Friday, September 8, 2017

Reconstruction?

This morning, I finally had a consult for my reconstruction surgery. My mastectomy was in December 2015, but they told me to wait until a year after my subsequent radiation treatments were finished so the skin could heal. That year was up in March, but I wanted to do some theatre before doing the surgery, and then it took a while to be able to get an appointment. Anyway, on to the appointment: in a nutshell, it was disappointing

I liked the doctor a lot. She was very realistic and candid. Just the right personality for me to consult with on something like this. However, because I had radiation on that area, the skin and muscle are kind of ruined. This limits my options for reconstruction, although there still are options. There are basically two. One involves taking fat and skin and muscle from my abdominal area to create a new breast. I had thought this sounded like a great idea--a tummy tuck and a new boob, all in one! Wrong. First of all, they have to take muscle as well as fat, which would impact my core strength. I could rebuild it to some extent, but it would never be what it is now. Secondly, there are several risks that could end up with a bad, irreversible result. She said most people in my situation who got this surgery end up being unhappy with it.

The other option is to take a flap from my back, where there's a muscle we don't use that much and probably wouldn't have an impact on my regular activities. "Probably." This surgery is less risky, but would require one surgery to put in the flap and an expander to start stretching the skin, then another procedure later to swap it out for a regular implant. And then that implant would need maintenance and probably replaced a couple times before I die.

In both cases, the surgery is several hours long and I would be in the hospital for several days. She described each one, and it was overwhelming how much they have to do. It is serious major surgery. The first would have about a three-month recovery time, and the second would be about two months. And that's  just to stop feeling crappy from the surgery. Then I'd have to rebuild myself AGAIN because of being cut up and rearranged and then doing nothing for a couple months. Of course, with any surgery, there's always risks of bleeding, tissue death (in which case I'd have no boob and the flab would be gone), the risks that come with anesthesia, etc.

All of this for...what? A little vanity? When I'm not even that invested in my physical appearance, and I've been walking around with one boob for almost two years? What's the point? In the end, I still won't have a spectacular rack, and I still would be limited on the clothes I can wear because of the scarring. I have a divot around my port scar that will never go away, nor will the scar itself. And, my ability to dance and swim and whatever else could be compromised. What would be the point, exactly? It doesn't even bother me any more to have just one, and Michael loves me no matter what.

So, I said I'd sleep on it, but I'm leaning toward just not doing it. Who knows, with medical science today, there could be a new procedure in a few years that would be less traumatic to the body and have better results with fewer risks, and I'll revisit. At first, the thought of being like this forever made me sad, but it's not like having the surgery would make me perfect or undo what cancer did to me. I can never be the person I was before cancer, physically or mentally.

Tuesday, March 7, 2017

One Year

One year ago today, I had my last cancer treatment. The culmination of nine long months of IV poison, surgeries, and radiation burns. Nine months of scans, blood tests, and palpations. Nine months of warnings, advice, commiseration, sympathy. Nine months of losing all my strength and energy while everything I went toward fighting this thing. Nine months of gaining weight because there was nothing I could do to stop it. Nine months of fear, determination, and hope.

Nine months of my life gone.

Often, when I think of things I did before cancer, I forget just how long ago it was, because it really was like losing a year. Now, it's been so long that I've been out of it, it feels like a dream. If it weren't for the wreck my body was left in, I could almost forget it even happened. Of course, there's some emotional baggage that stayed with me, too. Some of it is good, and some of it is bad: I am grateful to be alive and I'm driven like never before to live the life I want and do the things I want to do. But I have more anxiety and nervousness than before. It's even harder to control my emotions and my temper. I blow things out of proportion and am more easily injured.

Overall, though, I'm good. I'm crazy in love with a man who keeps me grounded. I'm happy, I'm having fun, and every day I get a little stronger. I still get wiped out a little too easily so I have to plan how much physical activity I do in a day, but there are worse things to have to deal with. One year ago, I could barely walk a quarter mile without feeling exhausted. Now, I can run/walk 2-3 miles, swim half a mile, do weights for an hour, and even be in a three-hour-long musical. Just not all in one day!

Life is good, and what's nine months in the grand scheme of things?

Friday, February 24, 2017

There's no business like show business!

Hello, blog! I haven't seen you in a while...there's hasn't been much to report on, but reading my last post from October, I guess there are a few updates. Plus I'm having some thinky-thoughts that are somewhat cancer-related...or at least, cancer-adjacent. So, bear with me.

First the quick updates: 

  • I will probably not get my reconstruction done until next year. I have a consultation in April for the interstitial tears in my shoulders (basically, the ligament that attaches under the blade of the shoulder has torn away--probably from years of dance and exacerbated by the cancer treatments for various reasons). They will probably need surgery, and that needs to be done before reconstruction. And who knows how long it will take to recover from that, and I don't know if they'll do it in two surgeries or one. 
  • Michael and I have been waiting for certain factors to fall into place before setting a wedding date, but we're tentatively looking at August 6. It will be a simple, intimate affair at our home. 
  • We're going on a cruise to Alaska at the end of May, and we're very excited! We're going on Celebrity with some swing dance friends. Given that we haven't done any swing dancing in quite a while, I think we really need to start practicing again!
  • Just in case I forget, which I might, I finished cancer treatments on March 7 of 2016. That's a couple weeks away. So...I haven't even been out of it a year yet.

But the thing that has been occupying most of my time and all my thoughts lately is my show! Most of you know that I'm in the ensemble of "How to Succeed in Business Without Really Trying" at Davis Musical Theatre Company. It opens tonight, and I'm feeling particularly thoughtful today about what this means and thought I'd share.

What made me decide to do this?

When I was younger, I did a lot of backstage work in the Nevada City theatre community, but I never got to be on stage although I would have liked to. I was doing horses at the time, I had to work, I didn't think I could sing, excuse excuse excuse. Then life took me in a different direction. I started ballroom dancing and did a lot of performances for events at our studio or at random parties for churches, in front of a choir, etc., participated in variety shows. We danced on the Garbeau's stage and at the State Fair. It was really a lot of fun, and it was a great way to get my performance fix.

However, that bug to return to the theatre never really left me. Teaching dance made it difficult because that always happens at night, when rehearsals are. I was too busy for many years, and there was still the issue of not being able to sing if I wanted to do musicals (which I did).

Then a few things happened. A few years ago, someone got me into karaoke, and I started feeling more comfortable about singing in public. Then, I met my awesome friend Andee, who is an amazing singer and actress, and going to see her in shows rekindled my love of theatre. I started thinking about maybe doing it...but I was still worried about singing, and I was still busy with work. Then I met Michael, who pledged to take care of me if I didn't want to work so much, but it was too early in our relationship to contemplate that.

Then the whole cancer thing happened and turned my world upside-down. My priorities changed. I was literally unable to work as much as I had before. I faced the fact that I could have died, in my early 40s, having not done so many things I want to do. I discovered that I can let someone take care of me.

I set the goal over a year ago to do a musical, but I kept it quiet. First I had to finish up the cancer thing. Then I had to recover and learn how to do some solo, stage-type dancing since I only knew ballroom. So, I started with tap because there was a convenient class near me (yay Dance 10!). At first, it was a struggle to get through class, but I kept at it and got better. I knew a musical would be physically taxing, so I was going to the gym and running/biking/swimming/doing weights as well. While I worked on the physical aspect, I worked on my voice as much as I could on my own, using some exercises Andee gave me.

I finally decided around November or so that I might be fit enough, so I started looking for audition opportunities. The timing of How to Succeed was good (coming up soon, but enough time to prepare), it's not a super dance-heavy show especially for the women, and I've seen a lot of shows at DMTC so I felt comfortable there. I auditioned and got in.

How's it going?

Although I was excited, there was a lot of anxiety at the beginning. Not because I would have to perform in front of people (that part is easy), but because I was worried about carrying my own weight. Was I singing the right notes? Would I be able to do the choreography and keep my energy up through a 2:40 show? I had a little emotional break down (thank you to those who listened to all my whingeing), and then I got some help. The musical director worked with me one-on-one one night before rehearsal, and then I started taking voice lessons with Carrie Hennessey, a local opera singer. She's freaking amazing. So, that gave me more confidence with the singing, and it turned out the dancing was easy. I settled down and just enjoyed the process.

It's been a lot of hard work, but it's been super fun. The cast is like a big family, and I honestly like everyone in it. I think I somehow simultaneously under- and over-estimated how much work it would be. Things I thought would be hard weren't, but then the long hours got  to me--particularly on set construction days. There were several days I spent about 6 hours working on the sets, and I'd go home so exhausted it was literally painful and I was barely safe to drive. In fact, there was one day I had to just skip because we  had rehearsal that night and I knew I couldn't do both in a day. I felt guilty, but what else could I do?

The last couple of weeks have been the toughest, and I cannot wait until Monday when I get a rest. My legs are sore and my feet are crying for mercy (why, oh why, did I insist on 3" heels??). During the show itself I do get a chance to rest between numbers, but I also have a lot of running around to do backstage, changing sets and clothes. I'm holding up better than I'd thought I would, even though I'm tired. I'm pretty useless during the day right now!

I am SO excited to open tonight and share all our hard work with an audience. It feels like the past few weeks have flown by leading up to this moment, and although this culmination of our work will last for several weeks, I feel like it's wrapping up and almost over. I don't want it to end; I'm  having the time of my life. And hopefully there will be more shows in my future.

So, I'll just have to make sure I enjoy the hell out of every moment in every single performance. And that is definitely something cancer taught me: enjoy every moment you have, and everything you do, because you never know when it will all be over. If you want to do something, do it now, before it's too late. Be grateful for the things you can do, because someone else wishes they could, but can't.

In the group photo, I'm in the back row, third from the left.


Friday, October 28, 2016

Chugging along

Just thought I'd post a quick update, although at this point there won't be any news to report until it's time to start thinking about reconstruction. I'm thinking that surgery will probably happen in the neighborhood of March, which will be one year after radiation was completed. If you don't recall, they told me to wait a year, partly I think because of my risk factor in case something comes up and they have to go in again, and partly to let my skin recover from the trauma of radiation.

The funny thing is, I thought it would be weird to walk around with one boob, but I got used to it when I couldn't wear a bra and it was taking so long to get a prosthetic. I thought it would weird, but I realized I really didn't care. Plus, it seems no one really notices. I guess it's probably helpful that my remaining boob is small anyway, so I guess it's not as noticeable, and people don't seem to stare at each other's chests that much. I suppose that's a good thing. I'll actually have people ask me what kind of cancer I had or if I've had reconstruction yet. I look down at my mangled chest and I'm like, "really?" It doesn't bother me; I just think it's kind of funny.

We had a great time at Disneyland, and as most of you know, Michael and I got engaged. No, it wasn't a surprise, at least to me (we planned it together), although we managed to surprise most of our friends and family! We're very happy and excited. We don't have a date yet, but I'm thinking next spring or summer.

The really great thing about our trip is that my energy held up really well. We bought a four-day pass thinking we'd only be able to do 2-3 hours per day, but I actually lasted 5-6. In fact, Michael tired out about the same time I did. So, I was really happy. And it was truly a magical vacation from beginning to end!

So now that all the traveling is done, I'm back on track with my fitness and nutrition plans. I'd gained a few pounds back, so I  have some work to do to get back to where I was a couple months ago. I've already lost a couple, though, so I'm sure I'll be there soon. Just in time for the holidays!

Wednesday, September 28, 2016

Lumpectomy and update

It's been a few weeks now, but I wanted to post about the lumpectomy for those who have to have one and want to know what to expect. Feel free to ask me any questions you have. Current update at the very bottom.

The procedure I had is actually called a biopsy/excision of breast mass/ lumpectomy with needle localization. The day began with getting checked in, vitals taken, and an IV started in the back of my hand. Unlike when I had my mastectomy, they actually got it in on the first try and it wasn't super painful. So, it seems my veins have recovered a bit from chemo. Yay!

Then I was sent downstairs to get a mammogram-guided localization wire installed and blue dye shot into the area so the surgeon would know where to go and which tissue to take out. This was actually the worst part of the whole thing, because the mass (technically, a mucocele-like lesion) was located about as deep as it could be and still be breast tissue--right in the middle against the chest wall. They had to try several times with the mammogram machine to get me in the right spot (you might recall we went through this with the needle biopsy), and none of them were comfortable. A couple were downright painful.

They finally got me in position, numbed my skin, and then injected something to numb the whole area (lidocaine, maybe?). There was a little bit of burning, which was unpleasant, but then it was a breeze after that. I didn't feel the wire or the dye going in, and then they bandaged it up so the wire wouldn't catch on anything and sent me back upstairs...but not before all the nurses asked me about ballroom dancing and planned to all go out together. See, Linda? I'm marketing! ha!

So then there was a little bit of a wait, and Michael was able to come sit with me while various members of my OR team stopped by to say hello. It was a little funny, because the anesthesiologist was the last to stop by. He was doing something with tiny bottles and my IV while he talked, and then the world suddenly started rocking back and forth and coming in and out of focus. It was very fast, and then we were rolling down the hall and Michael kissed me goodbye. We went on into the OR and I got on the table, I noticed the light above me was spinning (only to me, I suspect), they put a mask on my face, and I was out. The next thing I knew, I was already back in my little curtain room, trying to wake up.

Recovery was not terrible. I did feel weak and tired for a few days--I did not do the 5K the following Monday, nor any exercise for about a week and a half because that's how long it was before I felt really ready. I was a little tender and there was some bruising. I mostly just took ibuprofen for the pain, although a couple of times I went for the Norco, mostly after a lot of movement so stuff probably got jiggled more than it should have. My scar was glued together, so no stitches or steri-strips to deal with. It was three weeks ago, and I now feel about like I did before the procedure.

---

Fast forward to today, I still get tired every day. By 2:00, no matter how much sleep I got the night before, I'm generally unable to function, but lying down and sleeping (when I can) for a couple hours is usually enough to refresh me for the evening so I can do dinner and maybe go out. The other day I had a really long and hard day, and I was painfully exhausted at the end and it took me two days to get over it. I'm not doing much dancing as it's usually more than I feel up to. I usually mange no more than a couple of hours of work per day. I am exercising several days per week, which is good--and important for getting back to my old self.

I met with the physician's assistant at my oncologist's office yesterday for a sort of cancer debrief. Mostly she told me stuff I already know. But she ordered a blood test to check my thyroid in case the fatigue is from that, but she said it's not adrenal fatigue because then my sodium would be low, which it's not. [Update 9/29: my thyroid is normal, so I just need to be patient.]

So, things are fine. I'd like to recover faster, but I don't get a vote on that so I'm trying to accept where I'm at and do what I can.

Monday, August 29, 2016

MRI Results

I got my results from my shoulder MRI last week, although I haven't had the chance to sit down and write a post about it. I have tendinosis, which is a common degenerative malady, particularly for athletes (my years of dance). I also have an interstitial tear in the rotator cuff. The doctor is sending a referral to an orthopedist to consult with me about how to handle it.

From the reading I've done, they usually try to do physical therapy first in hopes of fixing it without surgery and often will just not do surgery, even if PT doesn't do the trick, unless you really need to lift your arms above your head. I'm thinking I really kinda do. But the PT has definitely helped a lot. Also, it looks like surgery is often indicated for tears greater than 3mm, and mine is about 4x5. So, we'll see what happens there. I would love it if we can just get it to heal without cutting me open again. My daily stretches have become routine.

My lumpectomy is Thursday. It shouldn't be too bad, but I'm not looking forward to it. I am looking forward to having it behind me, though!

Recovery is getting better. I still conk out every afternoon, but it seems like I can get more accomplished before that happens. I've lost about 18 pounds now since I finished treatment and getting stronger all the time. My trainer keeps making my workouts harder, yet I manage them more easily. I'm very happy about that!

Thursday, August 18, 2016

MRI done and surgery scheduled

I went to my MRI last night. When the lady at the first one (where I nearly had a panic attack and had to stop before it started) rescheduled me for this one, she assured me the tube at the downtown location was much bigger and shorter. IT WAS NOT MUCH BIGGER OR SHORTER. However, I did get a prescription for valium from my doc and took one about an hour before the procedure. And then I made sure to close my eyes before they slid me in (just in time--they could have warned me!) and keep them closed the whole time except for one brief moment near the end when I accidentally opened them for just a second and wished I hadn't.

The valium helped, although if I have to do another MRI I'll take two next time. I had to work at it a bit to stay calm. A lot of self talk and deep breathing, and then distracting myself going through dance routines in my head, then more self talk when I remembered where I was. I felt like I was in there for an hour, but Michael said I was gone for a total of 20 minutes. I question his math.

So then we were back downtown this morning to meet with my surgeon. The lumpectomy sounds like it won't be too big of a deal. However, we had to schedule it for September 1... four days before a 5K I'd entered on Labor Day. Michael says I'm not allowed to run 3.1 miles four days after I have surgery. So, now I'm pouting like a child. Yeah, yeah, I know. There will be other races. Poop.

On the day of surgery, I won't be able to eat or drink anything after midnight the night before. I'll check in at 11:30 and get a mammogram-guided wire and some dye stuck into my breast to guide the surgeon to the spot. Then he'll take out all the suspicious tissue--he said the size of a golf ball, and when I told him that's about all I have, he amended it to a marble. In any case, he said it won't be enough to change the size or shape or cause dimpling or anything. Then he'll glue it shut and I'll go home a couple hours later. I will be under general anesthesia, which is probably the hardest part of the whole thing to recover from. That and not getting to eat all day!

Anyway, so that's the scoop.

Tuesday, August 16, 2016

Feeling great

It feels really good to feel so good. For the most part, I have reasonably good energy. The scale has been going down steadily--I've now lost 15 pounds since I finished treatment. Although I'd hoped to lose twice that by now, I'm thrilled to have finally broken through that plateau. I think working with the personal trainer is a big part of that--he works me pretty hard with a combo of cardio and strength training, and I think that's made a big difference. And then because I'm seeing results, I feel motivated and have better willpower when it comes to what I eat.

Exercise goes pretty well, and I'm definitely seeing improvement. Bigger weights, faster times. But it takes a lot out of me. Between that and my physical therapy stretches, and then resting from doing it, it's most of my day. That's OK because I'm seeing results, but sometimes it means I run out of energy early in the day. I want to go dancing or to see friends or do something else fun, and I'm often just not up to it. But getting my body back is my priority right now, so that other stuff can wait.

I finally came to terms with the fact that doing the marathon this year is out of the question. My body just isn't up to that level of training yet. I'm disappointed, but I also know I've done absolutely everything I can and it's not my fault. The poison that saved my life causes a lot of damage, and it's just going to take time for that to heal, and there's only so much I can do about that. Plus, all this extra weight I'm carrying around makes it way harder. So, I'll keep running the shorter distances and everything else I'm doing and try to keep my focus on just getting better and improving and getting lighter. Next year, it's triathlons.

I'm so stubborn; it's hard for me to not think about training like a regular athlete. How many times this year have I had to accept that this isn't going to go the way I want it to? It's hard to give up on a goal. Michael says I'm not giving up, just postponing it, but it doesn't matter. I didn't get to do what I set out to do. Ugh. Anyway, I'm accepting it all in small steps and by pieces. One day it will stop being a revelation. But honestly, despite my whingeing, mostly I'm happy. Life is good.

Tomorrow I get the MRI on my shoulder to see if there's anything wrong besides the impingement from treatment. They've gotten way better with all the work I've done on them, but it will be good to rule out any other problems. Then Thursday I meet with the surgeon about my  lumpectomy. Would love to hear your stories about how your lumpectomy went and what recovery was like! I hope it won't set me back too much.

Monday, August 8, 2016

First hair cut! Also, claustrophobia.

My first haircut, 41 weeks post final chemo
Another one of those up-down days. Today I was supposed to have an MRI on my shoulder to rule out any other cause for the pain and range of motion loss besides the stress from treatment. It took a long time to get the referral and then to get an appointment for this issue I've been dealing with since March (but is steadily improving thanks to physical therapy and a whole lot of work on my part).

I've had a lot of scans in the past year, including an MRI, a PET scan, and several CT scans. I didn't anticipate this one being any different. Except it was.

The tech got me all prepped and gave me a squeeze ball to squeeze if I was having trouble and needed out RIGHT NOW. I almost laughed, because I'm such a rational, calm person and would never need that. Then she slid me into the tube. She'd had me close my eyes first because she turned on the lasers, but then she said I could open them as she was moving me. I opened them briefly, saw the tube was pretty small, and closed them again and decided I would just keep them closed throughout.

But then when she got me all the way in, I could feel how close the tube was around me. Much smaller than the ones I'd been in before. My chest constricted and I felt like I couldn't breathe. I tried to tell myself it would be fine, just breathe and relax, but instead the feeling got worse. She asked if I was ok, and I couldn't answer because I was trying to decide if I was. She asked if I needed to come out and I said yes. I just knew I couldn't take it for the 40 minutes or whatever the test would be. So we rescheduled for another day at another facility where they have shorter, wider tubes. I'll get valium from my doctor and Michael will have to drive me. That will happen the 17th.

So, that was frustrating. Generally, my claustrophobia has only been triggered when I feel trapped, like someone holding me down, not just from being in close quarters. I've noticed before that I have more anxiety since cancer, and this is a good example. And then not only can I not do the thing I was supposed to do, I feel awful afterward. I have a stress headache and just a general...I don't know. Discomfort--mentally and physically. As I write this, I've gotten past it somewhat but I'm still feeling some of the after effects. And it  happened two hours ago.

However, while I was out I got a bug in my ear to finally get my hair cut. I stopped at a place on the way home and they happened to have someone available right then, so I went for it. I like it! And one of the ladies working there recognized me from the dance studio, so that was fun. I think this will be my last hair photo, and when I get around to it I'll make my video of the growth to this point.

Thursday, August 4, 2016

Attitude successfully adjusted

My hair, 40 weeks post final chemo. I'm
waiting for the front to get just a little longer
so I can get a cute, short, sassy cut.
It's amazing how much my attitude and general outlook on life shifts around these days. A couple weeks ago, I was miserable. I worried about the possibly cancerous cells in my remaining breast, hated physical therapy, and I struggled through my workouts and life in general. I was mourning my cat. I felt like I'd used up all my strength and rah rah attitude when I was sick, and I just couldn't take any more. But, I kept going, kept doing my exercises, kept listening when everyone told me to hang in there and it would be OK.

And you know what? It is OK. The biopsy was benign, and although I have to get the lumpectomy to be sure, I feel like I've let go of that fear. I moved past my sadness and anger and bitterness (not that I don't expect to feel that again, but I'm past it for now). Physical therapy started getting easier, and although it still takes up a large part of my day and isn't fun, I'm seeing progress. I have way more range of motion than I did a few weeks ago, which is great. I've gone dancing a couple times and did reasonably well. My workouts still leave me pretty exhausted, but at the same time, my body seems to be responding and getting stronger. Weight loss is still slow, but I'm edging my way down the scale.

So, in general, I'm doing well. I'm reasonably happy with how things are going. They could be better, but they could be a whole lot worse. My consultation with the surgeon is August 18, so I'll find out what's in store for the lumpectomy, get it scheduled, etc. I will keep you updated, as always!

Wednesday, July 20, 2016

I'm beginning to see the light

I think I'm starting to come out of the haze I'm living in lately. I still have pain, physical therapy still sucks and has only minimally improved my range of motion, and I still get too tired too often. But I'm feeling more accepting about it all, having raged and cried until I'm sick of it.

As far as exercise goes, I've accepted that I just can't follow any regular training plan because I have to take it day by day depending on my energy level. This week, it's very low, and since I have a few dance lessons to teach, that's going to have to be my exercise a couple of the days. However, on days I feel good or don't have to reserve my energy for something else, I'll get a work out in (and I am still doing the personal training twice a week). I'm done being angry about it and just will have to deal with it.

So, I don't know which, if any, races I'll be able to do this year. When my energy levels improve, then I'll look at getting more serious again. Meanwhile, I'm still trying to be careful about what I eat although that's always been a struggle for me.

I'm feeling a little better about work, too. I'm getting some help with the writing work getting everything done, so the looming deadlines aren't stressing me out so much. At the dance studio, I'm teaching a few hours a week, and my boss there is great about not over-working me. It helps that I work for such supportive people!

So, I'm seeing the light at the end of the tunnel again. And that's nice.

Monday, July 18, 2016

Anxiously waiting UPDATED!

I should get a call some time tomorrow either telling me the results were negative (which is what we want) or that I need to make an appointment to go in and talk to my doctor, which would mean it's positive (which we don't want). I managed to not think too much about it over the weekend or today since I was focused on missing Isis. What thinking I did do, I managed to become resigned to to the fact that this probably is cancer. I know I'm supposed to think positive, but last year I was absolutely convinced I didn't have cancer, and I did. So, it's hard to think positive. But it's ok. I got through it last time, and this time we're catching it super early so maybe it won't be so hard.

In general, I feel better today. A little less sad, a little less overwhelmed. The support I get from you all really makes a difference for me, so thank you. Let's all keep our fingers crossed, and I'll post tomorrow as soon as I know anything.

Update:

There are no cancer cells. It's a mucusoidal lesion (i think that's what he said), which is basically pre-cancerous. I need to have it removed, which is an outpatient procedure. WOOT!

Saturday, July 16, 2016

Fun with needles

My update on facebook was pretty brief, so I thought I'd give more of the details.

So yesterday I went in for my follow-up mammogram. They told me they would start with getting the magnified images, and only do an ultrasound if they felt like they needed it. They took several pictures, squishing me in super tight, then had me wait while they looked at them. Ten minutes later, the ultrasound tech came and got me to do the ultrasound. This was painless and pretty quick, but she had me wait there while she went to get the doctor so he could take a look. As it turned out, the doctor and I know each other from dance. He was super kind...but then, pretty much everyone I've run into at Sutter has been.

He ran the ultrasound wand over me himself and said that the asymmetry and dense tissue they saw doesn't seem to be concerning. He told me to get dressed and we would talk about the calcifications. I did so, and in his office he showed me the mammogram pictures, including the ones from last year. There was clearly an increase in the number of calcifications (which are really, really tiny) since last year, which  he said is a concern. He also said the fact that they are clustered, rather than randomly scattered, is sometimes indicative of cancer but not necessarily. About 75% of calcifications are benign, but since I'm high risk, he wanted to biopsy it. He did say that there was no rush and I could do it at my convenience. I asked if we could do it that day, so they worked me in and did it. I'm going to drive myself crazy until I know, so no reason to wait.

Last year, they tried to biopsy this same spot, but because of its location at the bottom near the chest wall, they couldn't get to them and decided I'd been through so much with the biopsy on the other side (it was painful, they drained fluid, etc) and there was little concern about the calcifications at that time, they decided to just keep an eye on them. So, again this year they had a hard time getting to them and finally decided to go at it from the top of the breast, meaning a longer route to get to the tissue they needed to sample. Why do I have to make everything difficult? It was a good 10 minutes of one painful position after another before they finally came to this conclusion. The tech felt bad and I know she was trying her best, but it was not fun.

They did numb me, so there was only mild discomfort for most of it. There were a couple points when the needle was deep inside that there was some pinching and it was pretty unpleasant for a few seconds here and there. The doctor put in more anesthetic, but then decided they had enough samples and wrapped it up. They had me ice for about 10 minutes, then took a few more mammogram pictures (gentle this time) to document the metal marker he'd left inside to mark the biopsy site, and I was done. They will send results to my oncologist, and I should hear back Tuesday or so. I'm still a little sore.

It took all day to get all that done, and when we finally got home, we soon noticed that my 17-year-old cat Isis, who seemed fine in the morning, was acting very odd. She probably had a stroke or a blood clot or something, but in any case her condition quickly worsened and we took her to the vet knowing that in all likelihood we would not bring her home--and we were right. I didn't want her to suffer, and after talking it over with the vet, we decided to let her go. I think this was quite possibly the saddest day of my life. That cat and I went through a lot together, and she was a stalwart friend.

In general, I'm having a really hard time of it, physically and emotionally. They told me this might happen--that when the fighting was over, the enormity of it all would hit me and I might become depressed. I thought I'd escape it because I'm so strong and smart and blah blah blah, but it's hitting me harder and harder every day. All that I've lost, and how hard it is to get back. The fear of that biopsy coming back positive for cancer. The pain. Getting exhausted so easily. At physical therapy on Thursday, he told me I'm not stretching enough--I need to do each exercise three times, three times per day (so nine times per day), and I was only doing each one once, often only twice per day. They're painful. So by the time the ten minutes of torture is finally done, I'm a wreck. I feel like I have no tolerance any more. It's all I can do to get my work done, and I'm pretty sure i'm doing a shoddy job of it.

As always, Michael is my rock. I've soaked more of his shirts in tears than I can count. He understands me like few people do, and he offers perspective and comfort and lets me talk, but in the end I just have live through it and keep taking steps toward it being better. It's hard. I'll take all the love I can get, my friends.

Friday, July 8, 2016

Et tu, Lefty?

It's probably nothing. I'm trying not to panic. But...Tuesday I had my annual mammogram, and I got my results electronically last night. They said, "Questionable increase in left breast calcifications
for which further evaluation with magnification views is again recommended. Left breast asymmetry for which further evaluation to include spot CC, spot MLO, and full lateral view with possible
ultrasound is also recommended." They're going to call me for a follow up. Those calcifications were there last year, but they couldn't get to them to biopsy them and they were not concerned at the time because they were tiny. It was not fun trying to get it done last time, and I don't suspect it will be much fun this time.

Thank you to all of you who told me stories of your loved ones who beat this, never to have it come back. I need that like crazy right now. I try so  hard to just live my life and keep out the "what if?" thoughts, but then this happens. Statistically speaking, it would be very unusual to have a recurrence so quickly--but it was statistically unlikely for a 42-year-old non-jewish white girl to have triple negative breast cancer. What if I'm one of the "lucky" few? On the other hand, I just had a bucket load of chemo a few months ago, and it is systemic and should have killed everything. But what if it didn't? I had a couple friends who had something like this come up within a few months or a couple years after they were declared NED, and it was nothing. But what if I'm not like them, and it's something?

This is my life now. Worrying about every test, every lump, every pain. What if I am one of those people who spends the rest of their life fighting cancer? I know it's better than being dead, but it's a far cry from living a reasonably normal life. What if I never get me back?

On the bright side, I had my third personal training session today and it was great. Loving my trainer. Tomorrow I have my 5K at the Davis Moo-nlight, so wish me luck. According to the weather forecast, this should be the coolest it's ever been for this race--thank goodness. I know I made the right decision downgrading from the 10K, and I know I'm supposed to be grateful that I'm able to run at all, but I hate, hate, hate admitting I can't do something.

I'll keep y'all updated about when I go in for this biopsy, results, etc. Please pray for me and continue with those success stories. Thank you for your continued support!

Friday, July 1, 2016

Let's Get Physical!

My hair, 35 weeks PFC. I'd really hoped it
would be longer by now based on what I've
seen on other people, but alas I am not hair
blessed. Happy to have this much!
These days, I'm all about getting physical. I officially started marathon training for my event in December. But I gotta tell you, it is so much harder this time around. I knew it would be, but I didn't know what to expect of this new body. The good thing is, it's responding to training. I can do the workouts I'm scheduled to do. Slow, but I get them done. I'm swimming and doing some weights in addition to the running.

The problem is the recovery. I work out, then I go home and crash. I'm literally so exhausted, I have to take a nap or at least veg out for 2-3 hours. People tell me, "I get tired after a workout, too!" Not the same thing. I know what "normal" post-workout tired is, and this ain't it. So, I may have to back off a bit and take things more slowly. This may mean no marathon. We'll just have to see. I'm not giving up yet. I'll be doing a 10k (6.2 miles) next Saturday, so wish me luck!

I went to 24-Hour Fitness to re-join (I'd cancelled my membership when I got sick). I was talking to the manager, and he decided to give me this whole big sell on how important it is to eat right (um...I know) and how exercise is a part of that (um...I know), trying to talk me into his personal diet plan, telling me not to do things I know work for me, telling me I need to do things I know don't work for me, telling me to do things I'm already doing. He was clearly not listening to anything I had to say, and it was incredibly frustrating. I could tell he was another one of those who thinks fat people do nothing but eat bon bons all day and never exercise, and he has all the answers on weight management even though he's never struggled with it.

I was just about getting to the point of putting the kibosh on the whole thing, and he offered to pay for me to have two personal training sessions per week for a whole month. The only catch is that I have to show up no matter what, and if I do the whole month he'll keep paying for it. The implication being that I need motivation to go work out...well, he doesn't know me very well because that is the very least of my worries. But, hey, free training. I'll take it! So I took him up on that offer.

That was Wednesday. We set my first appointment for this morning, and I was braced for more of the same crap. I was already feeling defensive before I met my trainer, Matt. We started at a computer kiosk, where he went over their philosophy and got my background from me. He listened to everything I had to say, asked the right questions, and made no assumptions. We talked about my diet, and he completely understood what I talked about with making good choices most of the time, but having willpower failures that sideline me. He agreed with doing what works for me and made suggestions. He recognized my goals and talked about how he would design my program to help me meet them, rather than expecting me to follow some routine he does with everyone. I could feel the walls I had put up melting as the conversation went on, and I was excited to work with him by the time we were ready to actually get to work.

I don't know how long the workout was, maybe 20 or 30 minutes since we'd spent so much time talking, but it was a good level for me--challenging, but not overly so. He was clearly very cognizant of my limitations, checking in with me about how things felt, telling me to take a breather if I needed to. I left there feeling really awesome.

And then I came home and slept for about an hour and a half. And now I'm drinking coffee and trying to wake up and do a little work before we go out tonight. How is this cup empty already?

I started physical therapy last week for the pain and loss of range of motion in my shoulders and chest wall. They said it's not exactly frozen shoulder--there's just a lot of impingement on the joint from the stress. So, I have lots of super fun (not), totally comfortable (in opposite world) stretches to do to help get that range of motion back. It was really hard for me to be a lady when he was working on me in the office and not swear while he tortured me, but my momma done brought me up right. Anyway, I'll have four more sessions, with a lot of homework in between. I'm already seeing improvement.

Oh...and yesterday I realized I missed the one year anniversary of my diagnosis by a week. I had thought I'd make some amazingly wise and insightful blog post about it, but I forgot. I guess I'll have to wait for the next milestone!

Monday, June 6, 2016

You can take cancer out of the girl...

My hair, 33 weeks post final chemo.
Getting shaggy!
Wow! It's been a long time since I posted here--about two months. I'm happy to say that I've been too busy traveling and enjoying life and working! Things are going well in some ways, but not in others. My energy is good and I'm slowly regaining fitness. I can see improvement each week when I work out, and that's heartening. I officially started marathon training (for my event in December) yesterday, and I was able to do the required mileage and run/walk intervals. Other than the last week when I had a cold, I've been exercising six days a week--running, swimming, biking, light weights.

I finally got my prosthetic breast, two days before we left for our cruise (which was amazing!). However, I'm still so tender from surgery and radiation that I can't tolerate a bra for more than an hour or two, so most of the time I just go au naturel and lopsided. I'm used to it at this point and don't really care, but it is nice to have the option when I want to look nicer.

The bad part is my shoulders started hurting after I finished radiation. I did my stretches my surgeon gave me for regaining range of motion, exercised, used my little TENS unit, had a massage, used KT Tape, and took ibuprofen, but nothing helped and it just kept getting worse. I finally got in to see my oncologist, and he gave me a referral for physical therapy. They're full up, so I won't be able to start for a couple more weeks. I'm also supposed to get an MRI to rule out anything else, but he said this is pretty typical with all I've been through. Of course, this has a huge impact on my dancing.

Emotionally, it's still a roller coaster. I'm sure part of it is the sudden onset of menopause and my hormones are all out of whack. But part of it is that the whole experience was just exhausting and traumatizing. Sometimes I hear people say, to me or someone else, that it's "time to move on." But you know what? It's just not that easy. You don't just move on from having cancer; it's always with you, even when it's been physically removed.

In my day-to-day life, I do focus on what I'm doing now and making plans for the future. But in everything I do, I'm reminded how I've been changed. I get tired too easily. People tend to think I'm done with treatment now so I must be my old self, but I'm not. I don't have the stamina to work all day like I used to. To dance like I used to. Even to sit at my computer for hours. Because of the issue with my shoulders, a hundred times a day I do something that tweaks one or the other and it's agonizing. Even something as simple as putting on my shoes is difficult because of the ache and loss of flexibility in all my joints.

And then there's the things that blindside me. Someone tells me their cancer came back, and I wonder if that will happen to me. Three friends have died of cancer since I had my surgery and the pathology report showed no remaining cancer--in December. Each one reminds me that I could have died. Each one reminds me of how lucky I was. I manage to work through the feelings and get back to living my life, but have had some rough days. And I had it relatively easy. My friends with small kids? I don't know how they do it. The ones who have to fight tooth and nail to get their treatment covered, or whose treatment isn't working? it's awful. I feel blessed and guilty that it went so smoothly for me.

So, no, I don't know if I'll ever leave cancer behind me totally. But I am grateful I'm still here, and that I'm in a loving home in a life I enjoy. And you can't ask for much more than that, can you?

Thursday, April 7, 2016

Cancer teaches you patience! Not. Well, maybe a little.

My hair, 23 weeks PFC. 
When I first was diagnosed and learned I had many months of treatment ahead of me, I was impatient. I wanted it over with. Then, during chemo, I reached this sort of stasis. I gave in to the timeline, knowing it would be months until I was done, and I should stop looking at the horizon. Resolved. At peace with what was happening to me. And now, I look back on the whole thing and it seems like a dream. If it weren't for the drastic changes to my body, I could almost forget it happened. Almost.

So now I'm trying to get my body back. I want to do the California International Marathon (CIM) again this year and a triathlon next year. Intellectually, I know it will take a long time to get back to where I was, fitness-wise. In a way, I'm patient with myself. After all, I just finished treatment four weeks ago. I spent nine months doing nothing but lose fitness and gain weight. Radiation damaged my lung (hopefully only temporarily). I know I have a lot of work to do to get back to where I was, and I'm OK with that. I see progress every week, and that inspires me. Yesterday, I swam for 20 minutes without stopping and felt good after. Last week, it was 12 minutes with a break in the middle and I was exhausted. I'm watching what I eat and have lost four pounds so far.

What's hard is, I want to do the training to get to where I need to be just to start marathon training on June 1, but my body keeps telling me it's not ready. I have no choice but to listen. Some days it's good, and others not so much. Tuesday, I was supposed to walk/run two miles and go to tap class. I also needed to do some grocery shopping, and I was feeling a little tired. I realized I couldn't do all those things, so I skipped the walk/run and just went to the store...and I was still tired at tap class. I did get all the way through it, but I struggled. My energy levels go up and down like a roller coaster.

So, I guess I did learn to be patient while taking what action I can, but it's hard not to be frustrated. People keep asking if I'm serious about CIM. I am, but I'm also realistic. I have to at least try; I owe myself that much. But yes, I am listening to my body and I won't injure myself or something trying to do more than I'm capable of. But at the same time, I keep thinking I can do all this stuff, and really I can only do some of this stuff. So, who knows if I will be running from Folsom to Sacramento on December 4. I hope so. I'm also doing all kinds of reading on triathlon training and preparedness. I want to be in with the in crowd. For now, I'm slodging along.

Wednesday, March 30, 2016

Improving

My hair, 22 weeks PFC. I decided to spike it
with some gel. Not sure if I like it!
Short on time today, but I realized I haven't posted in about two weeks so I thought I'd do a quick update. It's been just over three weeks since my last radiation treatment (boy, does time go fast!). I'm exercising every day, either by riding my bike or taking a walk or doing light weights. Today I added some slow run intervals to my walk. My energy is really good, although my stamina has a long way to go. Monday, I was able to do tango class and then three songs of practice afterward, where last week the class was all I could manage. Yesterday, I rode my bike for 20 minutes (3.1 miles) in the afternoon, then in the evening went to tap class and then to the park where there were food trucks for dinner. Still had energy when I got home!

Really enjoying both piano and tap, by the way. Super fun.

I still don't have my prosthetic, although I'm just a little too tender yet to wear a bra even if I had it. As I suspected, the ones the lady ordered for me did not fit. I go back tomorrow to see how she did on the reorder. My skin continues to improve, and is now just kind of tan where I was treated--I'm all done peeling. I do seem to have developed some tendinitis in my shoulders, so I'm trying ibuprofen and gentle stretching to see if I can improve that. Apparently it's a common problem.

That's all I've got today!

Tuesday, March 15, 2016

About that positive attitude

Quick update before my thought for the day: I'm feeling a little better every day. The red burn is fading and turning to brown, which I suspect will all peel, but new skin is growing underneath so it won't be so painful as when I was getting blasted every day. Under my arm is MUCH more comfortable, and it doesn't hurt to move my arm anymore. My energy is returning; I went to tango on Sunday (danced two tandas, which is a total of six songs) and walked 1.7 miles this morning and didn't feel exhausted after. However, it's hit and miss--last night we went shopping at three different stores, and I was wiped out. I'm enjoying learning piano, and my first tap class is tonight. I'll probably go back to teaching pretty soon, although I'll keep my schedule light for a while.

Throughout this whole ordeal, people have commented on my positive attitude. I thought I'd talk about that a bit today. Several people said it's been shown that people tend to have a better outcome if they have a positive attitude. I don't want to get into whether positive thinking can actually cure you, because that's a huge, controversial subject and one I'm not qualified to discuss. But I can talk about how it affects me.

When I am miserable for whatever reason--I'm running 20 miles in the heat, I'm sick, I'm at a party where I don't want to be, etc., my attitude may not affect the actual situation, but it absolutely changes how I feel about the situation. If I stew in my feelings of misery, telling myself how awful things are, I am unhappy. It's like a negativity spiral: I'm in a bad situation, so I think about how bad it is, so I feel bad about being there, and that causes more bad things to happen. By contrast, if I resolve to make the best of it and look for reasons to be happy, I feel happy. Maybe that happiness then causes good things to happen, so now it's a positivity spiral. The situation didn't change, but at least I'm happy while I'm in it.

One of my favorite examples of this is when I was training for the marathon I did in 2014. About a month before the big event, I did a 20 mile race. So, first of all, that was the longest I'd ever run, so it was already a challenge. I didn't prepare well for it as far as hydrating, fueling, and getting enough sleep for the few days before (in fact I ate really awful food the day before, including jalapeno poppers), so I wasn't in a good position going into it. Finally, it was in early November and we'd had several weeks of cool weather and I had acclimated to that. Yet, on race day, it was quite warm which made things uncomfortable. So it was not an ideal race. Around mile 11, I started to feel nauseous. It might have been because I ate an un-tried flavor of energy gel, or maybe all the factors I listed above, but in any case I wasn't feeling too well. I started feeling sorry for myself, telling myself how this was too hard, and maybe I couldn't do it, and how miserable was I? Things just kept getting worse, I kept feeling more and more sorry for myself, and it was overall a miserable, miserable experience.

Flash forward to the marathon, which of course is 26.2 miles so quite a bit further. For the week before, I was resolved to not repeat the experience above. I prepared my body better, but perhaps just as (or more?) importantly, I prepared my mind. I actually visualized myself running the race, talking myself out of negative thoughts. It's too hard! No it isn't, you trained for this. I hate this! No you don't, you're doing something you never thought you could do. I'm miserable! No you're not, you're fine. Get over it. I practiced that over and over, and on race day, that's exactly what happened. I'd start to have a negative thought, and I'd replace it with a positive one. And although I was damned tired and in pain by the end, I was never miserable. I was never unhappy. I never pictured lying down by the side of the course and waiting for the sweepers to come get me. Although the race was harder because it had more hills and was longer, I had a much more positive experience.

Having cancer sucked. Hard. Doing the treatments was terrible. There was no way around that. And on those days when I was really feeling sorry for myself and reveling in just how badly I felt, I was unhappy. But if I could break myself out of it--sometimes by posting here and typing the positive words and forcing myself to get in the right mindset--I actually felt physically better. More importantly, I was happy even though my body felt terrible. When I got to the radiation phase and had run out of the willpower to stay positive, I spent a lot of time being unhappy.

Some studies suggest that when you think positively, your brain produces chemicals that support your immune system, while being depressed makes you more susceptible to problems. Whether you believe that to be the case or not, the bottom line is: you can be sick and happy, or you can be sick and unhappy. Why be unhappy? When you look for reasons to be sad or offended or angry, you spend a lot of time being sad or offended or angry. When you look for reasons to laugh or smile, you spend a lot of time laughing and smiling. How do you want to spend your time?

For me, life is too short to be unhappy. I choose to laugh and smile.

Thursday, March 10, 2016

I'm done, but it's not over


The Awareness Bear, my Radiation Complete
trophy, and my cancer memory jar. It has the
shredded chemo countdown loops and Dove
chocolate wrappers and gratitude lanterns
from radiation.
On Monday, I had my last cancer treatment. Huzzah! It is such a relief to be done. I cried, of course, and the techs hugged me and said they never want to see me again. Ha! The feeling is mutual. Sweet Michael met me in the waiting room with flowers, a pink "Awareness Bear" and a trophy he had made for me. Is it any wonder I love that man? I was an emotional mess all day, but they were happy tears.

So what now? Even though I'm done with treatment and in remission, it's really not over. I'll have follow-up visits with all my doctors for months for months if not years, next week I'll see if the lady at the Hanger Clinic managed to order the right prosthetic (who wants to take my bet that she didn't?), and I'll have my annual mammogram in June.

Then there will always be that niggling doubt. What's that weird pain? Is the cancer back? What does my mammogram say? Do I have cancer again? This is an experience that will never leave me. I refuse to live my life in fear, but it's hard to keep those doubts from trickling in from time to time. It doesn't help that I keep hearing about people who beat cancer, only to have a recurrence or new cancer a few years later that then metastasizes and they die. It's hard not to be scared of that. Today I heard about a lady who lost her fight with cancer at the age of 41. It's hard not to think, "That could have been me." So, if you have a survivor story where the cancer never came back, I sure could stand to hear some of those.

My hair, 19 weeks post final chemo. It's getting
almost shaggy!
And I'm not done healing. I'm still quite red, although it's turning to tan now. The patch under my arm keeps getting bigger as more dead skin falls off (sorry for the ick factor), but thankfully since it's not getting irradiated anymore, there is new skin underneath so it's not so painful. It gets a tiny bit better each day. I'm surprised that the itching isn't too bad, although I do have some. It's still uncomfortable to use my arm, but better. Hence, I haven't posted here until today.

It will take a long, long time to get my body back in shape. I walked a mile on Tuesday and again today, and it was a lot of work. But I have lots of motivation to get moving!

Of course, I carried some good things away from the experience. I have a whole new perspective on life and what really matters. I made some great memories as we partied our way through treatment and did all our little rituals. My friends and acquaintances showed me how awesome they are. And I learned that maybe I'm stronger than I thought. While I wouldn't wish this disease on anyone, it's good to have something positive to look back on. I certainly hope others can benefit from my experience and perspective as well.

I'll still have a few more posts to make. I never shared my "what I learned from chemo," and I'll do the same for radiation. I'm sure I'll have other things to share as well. So, we're not quite done here yet!