In 2012 I couldn’t walk properly, like not being able to lift my foot. It looked like a silly walk. My PPMS has moved up my left leg to my hip since 2012. Also it’s affected my bowel and bladder, got to get to the loo fast which is not possible with MS lol. I know it’s in my brain but I keep saying the MS has taken my knee or my hip, foot drop since the beginning. It’s weird to know that something is eating a part of my brain.