I love having my morning coffee with optimistic Dr. Beaber! I do believe it will get better. I am particularly excited for the newer high powered MRIs and AI and also how diet and lifestyle changes can help us to support our health, better manage our symptoms, and possibly prevent progression.
It's good to hear encouraging news about MS treatment. I wouldn't wish that disease on my worst enemy. My father died of complications of MS in 1982, as a quadriplegic of 12 years. At that time the `treatment` wasn't much. I've noticed the progress over the years, and it's good to see. Too little too late for my dad, but plenty of hope for the present and future.
I was on Copaxone back in 2015 when I was diagnosed then I switched to Ocrevus in 2019. I was scared of the side effects after my neurologist informed me of them but after speaking to his nurse, I felt relieved to know what even his nurses have huge belief in him. After switching to Ocrevus, I continue to have no major relapse like vertigo and going almost a decade strong relapse free. By no means have I been unaffected from MS though. After 7 years of being diagnosed, I finally got muscle weakness in my knees. I'm not happy about it but it could have been worse so I'm thankful it wasn't something horrific.
Every medicine has side effects and risks. People don't say they treated their fever naturally. They take antipyretics! Most people have never said the word lymphocyte and they want to avoid DMT bc they're scared. Not being able to see is far scarier
I too switched from the original drugs (Copaxone first - then Avonex - then Rebif - then Rebif + mycophenolate - then Tecfidera. After relapses seemingly every year (I always had great recovery, but went right back into inflammation) - I switched to Rituxan and then Ocrevus. It was life changing. They keep relapses at bay.
I am extremely grateful that my team was able to diagnose me right away because I heard stories of men that didn’t get diagnosed until later in life. I’m a 26 yo male and had my first symptoms December 2023. Diagnosed January 2024.
Moving from Kesimpta to Mavenclad shortly for my SPMS as none have had a "therapeutic" effect on my disease progression. My clinician at NIH thinks that my daily gym time has been my best therapy.
I love your thoughts processes…I agree that better more effective diagnostic and treatment ments are coming. I am a long termer and have around since before DMTs and have tried most. I am now in my 60s, and eat well, exercise and do all the things to a stay active amd healthy I think people forget that neuroplasticity is a newer concept and is real. I have mobility issues, and had to recently stop Aubagio from side effects but I stay hopeful, because why not…the alternative isn’t helpful either. I look forward to a belief that aggressive treatment is a a standard and remyelination to fix the damage becomes a reality…thanks for always sharing interesting takes on managing the beast!😊
I think expediting clinical trials so that exciting drugs like PIPE-307 and NVG 291 will be available to people who have progressive MS will not accrue more disability than they have to. As for future content I would be interested to hear your thoughts on new electrical stimulation technology such as Stim2Go distributed by Pajunk.
Thank you for your very helpful videos! I live in New Mexico, and we barley have neurologists, let alone MS specialists here, so its great to have access to your content. Just in case it helps, I'll go over how my new diagnoses and treatment of MS has gone. I was diagnosed with MS 6 months ago. I went to my Primary Care Doctor after loosing feeling in my hands, abdomen, and feet. She ordered a head MRI, after it came back with lesions she referred me to a neurologist and I was diagnosed within a month of my symptoms starting. My neurologist started me on Ocrevus and prescribed me a 1500mg vitamin D supplement to take weekly, since my vitamin D levels were really low. I feel like your prediction of MS being diagnosed more effectively and treated more aggressively with higher efficacy drugs is in alignment with my recent experience. I also feel very lucky to have an amazing Primary Care Doctor who immediately sent me for an MRI.
Hi! Preliminary results of the alpha-lipoic acid (LAMPS) study have been published. The difference in atrophy rates is striking. -0.58 cm3 (LA) and -7.18 cm3 (placebo) at p = 0.084. (not as little as we would like). It is also worth noting that proteinuria is very common among people who have taken LA
Terrific video! I really look forward to Wednesday mornings. I am thrilled by the varied research that is ongoing and I believe the next 10 years will be very exciting. Things I wonder about... How is the MS medical/research community organized. How do guidelines and recommendations get reviewed and sanctioned and then put into practice? E.g., Why would an insurance company ever deny a highly effective DMT when the data are so clear? What governing body recommendations hold the most weight when it comes to MS?
After hearing a lot of news lately about promising drugs getting on trials, like PIPE-307, I have somewhat become more optimistic than 2 years ago when I got diagnosed. So optimistic that I now believe I will live witnessing the discovery of a cure for MS. Even here in Greece we expect trials on Diaprotectome to start later this year, another drug for MS developed from a Greek-Australian doctor. As for faster diagnosis times, I feel there's still a big room for improvement and especially when non-specific symptoms come into play. In my case I got diagnosed with a 2-year delay and only after ataxia appeared. During the 2 years before my diagnosis I would have constipation that would appear, be insistent for a month inspite of using laxatives and then go, all that while still getting good amounts of fiber and water. MS is quite a tricky disease...
If they could find some way to reduce brain atrophy in people with MS (or brain atrophy as a whole), that'd be great. I know some DMTs can reduce atrophy somewhat, but not completely or for everyone with MS. I wish I could see into the future 100 years to see what the future of MS treatment looks like. Maybe an effective EBV vaccine could effectively wipe out MS (and other related conditions). I agree that AI and super computing has the potential for HUGE advancements for fighting MS.
Brain atrophy scares me, too. I've written here before how I'm apparently the last person on Earth still on Interferon, and that one does not slow down atrophy at all I think.
@Ennugia my old neurologist, while being very good at doing very thorough exams every 4 months, never went over my MRIs with me. He relied on what the neuroradioligist reported (that always said "no interval change"). When I finally looked at the MRI myself, I was SHOCKED at the severe atrophy I saw compared to my first MRIs years ago. It threw me into a deep depression.
I think your being practical-optimistic lol you covered alot of the practical things with a optimistic flair lol i read a post on a Facebook suport group of a lady who was diagnosed in the 60s by the hot bath test .... so like you and the wheelchair guy i was thinking of all the the way all people like me where so lucky to have the tech we have today compared to just the 70s ..... just a small time ago in the ms journey of the disease ..... I also was wondering have we hit a plateau of some aspects of ms ... like the mri ... mabye it will take longer for new tech to find itsway to find ms faster and more accurate.... but I do belive we will find better ways to treat progressive forms of MS now that rrms has been so easily treated .... grate video DR B
Hi doc, I know you already have a video on neurogeenic bladder & UTIs but how about one for UTI vacines being developed? And for pelvic floor PT? Very interested in these as I have combo incontinence and retention. I can cath but dont want to do it due to UTIs I keep getting. Maybe new technologies coming out for cathing? Better caths? Also one on neurogenic bowel? Anything new with the microbiome/gut flora? Just throwing all of it out there. Thanks for all the videos!
Thank you for these kind of videos! Is impossibile in your opinion that in the near future Will be Discover the cause of MS and develop a drug that stop Forever the disease?
I don't think a single cause of MS will ever be found. I think it's a complicated disease with several contributing factors. The closest thing to a "cause" is epstein barr virus, but some studies on pediatric MS find that
My lifestyle change of adopting whole food plant based diet with mushroom tinctures, proper vitamins, and microdosing psilocybin has actually given me sensation back in my feet, and my Lhermitte’s sign has diminished severely. I believe western medicine should adopt more holistic approaches. The benefits I have been gaining have been beyond remarkable! Not taking a DMT yet, but I can confidently say, I have reversed my poor balance, numbness, and brain fog completely by sticking to my holistic protocol. Would love to talk with you about my experience Dr.
Well the damage can't be undone I'd do literally ANYTHING to go back in time and have the use of my arms back Don't play with this. Please actually take a DMT or there's good chance you regret it. I work in ems and am likely losing my career. You're playing with fire
@ I am sorry for your experience but you have not adopted MY protocol and MY lifestyle. You have no information on what I am doing to fight this and it has been proven very efficacious. Please show some respect and an open mind and heart. It’s interesting that you perceive the human body to be incapable of healing itself.
Looool I am so fit and have been a strict vegetarian 18 years. I lift humans for a living. The damage is being done. People want to call food a DMT LMAO it's not. You want to gamble? Ok. Go for it. But don't get upset when you lose something you can't get back This disease happens to people with your "lifestyle". If it was your lifestyle that was working we'd stop giving out DMTs and diagnosing it and admitting folks to the hospital with it You didn't reverse your MS. That's not how this works. I'm tired of instant people trying to drag others down. I JUST got diagnosed at 35 because I'm a woman and my symptoms for 13 years were ignored. You don't have to deal with that but you'll just let disability happen to you? Ok then. 🎉
The damage caused by MS is often irreversible, and you will never be able to undo it completely. Over time, without potent drugs to control the immune system, the damage accumulates. It is your body and your decision, but think carefully.
I appreciate the optimist look forward. Remylenation and axonal regeneration would be amazing advances. AI may be a path to get there. I am also optimistic about neuralink and how that may play a part in helping our nerves to better communicate. I don’t think in the current form but the ability to generate nerve impulses and be responsive to task direction is promising.
I have the strangest case of MS. 1st symptoms 10 yrs ago, lost central vision lt eye, and along with it 10 plus other MS symptoms. MR shows stable periventricular and juxtacortical lesions that have never changed. I take nothing for it. FT worker, pump iron like a beast at gym 😛 and I'm 55.
Discovering the pathogenesis of the disease will be the only way rational treatment decisions can be made. Drugs may not be the answer, for instance diseases with a metabolic component can be managed with diet.
Do you agree with the fab Dr Boster that with the current highly effective DMDs along with supplementary diet and lifestyle changes, in the current era, MS can already be made 'boring'?
We are very good at stopping relapses and new MRI lesions, and many people with MS are stable. I unfortunately don't think we can stop 100% of progression with current technology.
I hope your predictions come true during my lifetime as well. I have my fingers crossed for CNM-AU8 in hopes it can recover some of my vision loss. I’d love a less suppressive version of ocrevus too. My neuro said as long as I’m not having recurring infections, I can continue on ocrevus despite having low IgA and IgM. G is normal, but not by much, and that concerns me a bit.
Thank you for another optimistic and informative video, Dr. Beaber! A question: you say ‘relapsing MS’ several times instead of ‘relapsing remitting MS’. Has terminology changed? And could you explain why?
Some relapses are not followed by complete recovery, and there is evidence of subtle progression in some people with relapsing MS, so I think the term "remission" is misleading. Also, many have significant symptoms during "remission."
Hello Dr.Beaber - I was wondering if you have come across any of the papers covering tDCS simulation in regards to alliviating MS symptoms and assisting in the repair of lesions? I was also curious on any info you may have regarding the papers which discuss tENS stimulation of the dominant-hand median nerve in order to enhance tactile sensitivity in the hands of MS patients in the long-term. Both of these areas seem to have very promising results for symptom management and restoring a nomial state of health, so it would be great to see your take on them!
It is possible to develop anti-drug antibodies against monoclonal antibody drugs for MS (tysabri, Ocrevus, rituximab, lemtrada, kesimpta, etc). The underlying immunology behind this is very complex and idiosyncratic.
Hey dr beaber , how are you i hope you are doing well, dr i have read some articles stating that keto diet help in protecting the brain from damage and being studied in Alzheimer’s and dementia Could it help in Ms ?
I love having my morning coffee with optimistic Dr. Beaber! I do believe it will get better. I am particularly excited for the newer high powered MRIs and AI and also how diet and lifestyle changes can help us to support our health, better manage our symptoms, and possibly prevent progression.
It's good to hear encouraging news about MS treatment. I wouldn't wish that disease on my worst enemy. My father died of complications of MS in 1982, as a quadriplegic of 12 years. At that time the `treatment` wasn't much. I've noticed the progress over the years, and it's good to see. Too little too late for my dad, but plenty of hope for the present and future.
I was on Copaxone back in 2015 when I was diagnosed then I switched to Ocrevus in 2019. I was scared of the side effects after my neurologist informed me of them but after speaking to his nurse, I felt relieved to know what even his nurses have huge belief in him.
After switching to Ocrevus, I continue to have no major relapse like vertigo and going almost a decade strong relapse free. By no means have I been unaffected from MS though. After 7 years of being diagnosed, I finally got muscle weakness in my knees. I'm not happy about it but it could have been worse so I'm thankful it wasn't something horrific.
Every medicine has side effects and risks. People don't say they treated their fever naturally. They take antipyretics! Most people have never said the word lymphocyte and they want to avoid DMT bc they're scared. Not being able to see is far scarier
I too switched from the original drugs (Copaxone first - then Avonex - then Rebif - then Rebif + mycophenolate - then Tecfidera. After relapses seemingly every year (I always had great recovery, but went right back into inflammation) - I switched to Rituxan and then Ocrevus. It was life changing. They keep relapses at bay.
I am extremely grateful that my team was able to diagnose me right away because I heard stories of men that didn’t get diagnosed until later in life. I’m a 26 yo male and had my first symptoms December 2023. Diagnosed January 2024.
Look up HSCT. I was diagnosed more or less at your age. Was a year on Ocrevus then went for HSCT. It’s basically a cure if you’re young.
❤ oh my gosh, I’m hopeful for everything that you said!!! And it can’t come soon enough.
Thank-you Dr Brandon, for another informative video, so much appreciated.
:)
Dr. B, you always give me hope! My ms is spiralling out of control… my neuro is useless! I really wish you were my neurologist! ❤️
Please get a new one! My first was terrible and I fired him after 1 appointment.
Moving from Kesimpta to Mavenclad shortly for my SPMS as none have had a "therapeutic" effect on my disease progression. My clinician at NIH thinks that my daily gym time has been my best therapy.
Thanks for sharing. Sorry you haven't had great results with these medications.
I love your thoughts processes…I agree that better more effective diagnostic and treatment ments are coming. I am a long termer and have around since before DMTs and have tried most. I am now in my 60s, and eat well, exercise and do all the things to a stay active amd healthy I think people forget that neuroplasticity is a newer concept and is real. I have mobility issues, and had to recently stop Aubagio from side effects but I stay hopeful, because why not…the alternative isn’t helpful either. I look forward to a belief that aggressive treatment is a a standard and remyelination to fix the damage becomes a reality…thanks for always sharing interesting takes on managing the beast!😊
I think expediting clinical trials so that exciting drugs like PIPE-307 and NVG 291 will be available to people who have progressive MS will not accrue more disability than they have to. As for future content I would be interested to hear your thoughts on new electrical stimulation technology such as Stim2Go distributed by Pajunk.
Thank you for your very helpful videos! I live in New Mexico, and we barley have neurologists, let alone MS specialists here, so its great to have access to your content.
Just in case it helps, I'll go over how my new diagnoses and treatment of MS has gone. I was diagnosed with MS 6 months ago. I went to my Primary Care Doctor after loosing feeling in my hands, abdomen, and feet. She ordered a head MRI, after it came back with lesions she referred me to a neurologist and I was diagnosed within a month of my symptoms starting. My neurologist started me on Ocrevus and prescribed me a 1500mg vitamin D supplement to take weekly, since my vitamin D levels were really low. I feel like your prediction of MS being diagnosed more effectively and treated more aggressively with higher efficacy drugs is in alignment with my recent experience. I also feel very lucky to have an amazing Primary Care Doctor who immediately sent me for an MRI.
Right now, NVG-291 is the one drug that is giving me hope
I am looking closely at this product as well, You make like this video I made on the topic: ruclips.net/video/JEEn1K6bRuU/видео.html
🤔 Food for optimistic thought! 🤗💭
Thank you
Also another thing i hope for is that the medications would be more accessible around the world.
Hi from Israel I always enjoy hearing your video God bless you dear doctor
Thanks
Hi! Preliminary results of the alpha-lipoic acid (LAMPS) study have been published. The difference in atrophy rates is striking. -0.58 cm3 (LA) and -7.18 cm3 (placebo) at p = 0.084. (not as little as we would like). It is also worth noting that proteinuria is very common among people who have taken LA
Terrific video! I really look forward to Wednesday mornings. I am thrilled by the varied research that is ongoing and I believe the next 10 years will be very exciting. Things I wonder about... How is the MS medical/research community organized. How do guidelines and recommendations get reviewed and sanctioned and then put into practice? E.g., Why would an insurance company ever deny a highly effective DMT when the data are so clear? What governing body recommendations hold the most weight when it comes to MS?
After hearing a lot of news lately about promising drugs getting on trials, like PIPE-307, I have somewhat become more optimistic than 2 years ago when I got diagnosed. So optimistic that I now believe I will live witnessing the discovery of a cure for MS.
Even here in Greece we expect trials on Diaprotectome to start later this year, another drug for MS developed from a Greek-Australian doctor.
As for faster diagnosis times, I feel there's still a big room for improvement and especially when non-specific symptoms come into play.
In my case I got diagnosed with a 2-year delay and only after ataxia appeared. During the 2 years before my diagnosis I would have constipation that would appear, be insistent for a month inspite of using laxatives and then go, all that while still getting good amounts of fiber and water. MS is quite a tricky disease...
Do you see patients outside of kaiser?
If they could find some way to reduce brain atrophy in people with MS (or brain atrophy as a whole), that'd be great. I know some DMTs can reduce atrophy somewhat, but not completely or for everyone with MS. I wish I could see into the future 100 years to see what the future of MS treatment looks like. Maybe an effective EBV vaccine could effectively wipe out MS (and other related conditions). I agree that AI and super computing has the potential for HUGE advancements for fighting MS.
Brain atrophy scares me, too. I've written here before how I'm apparently the last person on Earth still on Interferon, and that one does not slow down atrophy at all I think.
@Ennugia my old neurologist, while being very good at doing very thorough exams every 4 months, never went over my MRIs with me. He relied on what the neuroradioligist reported (that always said "no interval change"). When I finally looked at the MRI myself, I was SHOCKED at the severe atrophy I saw compared to my first MRIs years ago. It threw me into a deep depression.
@@andrewreisinger6860 how did you recognize the atrophy yourself? I have my MRI CD-s, but I can't read them myself, sadly.
@Ennugia very large ventricles, too much space between the solci (the folds around the outside of the brain)
I think your being practical-optimistic lol you covered alot of the practical things with a optimistic flair lol i read a post on a Facebook suport group of a lady who was diagnosed in the 60s by the hot bath test .... so like you and the wheelchair guy i was thinking of all the the way all people like me where so lucky to have the tech we have today compared to just the 70s ..... just a small time ago in the ms journey of the disease ..... I also was wondering have we hit a plateau of some aspects of ms ... like the mri ... mabye it will take longer for new tech to find itsway to find ms faster and more accurate.... but I do belive we will find better ways to treat progressive forms of MS now that rrms has been so easily treated .... grate video DR B
I have a friend diagnosed with MS but turned out to be Lupus :( Scary
Hi doc, I know you already have a video on neurogeenic bladder & UTIs but how about one for UTI vacines being developed? And for pelvic floor PT? Very interested in these as I have combo incontinence and retention. I can cath but dont want to do it due to UTIs I keep getting. Maybe new technologies coming out for cathing? Better caths? Also one on neurogenic bowel? Anything new with the microbiome/gut flora? Just throwing all of it out there. Thanks for all the videos!
Thank you for these kind of videos! Is impossibile in your opinion that in the near future Will be Discover the cause of MS and develop a drug that stop Forever the disease?
I don't think a single cause of MS will ever be found. I think it's a complicated disease with several contributing factors. The closest thing to a "cause" is epstein barr virus, but some studies on pediatric MS find that
My lifestyle change of adopting whole food plant based diet with mushroom tinctures, proper vitamins, and microdosing psilocybin has actually given me sensation back in my feet, and my Lhermitte’s sign has diminished severely. I believe western medicine should adopt more holistic approaches. The benefits I have been gaining have been beyond remarkable! Not taking a DMT yet, but I can confidently say, I have reversed my poor balance, numbness, and brain fog completely by sticking to my holistic protocol. Would love to talk with you about my experience Dr.
Well the damage can't be undone
I'd do literally ANYTHING to go back in time and have the use of my arms back
Don't play with this. Please actually take a DMT or there's good chance you regret it.
I work in ems and am likely losing my career.
You're playing with fire
MS comes and goes because you have relapses. The next time it may be your arms or legs or vision
@ I am sorry for your experience but you have not adopted MY protocol and MY lifestyle. You have no information on what I am doing to fight this and it has been proven very efficacious. Please show some respect and an open mind and heart. It’s interesting that you perceive the human body to be incapable of healing itself.
Looool
I am so fit and have been a strict vegetarian 18 years. I lift humans for a living.
The damage is being done. People want to call food a DMT LMAO it's not.
You want to gamble? Ok. Go for it. But don't get upset when you lose something you can't get back
This disease happens to people with your "lifestyle". If it was your lifestyle that was working we'd stop giving out DMTs and diagnosing it and admitting folks to the hospital with it
You didn't reverse your MS. That's not how this works.
I'm tired of instant people trying to drag others down. I JUST got diagnosed at 35 because I'm a woman and my symptoms for 13 years were ignored.
You don't have to deal with that but you'll just let disability happen to you? Ok then. 🎉
The damage caused by MS is often irreversible, and you will never be able to undo it completely. Over time, without potent drugs to control the immune system, the damage accumulates. It is your body and your decision, but think carefully.
I appreciate the optimist look forward. Remylenation and axonal regeneration would be amazing advances. AI may be a path to get there. I am also optimistic about neuralink and how that may play a part in helping our nerves to better communicate. I don’t think in the current form but the ability to generate nerve impulses and be responsive to task direction is promising.
I have the strangest case of MS. 1st symptoms 10 yrs ago, lost central vision lt eye, and along with it 10 plus other MS symptoms. MR shows stable periventricular and juxtacortical lesions that have never changed. I take nothing for it. FT worker, pump iron like a beast at gym 😛 and I'm 55.
Discovering the pathogenesis of the disease will be the only way rational treatment decisions can be made. Drugs may not be the answer, for instance diseases with a metabolic component can be managed with diet.
Do you agree with the fab Dr Boster that with the current highly effective DMDs along with supplementary diet and lifestyle changes, in the current era, MS can already be made 'boring'?
We are very good at stopping relapses and new MRI lesions, and many people with MS are stable. I unfortunately don't think we can stop 100% of progression with current technology.
I hope your predictions come true during my lifetime as well. I have my fingers crossed for CNM-AU8 in hopes it can recover some of my vision loss. I’d love a less suppressive version of ocrevus too. My neuro said as long as I’m not having recurring infections, I can continue on ocrevus despite having low IgA and IgM. G is normal, but not by much, and that concerns me a bit.
Some info on CNM-AU8 here: ruclips.net/video/zkkvE2xuOjA/видео.html
Thank you for another optimistic and informative video, Dr. Beaber! A question: you say ‘relapsing MS’ several times instead of ‘relapsing remitting MS’. Has terminology changed? And could you explain why?
PS idea for another video: is CAR-T therapy a treatment option for MS?
@ Thanks for the suggestion Laura
Some relapses are not followed by complete recovery, and there is evidence of subtle progression in some people with relapsing MS, so I think the term "remission" is misleading. Also, many have significant symptoms during "remission."
Yes, I recognize that, as I am one of those people
Hello Dr.Beaber - I was wondering if you have come across any of the papers covering tDCS simulation in regards to alliviating MS symptoms and assisting in the repair of lesions?
I was also curious on any info you may have regarding the papers which discuss tENS stimulation of the dominant-hand median nerve in order to enhance tactile sensitivity in the hands of MS patients in the long-term.
Both of these areas seem to have very promising results for symptom management and restoring a nomial state of health, so it would be great to see your take on them!
Dr beaber are you hopeful for seeing more specific and or rare/aggressive subtype meds in the future?
can you comment on how patients build tolerance to autoclonal antibodies?
It is possible to develop anti-drug antibodies against monoclonal antibody drugs for MS (tysabri, Ocrevus, rituximab, lemtrada, kesimpta, etc). The underlying immunology behind this is very complex and idiosyncratic.
Are any studies done on the effects of MS drugs on gut bacteria?
All the drugs are bad, take care of your gut that is the best you can do
Hi dear doc
Please tell ,when NVG291 comes to the markets, pleasssssssssse tell
Could I possibly see you for a consultation Dr Beaber I do not belong to Kaiser though ?
Hey dr beaber , how are you i hope you are doing well, dr i have read some articles stating that keto diet help in protecting the brain from damage and being studied in Alzheimer’s and dementia
Could it help in Ms ?
I have a video on this topic you may like: ruclips.net/video/egHRA4ZOLVM/видео.html
I'm doing another round of doramectin. This time with albendazole. (having corrected my vit D and calcium supp stack)
I like how you think!
Thanks 😊
Can you comment on car-t? It seems to be a cure for some autoimmune diseases
HSCT is the future.
Folks. You didn't fix your MS with food and exercise don't call your lifestyle a DMT. It's irresponsible.
Hoping on PIPE-307 and i'm thinking MS will get cured eventually. We've come along way.
What made you want to specialize in MS Dr Beaber?
Disagree here. Too many Drs slow get patients on DMT TREATMENT.
I don’t believe a single word you’ve said. Respect for the attention though.
So, you essentially have nothing new to say, and nothing to add to the narrative, only conjecture of what could happen.... yeah..... not helpful..
I give my hope on AI