Haven't been able to afford my MS DMD drugs in 7 years
Like most of American's, I live paycheck to paycheck and health insurance has changed greatly over the years.
To make a long story short, I haven't been able to afford any DMD drugs for the last 7+ years. Thank God, my MS is stable.
I take pills for tremors and PAIN (which is my worst symptom). If anyone can give me advice on how I can get the drug companies to give me a major help with this would be great.
FYI, I still work full-time and have SHITTY insurance through my employer, but it is better than nothing at all -- also, I cannot afford further supplemental insurance either. Any help would be appreciated!!!
Does your employer provide workplace accommodations due to your MS?