🔴 AMA Multiple Sclerosis: LIVE STREAM RIGHT NOW!

[@AaronBosterMD]

Never miss another LIVE! Click bosterms.com/get-boster-news/ to receive the monthly "Boster Corner" newsletter with times and dates of all upcoming LIVE STREAMS!

[@jude4896]

Dr. B , thank you for sharing your thoughts and rationale. I have RRMS I currently live in Fairfax VA and my first attack was in 2009. All other channels on KZbin on MS don't convey the information you do. Thank you! I always look forward to the live streams you share and the other videos from conferences and more. Thank you for sharing.

[@Nancy-dz1vo]

Again I say! thank you for your educational videos and caring for the MS community.❤️

[@ziqable]

Hello Dr Boster I am Zafar from Pakistan. I was diagnosed with PPMS in 2014.

[@raquintal]

I was diagnosed in 2010, I have a biology, chemistry, and mechanical engineering background. Solumedrol seems to be the most effective treatment it for me and seems to work better than any of the DMT’s I have been prescribed. I’m now on Ocrevus. Best Regards, ROBERT

[@Rose77745]

Hi Dr.B 🤗 I just found out, that I am no longer RRMS, and now I am at the SPMS stage. My Neurologist said, because my MRI came back, and showed no activity or inflammation with no new lesions from my last MRI that was done 4 years ago. I know talk about being neglected right by Neurologist in my neck of the woods?? 🤷‍♀️ 🤦‍♀️ Anyways now she is telling me that I do not qualify to go on any DMT, because she said it will not help me in any way, and also it won’t be covered by insurance from the Canadian Quebec Government. I don’t believe this is true, after watching all your videos for so many years, and especially the one on SPMS. Now this makes me really upset 😢 and heartbroken 💔 to find out that I cannot get on a DMT, to slow this monster down. I’m 45 yrs old, and I have a 3 kids ages 13,19, &22. I cannot go out like this, and refuse to give up. What can I do about this Dr B? I really need some advice, and help here 😢💔🙏

[@josephvered3991]

Hello from lsrael thank you for the information god bless you

[@gracerosa5249]

I have ms thank you so much i like my doctor. Sometimes i have questions between visits . This is so helpful. Please keep doing this.

[@Spitfirephotographs]

Glad I watched this later on today- see you tomorrow morning Dr.B

[@AaronBosterMD]

awesome sauce!

[@1life-2live]

Awesome congrats on 50k subs. I missed the livestream but enjoyed the replay tuning in from Newfoundand, Canada!!

[@AaronBosterMD]

Thanks so much!!

[@dutchyvan1669]

Hello from Queensland Australia I was diagnosed with MS 2013 which was after a bout of Trigeminal Neuralgia I have never been on medication for MS as TN is ruling my life my last MRI was 2017 so it’s time for a new neurologist who not only gives me pills for TN but Checks MS

[@tanjaketola1066]

Thanks For intresting live chat😊 Following you from Finland

[@kevinbaxter7390]

Sorry Dr was on my overwhelmed Fatigue sleep 💤🏴󠁧󠁢󠁥󠁮󠁧󠁿

[@dougtagg9162]

Good Monday afternoon. I am enjoying this day old livestream with my coffee in hand from Lyndhurst Ohio. Thank you.

[@Courtneyhorvath-i3n]

Good morning ❤❤❤

[@lemonpeelangelfish]

Great to spend my Monday morning watching replay with coffee in hand and my cat in my lap and my dog at my feet! Big hug to River she’s so gorgeous! Thanks for making Monday morning awesome 😁🔥🔥🔥🔥🔥

[@triciasproles5831]

I went to chipsa clinic for stage 4 cancer . In Mexico . They put me on coleys and my dr here put me on rebif better one a beta one A1

[@judehall2220]

Hi from the Upper Peninsula of Michigan 🙋‍♀️

[@shubhashah4022]

❤ Thank you .

[@AaronBosterMD]

You are so welcome

[@LarryLlewellyn]

Hello from Canada

[@raquintal]

Yes. STEM

[@davemassey2639]

Looking after my friends Doberman’s this week great medication 👌

[@desiredecove5815]

What a wonderful surprise to wake up to- sorry i missed this beaute. #StrongerTogether

[@desiredecove5815]

I was asleep/ was notified

[@boyd9919]

Good morning Dr. Boster

[@marilynlvsnails]

Hi 👋 from Miami Florida.. Late to the live chat.. But listening to yr chat.. Thank you for yr persistent videos.. Wish u had a "cone"of you here in Florida.. Waiting for Mondays live.. Whew hew!!

[@julieweber3398]

Good morning Dr Boster!

[@djbazaine]

Hi from Mexico waiting for my next session with my neurologist in order to program the semestral ocre 😊

[@tinateigen9230]

Hi! This is Tina from Idaho 🤗

[@kimloftis4724]

Hello from Oklahoma

[@archerseely2]

Archer Seely-Wilson from Albany Ga.

[@archerseely2]

Good morning

[@leonawilliams8102]

Aw sorry I missed jumping on live!

[@jackielavelle7974]

Crazy question Dr. Boster have you ever treated anyone who was wheelchair living ever gets out of a chair on infusion drug Thank you.

[@petras3953]

Hi from Germany! I'm just finishing 2nd year of Mavenclad 🎉

[@raquintal]

What are your thoughts about leaky gut and MS. I feel better the less I eat!

[@LoveRunsOver]

Are there ANY programs to help us with Job placement? Also I have new symptoms/lingering symptoms but my neurologist says my MRI is unchanged. Should I get a 2nd opinion?

[@raquintal]

Dr. Boster, I think you are on the right path…recently I had a Colonoscopy and after the Sutab drug cleanse I felt great for the next couple of days. Has made me reconsider occasional enema for some relief?

[@MamaV6531]

Hi! It's Delilah from boring CT appreciating you! I have had trouble with 5 different medications so my doc now suggests Plaquenil - what do you think? Also, any info on low blood pressure with MS and when to worry. Lastly, if you have a chance, any thoughts on alpha lipoic acid or adrenal fatigue if that relates to MS? Thank you! Take care everyone!

[@argentinarodriguez4170]

My MRI showed several lesions in the brain. I had a lumbar puncture a week ago, but no results yet. I was having a bad "MS Hug" and the doctor hospitalized me and placed me on a 5-day 1000 mgs of Methylprednisolone. The second day I felt better but I finished the 5-day treatment and even though the "hug" is better my legs are very weak. Doctor, please, do you think I am going to feel better? The doctor prescribed two 20 mgs Methylprednisolone a day for at home treatment. I also have a cervical instability, too. Thanks in advance!!

[@cardiomegaly5658]

Hi from Montana

[@sofiamelo8980]

Can you please focus menopause and MS? Im from Portugal. THANKS 🔥

[@kirstygeary6516]

I ❤ your channel, it's got lots of good nuggets. Unfortunately (& maybe just me) the background repeat music sound you've started doing recently is causing sensory overload when trying to listen to you. & have to disengage from listening/watching. 😕

[@VickiKnox88]

Are you still on at this time?

[@raquintal]

If MS is effected by EBV and mimicry can STEM or CRISPER (thus modify myelin proteins? I suffer from progressive ms.

[@fabianvazquez7476]

Hey doc ,can u explain wat is btk therapy?

[@MamaV6531]

Geez, I think I missed it! Sorry! :)

[@raquintal]

Hello from Tennessee

[@gloriaford2221]

Hi...I'm a 70 yr old woman....ms diagnosed when I was 40. I had new mri's taken last year & NO CHANGE in 30 yrs! However, I feel worse as far as energy & strength in my legs. Is there anything out there t9 help with the no energy situation? I'm in the Chicagoland area...

[@judehall2220]

❤❤❤❤❤Thank you!

[@michelekimmell1952]

Michele Kimmell from Kansas! My drug testing is going well.

[@michelekimmell1952]

❤

[@karenbragg3428]

What iz thd purple thing behind u.

[@jbaker6250]

How often do you hold live sessions? I keep missing them. :0(

[@AaronBosterMD]

Please sign up for The Boster Corner monthly newsletter, which includes the times and dates of all my upcoming livestreams! bosterms.com/get-boster-news/

[@jbaker6250]

@@AaronBosterMD Thank you! I'm all signed up. I didn't see the 📌 until after I commented. Doh!!

[@ziqable]

Now because of increase in lesions in last MRI, my neurologist is considering Ocrevus. The complication is that I had an episode of Hep-B in 2016. Although I fully recovered and my tests are negative but I fear that if I take this medicine then Hep-B may reactivate. Please advise.

[@hackett1181]

What about avascular necrosis due to steroid use?

[@heatherbuszka9208]

Is it normal to lose & gain weight without even trying?

[@karenbragg3428]

Also thd black big thing?

[@susanfabian6234]

The crap gap is real and I start getting it after 4 months. I've been on Ocrevus for 5 years. That's one quarter of my year feeling like crap. Then it takes me a few weeks to get my giddy-up back. Neurologist doesn't want to change med. Any suggestions?

[@kmcq692]

Thanks for posting

[@Milli2X]

Pretty much doing a fresh install of Windows after a HDD wipe

[@valeriealv7503]

My bp was low an now rising to normal after 5 months is this part of ms ? Dr placement in rehab .Nursin home my first real dysnilitong episode not official diagnosed

[@debbiewardcasey2362]

Hello

[@lee-annepatterson3045]

Howdy Dr. Boster got diagnosed 2yrs ago and have had Mavenclad treatment the first 2 treatments. I have less migraines and numbness has gone from my hand and arm. It was mostly upper right side of body that was affected aswell as co-ordination, memory, speech. But now I have chronic pain in hips and lower spine affecting my mobility could this be despite mavenclad having affect on my upper body problems could it be progressing causing the new lower body problems? Also fatigue just kills me when it strikes something I hoped the mavenclad would have helped with but hasn't and the warmer the weather the worse the fatigue. What is your view on Ritalin for the fatigue. I'm also on 120mg duloxetine for 4yrs for depression but have noticed that it help somewhat with pain. Any advice on living with the fatigue please? 😊

[@lesliemaletta3008]

I have a burning sensation across the lower part of my back is that and butt is that neuropathy

[@Hristo-Bushnyashki]

Hello from Bulgaria, iwas diagnosed 2009 with MS (RRMS), and 2016 progress to SPMS. On 04/25/2023 i got my STEM CELLS back (I go to Russia when make HSCT). I want to know what is your suggestions for people like me. What to do, what vitamins and medications to take so therapy to do it's best for us.

[@suelyttle8205]

i was diagnosed in 1982 with MS after several serious episodes, sudden blindness both eyes, cerebella attack total loss of purposeful movement, no walking no movement of arms. I was treated with massive prednisone DMTs were unavailable at that time After a few years where the big things were happening, I went into benign RRMS. Lived my very active life with no feeling of worry about MS. For the last few years I have had a few flairs, spasms and eye concerns. new spots on my C spine. My neurologist says this is most likely SPMS. She is talking about starting DMT. I am 82, would this be wise at my age? Sue - I live near San Franciso

[@faiththefrazzledfostermom983]

Hey! I did Lemtrada 2018 and it was a great drug for me! I did rounds one and two and my 5 years are up! Should I bed for a round 3 or consider these other drug options?? Kacepta, ocrevis and another drug I can’t remember.. but it was a new pill.. not the one that was already out! ❤❤ Louisiana here!! I understand your not my doctor and get get too deep!!

[@adrienne3334]

Hello there ive never been diagnosed with M.S thank the lord. But have known people with the condition! There is a neurological one off, of a disorder that runs in my late fathers side of the family though...peculiar name that was not discovered until long after the family members death, and only then because he donated his body to medical students, whom discovered or put a name to what he suffered with throughout his lifespan, that was cruel and insipid...and left him a cripple. The disorder mimmicked other well known neurological disorders including M.S,but was not any of them....Still i am interested in M.S because as ive already stated ive known some serious sufferers whom battle with this disorder every day of their lives...No cure either as yet!

[@raquintal]

I wonder, what are your thoughts and ideas on repairing myelin and nerve damage? Or is nerve damage 😢 unrecoverable .

[@junebee5128]

Google Clemastine fumarate and Ms. Some studies have been done in it helping repair… it’s an over the counter

[@rebecaenglish6422]

😊❤

[@djbazaine]

Regularly I get steroids the same day of my ocre, just before it.

[@kevineeverhart7869]

If you're serious about moving the printer out, I've got a fellow in West Liberty that wants it

[@AaronBosterMD]

sounds good to me. Call the office at 614-304-3444

[@beckymoran321]

IV steroids tend to work faster than oral, don’t they? Could it also depend on how severe the patient is is?

[@AaronBosterMD]

interestingly, the data doesn't look that different between the two routes of administration.

[@beckymoran321]

@@AaronBosterMD good to know! Thanks!

[@lee-annepatterson3045]

Forgot to mention, living in Ireland

[@Siberianpanther]

Hi, can you treat me? I live in California.

[@charliebucket7494]

You have to fly out to Columbus, Ohio. Get a referral from your insurance company.

[@cardiomegaly5658]

Is there any correlation between MRIs and getting cataracts? My eye doc is also not a fan of steroids for therapies or as diagnostic presurgery (I had 2 back surgeries late last yr). Both have been key in catching MS activity so I'm concerned.

[@hilarykerr7383]

👍👍👍👍🔥🔥🔥🔥

[@antoinettestickling866]

❤