Week 4 of Radiation Done! – November 9, 2015

Things are moving right along!  I finished week 4 of radiation with no difficulties at all.  I finally saw Dr. L on Thursday (he was busy Tuesday and Wednesday) and he told me that I’ll actually only need 25 treatments.  This means that this week is my final week of radiation!  The time has actually flown by, all things considered.  I really do think that Dr. L was able to increase my doses because I’m tolerating the treatments so well.  I don’t have any burns whatsoever; other than feeling more tired than normal (and feeling like I could take a nap any time), things have been “normal.”  Exciting!  I feel that when radiation ends, I’m 90% done with my treatment.

I mentioned in my last post that I hadn’t had to take any Imodium for almost a week. Well, I spoke too soon.  Almost as soon as I hit “Publish” I had diarrhea, and it didn’t really stop until today. I decided to take Imodium when I go to bed which helps the diarrhea in the mornings. I did contact Dr. S (GI doc) but I haven’t heard back yet. I think that this round of diarrhea is the result of chemo; the only way to test the theory is to see what happens after my next round of chemo. In the meantime, I’m managing the diarrhea.

My joints are sore, which leads me to believe I have a mild case of myalgia, which is a possible side effect of Herceptin. It’s hard for me to move if I haven’t moved in a while, such as driving to work (typically a 50 minute drive) or sleeping. It’s hard for me to take off a shirt, too. I’ll ask Dr. Priya about it again when I see her next week. I’d asked her about it before, but I talked about my knees only.  I can deal with it, but I’ve learned to ask rather than keep silent.

Only 4 more radiation treatments to go!

Two Weeks Post Surgery – August 27, 2015

It’s been 2 weeks since my surgery!  I was a pretty good patient and tried not to use my right arm at all for the 2 weeks in order to prevent lymphedema.  Let me back up.

The morning of the surgery, I reported to the Breast Imaging Center so that a locating wire could be placed in my breast to the clip which was inserted at the tumor site before I started chemo.  Then I was carted over to Nuclear Imaging so that a radioactive tracer could be injected into my breast, to help with the identification of lymph nodes. I will tell you that little injection hurt like nobody’s business – so much so that the nurse told me I could squeeze her hand as hard as I needed.  Fortunately the pain was short lived.  By then we were running late, so I was taken in almost right away at the Surgecenter, and my sister (who drove me) couldn’t come to visit.  After vitals were taken and I dressed for surgery, the anesthesiologist came to see me.  I knew that the surgery was scheduled for 3.5 hours, which meant I’d likely have heavy narcotics for the anesthesia.  So I warned the doc that I don’t react well to anesthesia.  He thanked me for telling him and said he would take extra precautions; we then discussed getting a patch which I could leave on for 1-3 days to help with post-surgery nausea.  I agreed, and shortly after the anesthesiologist left, I got a visit from Dr. White, my plastic surgeon.  He then “marked” me for the surgery, taking measurements and marking my breasts with a Sharpie.  Then Dr. Ching came in to check on things.  She reiterated that the surgery may need a follow up surgery if there aren’t clear margins from what she was going to remove.  I told her I had faith that everything was going to be fine – that I’d need only one surgery.

Soon thereafter I was wheeled into the OR, where the anesthesiologist was waiting.  I was out just a few minutes later, and woke up in recovery four and half hours later.  Dr. Ching came out to talk to my sister and let her know that everything looked good; she removed 3 lymph nodes in addition to the tumor area and a few other areas. Ted arrived at some point so my sister could go to work, and so it was Ted who joined me in recovery.  About an hour later I was ready to go home.

Despite the patch, I had nausea for the next day.  I finally decided to remove the patch and since I wasn’t in a ton of pain, to switch from Percocet to Tylenol.  Once I did that, the nausea stopped although I had very little appetite.  I’ve also had diarrhea pretty much since my last dose of chemo on July 31, and 10 days of antibiotics did not help. The diarrhea continues, but I’ve started taking Imodium again and that’s helped.

I’ve had experience not using my right arm before; in November 2011 I had right shoulder surgery.  My arm was in a sling for a while, although I was not 100% compliant, I know what it’s like to have to use my non-dominant hand for everyday tasks.  At least I didn’t have to worry about brushing and washing my hair one-handed! Actually, I wasn’t allowed to take a shower until my first post-op with Plastic Surgery, exactly a week after my surgery.  I tried my best not to use my arm, and since I was banned from using the computer, I’ve discovered the joys of Netflix and Amazon Prime streaming.

On Monday the 17th, 5 days after surgery, Dr. Ching called me with the pathology results.  The news could not be better:  NO CANCER ANYWHERE!!  The tissue removed around the tumor site showed all signs of having been changed from chemo; the additional areas removed had no cancer as well as the 3 lymph nodes removed.  No second surgery is needed.  Dr. Ching said that I was one of the rare people who is a complete responder with chemo, so all those months of chemo were totally worth it. It feels really great to know that I don’t have any cancer!

You might ask if that means my treatment changes at all, and it does not.  Because I chose a lumpectomy rather than mastectomy, I will still need radiation (for 5-6 weeks) and I still need Herceptin (targeted chemo) until May or so.  But to know that I have no more cancer has been the best news since, well, December 15, 2014.

My best friend Kim took me to my first post-op, after which we went to lunch.  After a lengthy surgery and a week of doing nothing, it was amazing how much that one little outing tired me out.  I went to bed very early the next two nights, sleeping a lot more the following day.  That told me that the surgery – and 6 months of chemo – has really taken a toll on my body, and it’s best if I rest as much as possible during my medical leave.

On Monday, I had an appointment with Dr. Ching, to which my friend Kim took me again.  Dr. Ching said that my breasts looked great.  I admitted that I hadn’t been 100% compliant about not using my right arm, and she said it was okay – that they tell patients not to use it at all, expecting not 100% compliance but maybe 70%, and that was actually enough to prevent lymphedema. Since I didn’t have lymphedema, and things were looking good, my next appointment with Dr. Ching is in six months.

I got clearance to be able to use a computer, knit and drive, so today I drove myself. First thing in the morning I had a blood draw because I’m scheduled to have Herceptin tomorrow, and then I went to Target to pick up a few things.  I felt faint in Target, another sign that I need to take it easy while building up my strength.  I came home and took a nap.  Naps are good.

I had another post-op with Plastic Surgery in the afternoon.  Dr. White came in to see how I was doing, and he seemed pleased with my progress.  I asked him about some areas which seem to “pooch” out; Dr. Ching mentioned that Dr. White could liposuction those areas.   Dr. White said he could but wants to wait for 6 months, when things should finally settle down from the surgery.  Then the PA removed the plastic bandages which covered my stitches. The stitches will eventually dissolve, but as the swelling recedes, some stitches get uncovered before dissolving.   The PA trimmed some of those, removed the glue using a type of “Goo Be Gone” for the skin, then dabbed antibiotic ointment around my scars.  She wants to see me a week before we leave for Maui, because if my scars aren’t closed by then I won’t be able to swim.  😦  Otherwise, I don’t need to see Dr. White again for 6 months.

I then went to Oncology:  I had an appointment with Dr. Priya, in which we mostly chatted about my nieces and nephew, and the pressure on high school students.  That was after we discussed that my magnesium was low (I’ll get 2 gr tomorrow), and that I can get my teeth cleaned now.  I told her that I was going to get an implant for the infected molar which was removed, and she told me to put it off until next year. I asked her why, and she said that with the chemo, surgery and radiation that she wanted my body to recover before getting an implant.

So how do I feel?  There is soreness in my right armpit, where the lymph nodes removal scar resides.  There is tightness around the scars under my breasts, and I need to wear a bra 24/7 (or as much as possible) for at least another week.  I’ve tried not wearing a bra, but after a few hours, my breasts get sore and tight, so a bra helps.  At least I can switch to a sports bra, or a camisole with a bra built in.  The bra which I received post surgery provides more compression than support, and I was getting tired of it.

Nerves were all messed up and jumbled during surgery, and it takes about 6 months for them to figure out what they should be doing.  What that means is there have been nights when I’ve been woken up by a shooting pain in my breasts.  It happens during the day, too, but when you get woken up by sudden pain…well, it’s just surprising.  At least the pain isn’t constant or all that painful – it’s more of a shock than anything else.

A work colleague set up a Meal Train for us for the past 2 weeks, and it’s been a big help for Ted not to have to cook in addition to taking care of me and the boys (our 4 cats). The generosity of people never ceases to amaze me, and I am ever so grateful for all the support we’ve received.  In addition to the Meal Train, I’ve gotten 3 beautiful bouquets of flowers, a gift certificate for dinner delivery, chocolate covered strawberries, homemade cookies, numerous get well cards – the list goes on.  I am a bit overwhelmed at my “village” and thankful for all of you in my life.

I plan to continue to rest as much as possible, but to start to resume some activities. After all, football season starts next week!  Fall is my favorite time of year.  I hope radiation doesn’t take too much out of me; I start in October and hopefully I’ll be done by Thanksgiving.  I’d love to host Christmas this year!

December 31, 2014

Happy New Year’s Eve!

I had a consult with Dr. Lundahl, the radiation oncologist yesterday, but couldn’t post because we went from the appointment to the Foster Farms San Francisco Bowl game. Despite the chilly temps, Stanford played very well and was victorious, so it was worth braving what for us were freezing temps.

Dr. Lundahl has a dry sense of humor, which I love.  His first words were that no, you won’t be radioactive during treatment.  He must get this question a lot!  He explained that they’d be irradiating the entire breast from 2 directions, that radiation therapy is 1-2 weeks after I finish general chemo (not the targeted therapy of Herceptin), and that the treatment will likely run 5-6 weeks.  Treatment is 5 days a week for those 5-6 weeks, but each treatment is only 30 minutes or so.  Not much new information for me, but it was good to meet him.  He also said that Dr. Ching does a great job of not being overly aggressive in removing breast tissue.  One of the questions I had was since Dr. Ching is concerned about how close the tumor is to my skin and that she may not be able to get clear margins, whether that will have any affect on the treatment plan.  He didn’t think so, but did reiterate that if clear margins aren’t achieved, a second surgery is needed.

While I was tailgating before the bowl game, Dr. Priya called to see how I was doing, and asked that I call her back.  I called her back today, but she’s out until Monday.  I did talk to her nurse, who said that Dr. Priya actually wanted me to come back in to talk to her, probably about the HER2 positive diagnosis and how this will affect the chemo treatment.  The nurse will call me back next week after she’s had a chance to talk with Dr. Priya.

I’m also expecting a call from Dora, Dr. White’s surgery scheduler, to book pre-op appointments.  This is my life now, going from appointment to appointment.

These arrived the other day.  I have awesome friends.

and reminds me of this post I saw on Facebook the other day:  IMG_3092.2014-12-29_174435

I’ve only told a few people about my diagnosis at this point, but everyone has been amazing. Thank you, Julie & Kelsey, for the beautiful flowers.  Love you!

Enjoy your New Year’s celebrations – stay safe!