multiple sclerosis
"I started Copaxone about six months ago.  I had been diagnosed with MS 10 years ago but didn't take anything for it but a giant dose of B vitamins daily.  Last December, I had my first real flare up and it was awful.  The nuero told me I had no choice now, but to take something.  So after researching with my husband, I decided on Copaxone.  Do not give up if you just started and are having itchy bumps and stinging when injecting.  It really did get better for me.  I did have one incident of the chest tightness and anxiety which lasted about three minutes but only once.  When I read the side effects from other drugs (Flu like symptoms and hallucinations!) I picked this drug.  So far, so good.  Neuro thinks I am not progressing at this point."