Wednesday, June 27, 2012

Camp Hobe and H2O


Earlier last week Taryn was lucky enough to go to Camp Hobe.  It is a camp for kids and teens who either have cancer or have gone though cancer, as well as their siblings. 

They really have it all figured out there... a lot of the counselors are nurses from ICS who volunteer to help.  Leaving Taryn there for 6 hours each day made me a bit nervous, but it would be really nerve wracking to leave your child who either has a central line or is on treatment.  It all made sense once I saw those familiar faces!  The volunteers and counselors make every child feel so special and welcomed.  The kids never want to leave!

Taryn did the day camp on Monday and Tuesday.... and by Tuesday she was ready to pack her pillow to spend the night!
I'm thinking next year I won't be able to convince her she's too little and she will end up doing the week long camp... which every parent says their kids are on cloud nine when they pick them up.

Taryn trying to ignore me when I came to pick her up - the girls after eating popcicles


Taryn with my cancer mom friends children.

Taryn and Isabelle...one of the many buddies she became friends with

Tenley was too young this year, but might be able to do the day camp next year with special permission.  She was having fun running around the dirt trails when we picked Taryn up.  I was bummed because I didn't jump on the opportunity to spend the night at a nearby hotel with all the other cancer moms who I have come to love and adore.  They are a special group of ladies who always have a listening ear, and just "get it."  Next year I'll for sure plan on joining them!



In th meantime while Taryn was having a blast, Tenley was having some pretty nasty diarrhea.  Poor thing had been having it all weekend, and it was still a problem on Monday and Tuesday.  Monday we spent the day at the park with all the other cancer moms and Tenley ran around for a good two hours straight.  It was over 90 degrees out, and I could not get her to drink very much, and sh did not eat anything at all. - which for Tenley is not normal. 

By Wednesday she woke up throwing up and was hardly moving around.  She layed in bed with me all morning and I was so beyond worried about her.  It's hard to go from cancer world to normal world when these kids get sick.  I wanted to know what was wrong, but at the same time I didn't.  One thing was for sure though, it was obvious she did not feel good. 
I took her into our pediatrician and he gave her a normal look over.  He is always so kind with his words and makes sure I understand everything he explains.  The conclusion was she was dehydrated.  After the diarrhea and vomiting, and the day in the sun, she was needing fluids pretty badly.  He had me go home and sit with her while she drank gatorade.  I was going to have to try and get at least 24 ounces in her before the end of the day.  I'm certain we didn't make that goal...

Next day, she woke up in a better mood, but as the day went on she got more tired and just wanted to be held.  Again, another scary sign for me knowing that was one of her symptoms before being diagnosed with Leukemia.  I was a wreck about her that evening... worrying about my instincts, not knowing if I should just give it some time for her to bounce back, or if I needed to rush her to the ER for an IV.

Friday came and I had decided enough was enough... I was going to take her in and get an IV.  She was still acting whiny and tired, and had no appetite.  I couldn't wait any longer.  After her nap, my mom and I took her and got right in.  I think of hospital visits so differently now.  Some might complain about an ER visit and the wait that usually comes along with it... but getting in and out of there in 2 hours was major speedy to me.  Of course as soon as we arrived she was all about eating the bag of goldfish crackers I had in my purse... the ones I had been trying to get her to eat ALL DAY!  And she was more than happy to take sips of apple juice.  Little stinker.

The nurses were so friendly, as always, and I'm sure after examining her could tell she really was just fine... but they took my concerns to heart and went ahead with a litte blood draw followed by an IV of fluid. 

She just lets the nurses do their jobs!

check out all that georgous blonde hair!

K, seriously... Tenley is a total champ.  My mom stepped out of the room worried about seeing Tenley upset when they poked her and got her hand ready.  Tenley didn't flinch, cry, or even blink when they did it.  It was like la-di-da... just a normal day.  Then after 30 minutes of getting that good juice flowing, and a thumbs up on the blood work, we were on our way! 


Ahhhhhhhhhhh.... huge sigh of relief!  I can't even begin to describe the worry this gal gives me when she isn't acting 100%.  I wish so bad I could just think of her as a normal little two year old who of course is going to get sick and have a bug or two go through her system.  I know it's going to take time... and quite a bit of it for me to get past those feelings. 
But I'm happy to say she is most definitely back to 100%
Our summer days are back to running, playing, and swimming... and I'm making sure it's filled wlots of water drinking as well.

 Oh... and here are the twins.  30 weeks! 
The countdown is on!

Our next chapter

Wow we have come a long way. 
This summer is flying by, and even though we are still going through trials, I am grateful every single day that Tenley is healthy and continuing to stay that way. 
Whenever I find myself looking through pictures or reading old blog entires, I can't believe we actually went through all of that. 

Tenley is an amazing fighter.  She still is.  Normal things that should make every child upset do not seem to phase her.

Like slivers for example. 

She always has one or more on her little hands from our back deck.  I didn't even realize that's what they were because she never complained about them.  Taryn on the other hand can't handle the pain of one!  (and neither can I for that matter) 
It makes me sad to think maybe Tenley is just so used to pain she thinks it's a normal part of everyday life.  I guess going through cancer will do that to ya.   

We have done quite a bit this summer....

We ventured to Disneyland and it was such an amazing fun wonderful trip.
We celebrated Taryn's 5th birthday and I have to say her party was a blast.
We've been swimming, eating popcicles, playing at parks, and enjoying new splash pads.
We have all marveled at the rapid growing rate of my pregnant belly.
but really...
We usually spend our days from dawn to dusk in our backyard.

And the best part of this summer for me... We have settled back into a normal routine of life that I so desperately wanted and yearned for.  My family of four is all under the same roof with my role as mother and wife.  I truly find joy in wiping away crumbs from the kitchen counter after little mouths have been fed.  Picking up shoes and toys and crayons and lipglosses that my girls are always leaving trails of.  Nightly routines with bathtime, picking out pajamas, climbing onto Daddy's lap (not me, the girlies) and reading a bedtime story, then reading scriptures and having family prayer.  Rocking Tenley and holding her close.  Robbie tossing Taryn into bed. Giving goodnight kisses and telling my girls I love them sooooo much and to have good dreams.

That has been the best part of summer so far.