Potholes in Brain and Spinal Cord, a literal description about Multiple Sclerosis
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- Опубликовано: 7 ноя 2016
- Quotes by Dr. Boster: "MS is a disease of Invisible Symptoms"
"Friendly Fire" Attacking the Body -- "Pathological Fatigue" -
"Functional Reserve" -
Listen to Aaron Boster, MD - literally describe Multiple Sclerosis as he Empowers those affected by MS with a very detailed description
Program date - October 22nd, 2016
Location - Dayton, Ohio
Program emceed by: Laura Kolaczkowski, a friend to MS Views and News
Website: www.msviewsandnews.org
Blog (MS News archives): wwwmsviewsandrelatednews.blogs...
For information email: info@msviewsandnews.org
Donation Link: www.donations.msviewsandnews.org
This doctor really gets it. Compassionate, articulate and personable. What a great role model for young physicians. ❤️
Agree
He's a gem
Hopefully you are registered with MS Views and News, so You can see more of his events.. To sign-up with us, click: www.register.msviewsandnews.org
I have had MS for nearly 10 years and I have never had it explained to me quite like this! I am so grateful for this information. Please keep sending it!
You are so welcome!
I was diagnosed with MS the week of my 60th birthday, two months ago. I've had random symptoms for at least 30 years but no doctor would connect the dots even though an MRI 38 years ago showed lesions. I was finally able to convince my PCP to refer me to a neurologist. I'm currently not being treated but my next appointment is in a week and a half and I hope my neurologist is on the same page as Dr. Boster. I've learned so much by watching him.
this guy truly understand s ms and what it does to us
Yeah I'm an army veteran, did my time in the USA nurse corps. I check this channel every day! Thank you Dr. Boster, for what you do. You have given hope and inspiration for those with MS, and even better you have made us VISIBLE!
Thank you for your comment
You're the first person who understands how I feel.
This Dr is a MS Hero! 👍🧡😍
Well said Dr 👏👍well said!! I have MS. Been following you almost 2 years, shortly after diagnosis. Everything you say has been dead on. You haven't said anything misleading, straight to the point. I think it should be a law if diagnosed with MS it is mandatory too listen to your lectures. You saved my life. I was depressed which in turn made me think about suicide. MS is a new way of life, but its my life. You gave me hope and knowledge. I hope you know how special you are. FYI I think you should have merchandise for you channel. I would buy a mug shirt hat etc. Saying something clever like "Team Boster PLEASE". Anyway in my head your my friend. Thank you for all you do.
This is the BEST talk given on MS that I've ever seen, or heard. I love Dr. Boster's communication style (he's kind of nerdy in a cool way. Love the Harry Potter reference), and he really gets it. He understands what we deal with daily while living with MS. So glad I watched.
Dr. Boster you really do understand us MSers, as I stated a couple of weeks ago you are an Earth Angel thank you for being you. Fantastic video so complete, you make it all understandable. Jane Co. Mayo Ireland
I am so grateful to have heard these You Tube videos. Now I just wish that my neurologist was a bit like him. Informative and compassionate.
He is so incredibly intelligent!!!! I’m 30 with PPMS,and recently had a seizure 😢!
Please make sure you get on the highest efficacy drug you can, I recently in December of 2022 was diagnosed after I started having debilitating issues and I am 41 and haven't been able to work but my issues are able to get better with Physical therapy and getting on a DMT for Multiple Sclerosis. I pray you are doing well and just know you can have a good life living with Multiple Sclerosis 😊.
We NEED MORE Dr B’s 🙏🥺👏🏼👌🏼
Absolutely incredible! Makes understanding MS much easier!
I was a mechanic....remember this: Maintenance is cheaper than repairs!
I'd just love it if I were able to see him! Been following him recently and he explains so much and u can tell he actually cares.i was dx 17 years ago....I do not have any health insurance now and I'm currently in my 3rd exacerbation in 9 months. At 48 years old I'm not ready to become disabled 😕
Oh and I am only about an hour away from Dayton Ohio
@@katloverstoddard4698 are u okay now ? Can you walk , see or speak well now?
Doc you are a great blessing!! I’m starting Tecfidera soon
Thank you for this video!!
GREAT JOB Dr Boster
Very very very informative
Fantastic
Approaching MS really well thanks Dr
Always welcome
Shared
I really like the this Dr. Especially after he said he jams to beastie boys! I like his spunk.he seems really concerned about his patients.
since starting lemtrada a year ago i have had no relapses and mri have shown no new legions, I feel great! and almost normal again. i hope all are doing well ;)
@@lordzmusic8461 Lemtrada
How do you feel now?
Wow,I sure learned a lot !
Some of these tutorials move me close to tears... Perhaps it’s knowing how much Dr. B , Cares- his supportive wife, and the Strength-of our Village !
👏 Bravo Bravo👏
I had Lemtrada in Oct 2015 no NEW lesions but my Pain is a 100x worse than before Lemtrada. No new relapses and the pain is SO bad there days I can't get my head up off pillow.
Jeffrey -- Though I never used Lemtrada, I can fully understand how bad the pain can be.. Want to chat? Write to me directly - stuart@msvn.org -- Regards, Stuart Schlossman, an MS patient
Copaxone year 2 - no new lesions
Thank God,I started with Copaxone And I could not Breathe So i switched to Rebif
After 18 yrs of injections (copaxine) I started having reactions to the med. I went off and haven't been on ms meds since. I know Dr Aaron wouldn't be thrilled with this. Because of the compromise on my white blood cells and pneumonia (interstitial lung dz. Is present), I am afraid of infection with a new ms med. Any suggestions? rmwsbe3@gmail.com
This dr gets it completely felt like he was talking to me. Dx at 16 35 now theres been alot of breakthrough
I wished this guy was my ms specialist. How can a person with ms contact and get a appointment with him. Reminds me of my past neurological doctor. I miss him
I would just love to get in to see him, unfortunately I currently have no health insurance so I would be interested in clinical trials. I am only 45- to an hour from where he is. Diagnosed 17 years ago, currently 48 yrs old and am not ready to become disabled. My disease went from rather mild to 3 nasty attacks in the past 9 months
@@katloverstoddard4698 are you okay now ..... before 17 years what the very first symptoms did u see ?? Can we see with our eyes still in optic neuritis?
I saw your post and hope you get this message but you can call the Ohio Boster Center and your first appointment will have to be in person but he can do Tele health visits after is what I was told when I called and he is approved for other states to treat.
I have a few to many potholes
Oldie but goodie
Where can I get interaction with my doctor like you provide for all of us? I know you might say you got to talk to your commission or your doctor and I do but it’s just not the same as I am watching the video I don’t feel sad or depressed when I’m watching your videos anytime I’m talking about my Mz with anyone at all I am very sad and very depressed almost all day I am on disability now I am not working for the past four or five years I am not like in my life I do not leave the house just like you said because I have bladder issues so I just sit here nothing even works I’m using catheters all day long that’s what I do with my time it seems to be thank you please teach all these other guys to be like you
This Dr is awesome. Why is his practice permanently closed?
His practice is not closed... Look for the @BOSTERMS Center in Columbus, OH
Dr. Boster this is off topic but need to ask you about a recent incident. I have tiny veins and receive ocrevus infusions. A Dr told me to always use a butterfly needle. So after being stuck with a regular IV needle 8 times. They finally got it but once again midway through my veun collapsed. So yes they finally used butterfly needle. So instead of usiing butterfly needle. The Dr tells me I need to get a port (surgerical procedure) or change my disgnosis so she can give me a different medication. I have PPMS. she wants to change it to secondary primary progressive. I feel as a patient if a butterfly iv needle works why cant they use it? My tuny veins like the butterly Needle. Is it me? My tiny veins await your answer.
we will share your comment with Boster
Just as a general question, what are the differences in treatment path between Lemtrada and Tysabri?
please send email to us at: info@msviewsandnews.org and we will send to Dr. Boster for his response ....
Hi there 🤗
On my Brain MRI it only show 2 single small lesions:
1 Brainstem (Pons)
And 2: very small lesion in my C5 (Cervical Spine)
But my reflex are OK
Just some bilateral leg buckling sometimes, stiffness and some mild tremors with fatigue..
Neurologist isn't worried at all..
It might just be that the lesions appear too small or is just the MRI machine lighting or refraction??
Help- anybody.. please!r
Get on a high edvicacy drug don't wait to get worse, my opinion and Aaron Boster says same thing but if you are not comfortable he will not force.
iv been on tysabri for a year and have relapsed many times. i think i may have permanent foot drop
If relapsing on Tysabri - you should speak with your neuro to put you onto something else
You convinced me to take a (brain )shrink-slowing rate of atrophy therapeutic medication... But I read at 65 I no longer am a candidate!- Other than diet Vit D, and natural anti inflammatory agents , biotin etc. what else can I do?
Dr Terry Wahl has a diet program that took her from being almost bed ridden to walking again! She has MS and you can find many of her interviews on RUclips and she has written books too!
no new lesions though
Dr b I would love nada
I'm 45 with rrms
a fever though can cause a flare
Ever heared of PPMS ????...
PPMS is discussed in most of our programs... There is medication for this too
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