Why BOTHER taking MS Medicines?

Why bother taking MS Disease Modifying Therapy? In this video, I provide you an answer.

The Boster Center for Multiple Sclerosis accepts new consultations and is actively enrolling several MS clinical trials! 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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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 educate 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!

[aymenmezaache]

I was diagnosed with MS in 2011 and I've been taking Avonex since then. My condition is stable, 12 years with no relapses.

[MC-ofre]

I have had MS for 15 years now and I have tried 3 different DMTS with horrendous side effects. I don’t and won’t try anymore. I’m too scared. It was so bad that it was worse than anything MS had affected me so far. I have been doing diet, exercise and cannabis. I haven’t had a bad attack in years.

[Jefff]

“Go hang out with your three kids.” 😂
That is so true I have two kids and believe me they motivate me for my vasectomy next week.

[fragariasec]

Thanks! 🎉 I was diagnosed three weeks ago, after my first really big attack. I had some smaller before, but nobody ever thought it could be ms. Having the appointment with my neurologist at the end of this week. I want to hit hard and early. ❤

[desiredecove]

The earlier you start a DMD the better.
It’s like putting on your armor- in a life long battle.
🤘🏻💪🏻 28 years of armor wearing- MS ass kickin and going.
Preach it Doc!
#SharingisCaring

[SorenArouet]

PPMS. I quit everything: appointments, MRIs, blood samples, treatments. I feel so free now and I'm happier than ever. My illness, my choice. I know my destination, I don't need to be reminded the path will be tough.

[stonz]

Thanks Dr. B - When I started Ocrevus just over a year ago, I felt my symptoms go silent about 3 months after the first infusions. Very thankful for these new DMTs and upcoming BTK inhibitors. I'm hoping to make the switch to reconstitute my immune system. I had a cold last week that lingered for a week (first time sick on Ocrevus), yet my wife fully recovered in 3 days. Before Ocrevus I was rarely sick, but I'd recover very quickly if I did get sick. That's been my only downside to Ocrevus so far and I will be even more vigilant in trying to dodge covid and the flu going forward.

[Yllohyllod]

I hope one day you'll make a video to talk about autonomic dysfunction. Everything I read says it's not common in MS but my very first REALLY bad relapse was when lesions formed on my pons. A whole host of things began at that time; swallowing difficulties, heart rhythm problems, BP irregularity, neurogenic bladder and bowel, and digestion problems (slow motility and slow emptying). As I've aged, these things have all slowly gotten worse. I had autonomic testing and it didn't show severe disability, but it has really slowed me down. I'd love to hear you talk about this subject.

[GoldenDelicious]

Hi doctor! I did give you thumb up and I do subscribe. But 5:40 was a bit worrying. I’m from Sweden and Was diagnosed with MS earlier this year at 44 years old. I’ve probably had ms for at least 14 years without knowing it, because that’s when I know half of my face got really numb and I didn’t bother to go to the doctor to look it up. So I’ve been told that i have more than 40 lesions in my brain and the medicine I’ve been given is Rituximab infusion. I’ve taken it twice this year. However what you say in 5:40 is not very hopeful in my case, but I’m thriving and I hope I can be the exception to what research shows. I’ll have faith in God 😊🙏
Thanks a lot for your content and work.

[nyrhockeychicklife]

I have watched most of your videos. While they’re all fantastic, I found this one most helpful. I’m untreated due to horrible life circumstances beyond my control. I’ve been convincing myself that I don’t need a DMT. This explained why I actually do. I still can’t take it until I’m settled again but this really helped me. Much appreciated ❤

[BenLeitch]

My DMT (Ocrevus) has slowed progression for me IMO. I am very thankful for this treatment and my previous neuro for getting me on it as soon as I was diagnosed. I just had my 12th infusion. Thank you Dr. Boster for all your videos. They have definitely educated me on MS.

[michaelkurtz]

Soaps, shampoos, conditioners bother us because they have lots of allergens. Soaps are especially bad because of the steric acids they use to harden soap. Steric acids used to be harvested from animal sources, now a days they are from soy.

[byron]

Yep! I find myself asking the same question. I have PPMS. I was told to go on Ocrevus. I asked, "will this reverse my symptoms?", answer NO! Since it will not reverse my symptoms, my career is over, my fitness goals are over. Not that I am giving up, I am setting new goals. But I am realistic, things that I have studied for and trained for years are no longer possible. Example, years of education and a degree are now worthless. I used to be an avid hiker, training to hike the AT (Appalachian Trail). That dream is now dead. I guess the only point in taking medication is to stay out of a wheelchair. But most of these drugs have dangerous side effects. With all due respect, how am I winning? I have PPMS. I have attacks 24 -7.

[programmingpassion]

How about possible remyelinators that may come in the future? That can possibly repair the damage and regain lost neurological reserve.

[bplatel]

A very important message, and incredibly well explained. Thank you Dr. Boster!

[georginal]

I always appreciate your honesty and enthusiasm. Thank you.

[josephvered]

Hi from Israel this video summarizes shortly the most important idea that good treatment is very significant to MS patients hoping to have a medicine that will cure the disease thanks dear doctor

[busygirl]

Thank you Dr Bostor !!
I had to go back to an older MS med because I had bad reactions to a newer one Doing what I can to fight this monster

[lemonpeelangelfish]

Thank you Dr Boster awesome informative video - I definitely agree we need the hug and the DMT! Hug back 🔥🔥❤️‍🔥🔥🔥

[adrianasandy]

Dr., thanks again! I’m in Europe, recuperating from a fall and experiencing the “crap gap” until my next Ocrevus. I’m so happy we have treatments available for MS. I’m totally committed to the treatment, and doing well. I hope people understand how lucky we are to have treatments available, differently than people from previous generations.