Multiple Sclerosis Vlog: SUPPLEMENTS FOR MS? Vitamin D3 and much more
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- Опубликовано: 18 авг 2019
- Supplements for Multiple Sclerosis? In this video I teach you about nutrition & dietary supplements for MS. Got Vitamin D3? If you want to up your food game, start watching this video! Content was originally recorded during a livestream on this channel.
What supplements do you take? Please share in the comments section below! I look forward to reading and responding!
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NOTE: Make sure to talk to your provider before ANY treatment decision. We hope to educate, empower and energize those impacted by Multiple Sclerosis. This channel consists of a collection of formal lectures and informal video clips about MS to help education others. These videos do not provide medical advice and are for informational/educational purposes only. The videos are not intended to be a substitute for professional medical advice, diagnosis or treatment. Always seek the advice of a qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read or seen in any of our videos. They are just to help educate you about the condition guys!
Thank you for another great video Dr. B 👍🏻🙌🏻👏🏻💪🏻
Thanks MiKe! I appreciate your support! #WeHaveMS
@@AaronBosterMD and I appreciate your endless knowledge of this disease. This is all new to me and I'm learning and I appreciate learning from you.
I was having a hard time getting my D to up normal. A friend suggested adding K2, it would help my body process the D3, and, it worked! I got above 50 in just a few months.
Wow Thankx so much
What dosage K2? I have continued to have trouble getting my D level above 50 even though I take 5,000U daily.
exercise while feeling WEAK is a challenge
I hear u..... Especially when the weakness is paired w/extreme pain in both legs.....
This video made me realize so many mistakes I have made. Trying not to take proper medication and trying to go more natural and not discussing with my doctors was a mistake. In my defense the medical has come so far in the last 20 years when I was diagnosised. And questions to many doctors were we don't know a lot about m.s. thank God for these doctors who want to find answers. Thank you.
Great video! Love the tips!
Howdy Dr Aaron, thank you for posting and taking the time,very informative video as always take care till next time, oh very true about the water liquid gold 👍😁
Love your lessons... Love the Summaries 💖 and the puns ! GI systems are often “Impacted “ with M. S.
Hi Dr.boster I really like this video. This video i give it a thumbs up. I really learn alot from this video.
Wisdom plus a kind soul and spirit, perfect!
Thanks for making this video. I tried taking vitamins while I was awaiting health coverage. I had no idea what I was doing but I took about 25 pills a day.
Such great information thank you so much to think about food for thought 😊
I have been dealing with MS for many years. currently SPMS and during those years have haunted the web for info. Yours has been the clearest and most useful I have found, thanks.
This is a really good approach. If people are eating garbage taking a few vitamin pills isn't going to help.
I love your videos they have helped me so much. Could you make a video for treatment for someone with RRMS that has latent or active tuberculosis as well? Thank you
Sheesh, this is blowing my keto diet up I don’t know what to think!
Your comment about the burger not rotting worries and scares me
Thanks Dr. Boster!!!
Thank you Doctor B!! "Real Food!"
I truly appreciate your videos Dr. Boster! You answer so many of my questions so I don’t have to wait until I see my MS doctor.
Thank you for the kind words Marie! Please remember these videos cannot take the place of talking to your doctor. I'm delighted this medical information/education helps you. I hope it helps you best prep to discuss with your doc.
I was put on 50,000 mg of vitamin D shortly after being diagnosed & still taking it! Honestly though I'm still not sure what, if anything, it's doing to help me but especially in the summer months I'm not outside often so that alone makes it worth it to me. I've been on Adderall for fatigue & it's the fourth one & only one that literally destroys my appetite! Other than sweets my taste buds don't work anymore so I know I'm not eating enough of any kind of food. Thanks Dr. B!
I am so glad that you spoke on these "supplements". I already take a one a day vitamin. I hv to get back to taking my biotin. I hv to get vitamin D2 back. I was already taking vitamin D2. I need to see if I can get D3 instead. I try to do my best when eating. I try to eat as healthy as I can. I eat a lot of chicken and now I've started eating fish as well. I exercise daily. I don't hv a vehicle so I don't drive. I will be back on my "Copaxone".I've always kept in my mind that ppl with MS die frm a heart related illness so I try to do gd by me. I don't want to leave this earth unexpectedly. I will be looking into the meds that you spoke on. I actually play Pokemon Go daily. This is a game that I am very fond of. When I "chase" Pokemon, I am traveling and exercising. I started playing this game as a bonding tool for my son and I. Being outside exploring different places, I am doing my very own "Physical Therapy". I know my own body and when my body tells me to stop, I do. That was the issue with regular physical therapy. My body didn't really like those excercises all the time. I also love drinking water. Especially when you quench that 🚰 thirst. I also love eating fruits and veggies. Thank you for another informative video Dr B.
I recently found your videos. Thank you so much for all the great info. I take Vit d 4000iu, vit b complex, and CBD oil 20mg twice a day. Have you done any videos on CBD oil for MS?
Great video again! I just wanted to comment and ask if you will be doing a video on paediatric multiple sclerosis? 😊 Thank you for all the hard work you put into making videos. They are super informative!
Reptiles& Rats I would love to see that video too!
Thank you so much for your videos! I just wanted to double check on your caution about immune boosters. Because theoretically this can negatively impact MS does that mean that we should also be cautious towards vitamins that support the immune system like vitamin C? I personally take 2 Flintstones a day along with 4,000 IU vitamin D3. Thanks again!
What?? No donuts? Lol I really do enjoy your segments. I’ve never had a doc take the time to encourage or recommend anything.
Great video!! What about magnesium?
What about magnesium for leg spasticity? Any research you can share?
Great video! I miss french fries and Dr. Pepper, but I doubt my body does. lol
Thnx for the memory.
This is like the Holy Grail of intakes and choices to heal MS. Be 🙏 Well doctor.
Thanks again Dr Boster! I’m just curious if you’ve ever heard about dairy being a bad food for MS. I’ve followed this for a long time. The supplements I take are D3, K2, Lutien, Circumen, vitamin E, and B12. Used to take others but dropped them after returning from Japan where many people take no supplements at all.
Scott Davidson /DOES all these vitamins help to prevent numbness,tingling in your fingers ???
They have found that safflower oil, canola oil, and a few others stay away from. I use avocado oil for cooking, olive oil, I am on keto and just one steak or fish or liver and maybe a sauteed veg that's it
I cut out soft drinks years ago even before I even had any symptoms of MS. I have always eaten red meat and chicken. Vegetables have been a challenge because we don't always buy them. I personally love broccoli and cauliflower. I'm not a big salad guy unless it's spinach, shredded carrots cucumbers and a little blue cheese dressing.
Thank you Sir ❤️❤️❤️
Most welcome
Thanks for the video, very useful as always. A few days ago in the Dutch news 500 sleep-specialists were warning about the use of melatonin to enhance sleep. Their message was that it is very good at recalibrating the biological clock, but that it could disturb this clock by as much as one hour per day of taking it for falling asleep. They also said that it might help you fall asleep 10minutes faster, but that the negative effects far outweigh the positive ones. What is your take on that?
I present this information to help empower you to talk to your provider about what makes the most sense for you. I hope it helps Bram!
Ty
Thank you. Good to hear this because people kept saying there's a wonder pill. One went on to say that if I do a massage with someone he knows, I won't be disabled anymore. Then another told me not to take medicines or DMD, but only natural supplements. This is really helpful. Whenever I want to take any supplements like magnesium, I'd ask my specialist first. Real food? My husband and I have been going on a journey of cooking organic, less salty, less sugary food. What we cook would most definitely go bad the next day (the latest) if we don't refrigerate. As for fruits, my husband has tried to buy fruits each week after I had another relapse while on DMD. By the way, Biotin 600mg and D3 (now increased to 2000IU+225mcg) is prescribed by my specialist for my case.
Are you sure it's 600mg of Biotin that your doc recommended?
@@aditya50499 I'm not sure why I didn't get any notification, but yes, I asked her and she said 600mg. I noted and bought it afterwards. After my latest relapse this year, she prescribed Neurobion. It's a challenge with my MS since it's so aggressive, highly active and unpredictable. By the way, my D3 is still low despite that increase in supplement.
❤️
Hey Dr. B! I have a deficiency of CD8 T cells (genetic) which prevents my immune system from adequately killing my EBV infected B cells, so I also have an elevated CD4/CD8 ratio. Is there any way I can increase my body's production of CD8 T cells? I think Ocrevus is great for this as it kills mature B cells, but I'd really like to know if there's something I can take to increase my Cd8 cells specifically. Thanks :-)
Thank you for making people aware that you should go to doctor about vitamins you're planning to take. My family have a weird thing where we just don't absorb vitamin D. I need to check my levels to see if I'm weird like this. No other numbers are affected, only the vitamin D. But if I didn't discuss with my family and with my doctor about it I wouldn't have known.
Otherwise I was told a general multivitamin was safe but all levels were within normal limits with only my potassium dropping one point below ideal at my last meeting.
I see a lot of people swearing by all these supplements without talking to their doctor or checking their levels and it worries me.
I will say working with a neutricianist helped a lot with confidence in eating. My husband has severe allergies which led to severely limited diet, now we are more aware on how to test for a new food and allergy. To the point we've tried coconut (one that came up on his list) and it seems it may be certain forms.
Random thought. Would you recommend allergy testing for foods etc?
Thank you
YW
Been eating this way for decades and taking vitamins and still ended up with this diagnosis. Keto since 2016. I am so discouraged.
Maybe some people are destined to have ms because of genetics and we can't do anything to prevent it
Thank you! This video is very informative. I have a question about the healthy diet tho. I know eating no sugar and no process food helps tremendously our health but it also helps with loosing weight witch is good. But in my case since my dx I lost a lot of weight and I am under my healthy weight now. How can we eat healthy without loosing weight? Whenever I quit soda I loose automatically. I tried increasing calories and exercises to gain muscles but it makes not much of a difference. Are the meds responsible for us loosing weight? I know some people with Ms gain but I am not the only one that noticed the opposite.
I think that Coinsides with us losing body mass.
no Omega 3 on the list ? i love everyting else you said though
Please plrease please talk about Dr. Gregor. My friend is a nurse and tells me I should try his diet for MS🙄
My mum is saying the same
Dr. Boster, what about coconut oil? Is this an acceptable fat?
If only I could take vitamin D3 knowing the importance of it but unfortunately it ramps up my insomnia…struggling with insomnia for over 30 years now, makes living a good life so difficult
Do you believe or have you ever heard of someone "aging out" of Multiple Sclerosis? Diagnosed back in the late 1990s, I'm surprised to hear a neurologist say something like this. So is anyone with MS that I've mentioned this to. Your thoughts, kind Sir?
What about the Keto Diet or Carnivore?
What about magnesium, b complex, and vitamin B12
My potassium levels are always low even though I take supplements. Any link between this and the muscle spasms I and many endure as part of our MS?
I have been taking 400mg Cheyenne pepper to help with cleaning up my cardiovascular system. I have not been told to take anything or had bad blood work. But at 61 I'm health conscience. I have noticed that my MS symptoms are milder. Is this a coincidence or do you have a professional opinion. I am also in my crap gap with my ocravis. Thanks
Hi Dr B! Can you give us any information on Sublingual NMNs? Can they help MS patients and is it something you would recommend to your patients?
what is sublingual NMNs Brooke?
It is a supplement made by Alive by Nature. It is supposed to increase your body's production of stem cells.
Is there a better time of the day to take vitamins like B and D night or day?
Hi Dr. I was diagnosed with MS recently and I started with ocrevus although my doctor wanted to give me Tysabri I had two aggressive attacks in three months how do I know if I should change the DMT Long term wise
And is tysabri a better therapy to start off with..
Good day Hassan can i ask you about ocrevus beavuse it’s my medication plan while you go this thripy can u share please
What is the concern of MS hug and thoracic upper back pain
Should we take probiotic every day? I have been taking mine 3 times a week.
What abouts a heavy metal detox and a parasite detox?
Can you take fruit and veggies supplements if you are afraid of high oxalates?
Wow so glad I do understand there's no cure no quick fix or a magic pill. So I started being my own advocate, yes I do check regularly with my dr with labs, mri's, ck up, mammogram, twice a yr dental ckup cleaning, so I do ck on regular bases so I can help myself at home along with my food menu, not big on fast food, package food, dont like chocolate never did not a sweets eat or big meat eater, guess I was born this way, but I'm still not where I need to be, my family dr said portion portion I like that. What I don't get is protein bars' their more carbs in the bars then protein read and count then. But they wouldn't call it a carb bar it wouldn't sale would it. So I just make my own if want one. I grow my own small garden herbs and even make medicinal, teas so I am trying but still get sick 😫 but it all helps out I can feel the difference.
Thank you for your great information I am looking for something to help me with SPMS I already take Vit. D3, Alpha Lipoic Acid, B12. I’m on Ocrevus every 6 months.
Hi JuNae I’m transitioning to SPMS and am thinking of taking Alpha Lipoic Acid too. How are you finding it? Do you take 1200mg like in the trial for it?
Melatonin gave me nightmares.😱
What's make your arms,started to get num or tingly in your hands,while you sleeping or standing UP ???...
Probably due to brain damage
Hey there Doc, I noticed you mentioned eggs being ok to eat; as it stands I eat a lot of eggs & try to make sure I go for the best I can get, usually pasture-raised or organic.
I've also heard others say that people with MS should not eat eggs, so what is the deal with eggs from your standpoint, truthfully; should I continue as I am or do I need to be mindful of my consumption of eggs?
Anyone with ms that has try immune 7 any info how it affected you
I have just started exercise as part of my ms plan. Will taking creatine supplements?
cant find much on this anywhere as I work out and taking it everyday but your body dose make it so a small amount cant hurt
Can I take citrus in MS?
Heart smart aka the Cardiologist's diet... If it tastes good spit it out.
lol
can possible MS tretment please answer
None of my neurologist want to give me intravenous and I have insurance. Gelenya not working for me my left Eye is going down Neuro op doc is Bad .
Question- I have a hard time eating. I eat like a bird but with fatigue factoring in it becomes tough....Now what? 😉
maybe talk to a registered dietitian about how to plan several (e.g. 6) small, calorie dense meals (e.g. nuts) for each day.
My vid D level was as low as a 3 once
wowzers!
Oh, believe me I suffered and it was my rheumatologist who found it in my blood work. That was a couple years ago.. Still take bit D prescription now and also eat really well and still only just "in range" but feel much better. No longer feel my bones may snap although they still hurt
What's a DMT?
disease modifying therapy
Vitamin D and Vitamin D 3?
Vitamin D3 is a TYPE of vitamin D.
@@AaronBosterMD TY
💉copaxone yay
What about B12, commonly low. Don't do any suppliment without proper blood work. I was told my mom being German and her sister having MS is why I got it. I said so why don't my two brothers or my aunts children have it. In other words it's guessing and saturated fats are bad for everyone. Also 17 years ago steroids and plasma exchange was treatment. Studies showed it worked?? Then studies showed that the miniscule help was not worth the long term side effects. So as a fighter, don't believe in disease modifying disease and the info he is giving is what EVER human should do for good health. Doesn't "improve MS". Beast still in the middle. He'll block me again. But please use your common sense. He ain't giving free MRI'S or Occurves treatments. And if you are looking to see if you have MS. Stop it. You don't want this diagnosis because doctors Stop looking for the real issue. And what you have may not have a name, but don't let them put you in this dam box🎉
What about smoking medical marijuana
Thank you
You're welcome