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I try to get me seizure medication covers and i am told no. some employees from molina called me saying fighting to try and get my medication covered because i am disabled with no income.

And they see this medication is covered for other people but not me. Its a medication i need for my M.S and seizures but i am told its not covered and i can not get reimbursed for the cost of my medication. all other seizure medications i have been on caused more seizures or other issues. my doctor wants me off copaxone because it causes me bad skin issues Note i have records from methodist hospital from 2004 sent to the government saying i can not work.

it is 2017 and i am still fighting the same case note they also reduce the help from my snap when i thought if i have no income it cant be reduced. My township got reduced also yet i am told i have to pay all of that back so why reduce it?It seems as the more progress i make to gain a quality of life i have a right to as a american the more effort is put towards making my fight harder. i feel if illinois would of took my word when i was 24 saying how cannabis helps my seizures we would not be the broke state we are now..But then i notice what my city peoria illinois in number 1 in. not only do i battle with my disabilities i battle with the hands that claim they came to help.

i have been told to suck it up and work for 16 years.

the years i was able to work was because i was smoking illegal things at work. can not find a cure without having compassion

Product or Service Mentioned: Molina Healthcare Medical Claim.

Reason of review: Poor customer service.

I liked: Helped me find out it me against the world.

I didn't like: Was told other get help but not i.

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Please email me as going though SAME frustration and problems I too have Molina and am under the care of OSF neuro institute in peoria IL we need to chat I think can help each other at least stay ALIVE!! Vmiller92@yahoo.com

Long Beach, California, United States #1356772
Molina Healthcare Verified Representative

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