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UPDATED: Thu, 11/01/2007 - 2:44pm

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Choosing the right summer camp

There are three basic kinds of camps for children and youths with epilepsy. Most of them are co-ed, meaning that while campers are segregated by gender during sleeping hours, they commingle for most programs and meals. Some epilepsy foundations, such as Southern California, also offer weekend camps for the entire family.

Epilepsy Exclusive Camps are only for children with epilepsy. An advantage of these camps is that children and teens with seizure disorders find themselves in a more sensitive peer group than at mainstream camps. In an epilepsy exclusive camp, the child or teen can meet and interact with others with seizure disorders without fear of being ostracized. Medical supervision is usually high.

Mainstream Epilepsy Camps are sessions held at a regular summer camp. Some of the campers have epilepsy. Most do not. The advantage of these camps, which are growing in popularity, is that they allow children and teens with epilepsy to meet and interact with others with epilepsy and also allow them to achieve a sense of "normalcy" while attending camp sessions with others who do not have seizure disorders. Medical supervision is usually by a 24-hour nurse with a neurologist on call and camp counselors who have received basic training in seizure safety.

Camps for Those with Disabilities often accept children and teens with epilepsy. They also accommodate children with other disabilities, like severe asthma, neurological dysfunctions, and mobility limitations. This can be the best option for children and teens with severe seizure disorders as medical supervision in these camps is usually high.

The appropriate camp should be determined by you, your child, and a medical professional. Check out any camp with your local Epilepsy Foundation affiliate, which also may have information on financial assistance if necessary.


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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
26% (30 votes)
How people respond to medicines differently
8% (9 votes)
Different medication options
14% (16 votes)
Support groups and epilepsy websites
8% (9 votes)
Social services for help with jobs, financial help and transportation
17% (20 votes)
Other treatments like surgery
10% (11 votes)
I don't need more information from my doctor
10% (11 votes)
Other
8% (9 votes)
Total votes: 115

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