A Change of Perspective

I’m a little behind on my blogging lately. I’ve been busy doing fun things. What a nice change from being tired as a result of cancer treatments and doctors’ appointments.

Last month, I had my first infusion of Zometa. Zometa is a bone strengthening drug, which also has shown to prevent recurrences of breast cancer in some studies. My oncologist wanted me to do this treatment since in July of this year, I was diagnosed with osteoporosis in my spine. Yes, the joys of breast cancer continue.

I was pretty bummed about having osteoporosis, but even more bummed about the treatment, since the drug is administered in the chemo area of the hospital. I never wanted to be back there. Ever.

My oncologist told me I could expect flu-like symptoms the first couple days after the treatment. So I scheduled the infusion for a Friday, giving myself the weekend to recover. It felt like chemo all over again – figuring out when my body would have the worst reactions to treatment and how long it would take to recover.

So I went to the hospital, as early as possible, to get it over with. The sooner I got there, the sooner it would be over. They start infusions at 9 a.m., so that’s what I did.

The nurses were so nice, as usual. I feel very grateful to be so well taken care of. Not everyone has that experience.

The infusion didn’t hurt at all. I barely even noticed the needle going in or out. I guess I’m just used to that by now. They started the infusion, I turned on my iPod, closed by eyes, and 5 songs later, it was over. As my oncologist promised, the infusion only took 20 minutes. The whole thing took about 45 minutes. Couldn’t wait for it to be over.

I went home and laid on my couch. I was pretty exhausted. Of course I didn’t sleep the night before. The first time I do anything, I’m always nervous. So getting rest that night didn’t really happen. The emotional toll was worse than the physical toll for this treatment.

My oncologist told me to drink a TON (her emphasis) of water. Zometa is flushed out through the kidneys. So water gets it out of the system. I spent the day on the couch, in and out of napping. I did get this souvenir from the infusion – a lovely bruise on my arm:

Bruise From Zometa Infusion

The next morning I woke up, feeling pretty tired still but not terrible. No flu-like symptoms yet, but I decided to stay in to rest and keep drinking that water.

Around 8 p.m., I decided to go to bed early to catch up on that sleepless night the night before the treatment. But that’s when the flu-like symptoms showed up. I started to get some chills and feel a bit nauseous. I actually haven’t felt cold in a long time. Hot flashes and overall heat is my normal body temperature these days, thanks to Tamoxifen and my oophorectomy (the removal of my ovaries). So in a weird way, it felt kind of nice to be cold. The nausea though, I could do without that.

The flu-like symptoms only lasted for a couple hours. As I laid in bed eating ginger to help settle my stomach and with a wool hat on my head to try to warm up, I kept telling myself, “You’ve been through worse. This is nothing.” It actually kept me calm and helped me not freak out about what was happening with my body.

Not that I really needed it, but the Zometa infusion and my body’s reaction was a reminder that I’ve been through the ringer in these last 2 years – a double mastectomy, 8 rounds of chemo that lasted 4 months, 1 reconstructive surgery, 32 zaps of radiation over 7 weeks (5 days a week), an oophorectomy, and countless tests and doctors’ appointments. My perspective has changed. A little chill and nausea for a couple hours? No big deal. I can handle that.

So, I snuggled with my dog Murphy for some body warmth and TLC. Then next thing I knew, the chills and nausea were gone and I went to sleep. Another cancer experience that I’m happy to be moving past.

 

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And Now … Osteoporosis

I’m 41 years old and have already gone through a double mastectomy, 8 rounds of chemo, 1 reconstructive surgery, 7 weeks of radiation and an oophorectomy (the removal of my ovaries). All because of my breast cancer diagnosis and having the BRCA 2 mutation.

That’s enough for a lifetime, if you ask me.

I went to see my oncologist in May for my 6-month check up. She wanted me to do a bone density test, mainly to get a baseline, she said. Having my ovaries removed and taking tamoxifen, my body is not producing or getting any estrogen, which helps keep bones strong. So I figured I would be at risk for osteoporosis, but not for a while.

Last week I finally did my bone density test, which, by the way, was the easiest test I’ve ever done. No IV, no drugs, no fasting. You lay down, they scan your spine, then they scan one hip. Then you’re done. In and out in 15 minutes. Best. Test. Ever.

Two days later, I got the call from my oncologist. My spine already shows signs of osteoporosis. DAMN IT!

So now she wants me to be given a drug called Zometa. Zometa is a bone strengthening drug, which also has shown to prevent recurrences of breast cancer. Both good things.

Here’s the good news – I will only have to be given Zometa once every 6 months (twice a year). It only takes 15 minutes to administer the drug.

Now the unsettling part – Zometa is given through an IV. That kind of sucks. But the worst part – I have to go to the chemo area of the hospital to get the infusion.

I never wanted (or want) to see that stupid chemo area again. When I said goodbye to those lovely nurses who helped me through chemo two years ago, I said goodbye. Not see you later. Goodbye. Have a good life. I’ll never see you again.

But here I am, being told to get an osteoporosis drug administered in the chemo area of the hospital.

Now, I know I should be grateful that I’m only going there for osteoporosis, and not because I have a recurrence of breast cancer or some other cancer (fingers crossed that’s always the case). And I should be grateful that my oncologist is aggressive and assertive on my behalf with any health issue. But that somehow isn’t making the tears stop flowing when I think about walking into that chemo area. Having to see all those people, who I used to be one of, get chemo – that’s going to be hard. Talk about PTSD.

I guess the other upsetting part is that this is just one more thing I have to do now because of stupid f*$%ing breast cancer.

I see at least 1 doctor every 3 months, I get blood work done every 6 months, I go for scans every year, and now I have to go get this drug pumped into me every 6 moths. It’s just one more thing that I have to do in a hospital with doctors. And that just sucks.

It reinforces the fact that you’re never really done with cancer. There’s always something.