Thursday, January 22, 2009

Monday 19 Jan 09

Chemo last Friday progressed well at a very steady pace. My chemo dosage was reduced by 25% again due to the vein inflammation. This means I am now at 50% of the original dose and according to the Dr’s it is still enough to keep the cancer at bay. I did make a comment to my chemo buddy, Anet, that it makes you wonder why I needed such a big dose initially and was very abruptly reminded that I am on a clinical trial so they are testing the correct dosage!!! So far the side effects have been milder in terms of the nausea. I am still very tired and feel disorientated when I do too much physical and mental exertion. I also saw a surgeon today regarding having a port fitted – this is planned for Tuesday 03 Feb all things going well. Tomorrow should be a normal day at work and then I head off to Antwerp again for 9 days and will see my Mom this coming weekend. Even in Holland things have had there moments of strain as my Mom’s husband fell last Sunday and broke his hip. He is still in hospital post surgery and from there will be moving to a care centre.

Thursday, January 15, 2009

Jacobsbaai

We have had a stunning 3 nights away and the boys were really on good behavior. They did not complain too much about the lack of internet and cable TV and both managed to get through a fiction book. This morning we got stuck in together to clean the house (my brothers seaside cottage) and left around lunchtime. Home in good time for me to get on top of the washing before tomorrow’s chemo session. I am feeling in good spirits as I prepare myself for tomorrow – more positive than I have been in months! Last week Dr T shared the detail of the CT scan. The one lesion that was close to my spleen cannot be seen anymore and the total diameter of the 2 biggest lesions was 32mm in the first trial scan and now measures 24mm. This is the best news that I could have hoped for and I can just hear God saying to me “where is your faith”! So for now, my decision is to remain on the trial for another 2 months and then we reassess again.

Thursday, January 8, 2009

4th round Patupilone rescheduled

This morning I headed off to the oncology unit by myself, feeling healthy and in good frame of mind. My normal partner Anet could not make today because it is her birthday… our thoughts are with you today dear Anet. Instead another dear friend of more than 20 years met me at the oncology unit and spent 90 minutes with me. All the normal tests where done… ECG, heart rate and bloods. The wait was much less than last time, but still took 2.5 hours to see Dr T. We had a good chat and after some deliberation it was decided to reschedule my chemo session of today due to the inflammation I have in my veins. I am now on more medication to ease the inflammation over the next week with chemo now planned for Friday 16 January. I have fortunately already made peace with the fact that chemo’s occur when they have to and am taking the change in my stride. It just means that our family holiday next week needs to be cut short by a few days and I can assure you all that a 17 year old teenager is very happy that he is coming home sooner. What is it with teens not enjoying family holiday!!

Wednesday, December 31, 2008

Welcome 2009

The CT scan this morning has delivered very promising results. The cancer growth is stable – this is wonderful news as it means that the clinical drug is halting the growth of the current and new lesions! With today not being a full working day I do not have the full CT results so I cannot report back on the state of my lesions – will do this later. This morning I saw Dr T regarding the terrible pain I have been having in my left arm since before Christmas and I have been diagnosed with inflammation of the veins (too much toxic substance causes this) …. Argh.. it is really painful! I cannot received chemo in my left arm again and will do some hasty work coming Monday regarding having a port fitted. I have been saving my right arm for all the blood tests, etc. So, in conclusion, I remain on the clinical trial with a reassessment of the lesions end Feb 2009. Lets hope and pray that the good news continues thru 2009. I thank everybody who has been supporting me the past 14 month and wish you and your families a healthy prosperous 2009. I will be having a few glasses of bubbly tonight to celebrate today’s news and the new year.

Sunday, December 21, 2008

3rd round patupilone

I was really positively surprised by my white cell and neutrophil count last Thursdays. Both were inside normal range – well done dear body for recovering so well! With the holiday season in South Africa the wait for the blood test results took really long – waited over 4 hours and then got the good news that chemo would occur… .Whoopee! The past 3 days have been much better than cycle one and two on patupilone. I ‘m still bit nausea and tired, but don’t have the intense nausea of the past two rounds. Dr T (clinical trials unit) has put me onto the same anti nausea meds that I had previously on taxol and carbo platinum, and it seems to be doing the trick! I have been having my afternoon siestas and early nights to rest the body. No rest for the wicked as I will do a few hours work from home tomorrow.

Thursday, December 18, 2008

11th round of chemo

Today I have risen with a heavy heart as I face the clinical trials unit and my 11th round of chemo. We start the day with an ECG and blood tests, I then need to wait for the test results (about 1.5 hours) and then see the doctors for some checks and balances, ‘anti’ medicine prescriptions and then I finally get to walk to the chemo rooms with my files in hand. I must admit that I am not looking forward to the treatment knowing how I am going to feel for the next week. In my heart I have had enough of this toxic stuff … it has been 14 months of chemo.

Sunday, December 7, 2008

Bron and Rory's wedding

Tuesday I decided not to take my cortisone (it was my last scheduled dose) and I really started feeling better from Wednesday. I still have the odd bout of nausea and tend to get physically sick in the mornings but managed thru Friday and Saturday without any medication. All is going really well this weekend and I have managed late evenings out and no afternoon naps, though I am not sure I will manage that today. Yesterday was my Goddaughters wedding day and Ian and I consumed an ample amount of bubbly. Bronwyn and Rory looked absolutely stunning and it was a wonderful ceremony and excellent party. Quite a few tears were shed as we raised our glasses to late Sharon (Bron’s mom passed away with cancer nearly 10 years ago).