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@grinch4567
Жыл бұрын
Thank you - will do 👍🙂🔥🔥🔥🔥
@MinkasTNR
8 ай бұрын
Any info would be great. I don't know what leukoencephalopathy means. Anything not well known is appreciated.
@jwsjws4812
25 күн бұрын
It costs money to join?
@khitir1500
Жыл бұрын
1. Don't smoke stuff 2. Exercise as part of your lifestyle: balance, core strengthening, limb flexibility, and cardiovascular endurance 3. Eat smart: drink more water, supplement vitamin D3, and avoid fast-food 4. Daily mindfulness: practice breathing 5. Take the most effective and comfortable disease-modifying therapy
@pauldavidober
8 ай бұрын
Work outside in the sun a lot , make your work as hard as you can. I have a vending company and I used to park my truck as far away from the location. Everybody would tell me to park closer but I didn’t. I’m parked as far away as I could so I can get the most amount ofphysical activity since I had to work and be sick I’m 63 still working first symptoms 24
@jenadeen
Ай бұрын
What is the most effective and comfortable dmt?
@Jcr2446
8 күн бұрын
What is DMT?@@jenadeen
@chrisc757
Жыл бұрын
Watching this video should be a requirement for anyone who has just been diagnosed with MS, it contains a tremendous amount of practical and useful information, wish I had seen a video like this, when I was diagnosed with MS 13 years ago.
@KatBrat38
Жыл бұрын
Totally agree when I was diagnosed 20 odd years ago, I only knew MS from the movie about Annette Funichello, so basically nothing, the doctor and my family kept telling me it was no big deal.
@kmcq692
Жыл бұрын
Totally agree. When I was diagnosed 30 odd yes ago, I didn’t know anything about it except that all the older people around me kind of turned weird when I told them I was diagnosed. Apparently they had a story in their head that I would become a vegetable of some sort. (I’m exaggerating, but they DID treat me different!) My neurologist seemed to be a Eeyore who was just waiting to see how bad it would get. Meanwhile, I kept riding my bike and walking everywhere and playing music and I quit smoking. It took this long for me to start a DMT but that’s because they are better now.
@thaliaventouris3855
Жыл бұрын
SO Agree!!
@dianaperez8780
Жыл бұрын
I absolutely agree 100%. I wish that I'd have known about this doctor & his video series when I was diagnosed w/MS in 2011....... 💯💯💯💯
@Shoeboxbears
Жыл бұрын
I'd like to say thank you, you've made me realise I'm doing most of the things I should be doing to help myself. I did have RR MS and was diagnosed as progressive a couple of months ago. I mountain bike 2-3 times a week and this is great exercise and mindfulness. You've also made me realise that I need to be honest with my neurologist and ask for help/support as I don't tend to do this. Thank you for being a fantastic Neurologist and explaining everything in layman's terms, keep up the good work x
@dalidzucheredi2495
Жыл бұрын
I have a son with Autism. I need to be able to help him for as long as possible.
@survivingtolive
Жыл бұрын
I've never been treated for my M.S. and have battled over and over for medicaid and tried disability. So for 16 years I've just suffered. I go to e.r when I go paralyzed they do steroids and then send me on my way. 5 times I've relearned to walk on my own at home. But I live in excruciating pain every day of my life amongst a million other things. I have no life. I really enjoy watching these videos because yt is the only education I get as well as getting answers to questions I have but no doctor to ask. I really appreciate the time taken to put out these informative videos. ❤
@chaisroom6631
Жыл бұрын
I am just like you...I have had it for 30 years but we cannot give up
@shelton191
Жыл бұрын
You have ms for 16 yrs and never had any treatment? Was it your choice to never get any treatment at all?
@shelton191
Жыл бұрын
@@chaisroom6631Are you on treatment?
@aalihte3378
Жыл бұрын
Get an appointment with a neurologist! Treatment earlier than later will keep you from getting worse. Medicaid won't help unless a doctor says to. Having a neuro will help with all that.
@starman9921
6 ай бұрын
Living with the pain is something we have to learn to live with it's horrible. I have been in M S pain FOR OVER 30 YEARS. I'm 64 now I've just about had enough. But I'm strong like you I will keep going
@KarenMaloney-yy9pu
10 ай бұрын
I am newly diagnosed and frightened! You helped me to calm myself with knowing this is not a death sentence. Thank you!
@hafssaserraj3943
10 ай бұрын
Same here. Got the diagnosis 2 days ago and am overwhelmed. I couldn't think of questions to ask.
@MADMPrecious
8 ай бұрын
I have MS. Get out of the US, and watch your body heal
@Idkchangethislater
7 ай бұрын
I’m bloody vex mate 😂 I’m floating between acceptance and anger
@arthurmiller9103
Жыл бұрын
Thank you Doc for helping the MS community worldwide. Be 🙏 well
@HazelRobertson-y3u
Жыл бұрын
Thank you. A must watch for anyone recently diagnosed. I wish my Neurologist was this honest and informative when I was diagnosed back in 2010. I was handed a pamphlet and sent on my way 😢
@Liam_100
Жыл бұрын
The best 21:53 minutes, I have spent on KZitem in a long time. It is so on point and helpful. Thank you Aaron. From over the pond.
@AaronBosterMD
Жыл бұрын
Thank you for watching @ljm!
@sabrinaabdul955
2 ай бұрын
I just got diagnosed with MS, i had symptoms for. 3 years and ignored them till i got blurry vision in my right eye. Hearing the news was shocking and confusing and scary. Im only 27 and i thought I was the epitome of health. Thank you for this video of everything i searched this has been the most clear and best explanation. I have MS but MS doesn't have me
@jlynnwms
Ай бұрын
Omg, that's how I found out I had it in 2022. I was devastated. I woke up with blurry vision and I went to the ER. You are so young. My son is 27. My mother had MS and I took care of her for years until I had to put her in an assisted living facility.
@billiejoe413
Жыл бұрын
I was diagnosed in 2017. I met with my neurologist regularly. As I have had symptoms I reported them to him. He never acknowledged any of my reported changing or new symptoms as an attack. I’m realizing I must be a stronger advocate.
@isaiahkirk4153
Жыл бұрын
When I wake up in the morning, I feel groggy, but listening attentively to this video boosted my moxie and motivated me to shoot past this ailment and smile! Knowing that I'm not alone makes me feel okay with this. 😌
@AaronBosterMD
Жыл бұрын
Right on! #StrongerTogether!
@Serenityisdestined
10 ай бұрын
I wish I had you as my doctor my doctor never explained any of this and now I understand it all because of you. Your an ANGEL 😇 God bless and thank you.
@take5512
8 ай бұрын
I just watched a video about how a physician HEALED himself from MS. And he is now healing others with MS. He spoke of a book he picked up during his sickness by a professor, and it spoke of all MS patients being intolerant of meat fats. None can have dairy, or meat fats. They also need to minimize saturated fats, so they cannot have meals with that, such as coconut oils, for example. He said the diet should be whole foods, plant based, zero meats, zero animal fats, no dairy. But seafoods are allowed. The doctor said this is how he has healed, via diet.
@chi_archive
2 ай бұрын
A pescatarian diet has been shown to help with inflammation but there is no way he actually healed himself via a diet, could you share the video?
@flandrensinteriors3428
26 күн бұрын
I've seen so many videos on ms ppl on carnivore diet where it has cured their ms. Odd how some doctors get it completely backwards. Meat fats are healing to the nerves and brain
@YaZzweb3
8 ай бұрын
An amazing holistic approach, I absolutely love your vids doctor
@dianaperez8780
Жыл бұрын
I'd absolutely love 2 meet this Dr. in person. I wish that my doctors were like him. I'd seriously consider moving 2 Ohio just 2 b able 2 have him as my MS specialist......
@destrygraves
Жыл бұрын
This is what I wish I had been given or told when I was originally diagnosed with MS. 8.5 years in and I’m learning most of this from watching your videos. Thank you.
@Asif49858
10 ай бұрын
How are you now?
@MohammadAsif-tu2os
10 ай бұрын
follow whal's protocol and ms will go
@anasantos-tp6os
9 ай бұрын
Thank you MS is frightening....
@josephvered3991
Жыл бұрын
Hi from Israel thanks dear doctor excellent explanation that summarises the MS it shows how dedicated you are to the MS patients and how you want to help them God bless you
@harmcity9934
Жыл бұрын
Imagine we had to go through MS without you sharing your knowledge with us. Nobody really compares and makes it easily understandable like you. Because of you i tell my nero what to do, not the other way around 😂
@ralsharp6013
10 ай бұрын
agree,
@andysings
9 ай бұрын
This moment is my first ever time finding this brother.. Very glad to have Been 10yrs official now Not on any meds They knocked me out too much and i thought, I've gotta see if it is any different without the meds.. Hmmmm - feel So Much better Been 6yrs since i haven't touched them. Yes, body in pain most days But i no longer have a walker Haven't fallen once Am So Much more clearer Just wanted to share with you all my brothers and sisters. Peace and kindness, andria in australia 🌿
@Jcr2446
8 күн бұрын
Please answer questions maybe in a video Q&A. It is so necessary and many have the same questions so would be very beneficial.❤
@cc34945
Жыл бұрын
Goal setting at 74 is very different than younger. The necessity of caring for my handicapped daughter is on that list. My husband recently died making me feel very vulnerable. While I have achieved NETA, recent events leave me gasping.
@markmattingly2929
4 ай бұрын
Thank you for your videos they give me a lot of courage and thought of positivity I have been fighting with my doctor for quite some time and it seems that it's too late for him to listen now so I thought I was going to give up on everything for your videos help me I've had so much stuff wrong with me that I've kept hidden for so long that it's just going to take time for me to understand why I can't process thoughts most of the time anymore and why my body is just so bad all over the things that I carry with this are embarrassing but seems no one listens and I can't make people listen I can only say my feelings sometimes keep up the great work It seems like even though I have no diagnosed I know what I feel and how I feel and I can't hardly put two sentences together when I'm trying to figure out why I feel this way it doesn't work thanks once again sir You're a true hero in the world of neuro such as what I have I guess
@jackielavelle7974
Жыл бұрын
Great Video, I sure do have to get it together. I have lost the desire to do anything. Can you just be tired of it all? I just don't get it. MS is a real pain in the butt~🤦♀
@cherylvl1036
Жыл бұрын
Thank you for another great video Dr. Boster! Someone very dear to my heart has been diagnosed with MS at the age of 79. She had an appointment with an MS neurologist who told her there wasn’t anything that could be done for her because of her age except Botox for very tight muscles. She can no longer walk and mostly uses a scooter. Do you have any newly diagnosed patients that come to you at an advanced age and what does your conversation look like with them? This could be a topic for a new video or a question answered in one of your livestreams. Thank you
@Emma-dh5he
11 ай бұрын
I really enjoy your videos. Your cheerfulness is contagious…..much needed when dealing with this awful disease. Thank you!
@VernaMarie
9 ай бұрын
this is wonderful introduction for anyone diagnosed with MS. I can't thank you enough, It really lightened the stress of it all
@janclebro6997
10 ай бұрын
Wow Dr Boster, thank you! My brother with untreated MS has just come to live with us. He appears not to care about anything. He is struggling to walk and seems to be experiencing cognitive symptoms. He is intelligent and highly qualified, but after a lifetime of good earning arrived penniless and disorganised. I can see I've got a lot on my plate. Thank you for this very clear video.
@robertsine8812
10 ай бұрын
Geez Dr. Boster. I didn’t realize how connected Mono and MS were. I had mono firstly in 2005. Was brutal for a couple weeks steady. Diagnosed with MS in 2018. 22 lesions were found throughout my brain. Also a couple being on the spine. I really cleaned up my act in many ways. Vitamins, exercise, eating “better” healthy mixed with junk sometimes lol. And I receive Ocrevus every 6 months. It’s a battle I must be honest. It’s a constant fight it seems to keep things calm. My main battle is cog fog now a days. Decision making, frustration, coping with stress, emotions. It’s brutal. Keep practicing with it I guess eh. Thanks for this vid. Happy to have discovered you this morning! I’ve liked and subscribed. Looking forward to following you onward.
@70Dandare
Жыл бұрын
Didn't realise about passive cigarette smoke as a risk for children. Does that risk decrease as they grow up with no symptoms? My Dad smoked alot and at 53 I'm heading to a neurologist to see if I have MS soon. Enjoying your vids here in the UK.
@Felice537791
Жыл бұрын
I have MS and teach leadership, starting this fight with “why” is important. Write down those goals!
@AaronBosterMD
Жыл бұрын
Amen!
@traceyhunt5320
Жыл бұрын
You are the best !! My son was diagnosed January 2023 and we watch you all the time . He is doing your “ 5 things “ 😊 He’s on Kisempta and trying to live his best life ! He goes for his first MRI since taking his DMT in a couple weeks 🤞🏼Thank you from Canada 🇨🇦
@Asif49858
10 ай бұрын
How's he now?
@tracieanderson4978
6 ай бұрын
How was your son’s MRI after his treatment
@giorgismama8024
Жыл бұрын
Ocrevus was my lifesaver!
@TMat0824
8 ай бұрын
Me too!!!
@proudtobe9932
Ай бұрын
What's that ?
@emmyeagle9596
Жыл бұрын
I really like your advice, as you are a very compassionate Neurologist doctor. I am a former medical assistant and I regularly study-research medical issues and nutrition. The root cause of medical issues in my opinion are key. Mindfulness practice is a great recommendation as this helps stress's, etc. Your recommendation to take vitamin D-3 is excellent and I believe adding Vit-K-2 with that supplement is very helpful. I don't have MS, I have scoliosis related to an 2020 injury from a pain management shot in my spine that injured a major nerve. Thank you for your uplifting video addressing many helpful ways to deal with medical issues and not just drugs!
@Callummullans
10 ай бұрын
Water hyssop was used in a mice model to relieve Autoimmune Encephalomyelitis (inflammation of the brain and spinal chord). Lions mane is thought to induce NGF which promotes the production of brain derived neurotrophic factor; this is involved in myelination.
@Uncle_Leezy
2 ай бұрын
Bruh the only person that understands ! I’ve had MS for two months what journey this life is going to be I’m only 26
@heatheremma3471
4 ай бұрын
Thank you for posting these posts. I live in Australia. My neurologists approach is not like yours. I really appreciate your point of view. It has helped me for years.
@fck.the.nwo.
10 ай бұрын
My neurologist said the treatment for ms can be worse than no treatment, im taking vitamin D ,lionsmane and magnesium plus b1 not on any other treatment was diagnosed in 2019 with extensive dyemylation.
@MJr-ku6wt
6 ай бұрын
How are you doing? Is it creating any issue in daily life ?
@Joanna-x7s
6 ай бұрын
Hi How are you doing with this treatment plan? What are your current symptoms etc? Would love to hear more of your experience? Thanks
@maggiecamperlengo6734
5 ай бұрын
He’s got a cat tree, therefore a cat, I like him already 😺… thanks for the information, I feel better about dealing with this new aspect of my life
@Jcr2446
8 күн бұрын
White cat walks by at beginning of video❤
@CherylLamping
9 ай бұрын
My 27 y/o daughter was diagnosed with MS 2 weeks ago. So much of what I’ve been reading has been overwhelming and frightening. I believe she has an outstanding medical team and they are starting infusions within the next month. This video has begun to restore my hopes for her future health and well being. Thank you
@scorpionsting2581
8 ай бұрын
Diagnosed at 30 I’m 33 been on ocrevus infusions it does me well
@pauldavidober
8 ай бұрын
Mavenclad, or stem cell transplant
@carmenbalan2188
5 ай бұрын
Take Alpha Lipoic Acid 600 mg/day and omega 3 krill oil 2 caps/ day. Helped me a lot.
@renaezelmar6718
Жыл бұрын
Thank you as always for your videos. Helps give clarity and a sense of control when confronting a medical system that can feel very very cold. We, and your patients, are lucky to have you.
@KipataSensei
11 ай бұрын
you have made this so much easier to understand. I thought getting diagnosed was going to end my life. thank you for what you do sir!
@starman9921
6 ай бұрын
The biggest impact on me is some physical disability but mostly pain. I have been in severe pain for over 30 years I take the best painkillers available but still in horrible pain. What amazes me is what we can put up with as humans and find the strength to overcome.
@incongeekome4167
11 ай бұрын
I have recently started watching your videos. Thank you so much for all the MS related information. When I first got diagnosed, I was completely in denial. But I'm slowly starting to accept my reality, and that's how I stumbled across your channel ❤❤❤
@AaronBosterMD
11 ай бұрын
You are so welcome!
@lisak2575
Жыл бұрын
Thank you! I am sure you would get along well with my neurologist. I am working on the exercise right now. I am walking each morning with my husband. I struggle with balance so he goes with me in case I need his assistance. I use the cane all of the time, but as I continue walking, I am feeling better. I like being outdoors for my 15 minute walk. Thanks for the information.
@AaronBosterMD
Жыл бұрын
You can do it!
@belmakanlic1113
Жыл бұрын
Dear dr. B, at 2:30, you say "People can have slow steady decline, but I'm taking over years and years". What is your opinion when this steady decline is happening in 16 months, not overnight, rather slowly but firmly from month to month. Like being EDSS 1 in 2021 and now limping all the time. And the decline was triggered by severe covid pneumonia. Best regards and thank you for all work you do on youtube for all MS people!
@phillyirish7370
2 ай бұрын
Want to be able to surf on knees or belly 😢definitely a goal. Grdw up swimming, ❤the ocean 💙 100% disabled veteran, 15 years with this beast
@BridgetMermikides
Жыл бұрын
Thank you Aaron so much for yet another outstanding video. You have been my main source of support since my diagnosis 4 years ago (symptoms for 12 years). I am envious of your patients and wish my ms team had a modicum of your intelligence! 🙌
@dermlover1
Жыл бұрын
Did you ever get tested for MS in the 12 years of having the symptoms? Why were you only diagnosed 4 years ago?
@goniaweg5559
10 ай бұрын
Czy ciebie też traktowali lekarze jak symulanta i wysyłali do diabła gdy uparcie wracałeś żądając badań?
@Scarlett_84
Жыл бұрын
bowel issues have ruined my life ... neuro says she can't do anything about that. I have a neurostimulator which doesn't work properly so she says I need to go to the surgeion and his nurse but I've lost hope
@tinawilson4120
5 ай бұрын
Hi Aaron, my name is Tina and I am 44 years old and I have been on Pax zone since I was 18 and recently I have been having flareups. My MRI showed a lot of lesions. Do you think my back zone has stopped working and I should try a new medicine
@kristylindstrom1
8 ай бұрын
I was recently diagnosed with MS and your videos are amazing. They have become a vital resource for me. Thank you for all you do to empower and educate. I start my Infusion treatment next month. Ocrevus. Looking forward to kicking those B cells out and living my best life. When I was diagnosed on the 22nd of December. I asked my neurologist if I could go on roller coasters the next day when I traveled to Florida. I went on the biggest, bad ass roller coasters I've ever been on, and I think I will be able to do that for quite some time!❤ Thanks again.
@AaronBosterMD
8 ай бұрын
YES!!!
@donnaacree9737
Жыл бұрын
Eating cucumbers carrots kale, any food from the ground, take walks or exercise everyday. Made me feel much better from attacks from M.S.
@donnaacree9737
Жыл бұрын
No pasta or bread, btw.
@Jcr2446
8 күн бұрын
I am big on detoxing and organic when possible. Lots of dandelion and senna tea, green juices, soup and veggies. Vitamin D is helping Gotta up my water game.
@patdaniel9512
10 ай бұрын
Thank you for taking the time to share yourself. Your informative videos are extremely helpful, informative and encouraging. It’s awesome to see physicians like you care! Your a rarity. God bless. ❤
@diannemason8857
5 ай бұрын
I wish I had watched this video 6 years ago when I was diagnosed with MS. This is a game changer for me - easy and practical info, but presented in a way that has me motivated to utilize all this info. I have been lucky with minimal issues and only 2 relapses (I'm 48 yrs old) and this video gave me a gentle nudge to continue down a "better" and healthier path -not to ignore my diagnosis but to live with it and be proactive with my health. Thank you!
@lorrainejohnson829
3 ай бұрын
Same here but I'm 52. MS finally dxd I was 42. Did ABCs/terrible home injections now unable to drive or do complicated engineering work. Still here tho I just mainly care for my dog now...walk 2h daily/no meds...its time to rest a little 😂
@lorrainejohnson829
3 ай бұрын
Thanks Dr. B 😊
@msme2400
Ай бұрын
I recommended to someone with MS they fight it and exercise, lift weights, eat lots of trout-it is easily available here..lots of good veggies and so now he is doing pretty well considering. I told him to grow his own food again too.. he did. He Is stacked now from lifting weights. He has bad days but overall he seems ok. We went for long walks and even though he felt sore in the days thst followed it was overall invigorating afterward and refreshing during the walk.. I think it was triggered by a ski accident?. I also told him to get as much sun as he can-rethinking some of his meds. His doctor agreed he could discontinue the med which caused sun sensitivity. What could someone with early MS do to delay the decent into disability.
@CallipygianMoose
3 күн бұрын
Would love to find a neurologist I could just pick the phone up to...I'm having to wait 6 months just to see one on the NHS
@BigGuy8059
3 ай бұрын
I had various symptoms for years before I was diagnosed with MS. At that time, I knew the strange blindness I was experiencing had to be in my brain, because it only affected one quadrant of my vision in both eyes! My brain essentially rewired and the blindness subsided after a few months, but in the meantime I got my MS diagnosis. I started taking Tecfidera and had no additional symptoms. At that time I did some research, and found that Vitamin D therapy looked promising. No risk, so why not? I stabilized at around 100 ng/ml. In late 2019, my CD4 level was low enough that I risked getting a lethal brain virus so my neurologist stopped my drug therapy. But I kept up the high Vitamin D intake. I suspect it made a real difference when I contracted Covid-19, but I might have benefitted by having very few CD4 lymphocytes! Anyway, my CD4s recovered enough by the time SARS-COV2 vaccines became available, so I responded very well to vaccination. For the last four years I have had no MS therapy other than the high Vitamin D intake, with no MS progression at all.
@Ohdatsjazzie
11 ай бұрын
You’re a blessing to us MSers
@EvenSoItIsWell
Жыл бұрын
I love everything about this video. You are the bomb Dr. Boster!
@landracriswell437
Жыл бұрын
Good evening Aaron! I try to watch all your videos on here Utube! I have to wait 11 weeks until I get to see my MS Neurologist, here in Indiana 😮. I don’t understand how & why I got MS? I’ve always been healthy and take vitamins daily! I appreciate all your information videos 😊😊
@romeoperales1986
11 ай бұрын
Doc good day i have a daughter diagnosed wth MS and the neurologist said the main cause is covid vaccine is it true doc. Pls. I need your answer..
@a.h.s5152
9 ай бұрын
Can SLE lupus cause MS, it seems like the SLE lupus I have is trying to cause me to get it, I'm not scared and worried anymore if i die i just die at least i will be out of suffering. I guess whatever happens, happens. I'm going to have to look for a new neurologist again. I been having a burning sensation in both of my legs with some tingling and numbness in my foot, I get these weird eye pains when I move my eyes one or both of them will hurt, it would feel like I have a rock stuck between my eye ball and eye socket when I move my eyes. When I have a bad lupus flare it feels like I can't get up I feel like my body weighs a ton my legs will feel weak it takes me some time to get up. I'm still freaked out about them two blackouts I had in July-2019 one morning when I got out of bed it felt like I went paralyzed from the neck down and it felt like my legs turned into jelly I lost control of my body and hit the floor hard I was awake and aware the whole time it happened it lasted a few seconds I slowly got back up on my knees. The second time it happened everything went black I almost went down it lasted a 20 seconds. I had a MRI done and seen that I have a lesion forming on my spine in my neck area right in the area that time I went paralyzed and fell down for a few seconds. I get bad brain fog. I run high lupus fevers alot with headaches and body aches and with burning lung pain and shortness of breath, I get extreme tired spells that hits me super hard at times. It's targeting my lungs it caused me to lose both thyroid glands. I can't believe how much meds I have to take every day to stay alive.
@PS-flyingbird73
Жыл бұрын
I’ve been doing all said on daily basis & works despite decided not to go on DMT for PPMS given diagnosis at age 45 (all lesions on spinal cord & maybe 2-3 on brainstem) Not the Brain lesion for past 10+ yrs. 5 yrs gone & no lesions though damage on spine is way ahead of me. Question on new biomarker MOG-IgA(new type of antibody called immunoglobulin A or IgA) may have a pathogenic role in CNS & I’m only positive for Zoster & EBV & everything else from blood to spinal fluid either normal or negative. So one of dietary approach is to keep EBV starving.
@ralsharp6013
10 ай бұрын
Its true, MS is from glandular fever type viruses. Thats why its very important for pple with ms, not to have live virus injections.. Please choose wisely, the country's you visit. Pubmed have alot of info about ms. 30 and 40 year Studies, on the Faroe islands.. You can find government information on any of the above, that I have mentioned.. I hope everyone is going ok with their illness ❤
@demetriusturner6997
Жыл бұрын
Thank you for explaining MS and sharing goals
@hackett1181
Жыл бұрын
Fantastic!!! Thanks ☺️
@randy1203
21 күн бұрын
What about the carnivor diet?? Or am I wasting my time????
@dianeaguero421
10 ай бұрын
Was dx in 2007 and this video was the most informative and clear and easy to understand. Thank you. I agree this should be required watching for newly diagnosed folks.
@susanwhite520
Күн бұрын
I just saw your video today. I am in limbo. I do have neurological symptoms, MRI of T spine shows "small chronic demyelinating lesions within the thoracic cord at T2-T3 on sagittal STIR image 6 and T4 on axial T2 image 12. Additional chronic demyelinating lesion in the lower thoracic cord centrally at T12" I have had 3 lumbar punctures that were all unsuccessful. No idea what is going on...
@alexmihajlovic4960
2 күн бұрын
Can you make primary progressive M.S. boring? No more attacks, but the damge has been done. Just going down.
@Itsme1.
Жыл бұрын
I feel my legs heavy and hurt since 2 days and don’t know if it’s a new attack because i never had something like this before and it’s not too much hard or bad i don’t know what to do it’s uncomfortable feeling specially in my left leg, doctors here don’t give steroids for any new symptoms unless it was hard and needed other than that they don’t do anything
@NiekopTube
9 ай бұрын
Is it possible that an infection with Lyme desease triggers MS?
@marystone5186
6 ай бұрын
I was diagnosed 16 years ago with R&R MS. Was on DM's for the first 5 years. I have had no significant attacks or new spots on my MRI's. I stopped DMs and have had no progression. I started farming after I was diagnosed, and I believe this has helped me live my best life. By farming I do exercise, it is what I call, Noah's workout. BUT I believe THC is the best medication for this disease. When I stopped smoking for 6 mths, I had my diagnosing relapse. Even being in the sun all day every day in SC, my Vit D is always low. I love being outside, with my 30+ Angora goats, listening to the birds and watching the clouds. Your advice is wonderful. But are DM's always the way to go?
@millennialhmong7121
Жыл бұрын
Please keep doing your gifted work. God bless🙏
@AaronBosterMD
Жыл бұрын
Thank you
@grinch4567
Жыл бұрын
Loving the channel, and love this video, so helpful. When you mentioned untreated MS being a monster, how much less of a monster is it once the patient is on DMD’s (which I have just started) symptom-wise?
@thaliaventouris3855
Жыл бұрын
THANK YOU Doc!! I don't know what else to say!
@BarneyMcD225
8 күн бұрын
I am currently under diagnosis. I have demylination and multiple T2 hyperintense lesions all over the place but mainly around the medulla and some T1. I’m waiting the results from my LP and the cervical MRI. However, listening to this, and many other, video makes me think I don’t have MS. I’d like to be able to think clearly and walk about after 1000hrs each day. Climb a mountain? 🤣 The constant pain, tiredness and general “I’m going to die soon” !!! I’d love to have what people on KZitem says is MS. Sorry about how that sounds but it’s true.
@fatimamirza2408
Жыл бұрын
Thank you for making these videos! I'm diagnosed with MS and these tips make sense for me!
@g_gaming2893
10 ай бұрын
Smart man that faces reality and doesn’t sugar coat shit is exactly what’s needed in this realm of study. Thank you for educating thousands of people sir!
@LynSteele-w8g
3 күн бұрын
I was diagnosed with PPMS 4 years ago and only discovered your videos a few months ago; they have been so helpful. I think there should be a Dr Boster clinic here in Northern Ireland
@desiredecove5815
Жыл бұрын
This is a great video for newly diagnosed ( and of course us OG’s) you explain everything ( including the EBV- which everyone of course questions)- Definitely a winner 🥇 in my book. #MakeMSBoring Have a great day Doc #StrongerTogether
@AaronBosterMD
Жыл бұрын
Thank you for the awesome feedback! #StrongerTogether
@sassy252
11 ай бұрын
I am 65 so -- tired of trying to get just one of my drs to put all the symptoms together for ANY DX..instead i get sent to another dr for each symptom. I am so tired of the pain. I did have brain MRI-Nonspecific bilateral FLAIR white matter intensities, with differential Diagnoses including demylinating disease or chronic ischemic microvascular disease. I am at a lossof how to get them to listen thank you
@AnnaArvanitis
Жыл бұрын
Thank you! I really appreciate all the information! So very helpful! 😌🙏
@anons1sefcik184
11 ай бұрын
My husband's is untreated right now, he is in 24 hour chronic pain😢😢 he doesn't walk.
@shelveyphillipsbowman8037
19 күн бұрын
You have a beautiful home..both my parents were smokers plus unfortunately I married a smoker.thank God I never did smoke.i beleive that's where I got it
@natileelipe7675
Жыл бұрын
I’m so thankful for you. ❤
@jenniferhart8733
Жыл бұрын
Dr B I would like to say Thank you for all the info, you have taught me so much in the last couple of weeks since I was diagnosed…been watching lots of your vids. Including on the meds I’m going to be put on, Mavenclad. I’m building up to doing my 5 for 5..must learn to meditate and up my water game tho. 😊from the UK
@AaronBosterMD
Жыл бұрын
You are very welcome
@michaelwhite5255
Жыл бұрын
Good luck with Mavenclad treatment. My daughter who had her MS treated with Mavenclad about 4 years ago in Australia has had very good effect. She also follows mainly with the overcoming MS diet. No further lesions in the brain or spine.
@colesteven1123
3 ай бұрын
Youre very good at communicating As an active cannabis and tabacco smoker(since 14yo, now 38) i can only hope my futute oncologist is as good a linguist as you. Love how you use so many "figures of speech" in your layman descriptions is awesome. Whether youre a believer or not, i believe god is saving a seat for you and others with as much compassion you show for desperate humans who want to stick around with their loved ones longer.
@knad7365
9 ай бұрын
man why cant all doctors be like you
@Geewdo
17 күн бұрын
Nothing helps my pain 😢. Every drug they give me either doesn’t help. Or renders me so l lethargic I can’t move. I can no longer walk due to spasticity. This is miserable!
@debradunbar6160
11 ай бұрын
I’ve also heard EBV mimics myelin and when it’s active, your body attacks your myelin by accident
@zuzanac951
8 күн бұрын
I have autistic brother and he was diagnosed with PPMS about 3 years ago .. he’s getting worse and his legs are so stiff , and shake out of nowhere.. we help him and hold him to help calm down the muscles when we try to move him around to sit down 🪑 and move to wheelchair 🦽.. we don’t know if he is experiencing any pain .. he doesn’t talk but he always keeps a smile on his face .. he is on a special diet due to having one kidney … he cannot take any medicine for MS so we just watch him getting worse and worse , it’s so heartbreaking
@LISALUV
3 ай бұрын
I really need motivation to finish because the time span diagnose is crazy
@jaynemcdowall497
Жыл бұрын
My husband always says “everyone has something”. I feel like I can’t talk about how I feel without feeling discounted.
@pelicanformation3802
3 ай бұрын
I guess that is true but it doesn't mean you can't talk about it and you will listen to him when he's feeling blah.
@dougcain250
Ай бұрын
Dr. Boster thank you for providing this service for both those with MS and those who want to better understand MS effects, I was diagnosed with MS in 1987. As a result of a bad reaction to a COVID-19 drug, I had to take 50, mg of prednisone daily for 6 months. The prednisone worked with the COVID issue it also took ten years off of my MS progression. Shortly after stopping prednisone, the MS symptoms came back. Was that likely a reduction in inflammation? I am not taking any DMT, is there any med that might act as the prednisone did?
@missannie8012
7 ай бұрын
Long history. Started in 2007 I kept getting too weak to walk. Especially during a 12* shift. (RN) Neurologist said that if she found lesions in my spinal cord I'd have MS for sure. Then she found lesions and said "that doesn't look like typical MS." My MRI showed "over a dozen lesions". Plus I had optic neuritis. But I keep getting told it doesn't look like MS. One neurologist put me on Gelenya (sp) been on that since 2018. Just had it changed to a generic. And I'm noticing more symptoms. That started 2 months ago. Started with severe fatigue and pain in my rt thigh then numbness. Sometimes it feels like my brain is swollen. Still waiting on a new neurologist. Mine retired.
@ope4r540
6 ай бұрын
Hope you find your next neurologist up-to-date on MS. Not all neurologists are MS Specialists. But there are some General Neurologist who are very good and will go the mile to listen and get to the bottom why your active symptoms are showing/causing pain or simply put, causing trouble. Even when you have the next appointment, continue to search for more MS doctors because, you never know if the one you like, will move or retire. Ask family and friends if they can recommend a neurologist. I ask the people I meet waiting in the lobby mg Neurologist office, who they’ve seen and do they recommend them. Good luck.🍀
@susancleveland5687
6 ай бұрын
10:32 I am a retired ICU nurse. I have gone thru so many neurologists and left with an ass. First one told me that because I was a nurse, it was drug withdrawal. It wasn't. I ended up going out of the area for my diagnosis. That was in 1994.. The reason for the MRI was I was driving and all the cars looked like they were going sideways. My sister just passed from a brain tumor. My GP ordered it, and didn't know how to tell me, he handed me the report. Long story. Now, here I am at 72 and really suffering.
@jwsjws4812
25 күн бұрын
Great video. I am diagnosed with CMT. They seem similar as they act out. Am I wrong. Are there similarities in how these two diseases come into being? Thanks Jim
@WeepingPillows
Ай бұрын
Hey! I've got a question about the 24 hour rule. If you have recurring, painful cramping of different muscles, where each muscle cramp lasts about 30 minutes, but they happen several times a day for the last couple of weeks. Would the reoccurrences of the symptoms count as lasting 24 hours, or does the symptom need to stay in a specific place for the 24 hour rule to be applicable? Hope that made sense. Thanks so much for this video!
@chrisdirects
2 ай бұрын
I was diagnosed with MS at 60. I also have Trigeminal Neuralgia and Lupus. ( a winning trifecta, I know ) good thing I had Gamma Knife surgery so as of now my TN is at bay. I am am an actor, I have e been for 50 years of my life. I also have and amazing job as a wandkeeper at. Ollivanders wand shop in Diagon Alley at Universal Studios Florida. That’s me in a nutshell. I have been loosing my ability to walk, I need to walk to do my amazing job. My list you mentioned, is a long run of doing this job for another 20 yers like my best friend did. I could give you my long list of meds I’ve been through but that won’t help here because it’s too damn long. So, if you can get me in with you, I have family that lives there or if you have other suggestions let me know. I know you must have 50000 people that want to be in touch with you, so here’s my story, if you can help then Wooohooo. If no response. Again, I’m sure your time is convoluted enough, so thank you for your time.
@autumn3035
7 ай бұрын
So I believe I might have this I been sick going on 7 months I stay supper dizzy and light headed migraines and my arms go numb I fell like static in my hand and fingers and my legs they fell heavy and fell like pins and needles and my feet burn I’m really struggling with my hole body when I walk I fell like I’m walking lobsited and I have lot of chest pains and trouble breathing what can I do I’m scared I’m only 23 and it’s only getting worser I’m scared I don’t wanna end up in a wheelchair I fell like I can’t function I fell weak and I’ve lost 34 pounds and I stay having chills but they did find out that I have a slipped disc in my neck c6 c7 woukd thag cause all of that ? And I’m staying depressed and anxiety I’m constant checking my oxygen felling for my heart checking my temperature I cry all day cause I fell like I’m dying I live in wv not far how do I find out if I have this ms
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