WHEN to switch your MS Medication? Neurologist Explains

In this video, I share 6 reasons you might need to switch your MS Medication? Listen to the end of the video and I share one big reason NOT to stop treatment.

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!

**********************************************************
COMMENT with your thoughts and questions below! I look forward to reading and responding!

**********************************************************

***********************************************************

***********************************************************

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!

[sweetrose]

I have MS and you can’t just rely on medication, but you have to start changing your diet as well. I’m on Ocrevus for one year and so far no complaints, but the muscle spasms are the worse. That is my only issue right now. Intermittent fasting has helped me because fasting activates your stem cells in your brain. I don’t intend on living my life dealing with these symptoms, so your mind set plays a major role in your health. I have tried muscle spasm meds for Ms and the side effects are awful. CBD oil has helped better for my muscle spasms.

[vickibowland]

Dr. Boster, this video is SO important for all MS patients!
My first 2 DMT's were fiasco's for me.
And it took for a different neurologist to say "well, some people can't tolerate Interferon based drugs".
My latest. neurologist assures me that should my DMT manufacturer decide to change the requirements for me to no longer be able to get my drug costs reduced; he will move heaven and earth to keep me on the med that works for me; no matter what anyone else says.
It is reassuring to have an MD who will fight for me as hard as I fight "MY MS".
And since there are more than 1, 000, 000 MSers out there; EVERYONE of which suffers from a different MS (including identical twins that I have personally met!) I am okay with that.

[denisebuckner]

I don’t see Dr Bolster until May 22nd. No available neuro appointments locally. This started 4/8, totally numb on left side, walking with walker, brain biopsy and no reports yet. Only two lesions but I’m tired and growing impatient daily. Only meds, muscle relaxers and steroid. Growing angrier every damn day…..I have a life to live and grandbabies to chase

[susanroper]

Thank you so much, always so grateful to you ✨ you’re a star 🌟

[Lacy-Nicole]

Thank you Dr. Boster for blessing all of us with your words of wisdom!!! You’re a brilliant man!!! I wish I could come see you one day!!! God bless you & all of you here in this community!!

[terijones]

I was on Avonex for over 3 years. I had 2 flare ups the last two years on it. My neurologist wouldn’t change my meds. My insurance company changed what they would pay for. I told my neurologist I didn’t want to take shots. He basically fired me and past me off to another doctor in the practice. She asked if I wanted to try a daily pill. I’ve been on this for about 5 years and not had any relapse. She’s also talking about discontinuing at 60……. My husband is retiring next year. I may be contacting your office soon.

[lemonpeelangelfish]

Thank you Dr Boster, this is such an important discussion! 🔥🔥❤️‍🔥🔥🔥

[Charles-fjtp]

Yes sir I've been following your channels I have been diagnosed with MS

[juliekranz]

Thank you, Dr. Boster. My doctor just switched me to Kesimpta from Mavenclad for just the same reasons you suggested. It gives me hope!

[Polly]

MS since 2015. I have been on Ocrevus since 2020 - no new spots on MR but general fast mobility progression since starting Ocrevus. I am considering a new medication.

[BenLeitch]

I totally agree with the age aspect. IMO I'll never be too old for a DMT

[desiredecove]

I’ve tried 4 DMD’s over the course of 28 years.
I find as with MS- they change- sometimes i couldn’t handle it- sometimes they worked for years…
It’s always different for everyone-
Switching DMD’s - always a scary time- but education on the meds- thoroughly explained by my amazing Neuro ( you) lessened the fear as. Understood what to expect.
#StrongerTogether
❤
Sharing is caring

[armandhyle]

Ocrevus for over 3 years. No new spots but physical symptoms while nothing new have gotten a lot worse. I noticed a little change before Ocrevus too. I really felt confident in trying stem cell treatment but can't get approval due to continuing trials.

[MichaelBorden-rtvi]

I'm a 40 year old male and, I was recently diagnosed. I have around 20 black holes and enhancing lesions along with non enhancing on my spine. My ears are ringing and off balance. I walk with a wide gate and have or had pretty much every symptom I've read about. I guess I'm a little scared.

[himanshidahiya]

You are a great doctor. All your videos are amazing and always helpful. Thanks for making such efforts.😊

[connych]

Thank you for the rant! My neurologist is one of those. He’s told me that he takes patients off of DMDs at 60… I’ve a few years to go before I’m 60, but now plan to flight back.
I don’t know if you’ve previously covered this in a video, but it would be good to get some advice on considerations & risk factors of changing from different types of DMD to another, such as Gilenya to Ocrevus.

[donalpaccio]

Thank you very much for this video! Greets from Paris

[EvenSoItIsWell]

Good morning Dr. Boster! I love spending Monday mornings having coffee with you. Thanks so much for this video. My MS center does not measure brain volume loss. Is this a critical measurement in your opinion?

[nazilakhademi]

❤thanks for your great informations and health advices 😊

[Allfunandgames]

Tried MS meds Has not made it better. Has done the opposite. try no processed foods and good stuff. Hope it works.