Retired great grandmother, age 67, diagnosed in 1993 after many years of symptoms being misdiagnosed as "stress." MRI and symptoms finally gave my problems a name...MS. My symptoms are invisible so I get a lot of comments like, "but you look so good." Only tell those who have a need to know. Started Copaxone in 2004 because of horrible fatigue, numbness in right foot, hand, face. No numbness now but continued with bladder issues and now take Detrol which took care of that. Depression is a problem along with fatigue. Frustrated with neuro who doesn't seem to care about my quality of life.