Hi everyone. I was diagnosed 3 years ago with MS. I first went on Gilenya, which made me so foggy I couldn’t drive or work. Next I tried Copaxone. Got used to giving myself shots but after an MRI my neurologist said she thought it wasn’t helping. So now I’m in my 3rd month of Tecfidera and managing this med well. December I get another MRI. I have experienced lots of bladder problem and have learned to manage these well, although it’s annoying. I wanted to know if anyone has experienced problems with their bowels? Yuck. I know it’s not a pretty subject. Sometimes I feel like I don’t have the muscle power to empty my bowels all the way. It’s not constipation. Just a feeling of not enough strength to do what I need. Anyone else having these issues. Thank you so much.
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