Tag Archive | MRI

The week that wasn’t

Sooooo…….two weeks ago was either the worst week or second worst week I have had since I started this whole cancer adventure. It is in competition with my very first week of chemo.

During that very first week my fatigue was so bad I could stand up for only a couple of minutes at a time and there were periods that I didn’t have the energy to hold my head up.  Continue reading

Brain MRI result

Doh……I forgot this bit.  And the last post was so long I decided just to make a separate post.

Brain MRI is clear!!  Yay!

I dread the thought of having something pop up on my brain.  Sadly, it isn’t even because I don’t want anything growing in my brain but because I don’t want to go back on the horrid dexamethasone that is used to control swelling during brain radiation and keep side

Continue reading

Come back 2016

I’m sorry, 2016, you weren’t so bad.  Can’t we just pretend the last 10 days didn’t happen and go back a year?  🙈 (This is new in Blogger, they finally have emojis……or maybe it is just that I’m using Windows 10 rather than an ancient Mac.  Apparently this is face with look of triumph 😤.  I always thought it was super angry face.  Hmmmmm.)

Right, back to this whole 💩 2017 thing…….

Last….Wednesday?…..maybe Tuesday, yes, Tuesday, my amazing elephant arm seemed to be a little more swollen than it had been.  It does go up and down a little bit, but it seemed Continue reading

Riding a Roomba, or what a difference a week makes

My last post, a whopping 10 days ago, left off with my comments about the lymphedema in my right arm and how much it bothers me. Since then things have gotten a tad more adventurous.
The motion in my shoulder has been somewhat limited pretty much since all the swelling started back in March. When I mentioned the decreased mobility at an oncology appointment a little while ago one of the annoying substitutes I had said that isn’t Continue reading

The Results are In…..

Last Monday, Leap Year Day, I saw my radiation oncologist to get my MRI results. Ian had the day off so  he came with me. It was the first time he had met my rad onc. We seemed to spend a long time twiddling our thumbs but it turned out my onc had a resident with her and any time there is teaching going on things just take longer. Fine with me, we need the newbies so they are ready to replace the oldies.
When my rad onc came in the exam room the first thing she said that the MRI was showing the skull lesion as being mostly stable with minor shrinkage away from the lining Continue reading

It’s October? What happened to summer???

I have been stalling a little bit, okay, a lot, on this blog post. No particular reason, just not feeling overly creative. Summer turned out to be a bit of a blur. The weather was absolutely amazing but the Bell’s palsy symptoms really put a damper on my activities.
I have regained a lot of the motion in my face……although I have to admit since I don’t spend a lot of time staring at myself in the mirror the motion part is really the least important thing to me……aside from no longer needing a straw every time I have a drink.
I am still not blinking as much as I should so dry eye is an issue. I alternate weeks of taping Continue reading

The saga continues

Hmmmmmmmm………….la la la la la la la la la………….I don’t remember where I left off in my last post (if I knew how you’d be listening to the Jeopardy theme as you read this) and I don’t feel like going back and rereading it. I think I’ll just wing it.

January has been chaotic.

I think I have already posted that the bump above my mastectomy scar and my enlarged lymph node were both positive for breast cancer and the node is estrogen receptor negative so the zoladex and letrozole I am on are not useful in slowing cancer growth.

The second week of January I was scheduled for a breast MRI and I also started getting a weird new thing going on with my tongue. Just before I went to bed on Monday I lost control of the back part of my tongue for a couple of minutes. It was very strange.
On the Tuesday afternoon I went for my breast MRI. Not overly exciting, lie on a bed facedown and don’t move. The machine used to take the pictures includes a large magnet (Magnetic Resonance Imaging) so there are a few interesting pre-test questions. The most interesting one, have you ever had any metal objects, such as iron filings, stuck in your eye from maybe an industrial type accident? Doesn’t that offer up a rather gross and extremely painful mental image? Yowzers!!
They also ask if you have any shrapnel, joint implants, a pacemaker, or other random metal medical items stuck inside you but the eye question is the one that really gets me.
The sucky part of the test is that while each set of pictures is being taken the machine makes an incredibly loud noise. The tech puts headphones on you and cranks music through them while the pictures are bing taken, but it still sucks. There are 5 or 6 sets of pictures taken and each set takes between 30 seconds and about 3 minutes. If you have decent hearing the end really can’t come soon enough.
I stopped to do some shopping after my MRI and the tongue thing happened again. It happened a few more times that day. So annoying.

On Wednesday the tongue thing started up just after I got up for the day. It only lasts for maybe a minute or two each time, but now that it is day 3 and happening more frequently I emailed my oncologist to tell her about it. She responded right away and agreed that it seemed very weird and she was going to send in a request for me to get a head CT done to see if showed anything new.

On Friday I met with my surgeon to discuss the lymph node issue. It is generally agreed that the lymph nodes should be removed. She had the results of my breast MRI and it is possible that there is actually breast tissue involvement right at the lymph node as well as the lymph node being cancerous.
Also, it turns out that when she removed my bump one of the margins was not clear so she needs to go in again and remove more tissue and hopefully get a clear margin then.
I asked about lymphadema and blood work and scans and treatment if I get the right side lymph nodes removed. I got the normal surgeon response of “there is no real proof that getting iv’s or blood work done will actually cause lymphadema” speech. And, as she pointed out, I have lymphadema on the left side so it could be used for procedures now since we are no longer trying to prevent lymphadema. True, and I have no idea why I got the lymphadema anyway. I had no visible cat scratches (probably for the first time in ages) or any other injuries I could see so having it occur when it did is a little weird.

I also learned at my appointment that the cancer in my lymph node is still Her-2 positive. That means herceptin should be effective but it is currently not preventing cancer cell growth. That is finally some sort of good news.

Immediately after my surgeon appointment I had to go zooming over to Vic General (my surgeon’s office is across from the Jubilee, so pretty much across town, and of course the appointment was late starting) to get my head CT. I am still a little stunned that I got fit in less than 2 days after the request went in. A little scary.
The head CT was uneventful, except for the 20 minutes it took to find a parking spot, and I was told the results would be ready early the following week.

On Saturday I headed off to Vancouver. I had a wonderful visit with everyone!! Thanks for all the distraction and fun, you all really help keep me from being boring and dreary and overwhelmed by all the crap going on. And extra thanks to Laura, Ian (Laura’s Ian, not my Ian 😉  ), Polo, and Pi and Keetah, David, and Satori for putting me up while I was over!!!

I had my PET scan at the Vancouver cancer centre on the Tuesday. It is the really fun test that does not allow any exercise the day before, no gum chewing the day of, and involves relaxing in a dark room for 45 minutes after being injected with a radioactive glucose solution.

I came home on Thursday and on Friday morning I received an e-mail from oncologist. She already had my head CT and my PET scan results.
There was nothing on the head CT to explain what is going on with my tongue. So after talking to my surgeon and radiation oncologist my oncologist put in a request for a head MRI.
The PET scan showed 2 areas of activity, the right lymph node and my right 6th rib. Neither was a surprise as the lymph node has been thoroughly inspected and I have been having random pain in the area of that rib for the last month or so that I figured was probably a met that was acting up.

I saw my oncologist in person a few days ago, after being seen by a resident. Since my case is nice and complicated any resident interested in breast cancer gets to see me so it turned into a long, tiring appointment. The decision for treatment is to continue to follow an aggressive path. This means my oncologist is recommending lymph node removal and mastectomy for the right side (yay! I really want the right breast off, the imbalance drives me completely insane and it is my only regret in all my treatment decisions that I didn’t have the right mastectomy done at the same time as the left.) I would then have radiation to the right armpit and to the 6th rib. The radiation to the rib should stop cancer growth there and reduce the pain.
I also requested at that appointment to switch from the clodronate pills for my bones to an iv drug. Having to wait an hour to eat after taking the pills in the morning drives me crazy these days and I am ready for a change. My onc decided to put me on something that is a monthly injection. I asked if that would be at the cancer agency because having to go to a walk-in for my zoladex injection is a total pain in the ass. She had a little hissy fit at me for not telling her that my zoladex was being done elsewhere and she said she would get it reinstated at the cancer agency for me in time for my March injection. The bone drug injection would also be at the cancer agency. Yippee! So much easier.

I had a few hours to kill post appointment so I spent some time with some old friends at the Jubilee lab. It is nice knowing people in so many hospitals 🙂
Then it was time for my head MRI (yes, already. I think this tongue thing of mine has really freaked people out. It is extremely disturbing how fast I am getting in for tests). This MRI was much better than the last MRI even though it was the classic type of MRI machine that is the long narrow tube.  Fortunately I have absolutely no problems with claustrophobia. I got to lie on my back which is more comfortable and I got earplugs that had the music piped in. Way better for blocking the sound of the machine!!! Good thing too since there were more sets of pictures and they all took longer. It seemed like about 10 sets and each set took between 3 and 5 minutes.
Finally with the pictures all acceptable I got to escape the medical facility. I ended up picking up Ian from and we met my parents for some sushi. An excellent way to end the day.

Since then I have visited with some relatives and watched the Super Bowl. No comment about that other than, it was 1 yard!!!!! What on earth made you think throwing the ball was a good idea??!?!?

So, a quick recap, node, bump, and rib are all cancerous, some of which is ER negative and I am waiting for dates for lymph node removal, mastectomy, and radiation.

Congratulations if you made it all the way thru this long, convoluted post. Have a drink.