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More time for Melissa

  • No more treatment

      28 April 2015

    After the news that the Cetuximab had stopped working Melissa had her 15th CT scan in 2.5 years. The CT results were good, in that the tumours had clearly shrunk since her CT in January and there has been no further spread. This means the Cetuximab definitely worked and Melissa is in better shape now than she was 3.5 months ago.

    That said, Melissa and her family discussed the remaining options with her Oncologist and have opted for no further treatment. The best she can hope for now is a few months of respite before new symptoms start appearing. Her life expectancy is now in the order of 6-9 months.

    Thanks again to everyone who has donated via this Givealittle site. Enough money was raised to cover the entire cost of Melissa’s Cetuximab treatment. As she will not be pursuing other non-funded treatments she is no longer seeking donations.

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  • Not great news this time

      10 April 2015

    Oh how quickly things can change. After my last update where I reported that Melissa’s CEA was still trending nicely downwards, she had two further decreases (52.5 after 7 doses and 51.9 after 8 doses), but given how small the decreases were they thought they were probably seeing the start of a plateau. A week later Melissa experienced her first increase since being on Cetuximab (53.7) and a week after that big jump to 78.3. The doctors have decided there is no longer sufficient evidence to continue with Cetuximab as it is no longer working.

    Melissa and her family now have a difficult decision ahead as there are only two remaining options. They can decide to try another expensive drug (Avastin) in combination with a chemo drug that she has had before (Irinotecan), accepting that the odds of it working are only in the order of about 10% and dealing with a new range of side effects (and revisiting some old ones such as hair loss and neutropenia) or they can decide enough is enough and try to enjoy the time she has left without the endless hospital appointments and side effects. Should she decide to proceed with Avastin any money left over from this Givealittle fundraiser will be put towards that.

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  • The good news keeps coming

      11 March 2015

    Melissa has now had 7 doses of Cetuximab and much to everyone's relief and delight, her CEA is continuing to drop. After two doses it had dropped from 265 to 132, and as of Monday this week (a week after her 6th dose) her CEA was just 56.5. The plan is to keep going until her CEA plateaus and then do a CT scan to see how things are looking. The CT results would then be used as a baseline for monitoring how long things remain stable after that.

    The other good news is that the only side effects she seems to be experiencing are related to her skin.

    She seems to be on top of the acne-like rash now and is experiencing extremely dry skin on her face and neck, however this is also largely manageable and she feels it is a small price to pay for the excellent results she's seeing.

    Thanks again for your continued support.

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  • Three doses down and Melissa has some good news to share

      11 February 2015

    Thanks to the generosity of everyone who has so kindly donated via this Givealittle page, I have now had three doses of Cetuximab and we have enough funding to cover the next two months of treatment as well. It is hard to believe that this site went live just 3 weeks ago and that as of today, close to $25,000 has been raised by 238 donors. The generosity of family, friends, friends of friends and even strangers has meant that the first 2-3 months of treatment will be taken care of. We have been completely blown away by the response and words don't seem enough to express our gratitude. At this stage it is unclear how long I am going to be on the drug however knowing the first couple of months is covered is a huge weight off our minds…..Thank you!

    Three weeks ago I had my first trip to Palmerston North for my first dose of Cetuximab. My Oncologist had told me that it probably wouldn't make me feel sick, although I was still quite apprehensive after reading up on the huge list of potential side effects. The good news (much to my relief) is that the drug went in, and I felt fine! And the next day was no different. After going through 21 rounds of chemo it was very odd to watch a bag of IV drugs go in, and not feel even the slightest bit queasy. As this is a weekly treatment, one dose quickly follows the last, however knowing that I am not going to feel sick or be out of action for several days following each dose is very comforting. The worst side effect I am experiencing is an acne-like rash on my face however that seems like a small price to pay for the benefit we are already seeing in my blood results.

    Earlier this week we found out that my blood results are strongly indicating that the drug is not only working to stabilise the disease, but may also be shrinking my tumours! CEA is a marker in the blood that can indicate tumour growth and shrinkage in people with bowel cancer. Most people without bowel cancer have this in the range of 0-3 however if you do have bowel cancer its not the number that matters so much as whether your number is going up or down. My CEA hit the highest levels I have seen (265) on the day I started on Cetuximab, and this fell to 211 a week after my first dose and to 132 a week after the second dose. So it looks like the drug is not only holding things steady but is more than likely shrinking the tumours. My Oncologist said he has never seen these kinds of results (ie an indication of such dramatic tumour shrinkage) on this drug so its all a bit exciting (and long may it continue!).

    Thanks again for your contribution and support. We are very lucky to be surrounded by so many caring and generous people.

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