Matrix Health Group

Spring 2007 | Are You Ready? / Tammy Davenport

For many of us, camp brings back memories of new friends, warm nights around a campfire, arts & crafts, and days full of laughter and fun activities. Why should that be any different for our children? It shouldn’t! That is why the forefathers of our bleeding disorder community decided to create their own camps. Hemophilia camp is a place filled with fun and laughter, offering a carefree camp experience that everyone deserves while maintaining the precautions demanded by a bleeding disorder.

Nearly every state has a camp specifically for people with bleeding disorders. The few treatment centers or chapters that do not will often arrange to transport the camper to the nearest camp location. Typically, camps last from five to seven days and are staffed by knowledgeable personnel, treatment center staff, industry professionals, and “veteran” hemophilia campers.

Activities may vary from state to state. Most will include activities such as arts and crafts, fishing, rope or challenge courses, swimming, horseback riding, and sports of all kinds. With so much fun, there is also time to learn. Education about living with a bleeding disorder is a primary focus at camp. Children can usually begin attending camp around the age of seven, a great age to begin to learn more about hemophilia and von Willebrand’s Disease. One of the goals of camp is to provide an opportunity to learn to self-infuse. Great role models and positive peer pressure is very effective at accomplishing this. At camp, one can often find an entire room lined with infusion stations occupied by a child learning to stick himself. Many times you will see the old pros (by that I mean teenagers) working with the little guys and celebrating in their successes. Learning to self-infuse is a monumental accomplishment and every stick is a big deal.

While most camps have primarily been geared for the seven to sixteen-year-old child with the bleeding disorder, many camps now allow siblings as well. Some states have weekend retreats for women with bleeding disorders and camp or outdoor excursions for the men. Many also have family weekend camps so that fun, friendship, and support is available for all members of the family.

Sending your child off for the first time is a daunting experience for anyone. As parents, it seems to go against every fiber of our being to put our little ones on a bus full of strangers. From the time my son started camp, about 6 years ago, I had a realization: I reasoned that with his HTC staff at camp, my son was probably safer there than at home with me. While I missed him terribly the week he was gone, my knowledge of the level of care he had available kept me sane. Keep this in mind when your child goes off to camp. It may help you too! The week will be over before you realize it. When the bus rolls back up, much to your dismay, you will find out he didn’t miss you nearly as much as you missed him. Kind of a let down after the week you had, but you will be happy at how content and excited he is and how much he is looking forward to next year.

Now that we have gone over how to keep your sanity, let’s talk about how to prepare for camp. It is recommended to keep your child on their regular medications for the week of camp. Medications for conditions such as ADD/ADHD should be continued. In addition to packing these medications, you will need to include enough factor and supplies for a week of prophylaxis doses plus two extra doses. If your child has a mild bleeding disorder and is treated on-demand, it is recommended to send no less than two doses. If your child is severe and is treated on-demand, it is recommended to send a dose for every day he or she will be gone.

Along with medical supplies, following is a list of items that your child will need. Keep in mind that specific camps will have other required items depending on the activities offered and on the location and weather of the camp. They will provide you with a checklist.

General Supply List:
• Sleeping bag or sheets and a blanket
• Pillow
• 3 towels (2 for bathing, 1 for swimming)
• 3 wash cloths
• Soap, shampoo
• Toothbrush/toothpaste
• Comb
• 2 pairs of sneakers (they will get dirty)
• Socks and underwear for every day, plus a couple of extras
• Clothes for every day, plus extras
• Swimsuit
• Sandals (I recommend something water friendly)
• 2 sets of sleep clothes
• Flashlight
• Camera
• Playing cards

Most camps do not encourage electronic devices such as Ipods, gameboys, cell phones, etc. Do not send money, there will be no need for it. Any additional questions should be directed to your local chapter or treatment center.

Camp is a wonderful experience for our children. It is a rare chance for them to be with a group of children who experience the same struggles they do. Camp fosters a sense of independence that nothing else can duplicate. The kids are given an opportunity to realize that they are not different from anyone else. In addition, the time at camp is a rare opportunity for the parents. After the first year or two of sending our child away, we can actually enjoy the week without our child as we learn not to worry the entire time. For many, it allows a chance to spend some extra time with our non-bleeding disorder children. Some parents even use this week to sneak away for their own little vacation. While I may not be ready to jump on a cruise ship as soon as my son gets on the bus, I have learned that he will be just fine with out me. He will be home in five days, completely exhausted, happy, and maybe even a little smelly. Yet, he is already ready to turn around and go back in a heartbeat! You and your child will truly enjoy their week at camp!

Attending Hemophilia camp has a huge impact on our children. It gives them a sense of independence and gives them tools to deal with everyday struggles. Hemophilia camp gives our kids memories for a lifetime and relationships that last just as long.

Most treatment centers will begin taking camp registrations in March, April, or May depending when the camp will take place. Many camps fill up very quickly. Call your Hemophilia Treatment Center and ask to be placed on their camp mailing list. When you get your registration form, be prompt about turning it in. This will help the Treatment Centers and the Camp Committee plan appropriately. If you would like help locating the camp nearest you, feel free to call Tammy Davenport directly at 936-628-3263 or e-mail her at tdavenport73@aol.com.


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