A Pill for Remyelination?!? (Clemastine)

[@TonyGonzalez-v5m]

Steve this information is hopefully. I have progressive MS. I was diagnosed back in 1999. I really didn’t have visible symptoms till 2012. It’s only gotten worse. Leg fatigue, muscle strength diminished, lack of balance, etc. I am going to speak to my MS doctor about remyelination.

[@3ZubUA]

Дякую, Стів . Як завжди дуже важлива і цінна інформація. Приємно бачити Вас знову . Ви виглядаєте чудово .✊🏻🙏🏻

[@SteveSolvesMS]

Дякую. Я знаю, що це було надто довго, але це було потрібно, щоб я міг розповісти вам усе, що я дізнався.

[@3ZubUA]

@@SteveSolvesMS Дякую щиро від усього серця за Вашу працю, за Ваш час, за Вашу допомогу всім нам у боротьбі з цим тяжким недугом. Будьте здорові і збережені.🙏🏻❤️🕊️

[@SteveSolvesMS]

​@@3ZubUA I find better results with a UVB lamp.

[@preciousramotswe4303]

Dearest Steve, I'm a 55 female Livingstone in Italy. I Washington dignosed with MD 10 months ago. West from dispare to hope. Don't know if I can get clamestine. Changed my diet, cut all sigarette e centinaia a trasporto of organico honey in the morning,started exercising everyday, and improving my walk. I hope to gain the ability to talk again. Wish you tons of health and love. Ps. I'm on my own. No family, no friends.

[@SteveSolvesMS]

I can relate. We can be best friends! Sound good?

[@albineg]

Regarding blood sugar: Apple cider vinegar is great. Another thing you can check out to help with blood sugar control is the herb gymnema. Many studies about it. Also cardamon, cinnamon and ginger as spices can help, The term holistic simply means: "characterized by the belief that the parts of something are interconnected and can be explained only by reference to the whole. This means when applied to medicine, that the practioner takes into account the interconnectedness of body systems, like the gut-brain connection, mind-body connection etc. But also the connection between your social environment, physical environment, your minds, thoughts, emotions etc. But the term holistic, just like the term science are being misued or are washed out as words. They have lost their meaning. There are many doctors out there claiming to be holistic, or claiming to be science-based, when in reality they are not. Also note to consider that there are a lot of limitations with scientific research in the areas of health and diet etc. Also tried clinical experience is worthy to take into account. For example the herb "gymnema" I mentioned before in this comment. It has been used for thousands of years for its benefit in blood sugar regulation. It was known before studies were conducted. The benefits of fasting, diet, exercise was also known. A truly holistic pracitioner does not ignore science or scienfitic results. As that would by itself be not considered holistic. You do not ignore any area of life. Be it physical, mental, emotional, social, environmental, scientific, genetic. Everything is taken into account. And what matters are precise diagnosis, treatment and positive results based on the diagnosis and treatment. A good example is the system of Functional Medicine. So yeah both the words "holistic" and "science" are misused and gets a bad rep these days. And there are many bad pracitioners out there. But there are also many good ones and people recover from all sorts of things that conventional school medicine (which clinical practice usually is 20-30 years behind the scientific progress) says can not be anything done about. The word curing "MS" or any other diagnosis is redundant because it wrongly assumes that all MS patients are created equal and have the same underlying genetics, and epigenetic triggers that caused the disease. Though there may be patterns, everyone has a unique constiution and an unique life experience and history of different stressors (like toxins, allergens, microbes, emotional trauma, microbiome, genes, etc). So people that claim they can cure "MS" I would not trust either. You treat a unique person, not the disease/diagnosis. Precise diagnosis is EXTREMELY important. But to be precise you need to go beyond a label like MS and look for underlying root causes. That's why I really like the system of Functional Medicine. It is not popular among conventional doctors and called pseudoscientific by some. While it may be hard to create studies that generalize people into groups like "MS-people" and matching them with a specific substance like "this drug" or "this herb", Functional Medicine is uniquely tailored for each person. You can measure the underlying root causes treated, and science supports how these root causes contribute to disease. But just like your program of applying several things at the same time to create a bigger synnergistic effect (combining diet, fasting, exercise, UV-light etc) is hard to prove with science the combined effect, the same goes for Functional Medicine. One study I do know about though, is a study showing the ReCODE program for alzheimers. You can find it on pubmed. "ReCODE: A Personalized, Targeted, Multi-Factorial Therapeutic Program for Reversal of Cognitive Decline". It shows the multi-factorial aspects of how Functional Medicine is applied and how it can be effective. I made this comment 20 min in in the video. Will continue to watch and maybe add something more. Welcome back to KZbin Steve :)

[@albineg]

Psychoneuroimmunology is a scientific field that is an example of a more "holistically" oriented one.

[@pattischmitz2680]

Recode for MS as well? Thanks!!

[@albineg]

@@pattischmitz2680 Applying a functional medicine approach by a good practioner that works with that method would work for treating the underlying causes no matter what diagnosis. In functional medicine you treat the unique person, not the diagnosis. There is a lot of underlying things that may or not be present and contribute to the symptoms and disease. Each case is unique. No MS person is alike, even though there are general trends that benefit many, there is still uniqueness in the application based on extensive diagnostics and personalized treatment plans.

[@ellie698]

So good to see you again Steve! I was only thinking about you yesterday 🤗 You look and sound great 🙏🏻

[@SteveSolvesMS]

Wow, thank you

[@CarlosLopez-tl9cd]

Congratulations keep on fighting and never give up! God bless you!

[@mujray]

You speech looks/sounds so much better than your videos from your videos 1 yr ago.

[@drakulie]

Thank you for the update, and all the research. Great to see you. 👍

[@SteveSolvesMS]

More to come!

[@pattischmitz2680]

Thank you for your hard work!! So sorry for your hospital stay!!

[@charlingocharlingo]

Have you thought about treating parasites? I’m trying that now. Keep safe

[@MagickIsPower]

Can I ask how you are doing this please?

[@pattischmitz2680]

Whats that suppose to do? Thanks!!

[@RickeyBobby-x2e]

I am dealing with Optic Neuritis as I write this: Once again, Im pivoting back to the Whals Protocol. I was doing better this summer, but, * As I thought it was okay to flap the diet, I went back to eating cookies, spring rolls, soy sauce, an occasional pizza since Late October. Oh, and those Christmas cookies, a few bags of fun size candy bars, and a few bottles of diet soda, slowly made me worse once again, so guess what happened.. I ended losing my balance again. Plus, I lost my right eye vision. Argh!! Its December 26, 2023, and my calendar log shows I began to slowly lose sight in my roght eye once again; Optic Neuritis. I can't see out of my right eye, except for objects; no detail. However, went right back as of Christmas morning. Already I am seeing slight color again in the eye again. *... Friends, I think I'm sold on the Protocol. If lucky, ill be back up the hill, playing the slot machines again and going to the ball game in preparation of baseball opening day, friends! Yippee! 😵😎✌️ Update: Optic Neuritis Vision loss; Right Eye; December 20, 2023, status Update as of Saturday, March 23, 2024 PM: * 😁👏🥴 Vision in Right Eye returned during week; March 18-23rd today. Can now see 10-12 point letters. I'd call that Empirical proof, at least to me, that Whal's Protocol clearly is helpful in mitigation of MS symptoms. Plus, I can walk in the house without the two canes I own. Next week: let's see if I can make it down the street and back to the Walmart without problems with balance and gait issues. ... I'm out. Peace ✌

[@grandaughters2]

I am 64 yr Female. Tripped 14 times. Have burning pain down back of legs.Sciatica all 5 branches.I have had 2 brain scans.No MS. Being told my Mylen Sheath has came off my Nerves. I have weird symptoms like water dripping on my Thigh,but touching my thigh it is dry. While walking in my house I jerk because I feel I am sliding on ice. I have had 3 back surgeries & knee surgeries. Every major joint is weak & painful. Seeing a Geneticist for Ehlers Dan los a connective tissue Disease. Steve, I have been like this since 2021. I am willing to try almost anything as I have constant pain & am very limited physically. I drive pillows under shoulders as I drive. Pillows in my chair and bed to hold me together. Cannot get clothes out of washer,pain in shoulders. Riding Scooter in my house.I am going to try your diet. I've had Thereapy at least once a year since my 30s.I always get repetitive injuries or agitation.Thanks for info ,Deb Ive been injured in therapy that resulted in knee surgeries when I was about 35.

[@SteveSolvesMS]

Wow, my heart goes out to you.

[@albineg]

Finished the video now. Scary with the ER visit. Glad you are okay and thriving. Keep up the good work with the channel. :)

[@albineg]

Also Clemastine has anti-depressant effects worth noting. "Clemastine alleviates depressive-like behavior through reversing the imbalance of microglia-related pro-inflammatory state in mouse hippocampus." You can also search for "Microglia in depression: an overview of microglia in the pathogenesis and treatment of depression".

[@ledomatt8797]

One of the worst things You can take for ms. Read from Medscape - In Unexpected Finding, Clemastine Fumarate Linked to Worsening Symptoms in MS ​@@albineg

[@MagickIsPower]

Good to see you. Please look into carnivore Steve. I've seen videos from people who have MS and have been wheelchair bound and are back to full strength on carnivore and high fat.

[@stupud818]

I was wheel chair bound and recovered through a vegetarian low fat diet. These extreme diets can work wonders. They an also do jack shit. Just be healthy

[@MagickIsPower]

@@stupud818 And that's why you need to try them out yourself and see what works...

[@FunWithCars716]

Good to hear positive steps in the right direction

[@juliekranz6899]

I am going to speak with my dr about this!

[@deannalopes8205]

I forgot to add that an MRI three years post report stated lesions are smaller and less noticeable in the thoracic spine.

[@justinkredible9628]

Hey Steve, Good to see you again, you look great. How is the drowsiness from clemastine? Do you plan on adding in Metformin at some point?

[@SteveSolvesMS]

I don't have any drowsiness. Never did. I think my lifestyle prevents it.

[@Pennystockid]

I have heard about this, but not taking it by itself. I thought you're supposed to take it with metformin for best results. Have you looked into Wim Hof breathing!? Check it out and the success stories

[@pattischmitz2680]

Success stories for MS?

[@SteveSolvesMS]

Metformin is a diabetes drug, which I consulted with my GP about. He said if I was to take Metformin, with my blood sugar levels, it would drop my blood sugar to life-threatening levels, instantly making me hypoglycemic. Causing many different symptoms.

[@pattischmitz2680]

@@SteveSolvesMS how do i contact you? Thanks!!

[@SteveSolvesMS]

@@pattischmitz2680 You can email me directly at [e-mail]

[@Star-mj9ku]

Steve, THANK YOU for doing the research. My Dr. prescribed 1.56 mg Clemastine 2X per day. I don't have type two diabetes so no Metformin. I do take 200 mg dihydroberberine. I know you aren't a Dr. and can't give medical advice. Just wondering what your opinion is...I am unable to take the morning dose of Clemastine. It puts me to sleep, and drowsiness follows me all day. Do you think doubling my nighttime dose and skipping the morning dose will work for remyelinatioin?

[@SteveSolvesMS]

I think that would work

[@theevilswan4053]

Hey Steve! Sorry if you answered this question before but do you know the relationship between gluten and MS? I notice my symptoms worsen when I eat gluten or use sunflower oil specifically, could it just be my own experience or is there any research about this?

[@SteveSolvesMS]

Hi Evil Swan, Although the exact mechanism is not clear, some researchers hypothesize that gluten sensitivity may trigger or exacerbate inflammation in the body, including the CNS, which impacts the progression of MS.

[@ilyaskharchi3392]

Thank you steve 🔥 ❤ is there any Clemastine alternative to regulate the M1 receptor!? Clemastine is not available in my country, so I have to order it from abroad. It takes time to reach my location...

[@SteveSolvesMS]

Not that I know of

[@jamesishmaelwilder8597]

I don’t understand. I’m learning new things I’m studying a new language I should be perfectly able to produce new myelin. Why isn’t it working to repair the damages caused by ms?

[@SteveSolvesMS]

It takes time. Remember, I really committed to start in 2013. It takes a long time, but it is more than worth it. I was able to take back my life from MS.

[@_ASK_]

Didn't the Clemastine research study conclude with it either didn't help or even made MS even more agressive?

[@SteveSolvesMS]

No, the results from the Phase 2 trials indicate that remyelination is indeed achievable. Watch this video from a Neurologist talking about Clemastine: kzbin.info/www/bejne/imfTZphoiciFb7Msi=PAOUobu4O5mCQ90p

[@arikcohen5525]

hi Steve what do you think about ng01 it's steam cell transplant with no chimo either to vain or spinel liquid Thank you

[@SteveSolvesMS]

I don't believe stem cells are the hope many wish they were. There are thousands on different stem cell drugs but there are still relapses. So ng01, yeah, its day in the sun now. But it will fade when something comes along

[@artempo8722]

Thanks for the research, Steve. I respect that you are trying to find a solution to our problem

[@SteveSolvesMS]

You are very welcome

[@tonnyncellist5910]

Hey Steve, thank you for ypur content. Do you use any DMTs currently?

[@desertskiesumc7262]

Sure do! Ocrevus

[@SteveSolvesMS]

Yes I do! Ocrevus

[@Mayen2002]

👍

[@bellatopiaaa8397]

Only the 2nd video of yours I watch… what do you mean by high days and low days? 🤔

[@SteveSolvesMS]

Watch this video and I explain why and how I do it: kzbin.info/www/bejne/bXTSk4evaNWWpJI

[@bellatopiaaa8397]

@@SteveSolvesMS Will do, thank you 🙏🏽

[@richardanjello2207]

Hey Steve, are you still using your vitamin D lamb?

[@SteveSolvesMS]

Definately! I do all the essential elements plus Clemastine.

[@richardanjello2207]

Thank you for your reply, Steve!

[@aluna_m888]

First time o heat about a Vit D lamp. Is that similar to the red lamp therapy?? Thanks

[@Star-mj9ku]

I have contacted my medical Dr.. What is the dosage?

[@SteveSolvesMS]

1.56mg twice a day

[@daniellove6002]

Umm, isn’t stem cell treatment combined with chemotherapy the answer?!

[@SteveSolvesMS]

This video is by my favorite Neurologist on KZbin, Dr. Brandon Beaber. It hits your question right on the head: shorturl.at/aU5sj

[@mballer]

Have you ever tried a carnivore diet?

[@SteveSolvesMS]

No, I like my salads and vegetables as well

[@mballer]

@@SteveSolvesMS There is a woman who has a channel @cabanachronicles, her MS went away when she went straight carnivore. Seems like a small price to pay if it could repair the body.

[@mballer]

Have you ever tried hyperbaric oxygen therapy (HBOT)? It is known to thicken myelin. ​@@SteveSolvesMS

[@mballer]

​@@SteveSolvesMS Sorry if I comment too much but, do you know your omega 3 blood levels and vitamin d blood levels, along with blood levels of common pesticides? Has your doctor talked to you about these things?