Hey all. I'm new here and am seeking some advice. I was diagnoised with Lyme around 7 years ago or so. It was late in the illness and I had started to have seziures. When they took me to the ER they found rashes all over my body. The most recent seziure I had was about a month ago. Is it possible that this is something that is a side effect of us not catching the Lyme sooner? I also get extreme migraines, have arthritis, and suffer with major depression. Has anyone heard of these being side effects that remain chronic after the illness has been treated? Drs are starting to think that I'm just a pill pusher and want pills when all I really want is to live a normal life where I can actually climb flights of stairs like a normal 22 year old. Any suggestions????
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