Saturday, February 19, 2011

February 16th Wednesday: A typical day of radiation

Following are some pictures from Charlotte's typical morning over at the Tom Baker Cancer center over at the Foothills hospital. We get all bundled up to drive all the way over there (its about a 5 minute drive). I feel like I should warn you that there are some pictures of her under anaesthetic and with her plastic helmet clamping her to the table. This is daily routine for us, but it might be a bit of a surprise for some people to see. 
Here I am all cozied up with Daddy, I get to ride in the elevator... going down to the basement.

Watching tv with Daddy while the nurses get ready for us.

I get to pick out a sticker for on my countdown sheet.
 
I sit nice and still and watch as they put in the anaesthetic.

Off to sleep on Daddy's lap.
Going through the radiation door.
 
The wonderful nurses, techs and anaesthesiologists who take care of me during treatment.


They are careful to keep my oxygen at a good level while I am moved into position.

Getting everything set up, I can't be more than 2mm from my original position!

This big machine rotates around to find the four angles that my radiation needs to come from.


Here it is moving around, the bed also swing around on the floor. Everyone has to leave the room, but they keep a close watch on the cameras.


All done! Now they can take off my mask and special helmet. 

Waking up on Daddy's shoulder. Some days are easier than others, sometimes I need to have a good scream to get it all out of my system. Then its time to get dressed and head back to the Ronald McDonald house. Mommy makes me my favourite Kraft Dinner for breakfast, sometimes I'm still too grumpy to eat.

Friday, February 18, 2011

February 7th Monday: Bingo Fun at RMD

Monday night bingo, everyone has fun when Brynn gets to call the numbers. I know I have written about bingo before, I just thought I would share some pictures of one of our games. There were not too many kids that night so the girls made a huge haul... more stuff to bring home!
Our beautiful bingo caller Brynn! (and her mom)

Yolanda is focused!
 
Charlotte has a full blackedout card... only 6 numbers have been called, this girl is good!

The prizes, we keep one eye on our bingo sheets while the other scopes out the cart.
  Here is Rob opening his birthday gift from the girls.I took Yolanda shopping and she helped me pick out a shirt, then the girls coloured up a few pictures. We didn't really do much to celebrate, anything that marks the passing of time is difficult for us to celebrate right now. We are getting closer and closer to the one year mark since Charlotte was diagnosed.
Charlotte is very pleased with her picture.
I am gearing up to do a post with pictures from radiation, thought I better put something fun up here too.

Tuesday, February 08, 2011

February 8th Tuesday: Prayer request

Charlotte is having a tough time right now. And therefore we all are. She is so tired and grumpy. Most importantly she is not eating, anything, voluntarily. We are trying everything we can think of, old favourites, fruits, new sweets and treats but she is just not interested in eating. Our healthy diet has taken a back seat. On someone who only weighed 11.4 kgs at the start of treatment there is not a lot of room for weight loss. Within two weeks Charlotte’s weight is down to 10kg, this is the number that in the past our doctors said they would want to see a feeding tube. There are a couple of factors here; one is that she is having radiation and full anaesthetic every weekday- this makes her very tired, the second is that she is on a chemo drug that knocks out her appetite. Rob and I have resorted to forcing in what Yolanda calls “Magic Juice,” basically a thick green sludge of blended spinach, carrots, and apples. We draw up a 10ml syringe every 15 to 20 minutes and pin her writhing little body down. She cries and puts up a fuss, some ends up squirted on the ceiling, most goes down with much gagging... and we do it again in 15 minutes. Once she has gotten a few of these in she seems to perk up a bit and not fuss so much. We can see the effects of getting food in immediately, the days we get more in the better disposition she has too.


We just found out today that her chemo is going to be cycled- take it for 21 days, off for 7. Today was day two of being off the drug; hopefully we will see her perk up for a few days.
We have two things that we would appreciate your prayers for.

The first is if you would please keep Charlotte in prayer at 8:00 every weekday morning, this is the time that she has her radiation. We are praying that God will heal her through this treatment. Some specifics would be that radiation does its job, succeeds in killing any trace of tumour. That anaesthesia goes well each morning- that we will not have to up her dose should her body become used to the amounts used. (Some days she comes out happier than others, some days we can sneak in her eating a cup of yogurt while she is waking up- before she is protesting.) Also pray that Gods protection will be over her and any side effects will be nonexistent, both short-term and long term. That damage to other areas of her brain will be negligible.

The second is for her appetite. That she will be given the strength to start eating again, without any drugs intervention. That she will not be too tired to eat, and that she will not be so tired from not eating. She needs her strength for her treatments and for that she needs to eat. This would take a huge burden off of Rob and me, not having to chase her down with syringes all day.

Thank you all so much for your prayers and encouragements. We appreciate hearing that we are in your prayers- facebook, emails, comments on the blog- these messages are all cherished.