effect are really kicking in and lasting longer and I was starting to get concerned if I was going to be able to keep up my current work pace for much longer. I love my work and this keeps me going along with my family and friends. The break from full blown treatment will be great. I am about to send all results to a very good Oncology Doctor in Melbourne who will now give a second opinion and he will also be make the decision on what to do with my bowel tumor. Hopefully I will know within a month whether I need radiation treatment or they can operate soon. I expect it will be radiation as the tumor in my bowel has not reduced in size but has not grown either. We expected this as the Chemo was focused on the liver, so all good. Thanks to everyone for all the support again and I appreciate it immensely.

Scan results next week!!!!!

As per my last blog I have just had treatment number 10 and dealing with the side effects best I can, but is not easy. I had a CT scan yesterday and really looking forward to the results on Wednesday. Any improvement is a positive. Some sad news, I guy who has been having Chemo the same day as me with very similar cancer, has been in Hospital for 3 weeks now and is not doing very well. I have come to terms that I will see some very nice people struggle with the cancer or not be able to win their battle as I continue down this long road to recovery and this is the saddest part of the whole journey.  It does make me stronger to keep the treatments going and keep improving, but in reality I have to be prepared I may have times where I could have complications, but will deal with this when and if they arise. My next blog will be after my Doctors appointment so please keep your fingers crossed and slip a couple of prayers in there and hopefully all will be good.

Thank you once again to everyone who is supporting me and I cannot begin to tell you how much the phone calls and emails mean to me.

Back on the Rollercoaster

I have just had the best period between treatments last fortnight than I have had for months.
It is Tuesday afternoon and I am currently sitting in the big blue chair at the oncology unit having treatment number 10. As I sit here for approx 3 1/2 hours and they feed the Chemo drugs into my body I can feel myself leaving the top of the hill on the rollercoaster and starting the descend to the bottom. I hope the bottom is not as far down as I have previously had and I can at least feel half normal this time round. It is strange to sit here and know how strong these drugs are going into my body. All the nurses wear protective gowns, face masks and gloves. Makes you feel a bit like a lepour! Some bad news. A friend of mine, who has treatment on the same day who has liver cancer as well, was not here last treatment and not here again  today. I asked the nurse and he is in hospital, and would not give more information than he may not be back. Hits home when you here this happening, but I need to get used to this as I work through my treatments and eventually beat this Cancer. There will be people who will not make it. It’s just a pity to see such good people be struck down in the prime of their life.
It really makes me appreciate every day a wake up and see the sunrise and the voice of my little boy Sammy as he shuffles in to our bed for his morning cuddle. I hope everyone who reads this will wake up tomorrow and feel the same as I do each morning.

Mind over body

Another fortnight nearly over in my rollercoaster ride of Chemo. This has been a much better fortnight than the last, as per my last blog. I seem to have shaken of the bug I had. Treatment number 10 next week which means I have been on treatment for 5 months. As my blogs reflect it is not getting any easier in fact harder each time, but all good as I am seeing results. Really looking forward to having scans at the end of next week which will give us a better indication of how I am progressing. To a lot of people what I am about to write, you might say "no big deal, I could do that", but for the people who read my blog and have cancer I hope you get inspiration from this.
On Wednesday I took my Executive Team on an afternoon Team Building exercise. Indoor Rock Climbing!!! What an excellent afternoon and everyone took away something from the afternoon. For me. I attempted to scale the 20 metre wall but could only manage about 6 meters when a ledge stopped me in my tracks and I just run out of energy. I came back down and let one of my Team have a go. He went up like a proverbial rat up a drain pipe. I took a big breath and focussed on getting back in the harness and setting my sights on the top. So I strapped myself in and started the long haul up the wall with these little pebbles to support me. I reached the spot which beat the on the 1st attempt and just set my eyes on the top and got over the ledge. From here you would think it would be plain sailing as it was just a straight 180 degrees (yes straight up and down). As I took each step to the next little pebble jutting out from the wall my body was losing any strength I had, but I shut out all negative thoughts and just zoned into reaching my ultimate goal,  the top. After 10 minutes of shear pain I made it. Yes a 48 year old stage 4 cancer patient climbed a vertical 20 metre wall clinging on by just fingers and toes. Was I proud of my achievement? What do you think? I reflect back and realise, this zone I was in to reach the top I am already in and have been in for the past 5 months. When your body says give up let your mind take control and you can achieve anything you want to. Maybe not first time but don’t give up. Photo inserted to just show you the wall which I conquered.

Turning a negative into a positive

I realize I only posted a blog yesterday but since then I had an interesting afternoon.

My temperature spiked up in the afternoon so as per the Doctors instruction any time I am over 38 degrees I need to admit myself into emergency. That in its self is an eye opener in the Darwin Hospital, which I will not go into now. I was in emergency for 4 ½ hours yesterday and every test you could have I had. In the end my temp came down and I was released with antibiotics to help my very low immune system to beat the bug I have. So the positive out of this bad afternoon. They contacted my Oncology Doctor to consult, and he had just received my latest Tumor Marker results. There are 2 separate markers which are based on overall cancer cell counts in the blood. The CEA result came in at +161 which were at 5510 back in October. The normal figure is -5. So huge drop in 2 months and 166 away from a normal count. The next is the CA result, which came in at 91 from 360 back in October. The normal figure for this test is 0-35 so another 60 points to go. I realize this will take a lot longer to get these last points down but how good to be so close so quickly. I put the great results down to everything we are doing from the dreaded chemo, to a couple of natural cures I have been taking,  to all the positive energy I receive from all my friends and everyone out there praying for my recovery. Obviously it is working. Thanks you again to all whom fall into the above.

4 1/2 months into Chemo and its taking effect

This Wednesday will be treatment 9 and I am really feeling the effects of chemo as it builds up in my body. Hair at this stage is holding on, but I am due for a haircut which will show the thinness of my scalp, so maybe soon the shaver comes out. I have my next scans coming up on the 29th of January so looking forward to some positive results which will give me the strength to continue on. I have had a bug since before Xmas which put me in hospital 2 days before Xmas. Since then my temp has been like a pogo stick if everybody remembers what that is! Ranging from 36 to 40.5. As my immune system is so low this creates difficulties trying to bet the bug. Yes something as a simple flu has put me in emergency. This is my life now and need to accept it, which I will admit is taking a lot to do as I have been so healthy until 4 months ago. The pain of the cancer is non-existent due to the drugs I take but it’s the side effects which cause the pain and frustration. I will not go into all of them but the biggest is the lack of energy and as I have mentioned in previous posts each day is a battle in its self just to get through. Work keeps my mind stimulated but need to listen to my body as well and take time out when needed.

I have contacted a very good Doctor down in Melbourne to be involved and give me a 3rd opinion, so I have doctors in Adelaide, Darwin and now Melbourne looking at my case. I have a lot of faith in their actions so we continue on. The Doctor in Melbourne is a leader in SITR research in Australia which is why I have chosen him for my case. What is SITR? please read the link and you will have a good idea of the treatment. http://www.umgcc.org/sir-spheres/about_sirt.htm   It is new into Australia but has had great results. Still looking to get the tumor in my bowel removed in the 1st half of this year by the Doctors in Melbourne and should have more idea after these next scans. Again thanks to all who are supporting me through this and I can not thank my Darling Wife Meghan enough who now wears alot of the day to day burden which normally would be shared in our relationship.