Just Diagnosed With Multiple Sclerosis - What's The Next Step?

[@kathrynmcvean2514]

Not new to MS but it’s always a good idea to hear these 6 ways to live best with MS. Thank you - again!

[@desiredecove5815]

This is great for everybody with MS, not just the newly diagnosed. Thank you for all you do to keep us as functional as possible. Much love and respect. #StrongerTogether #SharingisCaring

[@frankiegraham3918]

That drum scared the hell outta me!!

[@gebuikersnaam]

Just been diagnosed... 49 male healthy and i am still ok.. starting with ocrevus next week.. active leasures in spine and brain

[@Julien.gauth6581]

thank you doc, I was diagnosed last year and your videos allowed me to accept treatment (kesimpta) I hope that those who are looking for information will come across your always factual, educational videos... I would have liked to find an equivalence in French! take care of yourself 🤘

[@EvenSoItIsWell]

Brilliant video Dr. Boster! Such great advice. Thanks so much for being you!

[@AaronBosterMD]

Glad it was helpful!

[@PJ-bv9tc]

I really appreciate your videos Doc. I am not (yet) diagnosed with MS. Tests come back negative, which is a good thing, but I have certain MS like symptoms, which is a bad thing. But advice like this video helps me make healthier choices as I face…whatever this is. Thanks Doc!

[@MsY3sssi]

I actually just got diagnosed when you uploaded this video. 😅 great timing!

[@millymcrae3434]

You are one of a kind Dr Boster! Please come to Australia and do a talk. Your videos kept me positive as I battled through my first relapse in 10 years since initial diagnosis. Love your touch of humour too.

[@NickMaynard-hi4bl]

This is great advice! I’ve had 2 neurologist that said nothing like what’s in this video. Unfortunately I’m starting this advice 5 years after diagnosis. Please keep the informational videos coming

[@jtiahrt]

I was fortunate to be one of your patients at the OSU clint in Columbus😎 thanks for all the advice you give us!

[@AaronBosterMD]

Call us at 614-304-3444 and let's reconnect in Clinic! BosterMS.com

[@missapink6616]

Appreciate you and your content. I was just diagnosed last week and your channel has been so informative and comforting. I start tysabri tomorrow

[@JenAnty_JA]

Thank you for your videos, they helped a lot. I was diagnosed on October 2023, since then I'm taking Ofatumumab monthly, but today I found a new lesion. My neurologist does not know what to do, my CD 19/20 is zeros. No sugar, alcohol, drugs and no smoking, do exercise daily.

[@sashaSwetlowski]

water is highly underrated. each of these tips actually. Food, water, exercise, stress, and mindfulness are critical to everyone, but they make a bigger difference if you have MS. thanks for another great video.

[@cathypyper3977]

You're amazing, this is essential advice! My neurologist gave me a stack of Rx brochures and told me to call once I picked one.🤯 He only lasted one year.

[@Ian-fg7rq]

Sounds like I have the same doctor you used to have. Have to meet with him again next week with MY pic of medical treatment and if I’m going to take it with injections I give myself or if I will go somewhere twice a year for medication. Ask doctor what I should do (which was better) and was told it was more of a preference and basically woks the same….

[@rojinsamurai1]

Great video. I’ve been diagnosed with MS for a few years and find it helpful to have these reminders. I find Dr Bosters’ videos to be very helpful regarding MS.

[@jorgecastillo8110]

I was diagnosed on May 2010. Got a great job, lost 50k, got a great woman, everything was great, but I started to have a feeling of nothing matters, around 3 years ago, long story short, lost my job as an software architect and did not care, got out of the relationship and did not care, stop driving all together (I was loosing my mind every time I drove), I had lost a family member due to cancer and did not care. Last December I was admitted at a psychiatric hospital, I really wanted to ended all. now I gained 15kilos since December, rarely go out of the house only for my hospital appointments. I know how it is going to end. I believe MS is a weird illness. Since I have been a kid, I was not educated, but groomed and trained to be a good person a hard working person, to follow all rules. To the point our dad had a whistle to call us back like dogs lol. either way. I do not know if repressing as kid and as a grown man has anything to do with MS but I do know that repressing your feelings is not good for your body.

[@uzer-95]

Конечно играет роль. Вам нужен психосоматолог. Держитесь. Мне вас жаль 🤗🌹🌹🌹🌹🌹

[@arthurmiller9103]

Awesome and effective life saving protocol. Thank you🙏 Be Well.

[@lauraluffman6177]

Thank you Dr Boster you are an angel ❤❤

[@stonz42]

Thanks for the tips Dr. B! I've followed your advice after being diagnosed 3 years ago and doing well. For me, regular exercise (especially outdoors) and being strict with my diet and water intake have helped tremendously. All of that also helps with managing stress. My doc put me on Tysabri right away as well, which was switched to Ocrevus just over 2 years ago. All of the above have kept me at NEDA3 for over 2 years.

[@colleenstack210]

Thank you Dr. Boster for this video. This is a great video for us even not brand new to the dx to reinforce the basics. One thing I love is Pilates keep the core strong.

[@ktaylor6490]

What to do, Get your bucket list done & have no stress or Regrets

[@yogeshmalhotra9120]

It's a nice and great video to have more clarity on the disease. Thank you Dr

[@pasholnachui]

Dr Boster thank you so much for all the effort and energy you put into these videos❤🙏🏻

[@brettvogel3042]

I'm 51, and I got diagnosed with Primary Progressive MS back in January. I may also possibly have colon cancer, so I can't get treatment until they find out what's going on with my colon.

[@wilnahuffman8634]

Great information!

[@lisahope4582]

Thank you so much for all these videos ❤❤❤

[@lesliebarringer999]

On the water, can it be sparkling water? That seems to be the only water I can tolerate without severe bloating.

[@rebeccapetty5440]

Thank you so much

[@danielhernandez-fo3mj]

Hello doc .... dident knwo how to possibly get an idea for you to dona video onpelvic floor issue in ms spasifclly with males as there's so much on women and this issue in ms I just recently started learning men can have this issue also some times labeled as prostatitis or chronic pelvic pain syndrome.... I have been having these issues but most docs have no awesers at lest the ones I talk to...... weakness or spasticity in the waits or pelvic area I think is the culprit but there's alot it can effect with male down theres

[@karenclark-g5k]

Thank you always useful

[@geraldinebarcheski6376]

If you have lesions and also prior MRI of spine and brain that shows demylination but spinal tap shows no 0 bands does that mean you don't have MS?

[@busygirl4474]

I get really sick the day after steroid infusions are over terrible nausea Is there a way to prescribe oral steroids to wean your body off of them??

[@LuckyKat89TV]

I've been undiagnosed for about 13 years. How will my treatment be different?

[@valeriealv7503]

Just diagnosed very confused hasn't said what kind

[@willemdafoe9646]

I had mononucleosis 2 months ago and have started to have „electric/shooting pain“ in fingers and toes for two weeks, as well as tingling in my right foot for 3 days now 😞 Knowing that an ebv infection is necessary for the development of ms, how realistic is it to develop the desease so shortly after infection?

[@Darteghoster]

Hello! What do you think of vape? Cause i cant smoke cigs and nicotine vapes. It gives me massive tremors, but zero nic vapes works for me.

[@gnanashekar1579]

Hi Dr. @Aaron - I just figured Erectile Dysfunction could be one of the symptoms of MS. Is this a permanent ED or is this reversible?

[@Wendy-nv5cd]

Can the water be cups of tea with milk? What about coffee, or do this caffeine beverages cause dehydration?

[@skyeschallenge78]

Hi sir. I wanted to say thank you for this video and your caring nature. I live in Louisiana. I am being sent back and forth with neurologists and neuro ophthalmology. No one will tell me what’s wrong. I have had 2 MRIs and one reading says probability MS. The other report has a lot of fancy words that I don’t know or understand. To be very honest it’s frustrating and I am scared. Could you help me? Could I show you the MRI reports and you explain to me what they say? The only thing I have been told so far in this case is migraines. If you can’t I totally understand that. Thank you, Amber

[@LinhWithMS]

Doc i waa super fit through walking my dogs but also loved got to yoga clas at least 3 times a week some classes are heated someone arent. Even for the ones that arent, the room heats up bc if so many people ans that includes the humidity. Does this mean it should be off thr table for me?

[@dharmacharinipasadanandi7110]

Thank you

[@conniereeves2711]

Ive been having the ms hug for years but could never get a dr to help me. Now many years later i am having many symptoms, especially crushing fatigue. I told my dr that i feel that i have had ms for a long time, now recognizing symptoms ive had for years. She doesnt believe i have ms because i am 65 and wont advocate for the MRI to diagnose. So, my question is, how do i live my best life without medical treatment?

[@alleyes9911]

Hi , I will get right to the question , I have both cervical and lumbar stenosis and am worried I could develope MS due to some symptoms ?

[@suziwatkins5499]

That is too much! I don't think I can do it😢

[@beckypike355]

You can do this! It's probably not the best thing to do, but I motivate myself with fear. I don't want to have a flare-up. I don't want to be dependent on others. This makes all of Dr. Boster's advice something I welcome and cling to.

[@SMjeffkameny3711]

I didn't think I could either....7 years later I'm still living my best life.......

[@sashaSwetlowski]

start with the water. these things require practice, and any amount of progress will make you feel better, which will lead to more progress.

[@sannawiklund7298]

How do you drink that much water when you have to drive around for work and are lucky to get one toilet break in 7-8 hours? 😮 I usually drink practically nothing until I come home and then I can't drink litres of water (100 oz is almost 3 litres) if I don't want to wake up four times at night to pee!

[@BellBell-t1r]

Start doing one or 2 of his suggestions. Then when comfortable with those try adding a couple more. I know it is daunting to try all 6 from the start. And maybe just add one extra glass of water to start. I wish you all the best. Our daughter has MS. She is 42 years old. Was 22 years old when she was diagnosed.

[@valentinpopescu1156]

Hello, Dr.Boster. I'd appreciate your opinion about neuroplasticity in relation with spinal cord lesions. are they mutually exclusive?

[@Jr_thepro10]

What if you vape thc ? I feel like it helps with my pain and sometimes my mood

[@ItzDeDe]

I recently had a spinal tap can you please help me understand my results the anxiety is taking over and I'm not scheduled to see my neurologist for a month. CSF - Glucose - Normal - 64mg/dl CSF - RBC - High - 61 CMM CSF - WBC - Normal - 4 CMM CSF - mononuclear cell - 4 CMM CSF - IgG - High - 5.30mg/dl CSF - Albumin - Low -

[@Edhymbss21]

Thank you for these videos! Do you have any experience treating ulcerative colitis and Ms? My GI and neuro want me to take kesimpta but I’m already on Entyvio for the UC? Are two biologics safe together?

[@tonnyncellist5910]

Any news on BTK inhibitors?

[@ParisLeShea]

How might having ADHD affect someone who also has MS? Both are neurological conditions so I’d imagine it would make things harder?

[@butterflyangel1139]

How many years typically go by from an onset of RRMS to becoming SPMS? Also is it inevitable for RRMS to turn into SPMS (like after having RRMS for a long time?)

[@anaribeiro509]

No. With the DMTs we have now, the majority of us (with RRMS) never will be SPMS!

[@anaribeiro509]

In todays MS world, that is a mith.

[@anaribeiro509]

The majority of people with RRMS will never became SPMS. ❤

[@M.SsyMoves]

What if your neurologist gaslights you?

[@conniereeves2711]

😂 "in there like swim wear"!!! 😂

[@giaminh242]

can i switch to Vape or Pod, doctor ?

[@nomudnolotusnodragonnogold]

Its still nicotine. Nicotine bad. Plus, god knows what all is in a vape. No judgement here. I switched to vaping to quit a 30 year smoking habit. Now I've gotta quit vaping.😭

[@charliebucket7494]

House remodeling?

[@michorote106]

Can I get cancer with ms

[@ianpoulter1442]

No offence but my experience with MS is that you”ll wish u had cancer instead of ms 😢

[@desiredecove5815]

Yes

[@Ap9-q5f]

Why do you say this just diagnosed scared​@@ianpoulter1442

[@anaribeiro509]

Yes we can have cancer like anybody else. 🤷‍♀️