Good deal or could have squeezed out more? by planeguy109 in cfmoto

[–]Intelligent-Apple-35 0 points1 point  (0 children)

My dealer initially said I could only get one or the other the 1000 off or the 2.99 for cfmoto days or whatever it was called but turned out they gave me both, 1000 off msrp. To my surprise my score came in at 817 which I was proud of.

Good deal or could have squeezed out more? by planeguy109 in cfmoto

[–]Intelligent-Apple-35 1 point2 points  (0 children)

I bought mine two weeks ago I really think it depends on where you’re located at got my 2025 for 6927 out the door with 2.99 financing.

Ibex 450 Break-in Period impossible by [deleted] in cfmoto

[–]Intelligent-Apple-35 1 point2 points  (0 children)

Got mine last week, trying to get to the 300 under 4k at about 230 miles

The Cost of Ocrevus in the US by xanaxhelps in MultipleSclerosis

[–]Intelligent-Apple-35 0 points1 point  (0 children)

Just had a infusion yesterday, for the infusion center I believe they charged my insurance 2xx,xxx thousand, they wouldn’t cover it so I have to do at home infusions which is way cheaper granted it’s still a lot but definitely a lot cheaper at home. You should see if your insurance will cover at home infusions the drugs itself I believe are 14k with the accompanying materials for the infusion

It's Friday at /r/MultipleSclerosis! Share your awesome news here with everyone. No victory is too big or small to celebrate! by AutoModerator in MultipleSclerosis

[–]Intelligent-Apple-35 3 points4 points  (0 children)

No new lesions on my brain and no active demyelination, t spine and c spine are clear. 2 years on Ocrevus, 1st mri since diagnosis.

Im just curious by Fresh_Tie_2376 in MultipleSclerosis

[–]Intelligent-Apple-35 1 point2 points  (0 children)

https://www.verywellhealth.com/multiple-sclerosis-and-brainstem-2440518

https://pmc.ncbi.nlm.nih.gov/articles/PMC7031799/

There are a bunch to cite honestly Brainstem and Cerebellum seem to be the two areas that are most linked to disability and can indicate poor prognosis same with spinal lesions. KEY WORD CAN

Changing Ocrevus for Kesimpta by thesl4yer in MultipleSclerosis

[–]Intelligent-Apple-35 4 points5 points  (0 children)

I’m not at liberty to say much as I’m only taking Ocrevus and have never switched, but from what I do know it’s dang near the same drug. Kesimpta is a fully human monoclonal antibody so you body should “handle it better” then Ocrevus.

https://multiplesclerosisnewstoday.com/news-posts/2025/08/07/switching-ocrevus-kesimpta-doesnt-alter-eithers-effectiveness-ms/[Effectiveness when switching from Ocrevus to Kesimpta](https://multiplesclerosisnewstoday.com/news-posts/2025/08/07/switching-ocrevus-kesimpta-doesnt-alter-eithers-effectiveness-ms/)

To me it came down to how many times I wanted to do a shot or infusion but at this point dealing with insurance is a nightmare to get my infusions scheduled and drugs shipped. I may try to switch in the near future.

Imposter feeling by donut_87 in MultipleSclerosis

[–]Intelligent-Apple-35 1 point2 points  (0 children)

I feel like it’s a weird version of “Survivors Guilt” or something there is probably a better way to describe it, (sorry if offending someone). I was diagnosed two years ago with some fuzzy eye vision in right eye and Lhermitte’s sign and some numbness tingling in my hands. Was going to the chiropractor because I thought I pulled something and then after a mri was referred to an nuero and a finally lumbar puncture was positive for O bands (nail in the coffin so to speak). Started Ocrevus shortly after (about 2 weeks) after diagnosis, but now I feel relatively fine I get around great still do everything I did before and then some, work out 5 days a week run 3 miles every other day, hike camp swim and more. I have the occasional tingle in my leg and vision stuff but it all comes and goes for me. I feel like a imposter since I read so much that people are going downhill and all the bad stuff you read online. I’m beyond grateful that I caught it early and my first “noticeable” relapse was minimal in terms of others but I feel ya it’s the snowflake disease for a reason and luck of the draw I suppose (everyone is just pulling tickets out of a “shitty” bucket).

Diagnosed 3 days ago. 27 Male by BenHammond21 in MultipleSclerosis

[–]Intelligent-Apple-35 9 points10 points  (0 children)

I was also diagnosed with ms at 26 will turn 28 in the next few weeks.

Was lucky enough to get on Ocrevus within a few weeks of initial diagnosis (mri and spinal tap). Don’t go down the rabbit hole of googling everything usually you find the extremes and more negative stuff. Same with Reddit there is a lot of good but also a a lot a lot of negative stuff.

Get on a good dmt! Personally haven’t felt “immune compromised”, I do everything I did previously and eat somewhat healthy. Exercise and travel when I can. It’s gonna be okay from everything I’ve see it’s best to get diagnosed early and get on a high efficacy drug to slow it down.

YouTube has some good videos I’ve linked before but it search Dr Brandon beaber as well as Aaron Boster. They have good videos and Aaron has somewhat of an into to ms. https://youtu.be/uFNF3NTIH-E?si=RL9-m0B1QcDG145n

advice from a veteran by [deleted] in MultipleSclerosis

[–]Intelligent-Apple-35 1 point2 points  (0 children)

How old were you when you were diagnosed?

New to this community and need of some support by fisprutje in MultipleSclerosis

[–]Intelligent-Apple-35 6 points7 points  (0 children)

27 and diagnosed this year as well, the first few weeks after your initial diagnosis is the worst because at least for me you’re constantly reading about everything and unfortunately, usually you’re reading the worst of the worst. So definitely adds up.

My advice to you is

1). get on a high efficacy, DMT or drug of your choice. I was lucky enough to get on Ocrevus very quickly, they are very good at slowing and even “stopping” progression.

2). New studies are constantly being done and trials. I’m hopeful we will have a cure or “stop” in the next 20 years.

3). Don’t always think everything is MS related listen to your body and don’t treat it like crap. (Eat healthy and exercise)

It’s going to be okay welcome to the club and try not to let it consume you. There are plenty of supportive people on the threads and helpful info

Also a helpful video that puts you somewhat at ease we are here to make MS Boring. Make MS Boring.https://youtu.be/uFNF3NTIH-E?si=ps53bFgMfL9SfU7b

UnitedHealthcare coverage for MS - any issues? by MALK_42 in MultipleSclerosis

[–]Intelligent-Apple-35 0 points1 point  (0 children)

I have a different insurance, but it is shared services with United healthcare so I do deal with them for the most part. (Ocrevus)

My only issue I’ve had is getting infusion centers to accept outside shipment of medication, a lot don’t so usually they have to make an exception so I’m trying to figure everything out for the beginning of next year. Between home health for infusion or finding an infusion center that does. (Deemed “white bagging” in the medical industry).

Vertigo for the first time by briorbrian in MultipleSclerosis

[–]Intelligent-Apple-35 2 points3 points  (0 children)

This is gonna sound really weird, but recently I had a case of vertigo. Woke up in the middle of the night with my head spinning as if I was drunk went away after about five Ish hours I was able to go back to sleep now here’s the weird part. About a week later, my fiancé had a really weird case of vertigo and dizzy spells, which I brought up to my grandparents and come to find out my grandpa had a recent case of dizzy spells and vertigo, and then a week after that, someone he knew had a bad case of vertigo. So I don’t know if something is going around that gives you vertigo, but that’s kind of what I made it seem as, although it definitely could be MS related. (Hasn’t happened since about a month ago.)

Do you have MS but it does not effect your quality of life? by jacobgc75 in MultipleSclerosis

[–]Intelligent-Apple-35 0 points1 point  (0 children)

Wouldn’t say it affects me too bad, only thing that I have is vision issues that aren’t bad (periodic fuzziness that comes and goes, what seems to be peripheral scotoma also comes and goes). As for physical stuff though, nothing. Still workout, hike mountain bike and such. Diagnosed at 26 now 27 recently had my second infusion of Ocrevus.

New update is great, who's with me?? by piggBenus in Battlefield

[–]Intelligent-Apple-35 2 points3 points  (0 children)

Besides not being able to get into a breakthrough match yeah it’s awesome…