I’m on day two as well.

Starting Ocrevus in 2 days after Copaxone and Tysabri failed because of the side effects/reactions. But I'm really scared of starting Ocrevus..

Seb, are you okay? We haven't seen any posts for a year? Have you just got fed up doing these posts or are you really ill? People do care and are concerned about you. With much kindness. xxxxx

i didnt listen to whats been said on the vid will do later do u have MS

Just eat more carbs for fuller glycogen

Spot on! 🎉🎉🎉 Happy New Year my MS Warrior Brother and Sisters!

Do u have clonus in leg?

The burning sensation to my core & spine is almost like I’m on fire. I wake up in a panic and see whether I’m on fire. It’s winter here and shorts and a shirt outside brings me great relief. At night I sleep almost naked and not covered.m with a blanket.

Hi Seb is this still working for you? I’m going to recommend this to my brother who has MS.

I'm watching this as I sit on the bedroom floor, asking KZbin; how an MS patient can get up off the floor.off..😂😭

Hola! Se me cruzo uno de tus shorts y ahora estoy mirando varios mas... mi madre tiene essential tremors y estoy researching it (can't think of the word in Spanish). No quiere tomar medicamentos y buscamos todo lo natural. Eres multicultural con tantos idiomas jaja - buenisimo! Seb, te deseo mucho exito en todo lo que estas poniendo en practica para asistir tu cuerpo. I'll be looking into the Wahl's Protocol - at the moment we're trying "Essiac Tea" pero ella no es consistente Not sure if you mention more about Wahl's Protocol in the rest of your shorts but I've only gotten this far. I think your positive outlook is a real benefit so keep it up.

Cervical dystonia

How are you today ??? No updates why??😢

How’re you doing, mate? Hope you’re doing well 👍.

Your strength is inspirational, Seb. You really are a great person.

Just found this and so helpful to hear as I've been to two different doctors and then advised to go to A&E for persistent numbness/pins and needles, being off balance, feeling weak, tremor and twitching in my hands and fatigue and then facial/eyelid twitching which has started waking me up at night. Doctor said it didn't sound like it could be MS or anything serious as MS starts with loss of vision and paralysis in the legs. He went to check with a consultant. Without the consultant even coming to see me he sent the doctor back to discharge me saying he didn't think it had any physical cause and was most likely just a sign of stress and anxiety or maybe migraine. I've had migraines since age 10 and have never had these symptoms with it. I insisted he explain it to me and my face was actually spasming as he was talking to me and my hands twitching and he said that A&E was for people with serious conditions and was told to go back to my GP if I was still worried to ask for a neurology consultation which could be a 4-12 month wait. I felt so dismissed and as though I'd been accused of making things up. I'm a female teacher in my 40's and have no idea if there is an innocent explanation but it's seriously affecting my day to day life. I'm going to see the GP and ask to be referred so at the very least I can talk it through with someone who will actually take it seriously.

Great video but hard to watch. The visual effects are really hard on the eyes.

This is soooo true! And since ya look good, people can’t relate, or relate they have it ailments too. This video makes me feel sane!

Look into lion's mane mushroom as well.

Still looking good Blessings are enclosed. ❤

CBD is garbage, buying but a hippy myth. Does nothing for pain and nothing for neuro pain. THC is the only part of cannabis that works.

I'm so scared about the potential risk for PML. I know the risk is low but still

Thankyou for sharing

What was your life event that happened that you speak about in video?

I've had face tingling, I've got issues with my upper back, dizziness, nausea, pain, muscle spasms, twitches ect the doctor said its anxiety and a pinched nerve in my back but its getting worse so im now waiting on an xray.... 🫣 my finger twitches too. I get internal tremors as well.

Sir plz tell me can MS symptoms at early stages go away completely after some time

I'm on diet similar to wahl's diet. In my diet are included most legumes Beans, chichpeas, soy, bobsled(not lentils and peas) Gluten free grains are allowed. Yeast, mushroms and fermentated foods are banned. Eggs, dairy, gluten, merckel, hailbut, coffe, barley, oranges, plumps, potatoes and celery are banned. Because i'm intolerant and i want to be healty even if i don't have MS or other serious deseases.

Sir plzz all these symptoms are permanent or temporary

Does all symptoms go away after attack

I found out about my diagnosis at the end of the year

Those who will read this please try anulom vilom meditation and few streching and yoga. It will balance your symptoms more than any steroids. Check up on youtube for ramdav baba and his multiple sclorois video he is great Indian yoga guru. And also change your diet. Multiple sclorois cannot be managed well by suppressing immune system with steroids but with resetting your immune system by yoga, meditation (anulom vilom) and your diet. Please give it a try it wont cost you anything. Wish you all a speedy recovery and be consistent with it.❤ For female: don't do anulom vilom during periods. But do the period yoga.❤

I believe if anyone needs to heal then is the “Wahls protocol plus” Bananas are not allowed nor nightshades like red bell pepper.

Well said

Try ivermectin

Were they able to see any lesions on the cerebellum?

I started experimenting this in my head I tried hiding it at work for a month now but today a coworker noticed it.

I understand.🙏🏽🙏🏽😊🦋🐬🐝❤️ If you have a email, would like to share a tip.

My personal experience vitD3 for serious chronic urinary problems: I got chronical prostatitis and uretrithis for more than 12 years and since 8/2023 permanent urethral katether (PMK) for urinary obstruction. 7-8/2023 Starting taking vit. D3 20 000 IU/day for 1-2 months 11.9.2023 level of 25-OH vit.D 138,7 nmol/L 6.5.2024 operation of urinary bladder stone and BHP (-7g removed) 8-2024 again full obstruction again PMK, diagnosed with bladder neck tightening Since 5-2024 again daily dosage 20 000 IU D3 (drops D3+k2) 15.7. 2024 level of 25-OH vit.D 106,0 nmol/L 2.10. 2024 level of 25-OH vit.D 190 nmol/L, and Ca 2.53 mmol/L since 9-2024 increased daily dosage to 50 000 - 70 000 IU (D3+k2 drops) 15.10.2024 second urinary operation - widening bladder neck by holmium laser PMK removed after 1 week, during night 9-12x urination 29.10.2024 level of 25-OH vit.D > 375nmol/L ! not determined exactly, parathormon 20 ng/L Subjective observations: Big improvements in pain reduction, urinary frequency reduction since 30.10.2024. Since no experienced doctors in high dosing of vitD3 in my country found, so „ DIY Coimbra“ it is.. 1.11. 2024 organized a new measurement where blood will be dilluted 2x to be able to measure up to 600nm/L probably I will ask for measurement of Calcium again. Also taking chelated magnesium zinc and 1x a week Cu and Fe I wonder if somebody experienced might have any insights or recomendations?

My personal experience vitD3 for serious chronic urinary problems: I got chronical prostatitis and uretrithis for more than 12 years and since 8/2023 permanent urethral katether (PMK) for urinary obstruction. 7-8/2023 Starting taking vit. D3 20 000 IU/day for 1-2 months 11.9.2023 level of 25-OH vit.D 138,7 nmol/L 6.5.2024 operation of urinary bladder stone and BHP (-7g removed) 8-2024 again full obstruction again PMK, diagnosed with bladder neck tightening Since 5-2024 again daily dosage 20 000 IU D3 (drops D3+k2) 15.7. 2024 level of 25-OH vit.D 106,0 nmol/L 2.10. 2024 level of 25-OH vit.D 190 nmol/L, and Ca 2.53 mmol/L since 9-2024 increased daily dosage to 50 000 - 70 000 IU (D3+k2 drops) 15.10.2024 second urinary operation - widening bladder neck by holmium laser PMK removed after 1 week, during night 9-12x urination 29.10.2024 level of 25-OH vit.D > 375nmol/L ! not determined exactly, parathormon 20 ng/L Subjective observation improvements in pain reduction, urinary frequency reduction since 30.10.2024. No really experienced doctors in high dosing of vitD3 in my country found yet, so „ DIY Coimbra“ it is.. 1.11. 2024 organized a new measurement where blood will be dilluted 2x to be able to measure up to 600nm/L probably I will ask for measurement of Calcium again. Also taking chelated magnesium zinc and 1x a week Cu and Fe I wonder if somebody experienced might have any insights or recomendations?

Fasiculations are what they are called. 25 yrs of ms. I found a physical therapist whose specialty is neurological diseases. I tremor w his treatment but i know he is getting me stronger. Beware neurontin can cause meth like teeth. I would not recommend that med to anyone. Backofen prn. Look up clonidine 0.1 mg for your symptoms.

Today I got diagnosed with ms

My mom Is burning 11 years now

I also was diagnosed with Multiple Sclerosis in August 2024.🥀💔 But this injection is too much costly. I had my first injection of Ocrevus on October 14, 2024. And the second Ocrevus injection will be given 15 days later in ending days of October. And I will be injected with Ocrevus after every 6 months for the next 4 years. I hope that I too will feel better after the second injection of Ocrevus.

Hey Seb. I'm not diagnosed with MS yet but I have similar issues. I found an electric milk frother helps a lot with mixing things since all you have to do is press a button. I got mine at target for $5. Much love.

I LOST THE FEELINGS IN MY HANDS AROUND 2023. BUT BEFORE THAT MY BOTTOM HALF OF MY BODY WAS NUMB FOR TWO MONTHS. I THOUGHT IT WAS FROM MY SPINE.

My tremors feel internal. Its in my chest and feet i feel like a vibrating cellphone. But my Extremities don't shake visibly

I don't see the downfall. You are still doing something in the world ❤being the voices those who are suffering or frustrated about symptoms. I love your channel. There's so many big possibilities in this ❤❤

They tried to label with MS after they gave me a round of Ciproflaxon. The symptoms of being damaged by this drug is the same as MS. I took LDN a ND gave me , in time I got better.

Hi, stable now? I am stable now. Gr. Werner