Yesterday was my last radiation!!  I have some mixed emotions about this part of the journey coming to an end.   I am at the same time very happy that this treatment is over and a bit apprehensive that this treatment is over.  While actively treating the cancer, it is comforting to know that something is being done to kill all those nasties. When the treatments end, you just have to tell yourself over and over that one nasty cell is not hiding in a corner waiting to pop out and yell “I’m Back!”.

I want to give a HUGE shout out to the radiation techs at SCCA.  They are the best. Here are some members of a great team of people.  I am so thankful and lucky to have had them on my side for the last seven weeks.  I thank you all from the bottom of my heart.  You all helped to make the process as easy and enjoyable as possible.

I know some of you are wondering about Jody.  She finished radiation on Thursday and I finished on Friday.  Wednesday was actually a teary day for both of us.  We discussed our fear of radiation coming to an end.  Once again, it was nice to talk to someone who was feeling what I was feeling and understood what I am going through.  We have each other’s phone numbers and will keep in touch.

What comes next you ask?  Well for the near future, I will take a bit of time and concentrate on getting the rest of the house put together. Starting in January, I will add back more clients to my work schedule, which has been very minimal, to say the least.  I want to go on some trips in 2014, particularly a belated 30th anniversary trip with Scott.

I will have regular visits with the oncologist and the radiation oncologist.  I start hormone therapy soon and will continue that for a minimum of five years.  I also need to plan some “renovations” that are not associated with the house.  I will continue this blog as this journey is not over.  If you know of someone going through a journey of their own and they would like to talk,  I can be contacted via this blog or Facebook.  I am happy to help in any way I can.

Scott, David, Rachel and I went to a great restaurant to celebrate.  When Scott and I got home, this lovely surprise was waiting for me.  Thanks Diana and the Posts!  See the post Cheetos, Snickers and Peach Fuzz for back ground info.

This is the start of week seven of radiation.  The final week!  I will have my last radiation treatment on Friday, Nov. 15.  The original date was Thursday, Nov 14 but I got Veterans day off as a holiday.  There are four bracelets left.

The first 28 days of radiation focused on lymph nodes that drain the breast:  the  axillary nodes in the armpit, the internal mammary lymph nodes behind the breast bone, and the medial supraclavicular nodes located just above the collar bone. There are three levels of axillary nodes:

Level I is the bottom level, below the lower edge of the pectoralis minor muscle. Level II is lying underneath the pectoralis minor muscle.  Level III is above the pectoralis minor muscle.

Since I had a Level II axillary dissection,  those level III nodes still needed some attention.  The last five days of radiation are known as the “Boost.”  Basically the boost is radiation concentrated in the area where the tumor was located.  I get that site radiated from four different angles.  Not everybody has the same radiation protocol so if you expect to have or are having radiation treatments, your protocol may be different than mine.

I get the “Do you have burns?” question a lot.  Yes I do.  My collar bone is pretty affected.  I have skin peeling on my rib cage where a bra strap would be and my under arm is very tender.  I have a picture of my collar bone but thought that might be TMI!  Those area should start to feel better in another week or so.

Hair update photos below:

I think this last one is weird.  You can see that my bedroom is still a construction zone.

My hair is growing like a weed.  These eyebrows are mine, all mine!!  No enhancements necessary.  I have lashes that are now long enough for mascara. People like to rub my head, like Buddha’s stomach.  I hope all their wishes come true.

I have 13 radiation treatments left.  20 completed.  Every fifth day of radiation I have x-rays.  These are taken and then reviewed by the radiation oncologist to be sure that what is being radiated should be radiated and what should not be radiated isn’t.  After the second set of x-rays I had an 8 mm adjustment.  I really don’t like x-ray day.  The position that I need to be put into for treatment is extraordinarily uncomfortable.  I have to stay in that position longer on x-ray day.  My arms ache like mad and my hands fall asleep.  Did I say how much I dislike x-ray day?  But, better safe than sorry.

I have become quite friendly with the woman who has radiation therapy before me. Her name is Jody and it is good to be able to talk to someone who is going through what I am going through.  We started radiation on the same day and we will finish on the same day.  The radiation techs think it is great when patients get to know each other and support each other.  Actually, the techs are pretty darn great themselves.

For the last four weeks, only one of  the two linear accelerators (radiation machine) has been in use as they are being updated.  This has resulted in extended hours at radiation oncology.   Starting Nov 6, both machines will be in use which will result in a different appointment time.  When the radiation techs redid the treatment schedule, they made sure that Jody and I have appointments adjacent to each other. It is their thoughtfulness (and their humor) that makes having to go to treatment every day that much easier.

Before I get to molds, scans and tattoos, I will bring you up to date since my last post. I had the post op with the surgeon on Sept 5th.  Since I already knew the pathology results, we mainly talked about when I would see her next (March 2014), when I would have another mammogram (March 2014) and a little about plastic/reconstructive surgery.  I had great plans to have EVERYTHING completed by the end of 2013.  But, that is not to be.   I will need at least 4-6 months of healing after radiation before I can have any reconstructive surgery.  Best laid plans …

On Sept 10,  I had a consult with the radiologist.  We mainly went over things that were discussed at our first meeting way, way, way back in February.  When I mentioned that Scott and I were going out of town for Thanksgiving, she assured us that I could start radiation on Sept 30.  Since there will be 34 sessions (the first one being the practice and information session and the subsequent 33 being actual radiation) I should finish on Nov 14.

Before the meeting, I thought that the area being radiated was the tumor site.  Goes to show you what I know.  I will have the entire breast, armpit, supraclavicular lymph nodes (nodes above the collarbone) and internal mammary lymph nodes (nodes beneath the breast bone in the center of the chest) radiated.  The effects will be fatigue and burns.  This is a lot of area to be radiated.  The burns will start about half way through treatment.

Another side effect to radiation will be scarring of my right lung.  I was originally told a small bit of lung would be in the radiation field.  Well today I found out it will be about 30% of my lung.  I don’t consider this a small bit.  To me a small bit is 1%.

Today, I had the prep work done for the radiation sessions – molds, scans, and tattoos.  The mold was made so I will lay down in the same position every session. It was made from material in a big blue envelop that was filled with s substance that must be like the spray foam used for insulation.  The blue envelop grew around my head, neck, arms, etc like a mutant pillow.

Once that was done, the radiologist placed tape of some kind on various parts of my body that will receive radiation.  Since my head was turned and tilted, I couldn’t see them.  Then it was into the CT scan and out of the scan.  Tape adjustments were made.  Back into the scan and then out of the scan.  Then back into the scan for a few minutes.  Then out out of the scan.

After the last scan was completed and the radiologist okayed everything, I got my tattoos.  They will be used to help aim the radiation to the treatment area.   Yes, they are permanent.  Yes, they are very small.  Mine are blue.

This has been some kind of journey!   I will always have the tattoos to remind me of this year.  I don’t know how I feel about that.  I already have scars from the three breast surgeries, the axillary node dissection and the port.  I believe I will start looking at the scars and tattoos and instead of thinking of everything I have gone through, I will think of everyone who has been with me on this journey.

The pathology report came back yesterday and there is no further evidence of either DCIS (ductal carcinoma in situ) or IDC (invasive ductal carcinoma.)  Hooray!  This means that no further margin surgery is needed.  I still have to have radiation.  I will meet with the radiologist on Sept 10 to formulate the plan for that treatment. As of now, I expect to start radiation around the third week of September. This means that I should finish radiation by the end of the first week of November.

The house renovations are coming along.  The counter tops were installed yesterday.  Unfortunately, there are some issues there that I hope to have resolved today.  There is always something…  The master bath has been demolished and partially rebuilt and the tiling starts tomorrow.  The electricians are here now installing new ceiling lights.  By tonight we should be able to use our new stove and oven!  Pumpkin muffins anyone?

Some day the renovations on my house and my body will be complete.  I will have to come up with something really good to do with all that spare time. Perhaps I can grow some eyebrows?  I have completely lost the right side while the left is pretty sparse.  Anyway, I am sure I will think of something.

This is the partially finished kitchen island.  The chairs are in place to keep me from eviscerating myself on the brackets.  The bar height counter had to go back to the shop for some reworking. Kinda like me, last week.

We finally got home (the ferry was very late of course but the one that we just missed was on time) and Loretta is resting on the chair (we have two, actually) and eating a snack.

All is good.  We need a good report from the pathologist (Monday or Tuesday next week) to be sure that the surgery was successful but the surgeon was very optimistic.

Waiting for the ferry to take us home.  Loretta is a little loopy but otherwise good.

Spoke to the surgeon and she said she did really well.  She commented that Loretta must be a really cheap date because they didn’t have to use much sedation to knock her out.  They only did local anesthesia so she was really just napping.  So recovery should be easier.

We should be able to see her in the next 30 mins or so.

15 minutes early.  It should take about an hour.