untitled
My Battle with Breast Cancer
: How I Won

 
 
Lumpectomy & Lymph Node Dissection

 

The first surgery was to remove the tumor and determine how much if any lymph node involvement there was.  My surgeon went in under my left arm and removed several sections of the lymph nodes and sent them to pathology to determine if the cancer had spread to the lymph system.  It is important to determine how much lymph node involvement there is because once cancer gets to the lymph nodes it can spread to the other organs very rapidly.  The amount of lymph node involvement will also determine how aggressive your chemo and radiation treatment will be.  While the frozen sections of lymph tissue were being examined by pathology, my surgeon removed the tumor and surrounding margins.  Now what do I mean by surrounding margins?   Well, you want to be sure that there is no cancer left in your body, therefore the surgeon will remove a margin of healthy tissue surrounding the tumor to make sure that all of the cancer is gone. 

Sometimes the post surgery pathology reveals positive margins and additional surgery may need to be done to remove any remaining cancer cells. In my case the margins were negative as was the pathology on the lymph nodes.  If the pathology had come back positive my doctor would have removed the remaining lymph nodes as well.

 

The surgery was a day surgery, this way I could recover at home where I was comfortable and spend as little time in the hospital as possible.  You never know how you’re going to react to your treatment and you may end up spending a lot of time in the hospital so it helps to start by spending as little time there as you can.  I was in a lot of pain for a while and I sleep on my belly so it was almost impossible to get used to having to sleep on my back.  A couple of times I turned over in my sleep, OH MY G-D! Does the word ouch mean anything to you?  And the weirdest thing ever…well, the doctor removes a rather large portion from your breast and there is a space where that tissue used to be.  While it is healing there remains a space in there which is filled with a liquid anesthesia to kind of dull the area.  Well, no one told me about this and once the pain killers wore off I noticed a, I don’t know sloshing sound coming from my breast.  I freaked out!  I mean that is not a sound you expect to come from inside of you.  I called the doctor and found out it was perfectly normal, after that it was all my mom and I could do to keep from laughing about it.  All in all it wasn’t so bad, I was home that day and up and able to do little things like make myself a cup of tea.  My mom came in from L.A. to help me after the surgery, and though I didn’t need her there to do things like make me soup, I really needed my mommy just to be there.  To be there for when I couldn't handle being strong and needed to be a baby for a while.  Just knowing she was there if I woke up in pain or needed help with the laundry, made things so much easier.  Having her and my Papa come in the beginning made it much easier for me during chemo and radiation when they couldn’t be there.  Having their encouragement made me brave somehow and determined to be able to do what I had to on my own.

 
P.E.T. Scan and Chest Biopsy

After my lumpectomy my breast surgeon referred me to my oncologist.  In order to accurately prescribe my chemo therapy he wanted to make sure that there were no other questionable lymph nodes or masses any where else in my body so he sent me for a P.E.T (Positron Emission Tomography) scan.  So what the heck is a P.E.T. scan anyway?  Well, its diagnostic examination that involves the acquisition of physiologic images based on the detection of radiation from the emission of positrons. Positrons are tiny particles emitted from a radioactive substance administered to the patient. The subsequent images of the human body developed with this technique are used to evaluate a variety of diseases.  Still confused?  I thought so.  What they do is inject radioactive glucose into your bloodstream, you have to sit still for about 45 minutes while it works its way through your system, once that’s done you go into what looks kind of like a C.A.T Scan machine and it picks up the radiation.  You see, the glusose is attracted to cancer cells, inflamed lymph nodes (which can be caused by bronchitis), non-functioning heart muscle tissue, etc.  When you look at the completed scan anything the glucose is attracted to sort of lights up like points on a child’s Light Brite toy.

 

So, I had some lymph nodes in my chest that lit up and my oncologist sent me to a thoracic surgeon, who couldn’t have been old enough to be a surgeon.  I kept wanting to call him Doogy, surgeons are supposed to be old men not someone my age, anyway I’m getting off subject here…so he went in and took a biopsy of the nodes in my chest.  It was a rather miraculous procedure, rather than opening my chest he made a small incision between my collar bones and went down into my chest that way.  And that was surgery number two. To my great fortune the biopsy was negative and once my Mediport was we could begin the chemo

Mediport Installation..

Makes me sound kind of like a robot, doesn’t it?  As I mentioned before a Mediport is a kind of catheter inserted in the large vein leading to the heart that, in addition to being easier than having to tap a vein each time (especially if you have veins that collapse easily) allows for quicker administration of your chemo.  This in not something that is done under local anesthesia, you are completely out for this surgery.  And, as shocking as this may seem, it can be used right away. Mine was placed on the right side of my chest, the tube that was inserted into my jugular went over my collar bone and then down into the vein.  There was a small bump on my chest where the device was and it was a little tender but it wasn’t bad.  It was a little strange using the Mediport.  It is subcutaneous so they still have to pierce the skin each treatment and it seemed as though the needle had a difficult time finding its way into the opening in the port, but the chance of the IV coming loose is very small using the device, and I didn’t have to worry about my vein collapsing.

Removal of the Damn Thing...

Your Mediport should be removed shortly after you complete your treatment.  I ended up having to wait a while.  I was fired from my job, for reasons I’m still unsure of, three days after treatment ended and was left without insurance, so I waited. If only I knew then what I know now… How many times have I said that?  A million, but I only really meant it once.  I can’t tell you how important it is to follow all of your doctors’ instructions, take your meds, etc.  You’re given anticoagulants while the Mediport is in so that blood doesn’t clot in the port.  Well I didn’t know that that was the reason I was taking the anticoagulants and stopped as soon as my treatment was complete and ended up getting several blood clots in my port.  It was terribly painful and I ended up having to spend days in the hospital so that they could dissolve the clots with medication before trying to remove the device.  Let’s remember that a Mediport is a catheter to the heart and having one of those clots move through the catheter would have made all the treatment in the world a moot point. 

 

My dear friend Kelly was so wonderful for those five days.  She got me to the hospital and came every day (really she rarely left my side), she took care of my pet and my plants at home.  It made it a lot easier to be in the hospital knowing that I could count on her to take care of things for me.  And Kelly, if I haven’t said it enough already, thanks. 

 

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