hey I'm a 48 year old female diagnosed 9 years ago with Ms also a brain anyurism and then graves disease within 3 months of each other on nothing not a day of pain still driving and walking
I was going to bed when I noticed this live stream, so it was too late for me to continue watching, but living in the UK, i will definitely catch Saturday's live stream. I have learned so much about MS from your content DR Boster, so thank you! 😊
So sad I missed this last night. Sweetwater,Tn. Thank you Dr. Boster, I have learned so much from you. Gonna ask my Neurologist if he knows of you on my next appointment when he reads my newest MRI I had Tuesday. Even though he is much older than you, I feel like he could learn so much if he was willing.
Sorry I missed this! I’m from N central Illinois and at 70 wondered if there’s hope for me if I come to your center for possibly finally being officially diagnosed with MS. I had HepB 52 years ago and I understand biologics can reactivate the virus. IF I’m dx are there safer treatments? My daughter is willing to help get me there (as I’m going blind with optic nerve damage, etc), if it will help. Thanks for your time.
If it were me, I'd try to get diagnosed locally and then I would send all my labs and imaging to the doctor I wanted to see. You don't want to go all the way to Ohio to find out it actually isn't MS. I saw a doctor at first and then got a second opinion and that really helped me feel confident in my treatments.
Brain volume. Lol I still make jokes about the first time I was told I had "age appropriate brain shrinkage". I go to a 5 Tesla MRI. The first time I went I felt woozy after the test
Hey Doc, what’re you doing on here out of the blue? How’d I miss this beauty? Glad 🙂 I’m catching this now. Although I’m drinking now… so apparently will be up peeing all night… 😑 🙄🤦♀️😂 #sharingiscaring Ty for all this great information
I keep missing these but watching after is still so helpful. Thank you Doc!
hey I'm a 48 year old female diagnosed 9 years ago with Ms also a brain anyurism and then graves disease within 3 months of each other on nothing not a day of pain still driving and walking
❤ wow
Me to but I am not okay 😢
@mandiq7281. I love this for you! I pray you have continued great health❤❤❤
Thank you for explaining the importance of the strength of the mri.
Glad it was helpful!
Hello from Poland. Thanks for all of your videos. I am learning from them more than from my neurologist. Good job👍
Facts
I was so excited to see this last night! Like, wow an extra one?? Love it!
I learn sooo many things from you!!🙏🙏🙏🙏🙏
I was going to bed when I noticed this live stream, so it was too late for me to continue watching, but living in the UK, i will definitely catch Saturday's live stream. I have learned so much about MS from your content DR Boster, so thank you! 😊
As a previous smoker, I agree with the advice you gave! I really enjoy your videos. I have been listening for several months. In Ohio also!
So sad I missed this last night. Sweetwater,Tn. Thank you Dr. Boster, I have learned so much from you. Gonna ask my Neurologist if he knows of you on my next appointment when he reads my newest MRI I had Tuesday. Even though he is much older than you, I feel like he could learn so much if he was willing.
'Down Under' in New Zealand 2259 Thurs 21 Nov. Thank you for the educative, highly informative vids, of notable value. m
IM fasting lost 70, a1c 6.5, don't eat anything processed. No change in MS issues though
Congrats to you!
Watching replay .
Thank you for sharing.
yes
Sorry I missed this! I’m from N central Illinois and at 70 wondered if there’s hope for me if I come to your center for possibly finally being officially diagnosed with MS. I had HepB 52 years ago and I understand biologics can reactivate the virus. IF I’m dx are there safer treatments? My daughter is willing to help get me there (as I’m going blind with optic nerve damage, etc), if it will help. Thanks for your time.
If it were me, I'd try to get diagnosed locally and then I would send all my labs and imaging to the doctor I wanted to see. You don't want to go all the way to Ohio to find out it actually isn't MS.
I saw a doctor at first and then got a second opinion and that really helped me feel confident in my treatments.
Primary MS clinical trials? Enjoy your down to earth honest. Jupiter Florida 😮
Same sleep 💤 issues, it’s almost like I stagger my shitty days, don’t take adderrall, work out get obliterated so the next day is a real gem?? Yikes
When will the B2K Inhibitor be available to use?
Netherlands 3.40 am. Just seeing this...still hoping to get a few hours of sleep, so gonna catch up later...
Annette from Maryland
Replay…Florida…darn! Thanks!
I have PPMS would like something better the Ocrevus
Dang I didn’t see this I’ll be there tomorrow Dr B!
I have had almost every symptom of MS and yet, my neurologist says as she said my MRI is not typical. Yet she doesn't know what is wrong. Frustrating!
Ask for a referral for a neuro optomalogist. Maybe he/she can give insight.
Brain volume. Lol I still make jokes about the first time I was told I had "age appropriate brain shrinkage". I go to a 5 Tesla MRI. The first time I went I felt woozy after the test
Canada
Spokane, Washington
Hey Doc, what’re you doing on here out of the blue? How’d I miss this beauty? Glad 🙂 I’m catching this now. Although I’m drinking now… so apparently will be up peeing all night… 😑 🙄🤦♀️😂
#sharingiscaring
Ty for all this great information
Is there anything dealing with remilation?
this is cool
Anything on ocrevus zunovo
I really, really love that cigarette strategy for decoupling addictive activities to turn keystone cigarettes into dumb cigarettes.
Have you heard of bee therapy and if so what are your thoughts?
If your Lumbar Puncture was contaminated with abiotrophia defectiva. Would you trust the o band impression.
Like to hear from you
I'm late!!!😢😮
Post-Video Flames: 🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥🔥
From Beaverton ontario
I think I have spacity in my right ankle, do you see this a lot?
canada
The big city of Massena Iowa.
Replay…Idaho!
oklahoma here
Hi Dr boster, I'm from Australia, and have MS, love watching your videos, I also have heaps of questions and concerns, but don't know where to start.🫤
Hey
From uk, its 2.30 am...no sleep from ms
I understand, I struggle to 4 am here, lucky if I get 5 hours of sleep. 😮