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Starting ocrevus soon! Very helpful to hear your experience and helpful to hear the other lifestyle changes that have helped too! (So interesting to hear how hard it is to see a neurologist in the UK because it’s the exact same here in the US) wishing you the best ✨

Do you still take the meds or is it pure looking after yourself now that's helping you?

Cool!!😊 This is much better than 6 hours. Hour drive to and from hospital.

Tysabri was amazing for me Copaxonne awful lollie meds Ocrevus is okay not the greatest. Crap gap is awful. Ocrevus helps with lessions not symptoms I'm looking at kesimpta

Great video Tom. I didn't know you had MS. Good for you for doing vids to help others. I already saw you vid on Fasting Mimicking Diet. Good for you for turning a negative into a positive.

Nobody talks about ms hug, first symptom

Is it good to take antiinflammatories before taking those MS drugs

I am in the process of diagnosis and the truth is I am super scared, but it makes me feel good to hear that you are fine today, it is very scary to face this, thank you for helping me to be a little less afraid. I hope you are very well

Hope you're doing well mate

Just a quick question. I'm 33 years old. healthy guy, but I had a kidney stone in my CT scan.it also showed multiple sclerotic focus on my left ischium and bones.i some times feel numbness in my left fingers. Other wise no symptoms. I do regular jogging for 1 hour. Weight training too. Although My vitamin d was too low.What should I do further to prevent it?

Iv need diagnosed with in the last year I’m not worried there nothing I can do about it

How long you Are on ocrevus

Hey Tom, new viewer and I wanted to thank you for sharing your story. I am in the part of the story where the symptoms are all pointing in the direction of MS but we are just waiting for the diagnosis. 29 year old male. Main difference between the videos I've seen on your channel and where I am now is that you were at a much better weight from the jump and I am looking to improve my health. I want to get in front of everything and I am going to go full steam on the Best Bet Diet. I would love to hear exactly what foods, specifically proteins, work best and worst for you. Also, I see at the end they include desserts, do you ever have desserts? I fear that even Gluten, Dairy, and Soy free products seem counter intuitive so I'd love your feed back. Thanks!

I'm so happy for you! May I kindly ask you, why did you stop carnivore ( that's how I found you on the 1 place)? Was the last video about quitting it was also the time you completely stopped? Really curious because about to go carnivore 😅

this is great

Great news!

Fantastic clear video- great explanation. I know firsthand how much research goes into finding out what works for you and the differing advice can be overwhelming. I'm doing all that you are doing except the Wahl's protocol instead of the 'best bet diet.' I am also doing oxygen therapy but until I stop it it's hard to know if it's working. I found Gary Brecka fascinating and did the DNA test. The results show I have the gene associated with MS so I'm now beginning to supplementing with the suggested methylated vitamins- hopefully I'll see the benefits in the coming months. You are 2 years ahead of me on this journey and your positivity and hope has really helped me- thank you.

Very happy for you. Thank you so much for your videos!!

Great to hear. Out of interest what magnesium do you take and at what dosage? There are so many types.

Lumbar puncture yesterday for suspected MS. Arrogant Dr, hit a few nerves but im glad its over. My entire body has a headache right now and i cant sleep or do much.

Keep it up, Tom 👍🏼 Peace and Love, Everyone! ❤

whats the diet called?

Well done 👍 Tom great, food is important to heal any type of illness

Why omit soya and chick peas? Can you present an example of a weeks menu that you might undertake please?

Good on ya mate, glad you're doing well like me. Four years for me since my initial diagnosis-relapse free on Mavencald/Cladribine. Possibly relapse free for free without needing any more medication! OMS has worked for me, the mindset side of de-stressing whether that's by exercise or meditation is super powerful.

You're doing incredibly well! Very happy to hear you are keeping it under control :)

Congratulations, I’m glad you are doing so well.

Great to hear you are doing so well, and remaining vibrant. 👍

So my wife had vertigo...I guess a flare up. Multiple times.... She thinks I'm lying. It's so weird tbh.

MS is so annoying... my wife is confused about it. Denying it. Have you heard of that? Over 15 months now.

Congrats!!!! That is so nice to hear!

Wow I’m late to the party… had no idea they came out with this and I’ve been on Ocrevus for 4 years! It’s exciting news to me. I’ll have to research availability in the U.S.

I’m so sorry that you had to go through a lumbar puncture, I thankfully didn’t. Just the MRI and history. I’m now suffering a major relapse and in a lot of pain. I know things will get better.

Hi Tom. Thank you for very informative videos. A firend of a friend has MS, so this was very good. - Some years back I suffered from CFS/ME, but I managed to fight that and come back strong and healthy.

Keto diet really helps. No sugar, no processed foods, no seed oils. Eat meat, fruit and veggies only, and eggs and cheese and yogurt. Use butter, not margarine, and olive oil only. R ALPHA LIPOIC ACID helps with demilinnation (nerve pain, numbness, and itching) and bentophotomine. Vitamin D and B vitamins.

How you doing now Tom? I have MS too

Hi, as you told that your first symptom was numbness from elbow to wrist, how long it lasted, could you please tell me?

Thank you for the video I’m happy to hear that everything is stable 👍🏻♥️ My doctor said at end of the month I have to choose between ocrevus or kesimpta 💔🥹 I was going to choose kesimpta because I hate my doctor and the hospital that was a good reason for me 😂 but with this news it’s getting hard to choose between them + my doctor didn’t give any information I have to search but English is my second language so it hard to know everything especially medical terminology. If there’s any advice from anyone can help me ❤ stay strong 💪🏻

Have you tried Coimbra protocol? It’s basically much higher vitamin D3 doses. I’ve been trying 20-40 thousand IU of D3+K2 and magnesium, omega3, B complex, choline. I had a very bad relapse in June and now after 1,5 months of Coimbra protocol I feel amazing, I did blood test, my Vitamin D is 81 now and calcium is in norm. So I will stick to it from now on.

Hi Tom thanks for making the video been quite helpful. I’ve seen 3 doctors now and finally on the waiting list to see a neurologist. My symptoms started with my eyesight seemed to happen overnight couldn’t make out the figures on my screens but didn’t think to much of it. Then I’ve had numbness and tingling felt like prickly heat and static electric sensation which spread up my back into arms, also major fatigue and trying to walk felt like I was trying to walk under water. Also had a squeezing sensation in the tricep area and bolts of pain. Wish I’d of gone to A&E now my numbness started in April but didn’t get my referral till July and on a 18 week waiting list.

I wish you well brother

Thank goodness for A&E. That was ultimately how I began my journey to diagnosis too!

I have fought MS for over 50 years NO meds ever. to slow it down.

So is not new treatment just new form of the same drug.

I was expecting an actual new treatment. But this is cool. I'm looking forward to Frexalimab, NVG-300, and Lucid MS.

I've just seen your video even though it's a couple of years old, so helpful I really like how you explain things and shoulders a demonstration of the type of food you were eating, really appreciated your insight and explanation. Want to know more of your story, you look a picture of health I hope you continue to be strong and healthy.

Hi Tom, have you heard of/read Hal Huggins book and his research on MS?

Thanks for the update and you do look well! I was only diagnosed earlier this year and I am not on any treatment yet. Ocrevus was recommended for me but I declined as I did not like the side effect profile. This news will probably not have any direct impact on me until I decide to start treatment but it will perhaps lead to greater convenience for others. Tom, may I ask out of interest and for comparison with my own MS management, how many times a year do you have an appointment with a neurologist?

This sounds fab.

Thanks for the update. Hope all is well.