2012: It's Been Bitchin'

A couple months ago, in the midst of holiday madness, I made a very important decision.

I decided, with conviction and zeal, that 2013 is going to be my year.

I was tired of the cancer crap and everything that comes with it: the fatigue, the worry, the fear. So I made a decision. That next year, 2013, was going to be mine.

I was going to own it.

But before making 2013 my bitch, I had to get through my fist post-remission PET Scan since my recurrence last summer. It's hard to start the year off in warrior mode with a looming scan on the horizon. I tried not to fret too much about this one. After all, it's routine by now. I've done these scans so regularly for the last 14 months, it seems like my new norm.

But this scan is a big deal.

In the last year, I've been diagnosed and in remission, then diagnosed and again in remission. If the pattern were to hold true, it means it was time to be diagnosed again. The fact is, since first being told "you have cancer" I've never received two clean scans in a row.

And as much of a warrior as I pretend to be, that is a worrisome fact.

So yesterday, I went in for my first scan of the year. Trying to be more warrior than worrier, I took inspiration from one of cinema's greatest films: Cool Runnings. In an attempt to empower myself and spend more time wishing for the best rather than worrying about the worst, I took strength in repeatedly  replaying this scene in my head:

But even Cool Runnings can't completely get rid of the worry.

Luckily an email from my doctor can. Yesterday afternoon, in the middle of my fretting and only hours after my scan, my worrying was interrupted with this one line from my radiologist:

"PET scan is perfect!"

Perfect.

And while I'm sure the worrying won't be gone forever, last night I got a pass. I got a bonus night where I got to sleep free of the "what ifs" regarding today's appointment. Thank you, doc for rescuing me from the stress of the unknown for an extra 24 hours.

Must be because I am a bad-ass mother who don't take no crap from nobody. 2013, don't mess with me.

This year is mine.

Go Team Thunder!

Ten months ago, in this post, I announced that I had signed up to run a half marathon in this year's Detroit Free Press Marathon.

A lot has changed in 10 months: I rejected conventional treatment, accepted alternative treatment, got rid of cancer, turned 29, got cancer again, rejected a bone marrow transplant, accepted radiation, celebrated my fourth (!) wedding anniversary, got rid of cancer again.

Phew.

So here we are, just days away from marathon day and no closer to being able to run 13.1 miles than I was in January.

It's not that I didn't try. I really did. I set up a training schedule. I woke up early most mornings to get my runs in. I ran. A lot. But in the middle of this training, I started going through radiation, which in itself takes a toll on the body.

But I was determined.

So most mornings (with the help of friends), I would wake up and run before my 8am daily radiation treatments. The warrior came out. There was no way I was letting Cancer take this away from me.

But about two weeks in, I started to notice a shortness of breath. Not only did running become harder, breathing became harder (a common side effect of having radiation so close to my chest and lungs).

So I stopped running. I told myself it was temporary. That as soon as I was done with treatment, my lungs would improve and I would start up again.

My condition didn't improve. Here I am, two months later, still unable to take a true full breath and expected to run 13 miles on Sunday.

But, this will not be another thing cancer tries to take away from me. On Sunday, even if it takes me all day and I have to crawl across the finish line, I will complete my 13.1 miles. And luckily for me, I don't have to do it alone. Not only is The Hubby "running" with me, but my sister and a great friend are joining as well. We also have a team of friends coming to cheer us on throughout the day, decked out in Team Thunder shirts. It's pretty incredible to have friends that are willing to stand all day in a crowd of people, waiting to catch a glimpse of me as I walk a half marathon. That's love.

Even though cancer may have slowed me down (literally), it will not stop me from finishing the race. After all, it's not just my ego on the line. As I mentioned before, I am also running in support of the Make-A-Wish Foundation. And any foundation that strives to make a kid's experience with cancer a little brighter deserves our support and money. If any of you would like to support me by supporting the Make-A-Wish Foundation, please go to my fundraising page and give whatever you are able to.

Again, thank you all for your constant support throughout my journey.

See you at the finish line.

Go Team Thunder!

Breathe Easy

Last week I got good news. Really good news. Last week, after 23 radiation treatments, I got a clean scan. This officially puts me (for the second time this year) in remission.

But this time was different. I didn't run around yelling, "Suck it cancer!" This time, Mama Bear didn't cry when she heard the news. The Hubby, although ecstatic at the outcome, seemed more relieved than anything else.

This time we understood that this news, although reason to celebrate, is only the first of many hurdles.

Last time I got good news - the "you're cancer free" news - within a few months, it was back. And being told "you relapsed" is a prognosis that was, in some ways, worse than the initial diagnosis.

Right now I am extremely grateful, thankful, and excited with the news, but also cautious. 

I was told by my oncologist that it was expected to get a clean first scan, but it is the next several that really matter. His exact words, "After two years, then you can breathe."

Great. Thanks Doc.

In the meantime, besides holding my breath, I'm trying to stay focused on living a healthy lifestyle by juicing, eating right, and doing regular yoga. I'm trying to not let the fears of my oncologist's words flood my thoughts. I'm more focused on the optimism of my radiologist who believes in the success of my treatment path.

And most importantly, I'm trying to keep things in perspective. Rather than focusing on the uncertainty of the next scan, I'm constantly reminding myself that this holiday season (unlike last year) will be minus one Little Hodgy. I am constantly reminding myself that I am in remission.

And even though the future is uncertain at the moment, I'm looking forward to the day when I'm allowed to breathe. Then, I'll take it all in and finally tell Cancer to "Suck It" for good.

Waiting and Worrying

I'm not sure I can top today's post from The Hubby as he perfectly sums up what we're going through with such eloquence, but I think it's important to voice my thoughts as well.

This fucking sucks.

Here I am a year later and still waiting to see if I have cancer. This whole year has been one long waiting game.

And not just waiting, but worrying.

Waiting and worrying.

This is not to say that I don't thoroughly enjoy my life in the middle of all this waiting and worrying. I do. But underneath every thought, word, and action is "do I still have cancer?"

This constant thought gets really fucking old.

But tomorrow, I get my PET scan, which means by Wednesday, the waiting will be over.

And hopefully, for fuck's sake, the worrying too.

via

Georgia On My Mind

Yesterday I started a 5 day health detox at the Living Foods Institute in Atlanta. It was one of the original places I researched back when I was first diagnosed and - in Mama Bear's loving panic - booked us tickets before Little Hodgy had even a single second to grow.

As everyone knows, I ultimately went to a similar program in Arizona that I felt blended both natural and medicinal treatments, but leaving us with a credit to the program here in Atlanta.

So far this program has been less than healing.

When I think of healing, I think of the ocean and my toes buried in the sand. I think of music and dancing. I think of bike rides. I think of laughter with friends. And yes, sometimes healing means sitting on my deck with The Hubby enjoying a glass of wine.

I do not think of healing as sitting in room ALL. DAY. LONG listening to a series of lectures.

To be fair, I do have more knowledge than the average person when it comes to the alternative therapies. And I knew coming into this that I would have to listen again about the benefits of greens and wheatgrass and infrared saunas and all the other things I've already done. I just figured it would be spread over 5 days, in between actually getting therapies.

So far, I haven't left my chair.

Not very healing.

I'm going into today with an open mind (naive perhaps) and hoping we actual do something besides listen.

If not, this chair just might be the death of me.

Red, Red Go Away

When the doctors and nurses told me about the immediate side effects of radiation, no one mentioned the fact that I would start to look like the Batman character Two Face.

Currently, from my chest to the bottom half of my face, my skin is raw, peely, and a range of blotchy shades of red, white, and tan.

So not a good look.

I know this is temporary and if it means Little Hodgy is gone for good, it's totally worth it, but I'd really rather not spend the final days of summer hibernating because I scare away all the children I come in contact with.

I'll spare you pictures of what I currently look like, but here are a couple pics of the radiation room where I received my daily treatment:

The evil machine that made me look like Two Face

Me, in the radiation machine

Radiation, Check!

Today, after 4 and a half weeks of treatment, was my last day of radiation. 

I have to say, the process wasn't terrible. I've been a little more tired than usual (but that's what afternoon naps are for), my throat has been extremely sore, and my skin looks like I fell asleep in the sun, but nothing too unmanageable.



Like most things with cancer, it's the emotional toll that was the most taxing. 

Everyday for over four weeks I had to go sit in a waiting room with women more than twice my age. Not once did I ever see any patient under the age of 60.

This, frankly, is a constant reminder that I shouldn't be dealing with this.

What should I be doing? I should be finding my dream job. Or I should be traveling the world. Or, hell, I should be having babies (or at least another puppy). But early in this process I learned to give up on the idea of "shoulds".

As we all know, life doesn't always obey our "shoulds."



The mere fact that I had to start every day in a hospital took its own emotional toll. It's hard to move forward when your wake-up call is a daily dose of radiation.



But today, I am finished.



Now all I have to do is wait...

And wait..

And wait.

What will inevitably feel like a lifetime (aka 6 weeks), is how long I have to wait to learn if the radiation was even successful.

Everyone, keep your fingers crossed...

Because you should!

I certainly hope so!