Tag Archives: hospital

Wee Ghosties

I haven’t mentioned this to anybody yet, because I don’t want to sound crazier then I already am, paranoid. OK, I’m kind of nervous about this next sentence, but here is goes. I think Gage sees dead people.

Dead serious, ***no pun intended***. But do you remember the time in the hospital when Gage almost died? Well, I think that since he almost “crossed over” he was told it was not his time, and to go back. Thank you baby jeebus he listened too. I am not writing this to be funny, I swear. I truly and honestly believe with everything that I have, that Gage has become that creepy kid from The Sixth Sense.

He holds these long conversations, with absolutely no one. Conversations, with wild hand gestures and long pauses that make you believe someone or something is talking back to him. His voice rises and falls in excitement and anger. He offers his “friends” his sippy or snacks. He doesn’t talk to his living friends the same way he talks to these “friends” his whole demeanor changes, he is not shy with them or hesitant in any way. I think he feels safe with them, like a kindred spirit or something

Oddly enough non of this bothers me either. If he does have friends that are no longer in this realm, good for him. Good friends are hard to come by now a days, take ‘em where you can get ‘em Kid.

They Deserve a Chance…

So one of the many things I remember from the hospital, one that I would like to forget is when we would go down for surgery, ct scans, or ultra sounds the nurses would sit my adult sized ass in a CHILD SIZED WHEEL CHAIR! which totally is not what this post is about, but I just remembered this one time when trying to shimmy my way out I actually got stuck and they had to have someone help me out. Because my ass was not meant to squeeze into a pediatric wheel chair. UGH- embarrassing memories, thanks blog post.

Anywho, the other thing I remember most about those trips in the hospital was I would be in the mini wheel chair, and Gagers would be on my lap waving to everybody we passed. I wouldn’t at look anybody we passed in the eye ever, because I hated their pitying looks it was bad enough hearing the “oh, that’s so sad and poor baby.” Really? You totally think that is appropriate to say when I can hear you? It’s not comforting to me. In fact I want to scream “yes, this is fucking sad. But would you like to know what’s worse? Pediatric cancer research sucks.”

Did you know? The federal government has made only very modest investments in research through the National Cancer Institute (NCI). For every six research dollars per patient with AIDS and every one research dollar per patient with breast cancer, a child with cancer receives only 30 cents. To us, and the families of the 35 children diagnosed with cancer each day, it is clear that much more needs to be done to ensure access to treatment and the opportunity to fully recover.

30 freaking cents, that is all Gage is worth to them. It truly is enough to make me want to march to Capitol Hill and shove this blog down their throats. To make them see pictures of Gage make them look at his face, hear his laugh, show them that he is one amazing kid. Make them love him like I do. I’d tell them to get their heads out of their asses and do something about childhood cancer research funding. Because every baby deserves the chance to grow old.

Ethan Deserves a Chance

Caleb Deserves a Chance

Gage Deserves a Chance

And so do the 12,500 children and adolescents in the U.S. diagnosed with pediatric cancer each year.

Jovita

I did something very indulgent yesterday. I hired somebody off of craigslist to come to my house and clean up Gagers room, because even though we have been in this house for… OMG, three months as of today. The most I had gotten done in there was getting his large furniture put together, clothes and toys were always on the floor. Unpacked boxes, hangers, empty target bags I hide from the Hubs so he doesn’t see how much I actually buy ***target is like mom crack, totally addicting*** and a hospital overnight bag. Just in case. But on the floor it all was, taunting me.

Everyday I would go in Gagers room and then walk right back out again, promising myself and the Hubs that I would clean it tomorrow. Promise. Finally after three months of midnight diaper changes and almost spraining my ankle over all the crap on the floor, I took action and her name is Jovita. She is an angel in a denim jumpsuit and knock off Sketcher Shape ups. It took her two and a half hours and forty dollars but it was more than worth it for me, seriously it was like a weight was lifted off my shoulders. I swear Jovita is just like the miracle worker the rest of my day was totally amazing, my hair looked super shiny, my makeup looked flawless, and I fit into my skinny jeans!

OK, that last part was a total lie. My skinny jeans don’t fit and I don’t see them fitting for a long time. I’d like to blame the girl scouts for that. Them and their stupid cookies…thin mints sandwiched between dark double chocolate chip galato. Yumm-O.

Honestly though, sometimes a person just needs to do what is right for them. Jovita was exactly what I needed. Firstly, because I am super lazy much to the Hubs dismay and secondly, because I finally got to put Gagers new race track carpet on the floor in his room instead of rolled up against a the wall. He totally loves it.

Wordless Wednesday: We Be Rollin’


“We be rollin’”

Leukemia. The New Normal

I haven’t been here in a few days. Sorry. It all just got to be a little over whelming, people have been calling and emailing me, questioning me about what I am writing. Am I sure I want to be putting so much of our lives out their for the world to see?

The answer? Yes, I want to write about it. I want you to know that even though Gage is in remission, I will forever live in fear of relapse. And that even though it has almost been seven months since Gage was diagnosed I still have daily anxiety and at least a couple of times a week I have nightmares. To add to my nightmare Gage has been having nightmares. I rush to his room because his screams are so scary and heartbreaking. I wonder if he remembers like I remember. I hug him and kiss him, and whisper in his ear, that it will all be all right, mommy is here and I love you so much. He always falls back asleep almost instantly, into that peaceful baby sleep, curled up on his belly with his diapered butt sticking up in the air. I usually will stay and pat his back, rub his chubby little cheeks, rub the curls on top of his head. Wishing our lives were normal.

31-40

YOU KNOW YOU’RE THE PARENT OF A KID WITH CANCER WHEN…

30. You have more meds in your cupboard than food
31. You can read your son’s chart better than his nurse
32. You look like you’re tan but it’s really Betadine stains
33. You and your hubby get matching stress tattoos for fun
34. You start teaching your daughter the parts of her body, and you point to her chest, and she says that’s her port
35. None of the security guards on the pediatric floor ask for your ID anymore, and you’re on first-name basis with the operating room staff
36. Medical students ask to borrow your notes
37. Your toddler refuses to sit on Santa’s lap because he’s too germy from all the other kids
38. You wrap presents and packages with medical tape
39. Your main source of nutrition comes from aspirin
40. Your child is more familiar with CT scan & bone scan pictures than the portrait studio!!!

We Just Needed a Drink

When Gage was first in the hospital, I would not leave the hospital; seriously you could not get me to leave. I was afraid of what could happen if I was gone, and not able to be there with him. I didn’t trust anybody for me not to be there, not the family, not the nurses and sadly enough not even the Hubs. But gradually after about a month I started to go out with the Hubs once Gage was asleep we would tell the nurses we were going to Wendy’s when really we would head out to this little dive bar in the parking lot next door to the hospital. We’d sit silently not talking to one another, he drinking the house special beer and me a bloody Mary. Lost in our thoughts and emotions.

As a married couple the Hubs and I needed those nights at the bar, just to sit and be alone outside of the hospital, where nobody knew who we were and what Gage was going through. I mean we slept, ate, showered, lived at the hospital for like three months last year; and when we slept it was in separate cots. Not very romantic or conducive for a successful relationship, I am going to be completely honest with you people, because if I can’t be honest with 10,000 of my closest friends, then what am I doing here?

I wasn’t sure if my marriage would survive Gages treatment. I blamed the Hubs for not being with me when Gage was diagnosed, because it was a Monday afternoon he shouldn’t be at work. He should have been shopping at IKEA with me, then at the doctor’s office getting the most devastating of my life. Instead he was making a living for his family to live on, how dare he! I resented the fact that he went to work for those first few weeks, even when he wanted to be with us, and I demanded he go work. Gage didn’t need both of us at the hospital, going crazy with anxiety and fear; go work. I didn’t see that he was slowly killing himself because he was staying at the hospital, not sleeping and then getting up at 5am to work and not get back to our room until 9pm that night. All I saw was he got to leave, he had a “normal” life outside of the hospital; and I resented him for it. I pushed him to leave, and yet I resented it!

We got into mad, crazy yelling fight in the hospital. When I say yelling, I mean whispering loudly so the nurses can’t hear us, and quickly shutting up as soon as a nurse walked in to give Gage medication and change his diaper. Oiy- those poor nurses, the awkwardness of it all, I get so embarrassed just thinking about. None of those nurses get paid well enough to have been subjected to some of the looks we shot at each other those three months in the hospital. Those rooms echo, too! So I am sure they heard every word we said. No matter how quiet we tried to be. I said the most hateful things to him, while we were in the hospital. Things I wish I could take back, and never have said. Things I don’t think I have ever apologized for, things to this day I wont bring up to the Hubs because I am so ashamed of myself.

This was the man I married, the same guy I promised to love and honor, in sickness and health, good times and bad yada yada yada. And the first real hardship in our married life together and I freak the ‘eff out, on the one person who was giving me the most strength from anybody. Who for the last seven years has let me get my way in every argument, never told me no I couldn’t do something or buy an absolutely unnecessary item, I sure as hell didn’t need. He has always been there for me, during the good, the bad and the ugly loving me and supporting me; and I couldn’t do the same for him.

The bottom line is, this has been the hardest six months of my life as a mother and more importantly as a wife. But I love my Husband and if Gage can fight cancer and survive then we can fight to make our marriage work. I think coming to that realization has been what has saved us. Six months later our marriage is still on shaky ground, but we are slowly building our family back up, this time stronger than ever. I don’t know a lot, but the one thing I do know is I love him more and more each day.

 

Wordless Wednesday: This Is Spinal Tap

Ragin’ Gage

Gage started delayed intensification last Thursday. It was a long time in coming, six months in fact. Some days, I never thought we’d get to this point, and now that we are here I am scared of all the complications that can happen. I take his temperature like every hour just to make sure he doesn’t have some random fever. I call is doctors because his cough is back, and oh my gosh is that a rumble in his chest, did the cough move to his lungs? I have an overnight bag packed just in case we have to go to the hospital at the last moment.

The Delayed Intensification “road map” looks like this:

This is what Gage is going to be subjected to in the up coming weeks, he should also be receiving Pegasparaginase (PEG), which is two shots in his legs during week one. But he had the allergic reaction to the last shots of PEG he received, which in turn caused him to get pancreatitis and the ulcers on his pancreas that landed us in the hospital for three weeks before Christmas. So thank you Baby Jeebus, no more PEG shots!

Since starting delayed intensification, Gage has been so cranky. He is on seven days of dexamethasone, and seven days off for a couple of weeks and not only is he getting adorably chubby, since he is eating like a little piggy but he is getting not so adorably bitchy, as well.

His nick name from the hospital is back, we call him Ragin’ Gage. He screams and fusses all day long and as soon as Daddy comes home, he is all sunshine and lolly-pops. I have  actually called the Hubs at work, in tears begging him to come home, because there is nothing I can do to fix Gages tantrums. I know it’s the medicines fault that he is acting this way, but after seven hours of screaming fits, all rationalization is out the window.  Though the highlight to being at delayed intensification is once we are done with this round of chemotherapy we head into maintenance, which is kind of like the light at the end of the tunnel.


This is what Gage looked like last time he was on the dexamethasone. So cute and chubby! (sorry the picture is so blurry it was taken on my iPhone on zoom)

Ready For Anything

I don’t think that I will ever breath easy again. The panic attacks are back with a vengeance and I can’t control them. I don’t see things that have happened but things that could happen. Since Gage was diagnosed back in August of last year, we have had to be prepared for the worst. And by worst I mean I have his funeral planned out.  I know nobody wants to hear this but it’s truly been my way of coping with his leukemia. Sitting nervously in the waiting room at three o’clock in the morning not sure if he was going to make it out of surgery, I prepared myself. What Gage would wear, what the Hubs and I would wear, the colors. I knew then that no matter what since Gages life was such a joy and celebration to us, his funeral would be the same. A party in his honor, a celebration of his life.

It’s with a cold detachment that, when I think of it all, almost like it’s not happening to me. Like it’s not my baby. We all tend to think because he is doing so well right now, that he will continue to do well. Which is what I am begging for, because I truly do not know what I would do, if anything were to happen to him. But that can all change at the drop of a hat, he can end up sick and in the hospital, or worse. His life is just so unpredictable right now, as a family we don’t take a single day of Gage for granted. Which means he is going to be so spoiled because we can’t seem to say no to him, or take away his bottle.