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UPDATED: Wed, 02/27/2008 - 10:05am

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Adapting Plans to Summer Camp

Summer is a unique time in a child’s life – a time to relax, make friends, and have fun! It’s also a time of adventure and trying new opportunities. For children with seizures and their parents, it may also be a time filled with uncertainty and worry. Unfortunately, these worries and fears may keep children from participating in summer activities or camps, just when they need these programs the most! Camps can provide benefits that actually improve a child's ability to cope with and manage their seizures. For example camps can help build one's self-confidence, develop peer support and increase independence.

This preparedness module is intended to help parents think about the benefits of camp for their children, while recognizing inherent risks and concerns. The content is designed to help you consider issues unique to a child with seizures as you choose and evaluate summer camps. Use this also while preparing your child and camp staff to manage seizures safely and appropriately.

Parents of children preparing for camp should also read the other modules, especially Responding to Seizures and Developing Preparedness Plans. The resources and plans found in these sections can easily be applied to camp preparedness! Then visit My Resource Kit and look at all the forms you can use to communicate medical information to camp staff.

We hope that being prepared will help people be part of the process and take charge of their lives. These modules don’t solve everything or even address everything that a person with seizures or their parents may need to know, but hopefully it will give you enough information and skills to get started.

In this section, you will find information on:


Continue to Choosing a Summer Camp

Topic Editor: Steven C. Schachter, MD and Patricia O. Shafer, RN, MN.
Last Reviewed:5/25/07


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What is the most important issue that you'd like your doctor to talk with you about?

Possible side effects of medicines
28% (40 votes)
How people respond to medicines differently
8% (11 votes)
Different medication options
14% (20 votes)
Support groups and epilepsy websites
8% (12 votes)
Social services for help with jobs, financial help and transportation
17% (25 votes)
Other treatments like surgery
9% (13 votes)
I don't need more information from my doctor
8% (12 votes)
Other
8% (11 votes)
Total votes: 144

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