I have never been in this position before, I jsut lost my disability and I do not know what to do. I think it is amazing that they cut off someone on thousands of dollars a year in Epilepsy medicine, to not give any guidance on what to do when you lost it.
I have been on disability since 2005 conditions come and go, ulcerative colitis flares up now and leaves later. I do not know what to do for insurance or to pay for my doctors etc. I cannot even afford to leave my current epilepsy doctor if he doesnt take whatever other plan I have.
They do not even tell me how or why they think my condition have gotten better, which makes it all the more frustrating. All I know is my conditions have not changed in the long term.