Welcome to the E Club! For the last four years I thought I had epilepsy. I was about to have brain surgery, and then in the last several months it was discovered that I was misdiagnosed with epilepsy and have an odd form of migraines....but anyway I am still very much involved in Epilepsy research, the epilepsy community, and am currently applying to medical school so that I can devout my life to epilepsy and neurology, so I may not have epilepsy anymore but I well versed in the subject. If you haven't had a generalized seizure or blacked out for a significant period of time then you should be o.k. to ride...since I don't know your diagnosis exactly and I am not a doctor, just make sure you discuss it with your doctor and see how your react to your drugs before doing anything to outrageous. I would given him/her a phone call and talk to him about your concerns and ask if you need to take a break from some sports for a while. You may have to switch drugs several times, and it could take a few years (yes years) to find the right combination of drugs. Don't be afraid to speak up if the drug you are on impairs your ability to ride or function (makes you sleepy, dizzy). There are other drugs, and your doctor will be happy to work with you. A good neurologist will take into consideration your lifestyle, etc. when helping you choose a drug.

Also, it's VERY IMPORTANT that you get a MEDICAL ALERT bracelet, that way if you do seize while riding people will know what's going on and the paramedics can get easy access to your records. For a few extra dollars you can get one that looks like regular jewelry. If you just started having these spells and they seem to be varying in form, for the next few months while you adjust to new medications I would stay away from bike paths near high speed traffic that way if you fall, you're not likely to get hit by a car. And always wear a helmet!!! Most people with epilepsy lead normal lives. Since you were just diagnosed, I would suggest you hook up with the National Epilepsy Foundation. They can link you to a support group. The whole diagnosis can be almost more overwhelming than the symptoms themselves sometimes, especially because it's a very misunderstood condition in society. Don't worry though, your not alone. Feel free to PM me if you have any questions.