We are at 462 now. We are trying to get to 500. Please continue sharing and sign if you havent already. This is so important to my family. Epilepsy truly is much more than just a seizure disorder. The SSA must make more in depth consideration for epilepsy as a disability. They denied Shanes initial disability claim bc he has not had seizures frequently enough but no consideration taken for the side effects the AEDS he takes to control his seizures. The side effects of all his seizure medications coupled with cognitive impairment caused by seizures is what has caused him to no longer be able to work. Why is he being punished for taking meds to control the seizures? He either has to control them and live with the terrible side effects on a daily basis or not take them and have seizures every day. It is 100% unfair and we cannot continue to lose everything we have while we wait on the SSA to consider these things. Please support us in this endeavor we must do something to help people suffering like this. Thank you.
Posted on: Sat, 15 Nov 2014 06:55:44 +0000
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