Snapchat filters show YOUR personality. It does NOT take away from your other personality traits - dedication to learning and then sharing MS information. I like your personality.
since my covid, I've had such head problems. starting with ringing in my ears, and then after laying down too sleep. when awakening my brain at the top of head giving a lot of noise and taking me hours of sitting with head up quite a few hours to clear. I still have it after 2 years getting covid a second time. and it affects my head that i get really off balance and I can not do anything, but sit, and then sometime lasts for 4 to 5 days. THEN i can have 4 to5 very normal days. get my good days, and then the bad. IM 82 YRS old, and when this happens, I cant think right, then the following 4 to5 days I feel fine and my brain works great. I need help, but I live in Alamogordo, NM, and not too many doctors with this knowledge. Jeanne Houston
🔥🔥🔥 I applaud this young woman, our heroine, joining in the trial to help children with MS! I am crying, it breaks my heart that young people and adults face MS. I am SO grateful for souls like you Dr Boster, this brave and selfless gal, and so so many researchers and supporters! MS is by FAR the hardest challenge I have ever faced and it also shows me my greatest blessings. I give all thanks and glory to God! Thank you!! 🔥🔥🔥🧡🔥🔥🔥
Found ya here a couple days ago, im waiting to find out if I have ms 😢. But at least it would be a answer. Long story short started with sciatica issues which moved down my leg eventually my left left going numb at times and now my left arm going numb. I’ve had multiple MRI’s of my back which neurologist said I have multiple bulging discs in lower back but what has him concerned and possibly leaning towards ms is I have multiple lesions on my cervical spine. Next step is they want a mri of my brain and possibly spinal tap. In a way I hope it is ms in away so I would at least have answers to my issues but at the same time I don’t want it to be as that’s a scary thought. Neurologist said it could be a simple thing as vitamin deficiency but from my scans and symptoms he believes it’s ms. Here from North Dakota. I’ve been doing a lot of research the last few days after talking to my dr with anything from vitamin deficiency to ms to illness that may mimic ms ect…… trying to not get to worked up or jump to conclusions til after my brain scan and speaking to my dr about results
I missed the chat last night. I'm so bummed, I am not sure if you will see this. I have a guestion about JCV. I tested positive for the antibodies, and my index number was 3.75. What does that mean? My neurologist has not explained it to me, so now I am going to the University of Penn to meet with another MS doctor.
Tacoma Washington here like I said, I’ve had multiple sclerosis for 20 years exhausted every treatment out there and positive for the JC virus. They have me on mavenclad now I don’t believe it’s working at all right after I got put on mavenclad my MS specialist quit I had to talk to a virtual nurse via FaceTime once a week during my treatment on this drug recommendations.
Hey there, Dr Boster can’t answer specific questions about you in the comments. He would need far more information. You could phone his clinic and see if you could be seen? Just google the Boster Centre Ohio. Jane 😊
Paris Replay Crew here! 🇨🇵 I'm on Tysabri and I'm treated in Pitié Salpetriere and you sign at your first neurologist appointment if you want your results to be shared for purposes of research and if you're ok to participate in research programs. The only ones that are ok with my neurologist, because of my condition today, aren't the treatment trials but more MRI scans. For research purposes, the MRI machines are ultra powerful, I don't remember how many Teslas they have, but it's significantly more powerful than the standard 3 Tesla. But they are huge and intimidating. I initially was qualified for a research studying the suffering in neurons but when they've told me that I'll spend 4h in an MRI machine and get a break every hour, I just chickened out. It's so much anxiety. I understand it's important for the research but there are some things at this moment I just don't want to do.
Thank you Dr Boster for more info❤ keep doing what you are doing, do not change the faces, hats etc anyone opposed to these, needs to lighten up 😃. MS is a struggle we need light relief and you are this for us. I would love my Neurologist to be half as inspiring with a fantastic sense of humour as yours!
Watching from England 🇬🇧I found you a month or so ago in the plight to try and get to the bottom of my health issues. QUESTION: have you seen any links between Long Covid sufferers and MS onset or progression of possible MS which has been undiagnosed? Awaiting an appointment with a neurologist as my symptoms are not typical of LC and in retrospect have possibly had some symptoms pre- covid infection & vaccination. Thank you.
Thank you Dr Boster - so appreciate the live AMA I always learn so much! Love the Snapchat filters - they make me giggle 🤭 You are so awesome 😎 🔥🔥🔥🔥🔥❤️
Hi from kuwait 🌷 doctor thank you for all effort 💐 ♦️Question: I have very dry mouth and eyes for a year now what do you think ? ,I'm on ocrevus for 5 years
HI, Aaron. can you help me please?????? I am diagnosed ppms from 2015.... and am so tired of all experiment on me. honestly tell me do ocrevus or not? because I have to change some pills. .clonotrill... but other pills makes me worst.. I have to to take therapy for tuberkulios ( sleeping tuberk.) and then take ocrevus.Icant any moooore.... with changing pills, . even kortizon doesnt take my organism.. please tell me take ocrevus or not? because I have to suffer too much until there. and what it will help me..😏
Those snapchat filters are funny to me and I have been thru alot! I was blind in one eye from MS for some mnths and cldnt walk several times n had MS since I was 19 years old n Im 44!! So, these filters make me smile n laugh very hard! I think they are very cute!! I need the laugh!
Hi, I'd like to ask a question...I am 69,recently Diagnosed..but I have had since I was a Young Woman..so I have permanent damages..anyway..My question..I have a very specific issue..I know I'm going to relapse..I get severe Gut Cramps..usually about 4 Hours..fol.owed by severe Diarreah..fir about another 4 Hours.then..I'm left with My Urine smelling like the Diarreah ..then it will be My Skin and Hair will smell awful too..that can last for Weeks even Months..help!
I’ve had multiple sclerosis for 20 years I’m positive for the JC virus now I’m on this treatment mavenclad and it’s not working. Do I have any other options?
I wanted to ask you this last night but got nervous. What would you say if you found out a neurologist told his patient she had MS over the patient portal?
![BLACK BAG - Official Trailer [HD] - Only in Theaters March 14](http://i.ytimg.com/vi/Du0Xp8WX_7I/mqdefault.jpg)
I like the snap chat filters
Snapchat filters show YOUR personality. It does NOT take away from your other personality traits - dedication to learning and then sharing MS information.
I like your personality.
since my covid, I've had such head problems. starting with ringing in my ears, and then after laying down too sleep. when awakening my brain at the top of head giving a lot of noise and taking me hours of sitting with head up quite a few hours to clear.
I still have it after 2 years getting covid a second time. and it affects my head that i get really off balance and I can not do anything, but sit, and then sometime lasts for 4 to 5 days. THEN i can have 4 to5 very normal days. get my good days, and then the bad. IM 82 YRS old, and when this happens, I cant think right, then the following 4 to5 days I feel fine and my brain works great.
I need help, but I live in Alamogordo, NM, and not too many doctors with this knowledge. Jeanne Houston
🔥🔥🔥 I applaud this young woman, our heroine, joining in the trial to help children with MS! I am crying, it breaks my heart that young people and adults face MS. I am SO grateful for souls like you Dr Boster, this brave and selfless gal, and so so many researchers and supporters! MS is by FAR the hardest challenge I have ever faced and it also shows me my greatest blessings. I give all thanks and glory to God! Thank you!! 🔥🔥🔥🧡🔥🔥🔥
Coming off tysabari after 16yrs to Kesimpta and having a hard time, my walking is terrible 😫
26 years from the optic neurite I'm fine no medicine only yoga and vegetarian food ,I ' m lucky hello from italy
Wilmington, NC
Thank you for everything in arizona
can exercise help a lot or a little bit and is there a certain muscles to make sure to strengthen or is it different for everyone?
Hi, is medical cannabis a treatment?
I'd love to find out how I can switch to having you or your team of Dr.'s as my MS specialist?
With best intentions of watching live. I even set an alarm. However, it was 11.30pm in the uk and I had fell asleep 😴.
Is hypogammaglobulinemia common with Ocrevus and Kesimpta?
Found ya here a couple days ago, im waiting to find out if I have ms 😢. But at least it would be a answer. Long story short started with sciatica issues which moved down my leg eventually my left left going numb at times and now my left arm going numb. I’ve had multiple MRI’s of my back which neurologist said I have multiple bulging discs in lower back but what has him concerned and possibly leaning towards ms is I have multiple lesions on my cervical spine. Next step is they want a mri of my brain and possibly spinal tap. In a way I hope it is ms in away so I would at least have answers to my issues but at the same time I don’t want it to be as that’s a scary thought. Neurologist said it could be a simple thing as vitamin deficiency but from my scans and symptoms he believes it’s ms. Here from North Dakota. I’ve been doing a lot of research the last few days after talking to my dr with anything from vitamin deficiency to ms to illness that may mimic ms ect…… trying to not get to worked up or jump to conclusions til after my brain scan and speaking to my dr about results
Can here you.👍
I missed the chat last night. I'm so bummed, I am not sure if you will see this. I have a guestion about JCV. I tested positive for the antibodies, and my index number was 3.75. What does that mean? My neurologist has not explained it to me, so now I am going to the University of Penn to meet with another MS doctor.
Tacoma Washington here like I said, I’ve had multiple sclerosis for 20 years exhausted every treatment out there and positive for the JC virus. They have me on mavenclad now I don’t believe it’s working at all right after I got put on mavenclad my MS specialist quit I had to talk to a virtual nurse via FaceTime once a week during my treatment on this drug recommendations.
Hey there, Dr Boster can’t answer specific questions about you in the comments. He would need far more information. You could phone his clinic and see if you could be seen? Just google the Boster Centre Ohio. Jane 😊
Paris Replay Crew here! 🇨🇵 I'm on Tysabri and I'm treated in Pitié Salpetriere and you sign at your first neurologist appointment if you want your results to be shared for purposes of research and if you're ok to participate in research programs. The only ones that are ok with my neurologist, because of my condition today, aren't the treatment trials but more MRI scans. For research purposes, the MRI machines are ultra powerful, I don't remember how many Teslas they have, but it's significantly more powerful than the standard 3 Tesla. But they are huge and intimidating. I initially was qualified for a research studying the suffering in neurons but when they've told me that I'll spend 4h in an MRI machine and get a break every hour, I just chickened out. It's so much anxiety. I understand it's important for the research but there are some things at this moment I just don't want to do.
Missed the live stream. Checking in🧡
Hi Im in BC Canada
❤❤ love River!!! Thanks Dr. B for everything you have done me and the MS family!
Thank you!!!! Appreciate it so much
Thank you Dr Boster for more info❤ keep doing what you are doing, do not change the faces, hats etc anyone opposed to these, needs to lighten up 😃. MS is a struggle we need light relief and you are this for us. I would love my Neurologist to be half as inspiring with a fantastic sense of humour as yours!
Looking forward to the ask me anything livestream Doug coffee in hand from Lyndhurst Ohio.
Aww Doug you missed it 🫤. Next month? 😊
Do you know the fast mimicking diet of doctor Longo?
Can you please let me know when this actually is? Did I hear 1830 EST? On what day please
Ahh River is absolutely gorgeous girl xxx
Has anyone having had covid, has anyone gotten any signs of having MS?
Hello! Thanks for all your insightful videos!
Watching from England 🇬🇧I found you a month or so ago in the plight to try and get to the bottom of my health issues. QUESTION: have you seen any links between Long Covid sufferers and MS onset or progression of possible MS which has been undiagnosed?
Awaiting an appointment with a neurologist as my symptoms are not typical of LC and in retrospect have possibly had some symptoms pre- covid infection & vaccination. Thank you.
What is the difference from ms to function neurological disorder.
It was great. Thank you
My EBV tests came back negative. What are your thoughts about traumatic brain injury being a link to MS?
Thank you Dr Boster - so appreciate the live AMA I always learn so much! Love the Snapchat filters - they make me giggle 🤭 You are so awesome 😎 🔥🔥🔥🔥🔥❤️
You are so welcome!
Hi from kuwait 🌷 doctor thank you for all effort 💐
♦️Question: I have very dry mouth and eyes for a year now what do you think ? ,I'm on ocrevus for 5 years
I was told I have 25 new lesions since February this year. I have been on Kasimpta for the last few months. What would you recommend?
A question for next time. Which is the best to take flaxseed or fish oil? I cannot eat oily fish.😊
HI, Aaron. can you help me please?????? I am diagnosed ppms from 2015.... and am so tired of all experiment on me. honestly tell me do ocrevus or not? because I have to change some pills. .clonotrill... but other pills makes me worst.. I have to to take therapy for tuberkulios ( sleeping tuberk.) and then take ocrevus.Icant any moooore.... with changing pills, . even kortizon doesnt take my organism.. please tell me take ocrevus or not? because I have to suffer too much until there. and what it will help me..😏
I have MS and have been 8 drugs. Have SPMS now and just curious what you would recommend?
I rushed to get here I missed it tho 😞 next time
Those snapchat filters are funny to me and I have been thru alot! I was blind in one eye from MS for some mnths and cldnt walk several times n had MS since I was 19 years old n Im 44!! So, these filters make me smile n laugh very hard! I think they are very cute!! I need the laugh!
Hi, I'd like to ask a question...I am 69,recently Diagnosed..but I have had since I was a Young Woman..so I have permanent damages..anyway..My question..I have a very specific issue..I know I'm going to relapse..I get severe Gut Cramps..usually about 4 Hours..fol.owed by severe Diarreah..fir about another 4 Hours.then..I'm left with My Urine smelling like the Diarreah ..then it will be My Skin and Hair will smell awful too..that can last for Weeks even Months..help!
Does demyelination of brain mean ms or auto immune
I’ve had multiple sclerosis for 20 years I’m positive for the JC virus now I’m on this treatment mavenclad and it’s not working. Do I have any other options?
I have exonerated every treatment. That is why I am on Mavenclad Tacoma, Washington
My wife has little use of her left leg how about the Conic Sleeve should she try it?
Pickerington OH
Tacoma, Washington
I wanted to ask you this last night but got nervous. What would you say if you found out a neurologist told his patient she had MS over the patient portal?
I almost feel like no ms Dr will ever be good enough after seeing your videos. I do think I'll be in good hands if the MS center in OKC accepts me.
I've got my mom watching your videos now and my husband watches them. You have done so much to help me. You've done so much to help so many people.
Hi from San Diego!
Hello
🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥
Hi from Alabama, Roll Tide
Hello 1:09
I don’t think the filters are disrespectful just unprofessional
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