Showing posts with label childhood cancer. Show all posts
Showing posts with label childhood cancer. Show all posts

Sunday, August 26, 2018

Camp





One of the things that I always loved about working in the theatre is that everyone has the same goal. Yes, each departments specific goals might seem different... but in the end, everyone wants a successful production. Each persons definition of success is slightly different, but everyone has the goal of a successful production.

Camp isn't much different.
Our goal is to create an amazing week of camp. How we do that as individuals may be different, but that is our goal.

This year at camp had challenges, like every week of camp does.

But every-time I took a step back and watched these campers I was thrilled.

I was thrilled to see a camper return to camp and try many things that he had not tried the year before.
Last year this camper was always at each activity, but he was hesitant to really get involved. this year it was like a different person has arrived at camp. At our first campfire he jumped RIGHT in at every song. When it came times to go to the giant swing and the high ropes course, he tackled every challenge. To see the look on his mother's face when she picked him up told me that ... yes, we had succeeded in a successful week of camp for this camper. This camper challenged himself, pushed himself to do things he had never tried before. More importantly, he felt safe enough to take those challenges with us.


When the bus arrived at camp and the campers came barreling out the door one camper stood out to me. She certainly wasn't sure about all of us singing and dancing in our witch costumes. One of my favorite moments of camp was walking past her bunk and hearing giggling. She was sitting on her bed putting make-up on another camper. After dinner they were giglingg again trying to figure out how to use an eyelash curler.

We had 2 campers with mobility issues. Both of them used crutches to get around. one would think these would be the campers that needed the most assistance. Aside from buggy rides..... these two campers were some of our most independant campers of the group. During our water fight I was with one of these girls. I assumed she would need extra assistance. For your information, if you ever encounter this camper with water balloon, you will lose.... she WILL get you with the balloon.


Our other camper was no different. She wanted to go down the slip and slide. This was something she needed assistance with. So she sat down and two counselors made sure she could get down the slip and slide. this same camper was up and dancing more than others at our all camp dance.

Sitting back and watching our campers just have fun and enjoy themselves was THE best part of the week.

Seeing older campers take initiative to help with younger campers made my heart explode.

Hearing campers choose their names for when they are counselors helps me see the camp of the future.

I have so many other thoughts, and I may find time to write them down in the coming weeks. right now I am trying to get used to a quiet house, no slamming doors, not wearing a name badge, responding to my actual name, and not having all of my meals made for me.





Oh, in case you are curious.... washing cottage cheese out of your hair IS as gross as it sounds.

Thursday, October 20, 2011

Introducing Pat Pats Hats!!

Introducing Pat Pats Hats!!!!!

Okay, so in yesterdays post I mentioned knitting when I found out my nephew was sick. Well, here it goes. . .

On Aug. 30th my nephew was brought to Yale New Haven Children's Hospital Emergency Room. For a few days he had been complaining of a "boo boo " on his head and he was vomiting. The Doctor told my sister that it was likely a stomach bug when the symptoms presented, unfortunately, he wasn't getting better. The doctor told my sister to take him to the ER.

The Doctors int he ER were amazing, and immediately took Patrick into an MRI (he will never be an astronaut, he now hates space ships). The MRI revealed a mass on the back of Patrick's brain.

The next day, Patrick went into surgery to remove 3 brain tumors. We were informed that these tumors were malignant, and Patrick had Medulloblastoma.

We know that Patrick, after everything, will be okay. He will be enduring 6 months of Chemo to ensure that there are no lingering cancer cells, but in the end this little man is going to grow up and hopefully never remember this experience.

As a knitter, the first thing that I did when I found out about Patrick's impending surgery, I knit a hat. Then i found out about chemo, I knit another one. What else was I supposed to do, I'm a knitter and my nephew is bald. It's the PERFECT excuse to stash dive and cast on.

I decided that rather than only knitting for Patrick,I could knit for others (also, the stress of the situation made me forget just how big Patrick has gotten in his almost 3 years, and one of the hats was CLEARLY meant for a preemie). This got me thinking. . . . What if I asked people to donate hats to the hospital?

Thus Pat Pat's Hats was born

On January 6th 2012 (a few weeks after Patrick's 3rd birthday) we will be donating hats to Yale New Haven Children's Hospital. I am looking for hats of all shapes and sizes. . the softer the better. These hats will be donated to the hospital so that the children receiving treatment can take a hat home if they need one.

How much does it take to knit one hat? barely a skein?maybe a day or two?I know that you can do it, and these kids are sure to appreciate it.

I need to personally thank nutmegknitter and the yarn harlot who have helped spread the word about this project.

I hope to be able to donate hats every year, so keep those needles and hooks moving!!!

if you would like more details about the project you can check out our facebook page, or you can email me at
patpats.hats at gmail.com

Also, the Ravelry Group has been created
http://www.ravelry.com/groups/pat-pats-hats