Answering Viewers Questions: Multiple Sclerosis Symptoms And More
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- เผยแพร่เมื่อ 2 ก.ค. 2024
- In this video, I'm answering viewers questions about Multiple Sclerosis symptoms and more!
00:00 Thank you for learning about MS with me, Aaron Boster!
0:45 Are MS lesions still seen on MRI without contrast?
1:51 MS and Weight Gain
2:36 MRI of brain only, what about spinal cord?
4:07 MS and Psoriasis
5:16 MS and Depression
6:50 Is number of folks with MS in USA really 1M+??
8:04 Is Tysabri every 6 weeks ok if you're JCV antibody negative?
10:11 Does Physical Therapy impact Spasticity?
11:10 MS and HSCT
12:16 MS and trouble swallowing
13:25 Fampyra for MS?
16:26 Receptive Aphasia and MS
17:18 Global MS Village Shout Out!
The Boster Center for Multiple Sclerosis accepts all major insurance carriers and accepts consults in office and via telemedicine. www.BosterMS.com or call 614-304-3444 to schedule!
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COMMENT with your thoughts and questions on Multiple Sclerosis Symptoms 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 (and in this case Answering Viewers Questions: Multiple Sclerosis Symptoms And More) to help education 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!
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Good morning Dr. Boster. I like this way of videos your doing. It answers a lot of questions that some people in this community would have and some questions people would not think to ask. It's a great way to spread extra knowledge. Thanks
I appreciate that Chuck! #StrongerTogether #WeHaveMS BosterMS.com
Excellent Q&& A about MS & Gastric Bypass- I was just asked about this.
#SharingIsCaring
#wehavems
You are awesome Dr. Boster! Thank you 🧡🩰🧡
Oh no missed the live again 🙈 💜
Good morning Doctor.
You are AWESOME DR. Boster!! Thanks for all the info! Your videos help me and so many others greatly! Take care, Andrea
I am genuinely grateful for these videos and all that I have learned. Thanks so much!
Thank you Dr Boster, as always extremely helpful 💖
Great job again mate
Thanks again
THANK YOU! i watch your videos and feel better that i have access to such a great MS dr
I really appreciate your insight to MS. I have referred many to look your talks up on TH-cam. Thank you for all your information!
Super great video Dr. Boster. Love that you take information that would be confusing and hard to understand, and inform/teach us in easy to understand language. I have learned so much. Question, can a person go without being diagnosed or treated with MS ? Asking for a friend. Lol.
hahaha, have to get up early to catch up with Dr. B!! Love these helpful Q&A videos! Is there an alternative med to aminopyridine for someone allergic? Thank you.
Good morning Dic. B
I am curious to find out what the other 2 of 3 complications of MS could cause end of life.
About the trouble swallowing and throat problems, my throat flap thing never grew in right. So I’m always getting food and drink in my lungs, daily. I’ve had pneumonia, bronchitis, the flu, everything under the sun for lungs and throat. I hope it’s not just a countdown someday. It makes daily life incredibly difficult when just breathing or accidentally swallowing your own saliva down the wrong pipe could kill you. Not even 30 and I’m worse than some cases of people with PPMS in their 50s or older.
I’m scared and alone suffering this.
I was diagnosed in 2013, with symptoms that started much earlier, and my neurologist has not once in the last 8 years given me an MRI of the thoracic spine despite me asking for him to include the thoracic spine (at least for one mri). I'm angry at this point. What should I do?
Thank you for the video. Doug with coffee in hand from lyndhurst.
Good morning! How in the world did I miss it again 🥺🥺🥺 Is Tysabri ok for people w JC greater than 1.5? Scares me A LOT !
Has there ever been a recorded PML incident within 12 months of taking Tysarbi?
MRI noises are _monstrous_
I've recently had two falls. I go to Gahanna,OH for an MRI. I'm a little nervous about the findings. I was diagnosed in 2001.
Hi. Can you please suggest ways to help with fatigue. I'm allergic to the dye in the contrast. So my mri s are done without the dye. I have lost my desire for foods. I just don't get hungry. I can't taste foods either
My silly question is can I use flex seal to seal the leaky pool and then add water , I did think about asking this in the live stream but thought I probably shouldn’t. I do wish I could go back to when my pool had lots more water ,thanks for all you do to help us
Dr Boster was going to ask I start my octevus infusion Monday was going to ask does ocrevus cause breast cancer?
Hi! Long time since I’ve taken any treatment and my new Doctor here in Puerto Rico , Dr. Chinea is considering Mavenclad, but 1st he is going to do some more tests. Could you explain how that medicine works? Thanks
Hi this is Kirralea. This November 27th I completed Lemtrada 5 years ago. I just had MRI that shows repair and no M.S. progression. I don't know what to do. . . . . . . . .
Rejoice.
How common are focal seizures with RRMS? It is suspected that I may be having them. I have episodes where my whole body stiffens and goes numb. The last set of them affected my speech and swallowing abilities.
Hello Dr Boster. I'm a 62 year old woman and I am desperate to know if you can have symptoms of multiple sclerosis and all negative tests
Hello doc i have ms for one year almost .
I have trouble shallowing and some others stuffs but they to me that stres impacts the most of symptom not ms ,how we can stand out an ms symptoms from something to else .i have this symptoms for months. And the second question how is your honest opinion about drugs if the desease the next -5 years
Greetings, from Maine! Optic Neuritis question for you...I have optic nerve damage due to my MS (Diagnosed since 1991), recently my eye specialist noted significant loss of visual field & way elevated pressures & fears glaucoma is occurring. I'm now on Rx eye drops to reduce eye pressure. Question is: could glaucoma cause optic neuritis flare!? Am I now at extreme risk of blindness due to both these conditions impacting this nerve? I'm worried 🤔👀
I am just newly diagnosed with MS an randomly have coughing spells while/after drinking and or eating. This may happen once a week or so. Should I mention this to my doctor? Thank you
Why, and how, do old lesions get worse increasing the symptoms associated with them? Can lesions grow in size?
If there was breakthrough disease seen on an MRI while on 6 weekly Tysabri would moving to 4 weekly help much?
I am currently taking Aubagio and have noticed a lump on my left side of my base of the back of my neck and it's painful, should I be very concerned?? I see my neurologist at geisinger (Megan Esch) in 2 weeks and feel like it's something I should point out, also I'm pretty sure I relapsed , I feel like she sometimes is dismissive but I am concerned
How do you feel about botox for your bladder?
Do memory supplements help with memory?
If the symptom of leg weakness, or foot drop, or muscle atrophy, is asymmetrical (only affecting one leg) does that mean that the lesion location associated with that symptom is in the brain, and not on the spinal cord, seeing as only one side is affected? I was told that recently and just trying to figure out if that's true. Thank you.
Good morning Dr. B 😢 my question?
I have had ms 37 years . I am 72 . Can I still get ppMs??
Dr Boster, holla at your follower from Sydney Australia 🇦🇺 👋 👋
3rd year starter of Mavenclad, I really want to hear your thoughts on this. I can't complete week 5 because lymphocytes too low, hopefully they go back up but love to know what you think about a 3rd yr Mavenclad-er ☺️☺️
Why are you having Mavenclad for the third year. I am in Australia also and my daughter just completed the second year dose 2020.
Doing quite well. It should be given for 2 years and then be assessed again preferably with spine MRI.
I have ppms. My doctor says we cannot start treatment until I get vaccinated. My issue with that is I have a bad heart too and am worried about the vaccine doing more harm than good. What do you think?