I am unable to work due to my seizures. I am a person who has always worked and this is very hard for me. I never ask for help because I believe I can do it on my own, but it has gotten my breaking point. I am applying for SS disability benefits, but don't know how to express in words about my seizures. I guess one reason is because I don't like to complain and this makes me feel like I'm a complainer. Could someone please help me put into words how seizures are preventing me from holding down a full time job. From not being able to drive, to grand mal seizures, to everyday myotonic jerks, to side effects of meds, and even my depression. How do I put that into words so that the disability reviewers can understand?? Please help! Thanks for listening!