I have found epilepsy to be a very lonely experience as no one can really relate to all the ups and downs of it, all the side effects and the feeling that your falling behind every one else in life. Is this just me or have any other epileptics out there felt the same way?
#epilepsy
I had the same thing when I got diagnosed with epilepsy last year. One thing that I found helped me out a lot was just journaling everyday with a pen and paper. It also help me me keep better track of side effects.
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