Amazing Suppliment to Repair Myelin! | Multiple Sclerosis Recovery
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- Опубліковано 27 вер 2024
- Watch to find out an amazing supplement to control Multiple Sclerosis Myelin Repair!
It promotes axonal regeneration, survival, protection and differentiation of oligodendrocytes and facilitates migration and proliferation of oligodendrocyte precursors to the sites of myelin damage. It also directly regulates key structural proteins that comprise myelin.
#MultipleSclerosis
#remyelination
#Essential
#Myelin
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Man, one of my friends from HS passed away a few weeks ago from MS. my girlfriend was diagnosed with MS last year. Of course, I would never tell her that I don’t want to worry her, but it’s lowkey stressing me out.
But She is 23 and I’m 24, I don’t really know how to deal with it. The first time she had an episode she was bed bound in my house for a 2 weeks, unable to move and she would throw up whenever she’d try and look at anything. I took her to the hospital multiple times but they wrote her off as just being drunk. A few months later she started losing her eyesight, and this time they finally have her an MRI. She’s on ocreveus but I’m constantly looking for new drugs to follow to try and buy her as much time as possible. Hopefully one of these remylination drugs will be effective and she can participate in a trial. I’ve been with her for almost 4 years, I’m probably going to marry her. She’s the most beautiful kind girl I’ve ever met. Idk why I’m typing this, I just need to get it out.
aw you're so adorable. She is really lucky to have you
Pray you are both doing better!
@@thevcountdown9824 I urge you to look into the Carnivore Diet and the remarkable testimonies of healing from many serious illnesses, including MS. Best wishes!
I’ve had MS for 20 years & i’m almost absolutely fine! I’m sorry to hear about your loss. You can’t die from MS. So i’m not sure what happened. But please try not to think the worst. Read The Wahls Protocol. I’ve never taken meds but instead adopt the diet she devised which quite literally got her out of a wheelchair & back to normal function. Positive thinking is everything, too. X
no one dies from MS :)
I felt myself being so happy for you.
Thanks! I want you to be happy as well!
Thanks a lot. Trying now. For anyone reading, *theophylline* apparently does miracles, and fast, too, on myelination.
I will look into that also. Thanks. I want to try as many things as I can.
Was diagnoxed with PRMS back in 2009. Secondary Progressive now. I tried Lions Mane last yr & almost instantly felt calmer, better focused and had less pain that resulted in me doing more in a day, than usual. Making it easier to get out of bed each day. Good things were obvious to me. I ordered liquid Lions Main & put it in my morning coffee. I stopped using it for no good reason, (life happens) then forgot about it......Thanks for reminding me. Now, I'm going to order more.--Best wishes to you.
Good stuff
Where do you order it
Have you've heard of citicoline?? Or noopept?. Noopept increases BDNF as well and citicoline helps with nerve regeneration.
Thank you so much for sharing your progress and this information!
You're welcome, Suzie! Check back in a week or two for my next video. It's a big one!
Dude!!!!! I'm SO happy to hear this! I've been a mushroom enthusiast for many years. Just found out that I have as severe B12 deviancy after going to the doc for knee pain and hair loss. She gave me a shot and prescribed D3 as well, be but I JUST ordered lion's mane supplements yesterday without her knowledge, but will inform her on Friday for my follow up. I'm so happy you found it! No MS for me, but I think the symptoms are similar. THANK YOU FOR YOUR WORK!
Thats fantastic! B12 and Vitamin D are very important!
How’s the lions mane going for you Marie Lynn?
I can now put pressure on my knees again, so it's working nicely! Thank you!
@@marielynn3802 great! Keep us updated
Will do. I ran out of the lions mane and will stop it for a few weeks to see if the D3 and the B12 injections are sufficient for my issue. I CAN get on my knees again without the knives stabbing me in the knee joint.
Steve great news! Hope much are you taking? I've been taking it since I saw it recommended in Dr. Terry Wahls MD protocol for MS.
I just want to walk again. They just started me on ocrevus and I’m so depressed they didn’t listen to me as my walking faded away in 6 months. I am so angry still and while I want my myelin tissue to regrow I want my nerve damage to be repaired. If I didn’t have my little boy, I would have ended everything if I didn’t have my little boy. I am in so much pain and I feel like a Guinea pig to the doctors.
You are not a “test subject” for them. They don’t know how to recover because they don’t have MS. I do have it and know exactly how to recover because I have. It takes time, I was at your “it’s hopeless” point. I decided my life was worth fighting for. At that moment I never gave up
Steve makes a good point. You’re not a test subject, they’ve already tested ocrevus and don’t need more tests. But hopefully you’ve recovered a bit past few months
Started Ocrevus 6 months ago also and walking is fading too same feelings as you as I am a mother to a boy it's bulls#it. I'm done with meds
Very good for repairing myelin damage is BENFOTHIAMIN B1.
I heard about it and tried to get it but I still didn’t find a source on the net. Can someone help me in that?
I am located in Istria, is a region of Croatia, EU. Hear the pharmacies don’t have it.
PipingRock
@tottance77 It is simply vitamin B1(Thiamine). You can probably get it online in your country if you can't find at a pharmacy.
Do u have any relatives that had that ms experience with b1 ?
Jeste pronašli lavlju grivu@@tottance77
Thanks Steve, the Lion's Mane gives me crazy energy and I don't feel tired anymore.
Wonderful!
How much are you taking?
"Citicoline seems to increase a brain chemical called phosphatidylcholine. This brain chemical is important for brain function. Citicoline might also increase the amounts of other chemicals that send messages in the brain".
Are you taking it? I have been thinking of giving it a try.
Please do tell if you are taking it and have felt something after it.
I even asked a question to Dr.Aaron Boster in one of his live sessions. But he said " never heard of it".
Hard to believe that a renowned doctor like him hasn't heard of citicoline and phosphatidyl choline.
IV mannitol will open up the blood-brain barrier and allow significant and meaningful quantities of the erinacins and hericenones to reach your BBB pass through and reach brain tissue. 🧠 also take your omega 3's, 6's, and 9's with taurine. The taurine helps smooth out electrical impulses in the brain. Taurine is used in energy drinks to take that jittery edge off.🎉❤ much love, brother.❤😊
I take CDP choline for dysautonomia. It is definitely helpful. Thiamine is the more important supplement for me, and choline seems to boost the effects of thiamine. Choline is well known in dementia treatment.
Great video sir. And fantastic to hear of your improvement !
I don’t have MS but mercury toxicity which has damaged the nerves. Just started with twice daily Lions Mane. I’m positive it will help alongside my other health treatment.
Keep up the great work. 🙂
Add Coriander to your diet... Also spurilina and chlorella powder to your diet, you can even blend all 3 in a smoothie.... Powerful heavy metal detox...
Can I ask how it's going? Sometimes I am leery about things that seem to help in the beginning but then it turns out there is a tolerance or something
I use lions mane and I like it
@@jodybridgewater3062 some people get a delayed adverse effect so be careful
Hello. You posted it 2 years ago. Any news or changes on MRI? Thank you
You know nothing actually exist right,prayer or strong belief is more powerful than people realize.
I.agree,. thank you.
Thank you Steve!
Very welcome
Thank you God bless!
Same to you!
my friend grow Lions mane for me.
A Gingko Biloba extract I hear is good for MS
Yes sir! I do want to know.
Thank you Steve, just subscribed to your channel
Thanks for the sub! I'm happy you are here!
Great news!! I will try this out
Hope you like it!
I am so happy for you!!!
blessings on your journey. Namastè
Same to you!
wow simply wow.
Thanks for watching
Hi Steve, How are you? I just came across your video. I've heard of Lion's Mane when I was searching for some vitamins on amazon. I have a rare form of MS called Devic's disease. I was missed diagnosed in 2004 and in 2006 I went to the Mayo clinic for a 2nd opinion and that's how we found out I have Devic's. Now is Lions Mane a good supplement to help repair the myeline sheath? Please let me know. Thank you! And I'm glad it's going good for you.
Hi Julie,
It is. Not by itself; it needs to be combined with my other essentials and time. I can say that with confidence because I'm living proof!
Just subscribed, in baaaad relapse 🙄❤️
Hey Laura,
Thanks for the heart. Wish you weren’t relapsing!
@@SteveSolvesMS me too, I usually take lions mane but i lapsed a bit as take sooo much alternative herbs ect… we shall see, thanks very much for your reply 💪🏽💕
Lions main coffee is sold round the corner from me so I'm goin get some.
What about antigistamines? Curcumine? Taurine? There are so many. Even Trehalose(sugar substitute are used in trials)
Jury is out.... if they work for you thats great. But I can't find any science for MS.
Steve which supplement specifically do you use? Happy new year
This video explains what I take and why the benefits are not always apparent ua-cam.com/video/E6ZbzzuI9no/v-deo.html&feature=shares
Thank you Steve, very in formative, and omg, you responded. So cool. I will definitely consider these supplements. I have PML, which is obviously very different than MS, but curiously, I experience lots of the same symptoms. I am trying encourage my meylin sheeth repair, so I hope some things workfor me. Sending love from Atlanta. Keep doin y’a thing man. So inspired by your journey.
@@jose-luislopezjr.8167 how is it going I am trying to help a family member with PML
Hi! I’ve had MS for the last 14 years, do you recommend these supplements? I do have an active treatment with Tecfidera. Thanks
Hi Popescu, sorry it's taken so long to respond! These are the supplements I take. They might or might not work out for you.
Regardless, it's not the point. Supplements won't beat MS, and I'm sure thats what you really want. It can be done, but it takes more than taking a pill.
I've started a Patreon page, and I urge you to join. If you sign up for my Membership + package I hold weekly live stream chats. I offer much more like exclusive videos I don't publish here on UA-cam.
Thank you for your informative videos. Greetings from Australia. How long did you take lions mane for you to see results
Its a cumulative. Over time you will start to feel the effects.
@@SteveSolvesMS had brain scan for cellebular ataxia but mri show myelin being attacked but dr said ms symptoms but not ms but not see neurologist until mid may. I 55 years old. I enjoy your videos. Best wishes
I have a lot of neurological problems after I had covid in early 2020 that I'm still dealing with that fluctuate worse and better,but main!y stay bad. Concentration and focus problems, "foggy" thinking, constant tiredness and fatigue, poor sleeping ,muscle weakness, loss of dexterity in hands i once had, eyesight worsening, varying muscle spasms and twitching, nerve pathways in my pelvis and lower spine that are constantly making pain and irritation.
I've tried different regimens suggested by neurological specialists that they have been researching, like supplements NAC, Benfothiamine,(sp?), cucurmin extract, ginko Biloba extract, I'm adding tyrosine and lecithin and lysine but nothing seems to really help. I've kept having the lions mane come up to remind me to look into trying that and I got a powdered type that I can make a drink out of. So I'm hoping this will help me somewhat.
Thanks.
Does lions mane help with the motor nerves?
Don't know, but couldn't hurt!
I take Lions Mane. What are your thoughts on N-Acetylglucosamine and N-Acetyl Cysteine? Have you tried them?
Hey Justin,
I'll look into them and try them out!
@@SteveSolvesMSdid you try it?
@@SteveSolvesMS..did you try it?
@@sweetbeep Yeah, every morning when I wake up, then again when I go to bed.
Hi Steve, Do you still feel the improvement taking Lion's Mane? I plan to take rather higher dosage of 4g watching a guy completely being healed from MS taking LM.
It's hard to say, I'm experiencing massive changes that are growing. But I don't know how much Lion's Mane is involved, if at all. LM improves my sleep, and sleep plays a great deal towards remyelination.
Yes, I still take it every night. But there is a lot more that is better than LM.
I want to invite you to my Patreon community I'm building. Its in its infancy, Its by membership and all the films I post are for my Patreon members only. No ads, no UA-cam, no nothing, just my videos. I even have a there that includes a weekly Zoom chat where I answer any and all questions you may have. www.patreon.com/stevesolvesms
That's interesting and fascinating to hear!
@@SteveSolvesMS..what do you mean massive things that are growing?
@@sweetbeep I feel a lot of recovery taking place.
what dosage do you use a day?
I take 500mg morning and night
Steve thank you for liking my comment however you haven't addressed my question. I'm curious how much you take daily????????-Thx.
1,000mg
Where do you buy it? Do you buy the whole mushrooms and eat it? Or can you just take it as a supplement?
Amazon. Just the supplement, not the mushroom: a.co/d/1jVInKx
I have been taking Real Mushrooms LM for exactly one year and this is incredible for my small fiber neuropathy.
From my experience to get even better effect is to take it with acetyl l-carnitine(ALCAR) and fat soluble b1(benfotiamine).
Alcar also has NGF i BDNF mechanisms and benfotiamine strengtens blood brain barrier which is great because toxins can't reach into brain anymore and benfotiamine also has antioxidant properties and support glucose metabolism in brain.
I have no intentions to stop with this nootropic supplements because they are essentials and my last MRI showed no lesions in white matter anymore.
Citicoline I take also like one/two time in a week because it has very long half time.
My supplement list goes like 25 pills through day and few powders.
Every pill have purpose!
Hello : this supplement you take improved your symptoms of small fiber neruropathy?
Hello . Can advice me for small fiber neruropathy?
I suffering 1.5 year ago
Numbness.tingiling .......all my body
@@alshifaashifaa8599 yes.
R-lipoic acid, benfotiamine, lions mane+cordyceps, agmatine sulfate are best to take for SFN.
Can you tell us what all you take
This is great. How much white matter did you have before? How long has it take to go away? Are there any foods you avoid, or take?
Hey steve do you use lion mane supplements? If so do they have to be a specific one?
Not Anymore! Nasty stuff for remyelination. In my video about the M1 Muscarinic receptor, I explain how we need to not activate the receptor to activate remyelination. Lion's Mane activates it. Here is the link to the video: ua-cam.com/video/7CobTy3pcn0/v-deo.html
@@SteveSolvesMS Why don't you put an update disclaimer to a video description then though?
Lion's Mane
Hello. Nice to see you again. How’s your experience with Lions Mane today? Still part of your supplementations ? 🎁🧬
Absolutely not! It's bad for remyelination! Read the first sentence in the video's description.
I was watching your video while reading the comments and was going to look deeper into lions mane with excitement until I luckily read this comment! If it's an absolutely not, then maybe you should delete this video so other ms sufferers who haven't read the description or all the comments don't rush to take it xx
Steve what about alpha lipoic is it any good?
Hey Shawn!
I haven't tried it. What is your experience?
It is awesome. Be sure to get the "R" lipoic acid form.
@@tigerbunny6778 I agree - RLA (sometimes called R-ALA) is the one to get.
I take alfa r-lipoic acid and L-taurine as well.
@@tigerbunny6778 non ti abbassa la pressione? Purtroppo a me da questo fastidio...
So you don’t take Lions Mane any longer?
No, I don't
UA-cam is full with such videomakers. "I have no more symptoms". Just a fun. Full recovery. And what about clemastine? Actor.
Which brand of lions mane do you take ?
I don't take Lions Mane any more.
Why?
😎👍
Sorry, no clinical evidence for lion's mane regenerating CNS tissue.
I know. I stopped taking it months ago.
Hey why did you stop? I just bought some😭
Im suffering with demyelinating neuropathy. Is LM better for me ..? Please reply me sir..
I don't know. I have no knowledge about demyelinating neuropathy.
I’m going to add lions mane… have you tried medical marijuana? What are you doing for diet?
I have not tried medical marijuana. I don't have any symptoms, so I don't need it. Now, diet is something I'm passionate about. I want to talk about it here, but its much too complex to write about in a comment thread. I have an entire playlist and have made countless videos. I recommend you check it out! ua-cam.com/play/PLParAduBaLztmtx-1wYOYhWu6_IM6A9TX.html
Thank you for reminding me about Lions Mane!!
My dad has MS. I just order a lions mane extract from lifecykel. He is in a wheelchair and it is difficult for him to speak. I’m hoping starting lions mane will bring him back.
Don't forget to practice all of my essential elements!
How's it going with your dad?
How's your dad now?
Lions mane is good. also chinese senega has similiar properties :)
I have trigeminal neuralgia. I've been pain-free and drug-free for over 3 years. I take taurine, lion's mane, multivitamins, alpha lipoic acid, and turmeric curcumin. Giving the myelin sheath what it needs is where it's at and costs me 52 cents a day. I learned this from those who have beat MS. It's healing instead of drugging, so it takes time. I take the amount it says on the bottle, no more or less. There are over 30 supplements that restore the myelin sheath. Once I found what worked for me I stuck with it. I've been on the drug treadmill. It's not sustainable.
I know, its a fight that will never fully go away
Awesome video !
Look into the medical medium and celery juice. I have spinal cord injury and was in a coma for seven days and I just started celery juice in the morning on an empty stomach.
I am starting to get feelings in my hands and easily able to lift weights every day !
Go CELERY
It’s a miracle superfood 🎉
I understand that statin meds, anti cholesterol, degrade myalin coating on nerve fibre. Removing statins, going low/zero carb reverses or greatly mitigates this condition.
B1 supplements as therapy..thiamine and other various forms shown to help 👍🙏
After my mri scan, I have been experiencing some dangerous signs in my body for about 2 weeks now. I feel magnetic shock in my legs to my arms, heart beating faster, mri machine voice sounds louder in my brain 🧠 for about 15 munites am almost getting mad 😥. The following days, till today, I have been feeling the magnetic shock both legs arms and hearts beat anytime am alone thinking about it then it comes but if someone is close to me then I feel okay small. I want to share with you if there's any solution, please. My life is not in a comfort zone. Thank you
I’ve been there
@SteveSolvesMS please I want to know the type of disease of suffering from symptoms: knee injury for about two months now and it continues with magnetic shock in my body, one side of body becomes hot at times, heart beating faster, itching from the back my head 😢
Try the Mediterranean diet, use Herb's like turmeric, ginger and Asian ginseng and speak to a chiropractor, Blessed Be.
Thanks for the tip!
That’s such awful annoy8ng music playing it’s not music even why why why can’t hear this man??
sorry im really not out to attack you but gawdang person you use your freeking heart that "god" if wanna think that gave you the man can barely speak and you are whining about music ? do you grasp what ms does to the brain ?
Congratulations Steve. You spoke with God's love from your heart. He will bless you manifold for unselfishly sharing and reaching out to help others. ❤🥰
Man.. i took lions mane for a month and was blown away by the results. The only issue i had was that it effected my libido a negative way, and once i stopped it all the benefits went away.
Have you looked into zeolite to detox from heavy metals? TRS (Toxin Removal Support) is in nano particulate form and crossed the BB barrier. Also look into Paul Stamets and his work on psylosyben and lions mane.
Keep searching and the universe will lead you on your healing journey! ❤
Aho!
I take Lions Mane, but looking at heavy metals is misguided. MS is caused by an over-active immune system, not by toxicity.
Steve you are awesome 💪😊
Which dose of Lion's mane / how long does it take. And which way is the best to take it ? With or without food ?
I don't take it anymore, I used it take it once in the morning
@@SteveSolvesMS Thanks for answering so quick. But in which dosis did you take it ? I use 3x a day 600mg for about 3 months now. Why did you stop?
I am a member from you patreon channel but don't know how to contact.
@@Fam1974 I don't remember the dose, but I used far less than you! I stopped almost all of my supplements because they weren't effective and were just a waste of my money. If you're a Patreon member, welcome! We meet every Tuesday at 10am PST and we can talk more then!
Any brand recommendation?
I like Double Tree, but I think any are fine: a.co/d/icX2sNL
Pleased for you mate 👍
I guess different things work for different folks .getting anti oxidants across the blood brain barrier is a necessity..ALA supplements do that too..but if your magic mushroom does it great..
Hi where can I get magic mushrooms from in the UK? Appreicate if you send me the link to the website. Thanks
What are ALA supplements?
Does LM help with nerve damage from fluoroquinolones and/or benzodiazepines?
That is not what I'm focused on. You might find answers from a doctor.
@@SteveSolvesMS ..no lol. Doctors don't know squat about this stuff
@@sweetbeep 😁 I couldn't agree with you more. But I still know nothing about it, sorry.
@@SteveSolvesMS ..thanks
You're really doing a great work . Please I want to share my problem with u
How can I help you?
How do you repair the gut lining so we can repair the blood brain barrier so then we can stop T cells from entering the brain so the T cells can’t attack the nerves
Eat whole, fresh, and unprocessed foods. If you aren't on one already, get on a DMT.
What is DMT ?
Hi steve what about fasting if any u knows please share
Yes, I eat OMAD (one meal a day fasting). It's so important it's one of the essential elements of recovery. Browse around my channel, I make videos about it all the time.
So…don’t take Lions mane with your update?! If so just delete this video 😕 I’ve have been taking it for a week now, and have noticed some improvement, so I think I will continue to roll the dice despite your 2024 update warning. No two MS cases are the same, so I’ll continue down this path until my body tells me otherwise
I stopped taking it because research shows it activates the M1 Muscarinic Receptor. That activation prevents remyelination.
Do you take medication too?
The only medication I take for my MS is my DMT, Ocrevus once every 6 months
Glad💚💚💚🙏🏻
Supplement?
I saw a benefit from taking it when I made the video. But it activates the M1 Muscarinic receptor on the surface of OPCs, so I definitely don't take it anymore!
@@SteveSolvesMS why don't you delete the video then? it is confusing people...
God bless you my friend ! Thank you for the information !
You are very welcome!
I just had an MRI done and the results are that I may have myelin degeneration.
Thank you so much for sharing your experience
I am going to add this to my supplementation.❤
Are you sure ?
Thank u sir.. diagnosed 7 years ago. Stay in the fight playboy.
I have MS. Hello 👋 Steve
Hope you’re doing well today!!! Every day can be a wild ride. Much love your way!
You too!!
Is everything OK Now, after about 2 years.
It will never go entirely away, but I manage it perfectly
@@SteveSolvesMS OK, best wishes.