Multiple Sclerosis Vlog: Must we treat MS? What about Mild MS?

In this video I answer a viewer's question about if it's ok to NOT treat mild MS, or if it's ok to stop treatment after 5 years. To hear my answer, start watching this vid right now!

The Boster Center for Multiple Sclerosis accepts all major insurance carriers and accepts consults from around the globe, both in office and via telemedicine. www.BosterMS.com or call 614-304-3444 to schedule!
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COMMENT with your thoughts and questions below! I look forward to reading and responding!

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VISIT us on web: BosterMS.com

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NOTE: Make sure to talk to your provider before ANY treatment decision. We hope to educate, empower and energize those impacted by Multiple Sclerosis. This channel consists of a collection of formal lectures and informal video clips about MS to help education others. These videos do not provide medical advice and are for informational/educational purposes only. The videos are not intended to be a substitute for professional medical advice, diagnosis or treatment. Always seek the advice of a qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read or seen in any of our videos. They are just to help educate you about the condition guys!

[dianegonzalez]

Great question!! Your wow response 😂😂That play it down response is common among general physicians. MILD symptoms and occurrences mimic other diseases. This leads to we think, we don't know, Lets try this and that. A hamster wheel exsistance for years .

[youtubeuser]

My sister in law just received a diagnosis. They feel she's had it for 33 years!!!! Only thing she got was trouble with her bladder a few years ago which has been controlled with diet changes. Recently her leg has weakened and she requires a cane, that's what finally got her diagnosed at the Mayo clinic! She will now start treatment. She was blessed to have a wonderful enjoyable life never knowing she had Ms!!!

[Sharona]

I’m in the UK ...many neurologists here don’t treat “mild” MS. I tried to argue my case but was ignored. I’m seeing a different neuro now. I went from EDSS 1.5 to 6 in just two years with my “mild” MS.
Great video ...I’m sure the more this is talked about, the faster change will happen.

[modestinacolecchia]

Thanks Doc, great video. Fifteen years ago I had only 3 lesions and the radiologist said to me to run away from neurologist because "they put everyone in therapy". Today my brain and spinal cord are full of lesions but thanks God I still walk and go on with my life! I started my therapy too late. Please treat your Ms as soon as possible!

[annemacnab]

I’m keeping sending you ‘the love’ - another awesome video. Thanks from Edinburgh, Scotland

[EvenSoItIsWell]

Thanks Dr. B. I was one of those that was hesitant and afraid of treatment in the beginning. I appreciate your insight and sharing your professional opinions with us!

[elenastrong]

Great video, Dr. B!
I’m too was told that I have a mild MS and was put on Tecfidera.
2 weeks ago I had an appointment with my neurologist and, thanks to you and your channel, had a conversation about treatment approach. Looks like I’ll be switching to Ocrevus soon.
Thank you

[sandramoyse]

I'm on Avonex and have had no major relapses in 10 yrs. I continue on it because I believe if it ain't broke, don't fix it!

[lw]

Some of these comments with doctors that don’t want to treat people who have lesions and think it is “mild MS” are terrifying! For me, my symptoms are gradually worsening as I age, I predict I will be dx with SPMS. I was put on DMTs too late! Just because you feel reasonably okay now, doesn’t mean the disease isn’t active and that you will feel okay 10-15 years from now. I know from experience.

[stephaniekn.]

Love what you do for us. I learn something every time.

[marieb]

Another great video, thanks Dr. Boster! I have a question about MRIs...how come MRIs might not show any new lesions but a patient’s symptoms are getting worse?

[mikeecko]

Thank you Dr. B!! Keep filling our heads with your knowledge

[kyzone]

I did an MRI, they found a white spot in my brain. I have symptoms since 2012 and the doctor said "for the moment just forget about it, in the worst case scenario you have a very mild MS, otherwise since 2012 you should feel a way more bad" ... How can you left the consultant studio whit such a big question? I have MS or not? What mild it means? Why he didn't ordered some other test or put me on medication??? I think it's quite frustrating!

[johnscapino]

Very well put Dr. Boster.
I hope that you had an awesome 4th.

[rebecaapf]

I do haveild or benign ms
... been having it for about 10 years .. only two attacks and in remission for the last two years.. no medication except for cortison Therapie ONCE

[cementra]

Thanks Dr. Boster. Have a good weekend.

[lindsayrowell]

even if i had the most “mild” MS case in history, i would still never stop therapy. i might be totally okay now, but what about 5-10 years in the future? isn’t the idea that we’re on therapy for the future and not necessarily for right now? well that’s how i see it anyway, might not be correct. not a risk i’m willing to take 🙅🏽‍♀️🙅🏽‍♀️🙅🏽‍♀️

[ELZ_]

Your brilliant I've got ms but doctors investigating further to see what one I have I've had deeper MRI get results back next Thursday .

[j.svensson]

The last neuro I saw first said I didn't have ANYTHING wrong only to turn around three days later and say Yes I did have it "You have lesions on your cervical spine" but "I don't want you on medication because it is so mild." 3 months later he went back to the "You're 100% fine and I will refuse to see you again." Things have been shifting slowly here but I see changes. I'm so distrusting of neurologists (two have just been horrid) that at 62 I just don't know what to do. I don't feel well most of the time but I'm so tired of being called a hypochondriac or treated like an alcoholic baglady (I never ever drink). Any advice? I'm on medicaid so I'm at the mercy of the system.

[colleencalvert]

The first neurologist I saw told me that the spots on my MRI are irrelevant and I did not need to be treated for MS.