Welcome to Serbia. I hope you meet prof Gordana Toncev. Hope some things gonna change here in Serbia in comong years . Dr B in Serbia, its a great things. Lep provod i hvala na poseti
You should have an even larger audience than you do, Doctor B, given how many more people are being diagnosed with MS lately. Your info is truly valuable and hard to come by for many of us who have non-proactive doctors. Thank you! Enjoy your time away.
Wow this. Doctor.. Hes out and about again... Educating The 🌎 world in BOSTER style! :) ~ i think i figured it!out It must be one of those super expensive world globes.. You know the ones.. You gotta.. spin it as fast as you Close your eyes.. & its magic where ever you land is where.. You.. Educate.. Empower.. And... Energize! .. And where ever you land that is where u go.. To educate the.. 🌎 world... I honor.that fact.. Your compassion.. How passionate.. U are.. about the type of care you want to provide to this village.. To each and every patient. In this world. somehow we(as a village..) must reach every m.s. patient. Somehow. For.. We as this village. You.. See.. We brought. The Boster Light... "#Making m.s. boring #We have m.s." -Dr.A Boster Sincerely, Divine🙏 "Just one of the m.s.💛beat's Of this village"
I never catch the lives streams, but I’m from Athens, OHIO ! I was diagnosed in July of this year, I discovered your videos while I was impatient at riverside!
Dear Doc, greetings from Bosnia (neigboring country to Serbia). Here we had the same problems. There is no private medical insurance which will cover MS therapies. Thus, the state comes in. And of course, being a very poor country, MS medications cannot be paid for every MS patient. There is a committee which decides every 3 months which patients (from many applications) and they decide who gets the medication and who doesn't. Thank God, patients in Bosnia received access to superb MS medications few years earlier than Serbia, I was receiving Ocrelizumab in the time when you were making this video. Best regards!
Thank you Dr.B for all your love and care for us folks whom live with MS I do learn alot from you and your very knowledgeable and you understand this illness so well and you explain everything where I understand this easier I been Absent at least 5 months now without anything to control my multiple sclerosis I'm currently under care of my sister and she's bows abbly taking care of it which I don't think she is so thank you for your support and your channel you're an awesome doctor😊💙💜😉🙏
Wow Serbia, Must be so interesting. I can't stay long but will check back later. Just wondering if you heard of an inter stim device for bladder retention or if a supra pubic catheter would be better. I am 67 and between hand function, vision problems etc I can't seem to self cath. Even injured myself trying. So moving on from constant UTI's to another solution. Just confused as to what will be the best thing. I will also have my neuro weigh in on monday. Thanks for being here. Your trip sounds so interesting. Enjoy and be well.
Question - After Lemtrada, when can someone go into pool water again? What about the beach? Is it safe to swim in the ocean after lemtrada? (Thank you for all you do for the MS community! You are a HUGE help to those of us in more rural areas.)
Serbia!!!!??? Say hello to dr.Obradović...and thank you for your time here, please do best to help us, 88% of patients with MS don't receive any of medicines... I'm from Serbia, on Copaxone, i haved luck i suppose...
I have a question for you I believe I'm currently having a flare up and I'm not sure what to do I'm going to see another new neurologist and I don't know where to begin with my symptoms I was ready to start a therapy treatment but I had to move and now I have to start all over again and I'm scared that I have more damage to my brain I'm currently living in Turtle Lake Wisconsin and this weather does effect me with my mobility I have learned alot from listening to you and your very helpful advice for me to talk to my provider you've made it easy for me to talk to the Doctors I've seen I will continue to watch you Have a blessed week 😇🙏💙💜😊
I missed this live! Hoping this question can be answered in a future video. I cannot find an answer online as to whether an old optic neuritis is visible on a current MRI. I had problems with my left eye about 6 years ago. To this day it still goes blurry if I'm tired. But my 1st MRI was last month. Not sure if it could be seen that I had ON or not from that.
Question- when you are live, I forgot. I find I say that a lot more these days! Lol. Question is about dreams. Is it part of ms to have more intense and realistic dreams? What, if any, sleep disturbances are there, aside from bladder related issues?
Hi Dr. Boster! During this talk, I heard you way say that the immune system is overly active for people with MS (about at the 50-minute mark). When I was in high school, my sister got the chickenpox (I actually was poking at her pox because I thought it was a zit). I didn't actually get them! In Elementary school, she got walking pneumonia. As an adult with MS, I was tired of needles so I was trying to switch to fingolimod and was required to prove that I didn't have the chickenpox. I was tested for it, (which I KNEW I didn't) and I was laughed at because I never had them! So, my question... With those 2 diseases, could that have been a clue (way back then) that I would end up with this disease, or was it just luck of the draw that I ended up with it? BTW....the Lucy reference is from a movie called "50 First dates" with Adam Sandler and Drew Barrymore. It's hysterical. You should see it and let us know your thoughts. :)
@@AaronBosterMD it was just a crazy thought that I've had over my years with MS. Plus, I was so healthy physically growing up that it just hit me funny.
I also have a question about biosimilars. I have been on Rituxan and now am apparently being switched to Truxima. Can you speak about biosimilars and how these two drugs differ? Thank you Dr. Boster
I can't believe I missed this. I can't find something you said on another video but I wanted to ask you about it and what would you suggest to be on for SPMS after stopping Copaxone after 10 years use upon change in DX. I just had this conversation with my new Dr. Atrophy never came up. So not using anything for a while what would you start over with.
Thank you for this channel - I have learned so much! But I keep missing your live stream for my question. Question: Can cortisone shots for low back pain, between L4 L5, influence CSF results? So a person who is receiving cortisone injections bi-monthly is being tested for MS has a spinal tap and received negative results for the MS Profile. Could that person's results be a false negative?
Hello Doctor.. question i have a question for pain.i have a pain in my left neck its been 1 yrs n 3 months n m using gapapentin 300..but not improving.so i dont knw what m going to do..plz suggest me.thank u from Northeast India
Would taking steroids help reduce or eliminate recent symptoms of painful shoulder weak hand and heavy leg leading to odd gait? and which steroids would be most appropriate, Thanks
Can I have a ms hug in my thoracic in a straight line from armpit to armpit centered in my spine around to my chest into anxiety attack status in front? All in a straight line! When I have an attack pain is so bad I have to make baby breaths or hold my breath until i pass out almost or all together? Having trouble for 8 years in Columbus Ohio being treated at Riverside!??
I have brain lesions that are stable at this time! But still lost, Supposed to have neck fusion surgery but it was stopped when lesions were found after MRI because of balance issue! I do not what to do and in need of Help! Thank you for a reply!
Poštovani pozivamo vas u našu grupu koja se isključivo bavi temom Multipla Skleroze i vjerujem da će te u njoj naći mnoštvo zanimljivih i dragocjenih podataka o tom oboljenju. Srdačan pozdrav Ivan Novak facebook.com/groups/276128313060744/
![CAMPปลิ้น | EP.83[1/2] เปิดแคมป์หลอนต้อนรับ 2 ตัวพ่อแห่งวงการผี!](http://i.ytimg.com/vi/2uPuHYHgwiI/mqdefault.jpg)
Dear Doc, we are very delighted to have you here, in Serbia.
Will you be in Belgrade maybe? We can share some coffee.. :)
Your country is beautiful and the people are warm and generous. I won't be in Belgrade except to the airport, unfortunately. I wish I had more time!
Welcome to Serbia. I hope you meet prof Gordana Toncev. Hope some things gonna change here in Serbia in comong years . Dr B in Serbia, its a great things. Lep provod i hvala na poseti
You should have an even larger audience than you do, Doctor B, given how many more people are being diagnosed with MS lately. Your info is truly valuable and hard to come by for many of us who have non-proactive doctors. Thank you! Enjoy your time away.
Thanks for visiting :) I hope you loved Serbia ❤️
I did!
Doc B you rock! What a blessing that we have you.
Thank you Doctor, I have learned more from you than my Doctor. Thank you for all your videos.
Thanks for the program. God bless you.
Serbia,nice Dr.B! Missed your live as I'm on the Solumedrol train. Informative as always,4x4!!
Wow this. Doctor..
Hes out and about again...
Educating The 🌎 world in BOSTER style! :)
~ i think i figured it!out
It must be one of those super expensive world globes.. You know the ones..
You gotta.. spin it as fast as you
Close your eyes..
& its magic
where ever you land is where..
You.. Educate..
Empower..
And...
Energize!
.. And where ever you land that is where u go.. To educate the..
🌎 world...
I honor.that fact..
Your compassion..
How passionate.. U are..
about the type
of care you want
to provide to this village..
To each and every patient.
In this world.
somehow we(as a village..)
must reach every m.s. patient. Somehow.
For..
We as this village.
You.. See..
We brought.
The Boster Light...
"#Making m.s. boring
#We have m.s."
-Dr.A Boster
Sincerely,
Divine🙏
"Just one of the m.s.💛beat's
Of this village"
TY Divine!
Love this Divine!
~ Mikala, a beat from the Great White North
@@676dancer
I appoligize
i had missed ur comment.
Thx 4 the ms love
#wehavems
Godbless
~💛🌏Divine
I can’t wait to hear all about the conference’s. I know they are always filled with new information and exciting news.
Safe travels Doc ❤️🙏🏻
TY !
I never catch the lives streams, but I’m from Athens, OHIO ! I was diagnosed in July of this year, I discovered your videos while I was impatient at riverside!
You look great. All glowy. Travel must agree with you. Its chilly in Atlanta.
Hi from Sheffield, Uk
Dear Doc, greetings from Bosnia (neigboring country to Serbia). Here we had the same problems. There is no private medical insurance which will cover MS therapies. Thus, the state comes in. And of course, being a very poor country, MS medications cannot be paid for every MS patient. There is a committee which decides every 3 months which patients (from many applications) and they decide who gets the medication and who doesn't.
Thank God, patients in Bosnia received access to superb MS medications few years earlier than Serbia, I was receiving Ocrelizumab in the time when you were making this video.
Best regards!
Thank you Dr.B for all your love and care for us folks whom live with MS I do learn alot from you and your very knowledgeable and you understand this illness so well and you explain everything where I understand this easier I been Absent at least 5 months now without anything to control my multiple sclerosis I'm currently under care of my sister and she's bows abbly taking care of it which I don't think she is so thank you for your support and your channel you're an awesome doctor😊💙💜😉🙏
How Do i get notifications or a heads up for when these awesome live sessions happens 🤔?
Made me smile 😊 and as always extremely helpful Thanks Dr Boster
Wow Serbia, Must be so interesting. I can't stay long but will check back later. Just wondering if you heard of an inter stim device for bladder retention or if a supra pubic catheter would be better. I am 67 and between hand function, vision problems etc I can't seem to self cath. Even injured myself trying. So moving on from constant UTI's to another solution. Just confused as to what will be the best thing. I will also have my neuro weigh in on monday. Thanks for being here. Your trip sounds so interesting. Enjoy and be well.
Must coment one more time. You are and doctors like you some kind of life guru for us with ms.
Missed you again Dr. B I’m pretty sure it’s because I’m in GMT.
👏that is so awesome.
Question - After Lemtrada, when can someone go into pool water again? What about the beach? Is it safe to swim in the ocean after lemtrada? (Thank you for all you do for the MS community! You are a HUGE help to those of us in more rural areas.)
Serbia!!!!??? Say hello to dr.Obradović...and thank you for your time here, please do best to help us, 88% of patients with MS don't receive any of medicines... I'm from Serbia, on Copaxone, i haved luck i suppose...
Sorry missed live but from Houston
Hi from Wales
I have a question for you I believe I'm currently having a flare up and I'm not sure what to do I'm going to see another new neurologist and I don't know where to begin with my symptoms I was ready to start a therapy treatment but I had to move and now I have to start all over again and I'm scared that I have more damage to my brain I'm currently living in Turtle Lake Wisconsin and this weather does effect me with my mobility I have learned alot from listening to you and your very helpful advice for me to talk to my provider you've made it easy for me to talk to the Doctors I've seen I will continue to watch you Have a blessed week 😇🙏💙💜😊
Thank you for taking time from your conference, Doug coffee in hand from Lyndhurst.
I missed this live! Hoping this question can be answered in a future video. I cannot find an answer online as to whether an old optic neuritis is visible on a current MRI. I had problems with my left eye about 6 years ago. To this day it still goes blurry if I'm tired. But my 1st MRI was last month. Not sure if it could be seen that I had ON or not from that.
Question- when you are live, I forgot. I find I say that a lot more these days! Lol. Question is about dreams. Is it part of ms to have more intense and realistic dreams? What, if any, sleep disturbances are there, aside from bladder related issues?
Brandi, I get the WEIRDEST and most realistic - seeming dreams. Especially if I have to pee (drowning...🤭)
Hi Dr. Boster! During this talk, I heard you way say that the immune system is overly active for people with MS (about at the 50-minute mark). When I was in high school, my sister got the chickenpox (I actually was poking at her pox because I thought it was a zit). I didn't actually get them! In Elementary school, she got walking pneumonia. As an adult with MS, I was tired of needles so I was trying to switch to fingolimod and was required to prove that I didn't have the chickenpox. I was tested for it, (which I KNEW I didn't) and I was laughed at because I never had them! So, my question... With those 2 diseases, could that have been a clue (way back then) that I would end up with this disease, or was it just luck of the draw that I ended up with it?
BTW....the Lucy reference is from a movie called "50 First dates" with Adam Sandler and Drew Barrymore. It's hysterical. You should see it and let us know your thoughts. :)
TY for explaining the Lucy reference! I'm not sure I could connect those 2 diseases the way you describe Heather
@@AaronBosterMD it was just a crazy thought that I've had over my years with MS. Plus, I was so healthy physically growing up that it just hit me funny.
Hi Dr. Boster,
How do I find more information about stem cell therapy, specially about HSCT? What are your thoughts about HSCT?
How do you choose which conferences to go to? MS Research Australia just had theirs last month. Maybe next one??
Australia is on my bucket list! Please invite me for next year I'd LOVE to present/participate!
@@AaronBosterMD Will see what I can do. My little MS peer support group is always on the lookout for speakers too.
I also have a question about biosimilars. I have been on Rituxan and now am apparently being switched to Truxima. Can you speak about biosimilars and how these two drugs differ? Thank you Dr. Boster
I'm not familiar with that particular biosimilar.
I can't believe I missed this. I can't find something you said on another video but I wanted to ask you about it and what would you suggest to be on for SPMS after stopping Copaxone after 10 years use upon change in DX. I just had this conversation with my new Dr. Atrophy never came up. So not using anything for a while what would you start over with.
When will we hear the results of MD 1003 Biotin. I have followed this trial for years.
Thank you for this channel - I have learned so much! But I keep missing your live stream for my question.
Question: Can cortisone shots for low back pain, between L4 L5, influence CSF results? So a person who is receiving cortisone injections bi-monthly is being tested for MS has a spinal tap and received negative results for the MS Profile. Could that person's results be a false negative?
you're welcome Lorie. not enough info to be able to comment above
Hello Doctor.. question
i have a question for pain.i have a pain in my left neck its been 1 yrs n 3 months n m using gapapentin 300..but not improving.so i dont knw what m going to do..plz suggest me.thank u from Northeast India
Bio similars as a treatment
not my preference TBH
Would taking steroids help reduce or eliminate recent symptoms of painful shoulder weak hand and heavy leg leading to odd gait? and which steroids would be most appropriate, Thanks
Not enough info to answer you Maitube2
Are you familiar with ME/CFS?
Can I have a ms hug in my thoracic in a straight line from armpit to armpit centered in my spine around to my chest into anxiety attack status in front?
All in a straight line!
When I have an attack pain is so bad I have to make baby breaths or hold my breath until i pass out almost or all together? Having trouble for 8 years in Columbus Ohio being treated at Riverside!??
I have brain lesions that are stable at this time! But still lost, Supposed to have neck fusion surgery but it was stopped when lesions were found after MRI because of balance issue!
I do not what to do and in need of Help!
Thank you for a reply!
Question: if both parents have MS, what are the chances of offspring having or developing MS at some point?
1-3%
@@AaronBosterMD good to know! Thanks!
❤️
can anyone still have MS with a negative S.T ,THANK YOU DOC B
Anne, what is S.T?
Question can you have brain damage from ms without activity
Wirral UK Steve M
Poštovani pozivamo vas u našu grupu koja se isključivo bavi temom Multipla Skleroze i vjerujem da će te u njoj naći mnoštvo zanimljivih i dragocjenih podataka o tom oboljenju. Srdačan pozdrav
Ivan Novak
facebook.com/groups/276128313060744/
How I can find my number în serbia
👍
TY