LATHER, RINSE, REPEAT

(AKA, KRISTIE IS TOO LAZY TO WRITE AN ORGINAL JOURNAL ENTRY TODAY)

23 Days to Go

Two years and a month ago, give or take a few days, Kendrie was diagnosed with leukemia. It took me three weeks to discover Caringbridge. It took about three weeks after that for me to start using Caringbridge not as a method for keeping family and friends updated on her condition, which is how it started, but as the cathartic, therapeutic, beneficial tool it has become for me. I’ve said it all along, CB has kept me off the couch. Actually, this **is** my couch; virtual, online, cheap therapy.

But my very first, honest, laying-it-on-the-line Caringbridge entry took place on Thanksgiving, 2003. I was still pretty raw from diagnosis, and emotional, and exhausted, and felt the need to clear up a misconception that seemed to have occurred: That I was taking Kendrie’s leukemia diagnosis in stride, and was even pretty optimistic. That couldn’t have been further from the truth!!

So I wrote an entry telling people how my emotions were really running …. And you know what? Getting it off my chest like that felt gooooooooooood! And so you guys have been stuck with me and my absurd ramblings ever since. But I figured there was no need to ramble afresh today, since that Thanksgiving 2003 entry still rings true for me. Sure, things are slightly different now. We are nearing the END of treatment, not just starting out. Ignorance is bliss and I’m no longer ignorant to the unfairness of childhood cancer. The crap sandwich we have left on our plate is crumb-sized ….. we’ll be choking down the last few bites in the upcoming weeks and then OUR. PLATE. WILL. BE. EMPTY!!!

But, we’ll be required to hang out in the bar of the restaurant for the next five years or so. We won’t order off a menu, or make eye-contact with any employee on purpose, heaven forbid. For the next five years we will sit in the bar and keep a low profile and hope and pray the waitress doesn’t come back to our table. I’m not sure when we can ever pay our check and leave ….. and as long as we’re here, we’ll continue to see crap sandwiches being slung out of the kitchen on a regular basis. You don’t want one yourself, and you hate to see anyone else getting one, either. But you know they’re coming. So you just duck and pray you don’t get hit.

Anyway, those of you who didn’t follow along in our journal back then probably have no idea what I’m even talking about! (Although to be fair, do you ever? I do have a tendency to go off on some pretty bizarre tangents!) So I’m going to repeat the journal entry now, and hope that all of you enjoy it. Again.

Here goes:

Friday, November 28, 2003 0:21 AM CST
KRISTIE'S PATHETIC, LAME, COMPLETELY RIDICULOUS CANCER/THANKSGIVING ANALOGY:

First of all, I have to say how much we appreciate those of you who check on this web site and take the time to sign the guestbook. Several of you, and some who have e-mailed me privately, have made the comment you are glad to see me (try to!) put a humorous spin on things, and that you’re glad to know we’re coping so well. To be honest, I have no idea if we’re coping well at all. I just make it a point to do my crying and worrying and stressing in private, and put on a happy face, USUALLY, in public. But today, in this journal entry, I’m going to be a little more honest about things and the way I am really feeling. I’m not sure what has brought about this pathetic moment of self-introspection, but feel the need to get some things off my chest. If you don’t want to hear it, exit now, it won’t hurt my feelings. I promise to kick myself in the butt and be back to normal tomorrow. (No, I will not be taking volunteers for the chance to kick me, so all of you just put your hands down now. No, no, do NOT form a line!)

I think it’s the whole Thanksgiving holiday. Thanksgiving. Giving thanks. Something I’ve found pretty easy to do most years, and took for granted pretty much every year up until now. Sure, I know a little bit about worrying about the health of family members. Who doesn’t? My dad has muscular dystrophy. My mother-in-law is on dialysis for renal failure. My husband had two major surgeries to get rid of a cancerous tumor six months ago, and had a nice chunk of the inside of his head removed at the same time --- reconstruction still a work in progress. So I thought I was a veteran at worrying, but always managed to give thanks irregardless. WRONG. Nothing prepares you for the fear and worry when your child is ill. More than ill. Ill with a disease that, even in this day and age, still claims innocent victims. And now you want me to give thanks????? So here’s the lame analogy I came up with:

Imagine every year for Thanksgiving that you and your family go to a wonderful all-you-can-eat buffet. The food is always great and you look forward to getting the same delicious meal, year after year. So this year, you give your standard order to the waitress: an appetizer of “love”, a “caring” salad, the side dishes, “thoughtfulness” “compassion” and “laughter” and a big, juicy entrée of “good health and happiness for everyone”. The waitress brings you everything you asked for but the entrée. Instead, in front of you on the table, she places a big, fat crap sandwich. And the conversation goes a little something like this:

You: “excuse me, I didn’t order this crap sandwich”

Waitress: “house special. You got it without asking”

You: “but I don’t want a crap sandwich. I want good health and happiness for everyone.”

Waitress: “well, you got a crap sandwich.”

You (getting upset) “well take it back and give me what I asked for instead!”

Waitress points to a sign that says “Absolutely NO substitutions”

You say adamantly: “there is positively no way I am going to be able to choke down this crap sandwich and I think it’s really unfair for you to expect me to”

And the waitress replies “hey, look. You’ve still got love, caring, thoughtfulness, compassion and laughter, so try to appreciate those. Oh, I almost forgot, here’s your condiment tray for the crap sandwich. You also get big overflowing bowls of fear, worry, anger, guilt and resentment. Bon Appetit!”

And so you’re looking around the restaurant, feeling really grumpy about your crap sandwich, and you realize that there are a lot more people with crap sandwiches than you ever thought possible. And from the looks on their faces, none of them ordered them, either. Then you see a couple of tables with really, really big, Dagwood-sized crap sandwiches and you summon the waitress again. “Excuse me, why are their crap sandwiches so big?” And she explains that those people are facing situations even worse than yours. Their kids haven’t responded well to treatment, have had cancer relapses, or worse yet, died. And you start to think maybe your crap sandwich isn’t so bad after all. Maybe you should keep your big mouth shut, choke it down, and be glad when it’s all gone and everyone is well again. And then, right then, your waitress reminds you of one last thing: “Management reserves the right to serve you another, bigger crap sandwich, anytime they want”

That’s a little how I feel right now at Thanksgiving, living in this surreal world of leukemia. I know there are other people who are having a rougher time of things than we are. I know Kendrie is responding well to her chemotherapy. She is in remission and God willing, will stay there. But I am having a very difficult time Giving Thanks for this crap sandwich, and I’m unbelievably resentful that there are more crap sandwiches being made in the kitchen even as I type this, and terrified more than you can possibly know that our family might be due another platter.

I resent that “in remission” doesn’t mean cured. It doesn’t mean anywhere near cured. It means cured for right now. Today. Kendrie could relapse tomorrow; next week; next month; ten years from now. When are we ever supposed to relax? When will this knot in my stomach go away? It’s the last worry on my mind at night and the first thought in my head when I awake each morning.

I resent that for the rest of her (my) life, every time she complains of an ache or a pain or runs a fever, I will fear that the cancer has returned. Prognosis is no where near as good for kids who have relapsed. Dear God, don’t let her relapse.

I resent that I can no longer brush her forehead or cheek without covertly checking for signs of a fever.

I resent that despite my best intentions, my other two kids are getting the short end. There are only so many hours in a day.

I resent that I am so tired, and then feel frustrated with Kendrie for being the source of that, then feel ashamed of my frustration.

I resent that I saw Kellen had bruises on his shins tonight and for a split second, all I could think was “Dear God, not two of them.” It does happen; two kids in one family. What family could endure that? The ones that have to, I guess.

And that’s my point --- to all of you who say, “I don’t know how you do it” or “I don’t think I could do it” Well, of course you could. Do we have any choice? We do it because to do otherwise would be to shortchange Kendrie, and all the kids with cancer, which simply isn’t an option. And I try to do it with a little bit of grace and humor and optimism because quite frankly, if I wrote too many journal entries like this, I would depress the shit out of everyone, myself included. In fact, I don’t know what I hope to accomplish with this one, except maybe trying to explain that underneath the jokes and “looking on the bright side” is a terror so real that sometimes I lie in bed at night and can’t breathe. And I’m not trying to be overly dramatic. I’m trying to be honest. Leukemia kills children. Yes, the “cure” rate is 85 percent (For ALL, which is what Kendrie has. Other kinds have lower rates than that.) That means 15 percent still die up front, and the other 85 percent ONLY have to worry about a relapse for the rest of their life. I’m feeling a little sick to my stomach just typing all this, so maybe I should move on.

There are some things I am truly grateful for:

I am grateful that it looks like a CVS pharmacy exploded in my kitchen. That means there are drugs that can be used in an attempt to cure my child and beat leukemia.

I am grateful Kendrie has tolerated the treatment so well so far. I am grateful for remission.

I am grateful my husband has a good job with good insurance and that so far, finances are not one more worry to add into the rest of this.

I am grateful for the friends and family, both near and far, who have supported us so kindly, and who will read through this awful journal entry and love me anyway.

I am grateful that when Kendrie was diagnosed, my mother was able to drop everything to come to Georgia and be with us. I am grateful that my dad and my sister so willingly held down the fort in her absence.

I am grateful my husband had cancer this spring. Had he not, he wouldn’t have been placed on the “Do Not Deploy” list and he would have been in Sarejavo when Kendrie was diagnosed. As hard as that week was, I am grateful we were able to face it as a family.

I can’t come up with a reason to be grateful that Kendrie is going bald, but I’ll work on it.

I am grateful that my crap sandwich isn’t any bigger than it is.