When I found out about MS fatigue, I felt like I wasn’t crazy because I was always so tired before I was diagnosed & my husband always made me feel so bad about it. I get 8-9+ hours of sleep every night & I’m still so tired. I’ve tried caffeine pills, but it doesn’t help much. I feel like I can deal with the numb hands & feet, tremors, weakness, stiffness & even the vision probs that this lovely disease gives me, but the fatigue is starting to get to me a lot lately. I can feel it when I’m at work now & then I can’t think or I’m not as sharp as I usually am. I eat right, work out like a mad woman, take my vitamins, drink a shit ton of water & I’m still struggling with this awful fatigue. Any advice or recommendations on what else to do? Is it just going to get worse?