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Thanks for posting these ;-) very helpful in answering peoples questions and answering some of my own

Nice Video

That Cliff guy knows a lot 😁

very interesting and useful to get different insights

I appreciate your careful enunciation, and not being distracted by extra generic images and music

Hi from Israel interesting video thanks

Congratulations Jon, on 7 years of Real Talk MS! 👋👋👋 That's a huge accomplishment! I greatly appreciate all the information that you make available to us!

I am on Medicare and tricare.

As always was a great episode. And, as always I shared with my Face Book family of over 13k MS'ers. Thank you for all you do

So glad you had something for us progressives MS types l hope to see more .

6:55: to many level of corruption going on: FDA, Big Pharma to name a few…. We patient are living on false hopes only!!

Let’s not kid ourselves, 78yrs of history and exactly what did they achieve? mission statement: “pathways to cures” is a joke

Thank you for this information. I was diagnosed 2023 and it has been a challenging quest to educate myself on this disease but with podcasts like these I am happy to. Know I am not alone. Thank you.

I can report a symptom that went away- bladder urgency and control! It is such a common symptom that when it worsened I even tried prescriptions. I had already done pelvic floor therapy and their tricks were no longer enough. I finally had a good time to have an abscessed tooth pulled. I didn't even know it was an issue until I had a CT scan after a cleaning where I reported it felt "kind of odd". As soon as it was pulled- within a day- I no longer needed my Tolterodin and did feel the same urgency or loss of control. Amazing. A little infection like that was kicking off a pseudo attack that lasted for almost a year!

Hi 😊 What if I am getting worse on high efficiency DMT? But no new spots on MR? Thank you so much for your channel 😊

So good thank you

excellent interview. Relevant to many conditions other than MS

Hi from Israel thanks for the interesting data this is the first time I listen to your talk waiting to Your next talk

this is a lie,..people progress on DMT to SPMS....see "onset of secondary progressive ms despite long term Rituximab therapy "

Thank you for this video. Being a member of the over sixty crowd I appreciate all the information offered by Dr. Boster.

Thank you, this was awesome because I’m one of the black women

Thank you

Thanks so much, this was incredibly helpful!❤🙏

Thanks for sharing this info, it's difficult to find focus on progressive MS!

I would love to see more attention drawn to the developments in therapeutic vaccinations. Any treatment that can generate immune tolerance to autoantigens is likely to create a better future for anyone with an inflammatory autoimmune disease.

Regarding the anti-CD20 therapies, I vaguely recall from the research many years ago that CD20 had been identified on the surface of some T cells. The specific type of T cell had not been identified, if I remember correctly, but the point is that the effect on B cells may not actually be how those therapies work. Or I could be wrong about this. It was many years ago that I read about this, and my memory is not what it used to be.

From what I have seen of the research, the things most encouraging to me are therapeutic vaccines to generate tolerance to myelin antigens. I expect that tolerogenic vaccines are going to be huge for autoimmune diseases in general.

I found this so helpful. I have brain lesions but haven’t been diagnosed yet. I’m 62.my primary symptom is bladder disfunction and tremors. I’m also a nurse. I retired and got somewhat depressed because I missed my work family and my purpose to serve others. I love Dr Booster. He is very balanced in his approach and so relatable. Thanks for the support.

Thank you all ever so much for this!! I’m new to Real Talk MS and was delighted to find this gem 🙂 Cognitive difficulties are the most difficult part of MS for me. Also, have you done - or would you please - do a Real Talk on Brain Mapping Therapy and MS [mentioned in Norman Doidge’s book] please? 👍🙂

I’m 30 years dx this year. I was diagnosed at age 17. This is Such an important topic! I think that ,like everything with this darn disease, we just have to work harder, try harder, be more pro-active, creative and resilient than anyone else! We need to be on point with our diet, exercise, mental health management, social group maintenance, optimism, curiosity about the world and lifelong learning.. I’ve just started studying a degree in Cybersecurity - distance learning to challenge my mind. NEVER GIVE UP ON YOU!! Much love Xxxx

I just found REAL TALK MS GREAT. It was my Aunt Ethel's REHAB. She died in 1974 at the age of 60 from MS complications. Her daughter died 20 years later of the same thing. I only knew my aunt in a wheelchair, she could only move her head. She had to be changed and fed. She did as much as she could on her own for as long as she could. I was diagnosed in 2000. I am now a 68 year old man with secondary protrusive MS . My aunt inspired me to always be aware of what available on the market place to help me do better. I get teary eyed when I think of we have and what my aunt didn't. BEING AWARE of what is available makes me less scared of the future.

Social isolation is such an important topic in MS.

Courtney

Good morning boster ❤❤❤😂😂😂😢😢😮😮😮😅😅😅

So happy to hear Dr. BOSTER on your show. Thank you for posting

I share with my MS group 13k+ every Tuesday. I would like to hear more from Dr. Aaron Boster

Does A&W sell fish? If they want to help MS they should start serving health promoting food.

30:00 Exercise helps brain function with EVERYBODY, not just people with MS, this is nothing special.

Canada has high MS levels? Coincidentally Canada has low UV light from the Sun and low levels of vitamin d. Hmmmm.... Lots of Tim Hortons and McDonald's burgers eaten and not so much fish, eh? Omega 3 levels must be low too, eh? Exercise is good but over stressing the body with exercise may not be the best thing to do.

Dr. Burt saved my life. I had progressive Systemic scleroderma, the Transplant stopped the progression of the disease. He has a great book out, Everyday Miracles. He is great doctor.

So glad you had her on !!

Promo'SM 🙂

Thanks for this episode. These doctors are at my clinic.

Realtalk. you shared beautiful !so long~:))

I was waiting for something like this! Your content deserves a service like S M Z E U S.

We will want to hear about your voyage Jon.😃

I can relate to you 100% , faith -- I was diagnosed when I was 14 (so 13 years ago) and about 6 years ago, I also needed a plasmapheresis (I'm jealous of the location that you got that I'm, mine was in my chest lol) (but I think that my 4 back to back attacks might have been caused by my unstable relationship with my family.... Like I just escaped running away from my exhub, Mr Ms....... Getting kicked out of their house really took a toll on me...... But I've rebuilt my relationship with them and I'm finally doing allot better) ♥️♥️ your resilience is so motivating and we're so much stronger than our MS 🧡🧡🧡

AMAZING YOUNG GIRL. I'M 74 AND LIVE ALONE BUT INSPIRED TO TRY HARDER!

Nice interview

What a wonderful and inspiring story! She is a wonderful and giving young lady! Thank you both for sharing!