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Jun 16

Living with Leukemia: Cabin Fever strikes

This is day 23 of my baby, Serenity being diagnosed with and treated for Leukemia.  Day 19 is here.

A lot of the time, Serenity looks like this:

serenityhappy.jpg

A lot of the time, she also looks like this, often just seconds after looking the way she did above:

serenitynothappy.jpg

I’m not sure what set her off in this case, it may have been finding out she has to take meds soon, it may have been that she was in pain, it may have been that someone touched her bed or anything else.  Steroids and a 2 year old that doesn’t quite talk can be an interesting combination, anything will set her off.  As if being 2 isn’t hard enough, she’s got Leukemia and everything that goes with it piled on top – and it makes for a tiring combination as a parent.

Saturday night her zofran (anti-nausea meds) and her steroids met up in just the right combination and she went on an eating binge!  Literally about every 30 minutes she would wake me up and place her food order – eggs, yogurt, chips, popcorn, cheese, cereal, tortilla with peanut butter, bread with ranch – whatever she was craving at the moment.  She ate about half a dozen eggs, 3 cups of yogurt, and tons of chips, popcorn and everything else listed up there, she put me to shame in the eating department!  It then carried on through most of the day today although not quite as intensely. 

After spending a full week in the hospital, then being stuck in the house for 2 weeks with only going to the clinic, we’ve had on onset of Cabin Fever.  Earlier in the week we started venturing out to the back yard to swing.  Then on Friday we decided to have Talysa babysit the other kids while Adria, Serenity and I went to a 12:30 showing of the new Narnia movie.  We knew that since it had been out for a few weeks and it was the middle of the day that the theatre would be mostly empty.  We decided that if we sat in an isolated section of the theatre Serenity should be ok without her mask on – but she had to wear it into the mall and theatre in case anyone got close to her.

serenityatthetheater.jpg

She had quite a bit of fun hanging out with Mom and Dad and is probably the only 2 year old that will sit quietly through a movie.  On Saturday we took the whole family to the Orem Summerfest which is basically a big carnival.  She was able to have a lot of fun hanging out without her mask on, I wanted to enter her into a hot dog eating contest – she would have killed her age group :) While we were walking through the booths at the fair section, all the sudden she started freaking out and screaming something we couldn’t understand.  At first we thought she was hurt so we took her out of the backpack – but then she started pointing behind us and screaming, so we backtracked.  We went one both back where a guy was standing there innocently eating chips from a bag.  She pointed right at him and screamed what we now understood to be “Chips!”.  We actually had some in our day bag and got them out for her – but that guy is LUCKY that she can’t walk! :)

serenityatsummerfest.jpg

We normally use the Kelty backpack for hiking in the mountains, but this time it came in really handy in a different situation.  On a side note, if you have a toddler, I highly recommend the Kelty line of kid packs – they’re awesome and we love them!  Serenity also got to ride on the carousel – it was the only ride she could go on since all the other ones required her to sit down.

serenityoncarousel.jpg

She got a bit tired of it towards the end, and so did I!  So, in contrast to last weekend, which totally sucked, this weekend was a lot more fun, and a lot more normal with being able to get outside and do stuff with the family.  Normal now means lots of new rules though. 

Staying on the fun side of things, while we were at the hospital we were given a list titled “You know you’re the parent of a Cancer Kid when…(1-100)”.  A lot of these won’t make sense to most readers – which is actually number 45 “You don’t have to ask ‘what’s that mean’ to the previous 44 items”.  But for the cancer parents reading, I wanted to list out the ones that already apply to us and for eveyone else, give a glimpse of what’s different for us.

1. You carry a tube of Emla in your purse instead of lipstick.  (We actually carry almost an EMT’s med kit :) )

3. You can sleep anywhere, and anything that reclines more than 15 degrees looks “comfy”

15. Your child asks whats for dinner and you are relieved you don’t have to administer anti-nausea meds

16. Your 2 year old knows where all the medical equipment goes, and how to use it.

17. Your childs first word is a medical term. (Serenity uses several words, and now at least 5 are medical – including ‘port’)

18. You keep a bag packed at all times like you’re 9 1/2 months pregnant.

19. You can eat with one hand while you hold the barf bucket with the other.

20. Your childs bedroom looks like a Toys R Us store.

24. You know medical terminology better than your family practitioner. (for us, it was the ER doc)

29. You have a syringe in your purse (diaper bag) and you’re not diabetic. (I had one in my pocket the other day for some reason)

30. You have more meds in your cupboard than food.  (we have a whole cupboard JUST for meds and equipment)

31. You can read your kids chart better than the nurse.

33. You and your wife get matching stress tattoos.  (I’m working on this one actually)

34. You are teaching your daughter parts of her body and when you point to her chest she says “port”.

57. When the siblings want to know what the child’s counts are so they know whether they can go inside and eat at McDonalds.

58. When your kid asks for a Happy Meal, you immediately turn around and start heading to McDonalds as fast as you can, before the craving wears off (and if they’re on steroids, ask “A Happy Meal or a Super Sized one?”).

79. When you can whip up a 7 course meal in minutes for a child having a steroid pig out – and you’re happy about it!

82. You are totally comfortable in an examination room and don’t think twice about getting items out of the supply drawers.

84. When its time for your 2 year old to have her vitals taken and she lifts her arm and extends her finger without being told, or complaining – all without looking away from her movie.

87. When you have a collection of barf buckets in every room of the house.

91. When you think of anything your child will eat and keep down as a “nutritious meal”, even if it’s cookies and candy.

100. Your child has her own website to keep friends and family updated. :)

The story of Serenity’s battle with Leukemia begins here.

UPDATE: Day 36 is here.

5 comments

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  1. Laura

    Bless her sweet, little heart. She is precious! Hugs to all of you, I am praying for you daily.

  2. amanda

    If we can’t get to the park or (insert much desired destination) we tell “Princess Briar” stories at bedtime. Princess Briar gets to do all the things we would have liked to have done, and, she gets to do it with talking squirrels and the like.

    Hope you can find ways to give Serenity the flights of fancy she craves.

  3. tara

    I am not sure if you all can venture to Disney but i wanted to invite you to the emla website. We’ve built it thinking of families like yours, hoping they would share thier stories and words of advice. Check out the site: http://www.ihateneedles.co.uk. We are giving away a trip to DIsney and some other goodies at the end of summer for the best videos so join in. There are tons other emla users who would appreciate some words of advice.

  4. drt

    Like Laura, we are praying for Serenity daily.

  5. Corri

    that poor child shes so cute

    x

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