APRIL LIVE STREAM - Ask Me Anything Multiple Sclerosis
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- čas přidán 26. 04. 2024
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The Boster Center for Multiple Sclerosis accepts accepts new consults and is actively enrolling several clinical trials. www.BosterMS.com or call 614-304-3444 to schedule!
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AMA Multiple Sclerosis: 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!
I wish every person who has MS could find you like I did. You are the best ‘treatment’ for MS. Thanks for all you do. ❤❤❤
I agree 100% with you @kathyeyesopen4078 ✨Dr B deserves more praise than he gets for his clear 🔥passion 🔥towards helping the world fight back & against MS. One man CAN make a difference! 🤍
I agréé!🙋♀️ I wish everybody would know your channel and have a neuro like you! ❤️🩹 You're too good to be true 😂.
Hey , my wife is a patient of yours and I just want to say that as her husband and biggest supporter I am glad that you have the confidence to call out BS . Somehow that’s comforting to me . Thanks
RI
Ips stamcel terapiye Amsterdam turkey 🌎🥊❤️ms
You’re the best Dr B. I’ve never been so supported by any doc like you! Can’t believe it’s been 14 years!
Wow, thank you!
Yes the same think and the threu ,sorry my english whrite is not so perfect but humantiy🌎❤️❤️idea i vote mister arion of 🌎asmadeur ms 🌎🙏🤲like this🌞🌞sun ❤️🌎may be tekst onther the video alfabet than can i whrite slowy again again 🇹🇷
Dr. Boster, about three weeks ago I started going to the gym to do workout classes and that is almost entirely because of you. It has been on the front of my mind about movement for MS and it’s because you’ve drilled it into my brain since I started watching your channel. It may have taken me a year and a half to get here, but better late than never! Keep on hounding us on 5 for 5, it sinks in eventually. ❤❤
What is 5 for 5?
@@georgettebrewer9905you can find CZcams videos on Dr. Bosters 5 for 5,; it has also been 4 for 4
He Just came out with a Sixth: 6. Be Your own advocate.
@@georgettebrewer9905He has several videos involving his 5:5. The things he highly recommends to everyone to live your best life despite having MS. These are: 1. Don't smoke stuff 2. Take Vitamin D3 3. Exercise as part of your lifestyle 4. Eat real, whole foods 5. Severely limit alcohol 6. Be your own advocate.
Queens, NY here. How do find a new MS doctor? Many red flags are waving with my existing physician. M, 69, diagnosed’07. Main issue: Bad walking problems.
Hi im 45 female suddenly started having falls, numbness etc.. 8 years ago 1st symptoms vertigo and got better after few months. I have altered sensations mainly to heat. I have Multiple scattered leisons in both cerebral hemispheres where my neurologist found it hard to diagnosis.. in the end I was diagnosed was FND, some vascular change, small vessel disease and maybe in 5 or 10 years will have MS. Sent home with a amitriptyline. Cant walk far feets burn n heat up, blurry vision and memory issues. So difficult to live not knowing or waiting.
Sounds so similar to my experiences...52 now. Mavenclad was my choice after a previous one meaning medicine. Feeling much better now, I think just not working for the past 7 years might have something to do with feeling better...best of hope for you ❤
Thank You Sir
I get so irritated by people with MS blaming everything on MS. As we age, lots of things happen to us
This!!!!! As I say to the neurologist I don't know if it's normal wear and tear or MS!!!!
Please don’t be irritated. Sometimes s… happens. As a senior ppms person, when I have something new happen that affects my functional ability it’s easier to blame ms. That’s my prerogative even though I know my age is part of the problem.
✨From 🇬🇧 - Diagnosed with MS since 2012. Watched you for years now. 🤍 You have been the best source of practical, helpful and current MS. information I have ever found! I love your clear 🔥passion🔥 for treating and helping people with MS (patients & strangers alike) ❤️🔥🌟 Your energy is contagious and lifts my spirit when watching you. Thank you 🤗
Thanks for a wonderful Livestream Dr. Boster, I always learn a lot and it helps me to feel more confident that I will be able to successfully navigate my life with MS.
Comox British Columbia Canada
Are you ready!
🔥🔥🔥🔥🔥🔥
Thank you Dr B 😊
this is my first time on your live. I just found you last week and have been binging your videos. You have been extremely helpful. I have learned more about MS than I’ve ever known. I was diagnosed 2015. Thank you for doing these videos. I am very excited to be here on one of your lives, could I possibly get a link to a list as well of when you come live? I just happened to find you this morning accidentally I am from Las Vegas Nevada.
Hello from New Zealand
When is the next live stream?
Hello from Winnipeg Canada
Hi,from Scotland Glasgow
Hi from france ! ✌
Las Vegas, Nevada
Hi Doc from Janine, Sydney Australia!🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥
I'm on infusions now I noticed extreme stiffness and working out helps but not long
Kathy in Delaware. Dr Borster, I didn’t know your answers start about 30 min in! No wonder I missed the other answer shows!
From Amsterdam
I just found out my spine MRIs are being done on a low strength MRI machine (in a trailer). Techs at last brain appt said I should be coming in the office to have all done on the high strength MRI machine. Thoughts?
❤❤❤hi boster. Michigan
Ft Worth Tx
Hi from Israel very useful video answers to alot of problems which Ms patients deal with I will send it to my daughter thanks dear doctor
Hi, this is Betty from Austin Texas.
Question for your next video - I have MS….is itchiness, unrelated to any allergies, another symptom? Like my tingling or the burning sensations associated with MS, it seems to come and go and is louder when everything else is quiet.
Congratulations John on your new marriage❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤❤
Just wished to see you via video out of state
Doctor, I am having a problem with constipation. I've had MS for some 30 years and I am now70. I am finding that it is harder for me to swallow while eating. my last issue is that I also have a very weak bladder. I'd be interested in your feedback, thanks.
In lieu of Dr. Bosters standard answers: Against constipation, start by upping your water game. It can only improve your bladder issues to empty it often; try to finish up with the extra water by 6PM. Swallowing is a serious issue, try tucking your chin in when you eat, and request a referral to a Speach Pathologist. Blessings from Jerusalem!
From Opelika,Alabama
New jersey
Greetings from Ireland
Hello from Miami! Thank you for being such an amazing person!!
Q. Have you ever had a patient that you diagnosed without an MRI w/contrast? I had a CT scan with contrast of the chest in 2014 that caused way to much pressure. Couple wks after started with on and off numbness and tingling on left side of my body, and still going. I'm terrified now to get contrast in my brain, but can't get diagnosed without it😢😢
Really sorry to the folks that have this illness , I have cervical & lumbar stenosis from spondylosis but I am really concerned that I've read that there could be a percentage of developing MS , from an educational view .....is this true ?
Susanville California
Hi! Can you please address Tumefactive lesions. I had one on 1st MRI - what causes the size, etc. My neuro dc'd meds given 65 yrs old; I'm scared now.
@AaronBosterMD - what does it mean when you have 8-9 brain lesions, positive LP, numerous MS symptoms and the MRI report says possible no demyelination on the report? My doctor doesn’t explain it very well at all.
I have tried to submit a request for your Monthly Boster Corner. I get a message stating unable to submit. I need help with this 😢
Hi I'm Sonia from Pennsylvania
QUESTION: how long does it take to get an appt with you in your office? I submitted forms about a month ago. Didn’t want to be a nuisance and call to see where things are at with getting my records from previous doctor.
I am waiting to get in as well. The medical records department has 30 days to get the paperwork in. They told me to call them myself to hopefully expedite it. Good luck getting in!
Thank you Doc
Awesome as always 🙏
Can prednisone affect a mri reading? If a person has ms and takes prednisone for 5 days prior to the mri, would that hide lesions?
Can MS contribute to / cause sleep apnea (blood oxygen of 90 and below)?
Montreal 🇨🇦
Going for my spinal lumbar tomorrow. I’m so nervous. My body is vibrating so bad and margines getting so bad . Plus all the numbing throughout my whole body . Was at the er the other day for the 10th time just blow me off and give me a “ migraine cocktail “ which helps for the day . I need answers.
Also do you accept upmc for you insurance ? I’m in PA . Thanks
I think I figured out where I went wrong with this Q&A video. Should I stopDMT before getting total knee replacements? My ortho won’t perform TKR on anyone who has been on my DMT, Ocrevus because of high incidents of nasty infections. What is your advice?❤❤❤
You have MS. Doesn't sound like a TKR will make things better.
From Amsterdam i use Fampyra en ocrevus but walk 2023 20 minuten now 20 seconden what happening body vert strange to gether 🌎🌎🥊🥊we are strong
How do you ask a question?
How to prevent osteoporosis in ms?
Vicroria
can the continuous singles trying to be passed cause fatigue
My worst symptom is vertigo , how can i get rid of it? 😢
Hi
Australia 👋
Lorazepam
❤❤❤❤
Does progressive MS have different Stages?
I was recently diagnosed with secondary progressive MS.
Hi!
Also from pa!
❤
🔥 🔥 🔥 🔥 🔥 🔥 🔥 🔥 🔥 🔥 🔥 🔥 🔥 🔥 🔥 🔥
If you were referred to neurologist and had exam, MRI (8-9 small lesions on brain) and positive LP with several MS symptoms. Would you put your patient on DMT? If not, why?
Thats a hard question to ask .... very personal to your ms experience... everyone with ms should be on dmt some neros feel age is reason to stop dmt once you hit 60 ... I also have 8-9 lisons and am on ocruvus
I just heard of Ocruvus. Do you notice anything from taking it?
@cieloview1329 well it has helped me recover better after a relapse.... though while taking it you are at increase for infections I like it cuz it helps plus I like not having to take a pill or shot daily or monthly it's every 6 month or longer so the day ad a few after the infusion I'm alittle out for the count but the rest of the 6 month I'm pritty good ....
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I called the office on Thursday and I thought they mentioned the live started at 3pm EST. So bummed because I wanted to ask about taking LDN. Please let me know, what do you think of low dose naltrexone?
Take it. Did wonders for me for 4-5 years. Some say it's a placebo, I don't care, it's worth $1 for a night's sleep.
@@Jerusalem_Warrior Oh my goodness thank you for the reply!
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hallo