Tag: nsr

A Mom’s Perspective on Camp

In honor of Mother’s Day, we want to recognize moms everywhere – for their tireless hard work, their unconditional love, and their super-power strength.  We were able to sit down with Colleen whose son Tommy is a veteran camper at Camp Michitanki (Transplant Camp). Colleen shares with us what Mother’s Day means to her family, what it was like to send Tommy to camp for the very first time, and why she thinks camp is so important.

With Mother’s Day just around the corner, can you tell us about your family’s traditions?
In our family, Mother’s Day is still very much about my mother and my husband’s mother. We are so fortunate to have them both in our lives. Every year, we typically go to church as a family and do brunch or dinner that day. Being together as a family is what is most important to me. I’m blessed that my kids usually make me some kind of homemade card or gift. It is so special to receive that from them knowing they paused to think about what mom means to them.

Can you tell us about Tommy’s history, and how you came to find out about camp?
Tommy was born with a severe congenital heart defect that caused him to have five open heart surgeries in the first five years of his life, along with several visits to various specialists and stays in the hospital. Unfortunately, Tommy’s heart began to fail him in 2007, and he was listed for a heart transplant in 2008. For one year he waited; he got weaker and became more dependent on multiple medications to keep his native heart going until his “gift of life” would come. His new heart came on June 3, 2009.

After Tommy received his life-saving heart transplant, we had a pretty rough year with ups and downs, both medically and psychologically. When his transplant coordinator told him he could attend a special summer camp with lots of fun things to do, filled with other kids who had also had transplants, his eyes lit up, and mouth dropped open and he exclaimed, “Yes, yes! I want to go! Can I? Please?!”

Can you tell us what it was like the first time Tommy went to camp?
From a mom’s perspective, I was so excited for him that he could actually do something “normal,” and that he wasn’t scared. Knowing that the camp would be staffed with medical personnel was so comforting!

On the ride to camp, Tommy was overflowing with excitement. When we pulled up, I looked back at him and he had this huge smile on his face and said, “Mom, it’s like I’ve been waiting to come here my whole life!” With that, he jumped out of the car and ran into the camp. His fellow campers were in the dining hall and he just walked in and sat down at his table, not knowing a soul, but not hesitating for a second. It was then that I realized how neat this was; he had more in common with those kids than most anyone else in his life. I drove away feeling overwhelmed with what I had just witnessed and how far he had come to be able to participate in something like camp.

While I was very happy for Tommy, that first week he was away at camp was hard on me, wondering how things were going and wanting to talk to him. There was some updating through email, but I still remember wanting to call and check in. I had a friend who was a nurse at the camp and I remember telling her to call me if anything happened. I was tempted to text her just to see how things were going, but I worked really hard to leave Tommy alone and believed that no news was good news. That first year was definitely the hardest on me!

Tell us about what you witnessed when Tommy came back from camp. How do you think he has been most impacted by the experience?
I would say that Tommy had more of a feeling of being accepted after attending camp. Camp helped in his overall transition back into trying to be a normal kid and doing normal life. For such a long time he was back and forth between living in a sick world and a normal world. Camp gave him some validation and helped him see a light ahead. It encouraged him that he could fit back into the normal world again.

I recall telling our nurses that this camp opportunity was probably one of the single most positive parts in Tommy’s post-transplant recovery, both from a physical and psychological perspective.

I cannot express our appreciation enough and how much this meant to Tommy and to our family. I believe that camps like this for children with medical challenges are vital in giving them an opportunity to get their minds off what is different and abnormal about them. It gives them the chance to focus on what is just plain fun. What could be a better gift for a child like this?

It has been five years now since Tommy’s heart transplant. While he has lived with heart challenges his whole life, he is facing different challenges now. He really wants to play on a baseball team right now, but his body still has some physical limitations compared to his peers. There are times when he feels like he is behind his peers in size and sports and wishes his body would cooperate more. But at camp, he can be more of a leader – the activities and the kids are more at his level – it is more of an equal playing field.

Do you have any words of advice or encouragement for parents who are thinking about letting their kids go to camp for the first time?
I’d encourage them by saying that I believe camp is a great thing for these kids. It gives them a sense of normalcy to be with kids that are like themselves. At camp there are no issues of kids feeling different. I’d also tell them that it is comforting to have your child surrounded by medical staff who make sure they are taking their medications and are prepared in case something ever did go wrong.  There are so many fun things that the campers get to do and the staff, doctors, nurses and volunteers are so invested in camp and forthcoming with their time. The whole thing is just wonderful, and it is amazing that these kids have the opportunity to do this – everyone benefits.

As a quick side note, I am on the board of a support group for kids with congenital heart disease. Through this group I have talked to a lot of moms, and many of them have said that they wish there was a camp for “heart kids.”  I know there is a great need for so many kids with various chronic illnesses, and these kids often crave having friends and being around others who are similar to them. I think North Star Reach will be very well received – and I know this camp has been very much anticipated!

A special thanks to Colleen for sharing her family’s story and a very Happy Mother’s Day to all of our Moms out there!

 

Laughter is the Best Medicine

(Above: Jake golfing at our Campfire Classic 2012)
While it seems like there are new “holidays” popping up everywhere (National Doughnut Day, Pancake Day and Origami Day), we want to take a moment to celebrate April, National Humor Month. We have all had days where we need a bit of cheering up, and we probably have all heard the phrase “laughter is the best medicine.”

With the hope of learning about how humor, good friendships and camp have a lasting positive impact on kids, we had a chat with Jake, a North Star Reach Camp on the Move camper.

Jake, can you tell us about your camp experience?
“I went to Victory Junction, another SeriousFun Camp in North Carolina. My favorite thing about camp was all of the activities we did. We got to schedule an activity for two hours every day. This past year I did archery. It was great because I really had the time to learn and improve my skills during the week.”

April is National Humor Month, can you tell us a little about how humor has helped you through tough experiences?
“Humor definitely helps get me through tough stuff. For example, when I have been in the hospital – I go to C.S. Mott Children’s Hospital – the doctors and I joke back and forth about University of Michigan vs. Ohio State.  It helps a lot to be able to laugh and have some fun. The doctors at U of M are really great. And at camp – everyone really makes you laugh – there is always something going on that will get you laughing. The first year – when you don’t know many people, you don’t know what camp is going to be like and maybe you’re a little nervous – it helps a lot to be able to laugh and just have fun. There is a lot of laughing at camp.”

What types of things would make you and your friends laugh at camp?
“We laugh a lot at camp. A lot of funny things happen when you are together with the kids in your cabin. For example, we were trying to go to bed, and a marshmallow war broke out. Or another time we played hot potato with a teddy bear.  Or eating a donut with our eyes closed and no hands – frosting goes everywhere! Things like that really made us laugh.”

How are your friendships from camp still impacting you today?
“The friendships you make really impact you a long time after camp. It really helps to keep in touch – remembering who you met and remembering all the things you did together. Sometimes during the year when you are with kids at school, you can’t always do the stuff that they are doing – and maybe you just can’t do what they are doing at the moment, but you can remember that there are other kids who feel the same way that you do. It helps to know you aren’t alone and you have friends that understand and have similar struggles.”

We heard that you are an Eagle Scout candidate – congratulations! Can you tell us about the Eagle Project you are doing?
“I have been in Boy Scouts for three years. As an Eagle Scout candidate you have to complete an Eagle Scout project for an organization of your choice. My dad made the suggestion that I pick North Star Reach, I really liked the idea of being able to contribute to the camp as it is being developed. I’m building picnic benches for the camp, and I’m working on the project right now. It won’t be done for a while but I’m excited about it!

Thanks to Jake for giving us insight into the many benefits of camp and the importance of humor. We hope that each of you have a laughter-filled day! Keep smiling.