Hi, I have been uninterested in any treatments for my MS. My mom has it as well & took copaxon a while back & all it did was make her sick. It definately gave me a bad image of the treatments. I know, I'm babbling. I'm sorry. I have fibromyalgia also, & I take a lot of pain meds as well as nuerotin & flexaril for when the spasms get bad. Sorry, babbling again. This is my 1st step in deciding about treatments. I am getting worse all the time, & it's relly starting to scare me. So I want to 'pick' your brains. Please give me any advice or info you feel might help. Like I said, denial isn't working. I tried it for years. Thank you, tracy
I have problems with urine just leaking out. I'm not talking gushing, but dribbles that are significant enough to know about. What can i do? What should I be doing? I wear a pad, but I just don't feel it coming until I feel the warmth. Any suggestions?