I know mine is here almost always. Different levels of fatigue but I usually start the day already tired. Everyone is different, even though we all have the same disease.

I was told my RRMS lapsed into SPMS & I'm getting weaker all the time...but, I am not giving up! My will is stronger than ever, my physical strength is weaker but I can still work out in the MS Gym & surprise myself@ what I can STILL do! HOPE LIVES!🧡💯🙏

Try to remember you are the same person as you were the day before a doctor told you it looks like it's MS. There are things you can do once you know about the fatigue. For example, trying short breaks from everything for like 5-10 minutes every couple of hours really helped me. For you, your diagnosis of MS is newer with a ton of things your noticing now. You'll figure out what they are and then start to see what might help you. You get to explore now!!

Yes fatigue can come with walking to much, driving to much, stress so you must always be careful

@A MyMSTeam Member I still have symptoms I just haven't had any changes in my MRIs since 2018. I have my yearly MRI on the 16th but won't see my neurologist until Aug something. I'm not sure it's in remission since I haven't seen my neurologist for a year. I did see her PA but we didn't discuss that. I guess I don't think about it that much.

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