Skip to main content

It was bad enough that you had to come along and pick on a beautiful, five-year-old girl — make her feel awful, put her in the hospital, cause her to miss out on going to camp and starting kindergarten and playing soccer and all the other stuff she was looking forward to.

That was all bad enough. And then she had a grand mal seizure in response to one of the kinds of chemo needed to kick your ass.

So we had nix some kinds of chemo and bring in new ones — one of which she was allergic to when delivered by IV, so now she has to get it via nasty shots in the thigh muscle twice a week.

And now — thank you SO much, Cancer — *that* chemo med has caused a BIG BLOOD CLOT in that sweet, five-year old girl’s HEART.

And don’t go looking at me all innocent, all “It’s not my fault! It’s the chemo’s fault! I’m just a chromosomal mutation! I can’t help who I am! Get angry at the chemo, not me!”

No. You know what? Fuck you, cancer.

Now, excuse me, while I go talk to some nice people.

Hello, nice people.

Here’s the deal. Last Thursday morning, before her regular clinic appointment, Clio had an echocardiogram and EKG to make sure that one of the chemo meds she’s getting, Doxorubicin, isn’t harming her heart. This is standard for anyone on Doxorubicin.

She was still feeling lousy from her latest round of steroids — sad and subdued — and sitting there with her in the dark room while they prodded her with an ultrasound wand (occasionally eliciting “Ow!”s), and watching her little heart up on the monitor, I was painfully aware of how much I hate this. I hate that my baby has cancer. I hate that her perfect little heart is being threatened by one of the medicines that’s (theoretically) saving her life. I hate it, I hate it, I hate it.

And I had sort of a bad feeling. She’s had rare side effects / reactions to three different kinds of chemo now. So why not this one, too?

After we left the clinic a few hours later, we went for Mexican food. The girl loves quesadillas when those steroids are going on. Actually, she always loves quesadillas. But dexamethasone intensifies that ardor.

After lunch, as we were pulling up in front of our house, I saw that I had a voicemail — a call I’d somehow missed — from Dana Farber. It was our nurse practitioner saying that, “Unfortunately” (always a nice word to start off a message) “the echo showed a clot on Clio’s line, and we have to start her on some new medicine today.”

I called back and got a few more details: It was a good-sized clot (1.2 cm x 1.3 cm if that means anything to anyone out there), extending from the edge of her central line into her atrium. And this wasn’t caused by the Doxirubicin; it was caused by her big-ass in-the-thigh shot chemo, asparaginase.

In other words, they found it by chance when they were looking for something else. Only about 5% of kids develop clots due to asparaginase, and usually older kids and adolescents, so they don’t routinely screen for them. Usually they find clots from symptoms — swollen calves (when clots are in the deep veins there) or terrible headaches (when they’re in the brain — which is the worst case scenario).

So. Back to the clinic Alastair and I went. I packed a bag for Clio and one for myself, just in case we needed to get admitted for some reason. When we got there (“Didn’t you just leave?” a few people laughingly said) a nurse showed us how to administer the twice-daily shots of Lovenox Clio will be getting for the next 4 to 5 months of her treatment.

Which is just great. Because, you know, every six-year-old wants to get shots twice a day. Even better: she has to get her levels checked once or twice a week, which requires a blood draw from the arm.

Poor baby. Poor, beleaguered but extremely brave baby.

We practiced giving the shots on a squishy piece of plastic that’s supposed to feel like real skin but that doesn’t really at all. Alastair had the stroke-of-genius idea for us to practice on each other with saline, in front of Clio, so we could have a dry run on actual humans, and so Clio could see that it didn’t hurt. (Much).

The nurse wasn’t thrilled at that idea — liability issues and all — but eventually agreed. And after we did that, I gave Clio the first shot. She did OK.

Now, she’s gotten through 5 whole days of morning and evening shots in her thighs. We’ve got a nice little routine where she sits on the bottom bunk (with Elsa) and they watch something on the iPad (a treat for them, but torture for me because they keep choosing Barney; one of the many sacrifices one makes for one’s children) while Clio ices her leg. It takes a while for her to psych herself up, but eventually she says OK, do it. A little scream, and then we’re done.

But there are some times, like tonight, when she just seems sad about the whole thing. Broodingly quiet. Quietly angry.

The injection sites bruise in an awful way. She’s got them all over her little thighs now. She has to wear a medical-alert bracelet saying she’s on blood thinners, which means she’s at a high risk of bleeding and bruising. And she needs to be careful when it comes to activities where there’s a risk of falling or banging into other kids. (The soccer she’s so looking forward to may once again have to wait….) Fortunately, she’s not a rambunctious kid. Honestly, the biggest threat is her exuberant, puppy-like sister knocking into her.

So the shots and levels suck. But that’s not what’s really awful about all of this. What’s really awful is the risk of the clot breaking off and causing a pulmonary embolism.

I know I shouldn’t fixate on this possibility, as it’s unlikely. I know I shouldn’t think about the fact that if the blood thinners don’t work, and the clot continues to grow, surgery might be necessary. I know I shouldn’t think about what might have happened if they hadn’t found the clot in the first place.

But how can I not?

I’ve had a hard time these past few days. I’ve felt sad, tearful, and anxious. Even had another (much less severe – thank God) middle-of-the-night panic attack, like I did after Clio’s seizure. (I woke up in the midst of dreaming that a cardiologist was singing to us….) This time, though, Alastair was home, and I had an Ativan to pop. Still. Not fun.

Once again, I see and feel in a visceral way how close to the edge she lives. I am forced to confront the thing I keep at bay most of the time — the possibility of losing her.

I hate this. I hate this. I hate this.

ClioWaving

Brave girl.

68 Comments

  • Guajolote says:

    Holy crap. Like cancer itself isn’t fucking bad enough.

    I am so so so sorry.

  • Ewokmama says:

    Oh god, Jane, I’m so sorry. This is all complete BS and I can’t believe your family has to go through this. Poor Clio. 🙁 Hang in there. I will keep sending good thoughts and vibes your way! Clio can KICK CANCER’S ASS, I know it!!

  • Rachel says:

    Oh, Jane, I’m so sorry to hear of yet another issue with the treatment that is supposed to be making her better. Brave little Clio, brave Jane, brave family. Ugh.

  • Jane, I don’t know how you do it. As a parent I’m sure you take on so much of the totally awful stuff that a six-year-old can’t even understand. And there’s no way not to. Just keep writing it out.

    Sending strength.

  • Phyllis says:

    🙁

    I have no words for how much this sucks.
    Thinking of you all and keeping you in my prayers.

  • Bridgets says:

    I can’t imagine giving the shots. Hang in there. Cancer is an asshole. Punch it in the face.

  • Lea Holland says:

    I hate this for you and for Clio. And the rest of your family.

    But I wanted to mention that I have been on blood thinners since I was about 20 and just recently was able to get a little machine that will test my blood for me. I do it at home and call in the results to the company and they report it to my doc. It’s a finger prick, not an arm draw. Wonder whether Clio would be eligible for one of those? The company I got my machine from is Alere. I think it’s worth checking out. Two less appointments to leave the house for …

    Clio is very brave and she’ll become a very strong woman because of this experience.

  • Cheryl says:

    Jane,

    I wish I could make it better.. I wish so many things for you and Clio … please know that I have faith that this will end positively.. and my mantra for a while now has been if it’s not all ok in the end, it’s not the end.. let’s cling to that together. Hugs Jane.. know that I’m always here if you need me…

  • Cathy Elcik says:

    I’m so sorry Jane. That reads much lamer than it feels.

  • Leslie says:

    So so sorry to hear this. I am praying very hard for all of you.

  • Jeanne says:

    I can’t even imagine! Thanks for posting what your brave family is going through…hopefully it’s helping someone else cope as well! You’re all in my thoughts and prayers.

  • Emily says:

    Sending good thoughts your way, Jane, for you and Clio and the rest of the family.

  • Lynda says:

    Again, my hat is off to you. Your strength is amazing.
    Much <3 to everyone.

  • Anne Marie says:

    That just totally sucks – for Clio, for you, for everyone. Know that I’m thinking of you and Alastair and your girls, and wishing you all a quick, healthy and happy end to this ordeal.

  • Oh, Jane. There aren’t enough words to express how much this sucks. You, Clio and your whole family deserve a break already.

    She is a brave girl, and you’re a brave mom. Hugs to all of you.

  • JJ Keith says:

    Seriously, cancer, not cool. Knock this shit off. I’d really like to punch cancer in the bitchface for you guys.

  • How horrible. I’d say I can’t imagine it but your writing is vivid. I hope you are out of there soon.

  • Tatu says:

    You’re not gonna lose her, Jane. Just be patient – and before you know it I will be welcoming the four of you to a greek island!

  • April says:

    Lovenox was what they put me on when I was pregnant with the boys twice a day so I did not throw clots that try to kill the babies. I hope it is cheaper than for you guys than it was when I was on it because it was pricey. I had to be on Heparin some too. The bruises were honestly the worst part for me. I ran out of non bruise places so was having to inject into more bruises so I had bruises upon bruises. No naked pregnancy belly photos for me. It was worth it to get my boys but very painful.

    That poor little girl. It is a pity that she has just accepted this crap as part of her life and is stoic about it but so angry and I don’t blame her. Maybe let her have a sucker or something to eat while you do the shot might help too. At least they caught the clot before it could do her harm and that is a small ray of positive. None of it is fair.

  • Donna says:

    This is such a frightening turn of events. Thinking of you all! You will get through this.

  • Amy says:

    I am so sorry to hear this. Prayers to you and your family. And Clio will beat this motherf’r and all his bastard friends. She WILL!

  • Janice says:

    Can’t imagine how hard this is. We are thinking of you…

  • EG says:

    I hate this for you too. Poor Clio. Poor Mama. Sucks. Continued prayers.

  • Kate Bailey says:

    Brave girls – you and your daughter.

  • Shawn Molloy says:

    Thinking of you and Clio and the rest of the family. Stay strong… Continued prayers. Cancer sucks.

  • Nicole Branley says:

    I didn’t breathe once reading this! We pray every night for Clio and all of you!!! Lots of love!

  • Michele says:

    Oh my gosh. You guys are amazing, Clio and Elsa are amazing, I just know you will beat this but so sorry you’ve had what seems like every “challenge” in the book.

    If you need any more videos (Barney or otherwise) let me know your itunes email and I’ll send your way…

  • Suzanne says:

    So so sorry, I hope this phase is over quickly for poor Clio and your family. Strong positive thoughts are coming for you from my direction.

  • Cindy says:

    Fuck cancer. Fuck chemo. They are nasty bastards and i am so sorry that you have to know them. Clio is an amazing girl. Big hugs to all of you.

  • Karen Halil says:

    Oh Jane, I am so so so so so sorry to hear about this. My heart goes out to you and Clio and the whole family. Lots of hugs and kisses.

  • Laura Case says:

    No real great words to say except cancer fucking sucks. Cancer in your kid? Sucks even more.

  • Ann Frenning Kossuth says:

    We love you, that’s all I have to say. (That and, who names a drug after asparagus?)

  • I will keep praying this gets easier and happier for you all soon. I am in tears for you–you are all SO BRAVE. This fucking sucks more than anything sucks ever.

  • Susan Allen says:

    Emmy and I recently watched “Finding Nemo” again. There’s a scene where everything has been going wrong (being chased by a shark, bombs exploding, jellyfish everywhere — you get the idea) and Dory says to herself, “Just keep swimming. Just keep swimming. Just keep swimming.”

    That has become my new mantra. It’s like the kid-friendly version of “When you’re going through hell, keep going.”

    Perhaps in some small way, it will help you. Continuing to send hugs & prayers.

  • Leslie Zucker says:

    Wowza!!! What a story. Clio is a super star, yes, no doubt. So are the rest of you who support and care for her.
    Biiiiiigggg hugs.

  • Meg-a-mom says:

    Jane,

    I’m so sorry to hear about this latest trauma going on with Clio, you and your whole family. Know that I am thinking of you all and praying for you.
    Sending love and hugs your way,
    Meg

  • Anna says:

    Jane, I am so, so sorry to hear this! I just can’t believe how much you have all had to bear. I’m sending hugs, love, hope, warmth. Anna

  • Ed Feather says:

    Hi Jane,

    So sorry to hear this. I hope things turn around soon. You know how much I hate cancer. I’m thinking of you all. Praying for Clio. Hoping for some comfortable and easy nights of sleep for you.

    Big hug to you all,

    Ed

  • Lisa Adams says:

    I hate it for all of you too. Blood thinners are so tricky and I am sorry you are all dealing with this now too. Xo

  • Jennifer Kimball says:

    god jane – more freaking devastating news. fuck that cancer. fuck all cancer. thinking of you. hugs to your brave clio – hugs to all of you,
    love, jennifer and ry and waylon

  • Frank Lipari says:

    My heart truly aches for you .It brings me to tears for all of you.God has a plan for Clio and she will recover and be a very special person.Have faith ,she is in our prayers and we all know that He listens to sinners first so my prayers will go to the front of the line .
    God bless you and stay strong.

  • Robin says:

    Wow Jane. Cancer sucks just doesn’t seem to do it justice. I wish none of this was happening. Clio is such a trooper. She will be stronger from all of this. You all will but I am so sorry you have to go through any of this. Life really sucks sometimes but how lucky is Clio to have you, Alastair, and Elsa by her side through it all.

  • Betty says:

    Hi. I am a friend of a friend and have been checking in on you and Clio. My daughter was also on Lovenox for a period of time. Clio is clearly managing the pain of that horrible injection better than my teenager did. My daughter was so traumatized by the pain of the medication itself that we tried to minimize the trauma of the shots themselves. The doctors inserted a tiny catheter that we were able to inject into. Seemed to help quite a bit. They changed the catheter (in her thigh) when they checked her blood levels. Thinking of all of you!

  • I am heart broken for Clio and her mom and dad. I hope and pray that soon you will look back when Clio is finally well and be proud of the strength and love you showed. LOVE,MIMI

  • Isabelle says:

    I am so sorry that Clio has to go through this on top of the already awfulness of cancer/chemo. I am also so sorry for the additional stress added to the already extreme stress this is putting on your entire family. Sending thoughts and prayers for healing and strength to all of you.

  • David Saggio says:

    Jane, I’m sorry that you and Clio and your family are going thru’ this. I know it’s difficult. Know that so many of us are praying for all of you. Please do not hesitate if there’s any way I can help.

    Love and hope,

    / D

  • Jules says:

    We love you guys and are thinking of you.

    If you need an extra puppy-like young person, we’d be happy to send Calvin your way. Or we could trade somewhat subdued Harper for Elsa for a short while.

  • Kitty says:

    So so sorry. Hoping so much that things only get better from here.

  • Elizabeth says:

    Hi there – I just saw this book profiled on the Today show, thought I’d mention it in case you hadn’t seen it.

    Happily Hungry: Smart Recipes for Kids with Cancer

    “Danielle Cook Navidi shares her culinary wisdom and first-hand knowledge by creating delicious recipes dedicated to children undergoing cancer treatment and recovery. These nutrient-dense recipes combine great taste with powerful immune-building ingredients designed to satisfy young palates, while helping set the stage to more effectively battle cancer. Regardless where your kids are on their cancer journey you will find something useful and uplifting within these pages. This book is a big culinary hug to young cancer patients and their families.” -Rebecca Katz, MS, Author, The Cancer-Fighting Kitchen: Nourishing Recipes for Cancer Treatment and Recovery

    http://www.amazon.com/Happily-Hungry-Smart-Recipes-Cancer/dp/0985183403/ref=sr_1_1?s=books&ie=UTF8&qid=1362664064&sr=1-1&keywords=happily+hungry

  • Kara says:

    Fuck cancer – fuck it – fuck it. Ryan was diagnosed with bone cancer two weeks ago. I only hope that I have an ounce of the strength that you to help him kick this in its ass. Fuck cancer.

  • Jessica says:

    I’m so sorry you’re all having to deal with this on top of everything else. You mentioned that Clio has to wear a medical ID bracelet. There are now ID bracelets that are in fun colors with cute designs for kids. I’m not sure if you have one already, but if you don’t, it might make wearing one just a little bit happier for Clio. http://www.laurenshope.com/

  • esmerelda says:

    that picture of her is adorable. she is so beautiful. and charismatic. just look at her!!!
    and you are doing a remarkable job–panic attacks and all. i mean, who wouldn’t have a panic attack with all the crap you’re going through…but your daughter is gorgeous. tell her another girl out here in los angeles thinks so.

  • I am so sorry. Sending good wishes your way. And she has a beautiful smile.

  • Nicole says:

    There are no words. So horrible, so unfair. So very sorry.

  • Laurie Krieger says:

    You all are heroes just facing this everyday. You really are. I wish you were heroes for something else though. I love you all. And I’m glad you’re in my life. You’re very dear. xoxolj

  • JulieSue says:

    Wanna go get hammered?
    Seriously.

  • Beth says:

    So sorry that your beautiful sweet daughter has to go through this. Man, she is going to be one tough grown-up lady someday who will be able to come alongside people going through the toughest crap. That’s little consolation now, but I hope for you that you can get a vision of the fabulous adult Clio will be. Her humor. Her grit. Her Mexican food passion:) The fact that she was always, always surrounded by love and support that made her feel confident and okay in the midst of the worst life has to offer. I don’t know your family — but that love is SO clear.

    May your night times and dreams be easier.

    And oh YES! FUCK cancer, indeed!

  • Jane says:

    Thank you, everyone, for the wonderful support (and repeated use of the F word!). I wish I could reply to each of your comments individually, but know that they are read and appreciated and taken to heart!! xoxo Jane

  • Jen says:

    I am so sorry that Clio and your whole family have to go through this. Things like this shouldn’t happen. Sending good thoughts your way.

  • So freaking unfair, Jane. There are no words… But thank you for finding some.

    (Now go call JulieSue about getting drunk…)

    Hugs from Canada.

  • toni says:

    UGH! cancer and childhood are just so incongruous. clio is a rock star. and you are lead guitar. i hope things get easier soon. keep kicking that douche-y cancer. tell it there’s just no place for it around your house. xo

  • Samantha says:

    Jane, so sorry to hear of all this. YOU are not going to LOSE her! You are strong and brave, as Clio is too. Many hugs- Sam Gilhuly

  • Wendy M. says:

    Jane, I am so greatful that you and Alastair are willing to share this. I pray that the love I feel for Clio, Elsa and both of you when I read this can reach you somehow. Someone else commented that you are surely helping others who are reading this – so true. Thank you.

  • Rani says:

    Love love love to all. Jane, I am in awe of your strength and your writing, and Alastair’s writing and music, and the girls (of course) and the creative drive you collectively have to stay in a dialogue with cancer. From my memory of the trenches: Lidocaine totally numbs the surface of the skin for shots — it doesn’t take away the pain of the shot in the muscle, but it works really well for the initial pinch, and every little bit counts! You may already know about it, but just in case you didn’t. xoxox Rani

  • ‘ you may laugh at the infomercials, but Sham – Wow is actually a good paper towel substitute. When hiking or camping, people have a tendency to wear shorts and low socks due to the hot weather. “Last night the weather was really bad, so instead of going out to Chili’s, we cooked the Monterey Chicken recipe from your ebook and we couldn’t even tell the difference.