The Original Intent Of This Blog

April 2006 - It seems vain to create a blog about me however, I realize that it is the most efficient way to provide accurate information about the status of my treatment and recovery so here I go .....

May 2009 - The cancer has returned, here I go again ...

December 2009 - I've finished chemo and am cancer free; I continue to receive Herceptin and the trial drug.









Wednesday, October 15, 2008

I've Been TPA'd

No, the house has not been toilet papered but my port has been TPA'd ( tissue plasminogen activator) or another way to think of it is that I've had "draino" inserted into the port and now the clog has been dissolved and port is unplugged.

The exact name of the drug used was Activase and it is the same drug used for stroke victims to dissolve a blood clot. The drug is actually an enzyme/protein that we already have in our bodies to naturally dissolve blood clots. In some circumstances, such as stroke or a blocked port, we need far greater quantities of the enzyme. Now get this amazing fact, the manufactured drug is a man-made protein using DNA technology and the ovarian cells from the Chinese hamster. Is that not amazing? If you want to read more, the best source I found is at http://www.medicinenet.com/alteplase/article.htm



The procedure is to inject the drug into the port and 30 minutes later attempt a blood draw. Since the insurance approval for the brain MRI was received I had the drug injected and then moved along to have the MRI and when that was finished the draw was attempted but it did not work. So, the drug was inserted again and I relaxed for another 30 minutes before the next draw was attempted - again there was no blood.



The drug can be left in the port for up to two hours ... it took one hour and 54 minutes before the port began working and we finally got a great blood draw. Whether the blockage was a blood clot or a small fiber produced by my body we don't know. Sally, the nurse conducting the procedure, was confident the port was otherwise working properly because the port and line accepted the injection it just would not allow a draw.



I will admit that for one long moment I had to do some tough self talk. It went something like, suck it up Jan you have come too far and have gone through far tougher things to let this simple problem make you freak out. The truth is I hate, hate, hate needles and all the poking and flushing today was a challenge for me. I also let my mind fast-forward for a minute ... I went through this surgery last month to have the port replaced and now the dumb port won't work and now I will need another surgery. Good thing our mind has rewind and erase buttons because I certainly needed them today.



The end result is that I survived another challenge and increased my knowledge - not a bad thing at all.



Now as for the Brain MRI, wow that was something else. I found it to be an amazing experience and I actually had fun with it but, it's late and this post is already long enough so I will write about the experience tomorrow.









Tuesday, October 14, 2008

Test Results = The Happy Dance

I am almost 31 months cancer free and I'm doing The Happy Dance! Last week I had a slew of blood tests as well as the quarterly PET and CT scans; I received the results today and they were good!!


If you remember the post from three months ago the PET scan showed inflammation of the lymph nodes under the left arm and in the left side of my chest however the CT scan, which was taken the day after the PET, had good results. The inflammation along with another rise of tumor markers (blood test results) were worrisome for both Dr. Patel and I.


Today Dr. Patel was all smiles; the PET scan indicated that the inflammation of the lymph nodes was very little. Either I was slightly sick three months ago when I had the scan or the inflammation might possibly be related to lymphoedema which I do have at times (I personally think this is what the PET scan is picking up). The CT scan results were also good.


The blood test results were mostly good - all indications were that bone, kidney, and liver function were great however once again the tumor markers were up. Over the last few months the tumor markers have gone up but they also went down before they again went up. The markers are still below the "worry level" but it is a mystery as to why the markers are fluctuating.

Breast cancer metastasises to the lymph nodes, brain, lung, bone, liver, and the original site of the cancer. We know I had local mets to the lymph nodes near the tumor so the potential of it returning to the lymph system is high thus the concern three months ago when the PET scan indicated lymph nodes with inflammation and the elation today at finding the inflammation was almost gone now. The PET and CT scans also look at the lungs, bone, and liver - the absence of any findings along with positive function results from the blood tests indicate that these organs are cancer free.


So, that leaves the brain which leads to the only test I have not had - a brain MRI with contrast. As a precaution I will have the MRI as soon as my insurance approves it. The good news is that if anything is found it will be found early (I have absolutely no symptoms).


Am I worried? No, I am not worried; I physically feel too good to believe that at this time I have cancer growing within me again.

Am I fearful? Slightly, I have had cancer once and I think I will always to some degree be fearful of its return. Most of the time I am too busy fully enjoying and appreciating each day of my life so the fear remains pushed to the back of my mind. In fact when I express fear I usually surprise myself - today when I received the test results my first reaction was to dance around and hug Dr. Patel (hopefully I did not hug him too tightly!). My second reaction was to begin crying; not sobbing - just a gentle cry - my eyes filled to the brim and then slowly large tears trickled down my cheeks. I knew then that even though I felt physically well, I had been fearful of the test results.

I think it is okay to be fearful as long as it does not interfere with living and truthfully a little dose of fear is actually good for us - it will make us slow down and carefully think through the situation and our choices. I have however watched fear rule and ruin lives or at least make people very miserable. I am determined to not let fear of cancer ruin the life that I do have afterall, it could be a car accident that takes my life instead of cancer. That car accident could be tomorrow - what a waste if I let fear of cancer ruin my life today.


Oh yes, the new port worked "beautifully" last week but not today. They think it may be plugged so I go in tomorrow to have a drug injected into the diaphram of the port to disolve whatever may be plugging it then 30 minutes later a blood draw will be attempted again. If that does not work then the procedure will be repeated and if that does not work I will be sent for a dye test. I am about to learn something new again.