Tag: seriousfun children’s network

Swimming to the Moon for Camp

In just about one month, I’ll be stroking my way through the calm waters of the Hiland Chain of Lakes, joining approximately 200 other water lovers for the 2015 Swim to the Moon. Presented by Epic Races, Swim to the Moon is one of Michigan’s premier open-water swims, offering participants the option of swimming a half-mile, 1.2-mile, 5K, or 10K course. More importantly (for me, at least), Swim to the Moon is a fundraiser for North Star Reach, a camp for children with serious health challenges.

I first heard about North Star Reach several years ago at the University of Michigan Pediatric Congenital Heart Patient Reunion, held every other year at Wiard’s Orchards in Ypsilanti. My youngest son, Bryce, is one of the U of M’s heart patients and, coupled with multiple other chronic conditions, was unable to participate in preschool, much less the summer camp his older siblings attended. We added our names to the contact list and began to look forward to the opening of North Star Reach.

In 2013, I decided to participate in Swim to the Moon’s 1.2-mile event, along with my friend Patrick. 2015-07-18 11.48.23Both of us had swum competitively in our youth, Patrick in high school and myself in elementary school. Decades later, we were eager to see how our old sport stacked up. Imagine my delight to find out that North Star Reach was Swim to the Moon’s charity partner! I signed up to become a fundraiser, had a surprisingly good swim, and raised several hundred dollars for North Star Reach.

Swim to the Moon and fundraising for North Star Reach has now become an annual tradition for me. Last year, I swam the 5K to raise funds for North Star Reach. Bryce and I attended the grand opening celebration for camp at the Polo Fields in Ann Arbor and got to meet several of the campers who’ve benefited so much from attending Camp on the Move (camp at other SeriousFun camps in the US; in 2016, North Star Reach will open its doors here in Michigan). We’ve had fun seeing the photos of the facilities being constructed on the grounds of North Star Reach.

I’m very excited to see all the buildings first hand as I once again tackle the 5K on August 23. The starting line is on the shores of Patterson Lake, the waterfront for North Star Reach. I’ve been training regularly, alternating between 50- and 100-yard sprint workouts and long swims in the pool (swam a 5K this past Saturday) to open-water swims, with and without wet suit, at Silver Lake in Pinckney Rec Area. Bryce has been my chief cheerleader; due to a coordination disorder, he cannot swim, so I’ll be swimming for him, to the best of my ability. While I hope to beat last year’s finish time of exactly 2 hours, the swim is not about awards and accolades. It’s about raising funds so that kids like Bryce can experience the summer of a lifetime at North Star Reach.

To learn more about the Swim to the Moon race, visit their website.

To make a donation to Ana’s fundraiser for camp and help her reach her fundraising goal of $1,000, go to https://runsignup.com/anahotaling.

The CEO and Founder of North Star Reach, Doug Armstrong is swimming the 5K for the first time. You can support his efforts to raise $5,000 for his 5K at https://runsignup.com/dougswims, Your support will help sponsor a life-changing camp experience for children with serious medical challenges! Thank you.

Blog post by Ana Hotaling

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!