Hi All,
Due to the fact that I lost my job 2 years ago because of what I now know was MS, I also lost my insurance. I am now on MaineCare, which used to be called Medicaid. Does anyone know if the State run insurances pay for the expensive MS drugs, the ones used to slow or stop the progression? After a recent trip to the emergency room with a serious viral gastroenteritis, I was unable to fill the script for the anti-vomiting drug because the State would not pay. Also, my Dr. wants to up my gabapentin (neurontin) to 1800 mg a day, but the State will not cover that. I hope this is not a sign of what's to come if national health care passes. It has me nervous. As much as I hate needing to be on State insurance, it grieves me that I paid soooooo much in taxes over the last 10 years of my career and so far the Feds keep turning me down for disability. That's a little off the subject, but any feed back anyone could provide about drugs covered or about their SS disability experiences would be appreciated.