What have you found to be the most beneficial since being on it?
Now, you know, I will be the 1st one to tell you that ALL DMTS are to slow the progression down! They do not heal us.😒 😂
Some of you have said that you have had good things.😊 Please share! 🤗💕🌠
My balance and gait are better. I also noticed that my mood is better as well. Perhaps that was a side effect of being on the prior DMT. My neuro hasn't seen any disease progression with regards to lesions, but I haven't had any new lesions or flare ups since being diagnosed. 
Well. It was a long list of benefits and I guess I’ll have to revisit this again when I’m back on it. I don’t think I could pick just one. Hot tubs? Man, I sure did miss those!
Not feeling like crap all day every day?
A healing cord lesion? That may be the most beneficial, actually, technically, but was it Ocrveus alone or a combination of lifestyle choices and my genetics 🤔
Who cares! I still don’t know anyone else who has had a MRI like that.
I dunno. Maybe next time I’ll get a super power or something.
I have had zero improvements that I can attribute to Ocrevus. I didn’t expect any either. I’m coming up on Ocrevus infusion #5. Keep in mind that I’m on the “mature” side and our body’s ability to repair itself naturally declines with age. However, I have improved my balance somewhat through hard work in PT and yoga the last few months.
I’m about to have another MRI so hopefully it still shows stability. Fingers crossed!
I have noticed improvement since I began the Ocrevus infusions. I,too, didn’t expect anything but I do have a bit more energy and feel more confident that I won’t fall down 10 times a day. My last MRI hadn’t changed. I am happy that I decided to try one last thing!
I just had my 2nd full dose last week. I am doing great. Almost all of my MS symptoms are gone except for a little numbness in my toes. The CogFog is gone, the heat sensitivity is gone - I was able to be outside and garden this summer without a relapse. The muscle spasms are gone along with the restless leg syndrome at night. I still have some cognitive problems with recall and comprehension when someone is talking to me. The fatigue is also gone. I feel really good most of the time.
I think I missed your good news, so a late congrats to you on the escape from your MS symptoms!! 🎉🙌🏻👏
my balance and gait has improved. my spasm has relaxed.I.m less fatigued.
earlier this year I had to go from a cane ( used from 2.016-Jan 2019) to a walker (Jan 2109 - present) because my balance has improved I have been practicing walking without the walker and cane at pt and home
I can feel my feet and legs; balance still iffy, but overall, much better and waiting for my 4th dose in December and looking forward to it!
use to have to use a cane all the time and if i squatted down took for ever to get back up ...only use if going to walk for a long time ...can be out in the heat longer with out any problems ..worked in the yard a lot this summer couldn't before if warm at all ...my dizziness is nothing compared to what it use to be ...it was just terrible i still can have it if i have gotten over heated really bad....don't fall as much as i did before ...it just has really helped in so many things ...i know it isn't to fix it but has brought back things i couldn't do before ..fatigue isn't as bad as before ...when i was first on Avonex i would sleep eat sleep eat ...it was so terrible ..i have a very full figure now ..it is hard to get it off though...i use to think 130 lbs was fat now i wish that was what i weighed now ...anyway i do feel it has done wonders....
Hi I’m on Tysabri and it’s sorted out progression and no new lesions but I still have my symptoms- crap balance and overactive bladder! So I don’t know if it’s the answer or not! The bladder is being sorted out, I’ve got single use catheters and medication - so I will see how I get on xxxx
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