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Thanks

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Thanks for all your support on this amazing journey! Love you all 🫶🏻

Recently diagnosed

Congratulations that's brilliant!!!!🌵

Gidiup! I think i spelled that wrong.😆🌵

That is some great ink. My Husbands son and his family came to visit us here in hot Arizona, all the way from Hull, UK. They are doing all the stuff the West has to offer. How is the Ocrevus treating you my friend? 😊🌵

I was diagnosed with RRMS in 2015 and progressed to SPMS in 2021, as my issues and condition got worse with worsening mobility and many, many issues I experience both every day & every night. I’ve lost 95% of my independence and annoyed with myself, as I want to do what I did 9 years ago prior to diagnosis 😢.

It seems like MOST people have ms hugs come and go, almost like a flare up but mine never stops. I’m literally being squeezed 24/7. The only difference is, it can vary from a tight squeeze to a tighter squeeze. I’m unbelievably depressed about it

I think I have both 😢

I can very well relate to you.. Even I have gone through some strange symptoms which is soooo hard to understand.

hell yes , on it since 2021 after 7 years of tecfidera, it is smooth and great , the throat thing (if you had this feel) is happening only in first ones and having no b cells all this years, never felt sick since (only delta covid one time without suffering much else than 24h fever) , welcome to The Ocrevians

I understand. I was diagnosed with MS in 2016. My son has been diagnosed with ADD. The symptoms are so very similar. Please check out David Lyons MS Fitness and Optimal Body Fitness. The workouts are structured and planned by, David himself, who also has MS. Highly recommend.

You're such a delightful person and a dedicated doctor, you are truly an inspiration Dr Emovon on TH-cam, I'm finally free from bad breath and acid reflux stay blessed sir.💐😝😝🎁💐💐😅

Is ms sexually transmittable

Omg so ive just been diagnosed with adhd but been struggling with nerve pain and more. So just looked it up and found out ms and now ive found out there is a link with the both

Since I’ve had 4 flares already this year, I can’t help but worry. No DMT reduces said flares. Find a cure, and no one will ever “worry” again.

🧡Much love and light🧡

🧡🧡🧡

I’ve got the mint green Nordic Pioneer and I love it. ByACRE have done such a good job of making aesthetically pleasing and extremely functional rollators. I recommend them to anyone who is looking for walking support.

I have MS and VKH I smoke cannabis with my mother my twitches and seizures suck my doctor told me to smoke cannabis

Congratulations 🥳

You will be an awesome ambassador!

Congratulations!!!

congrats!

I'm so happy! Can't wait to start working together 👊🏻🧡💙

Nice ink ✍️

I got diagnosed with trigeminal neuralgia a few years ago. I also have addison's disease. I haven't seen a neurologist in 2 years =/ but they said i may have ms?? I feel like my body shuts down..

A Dr Sam Gartland and Professor George Jelinek claim to have reversed their MS, what are your thoughts and have you followed their guidance?

I’d love to get something in regards to M.S, I just don’t know what

Around 2016 i went to the hospital thought I was having a heart attack dr said no and this before i was diagnosed with MS diagnosed in 2017 but having discomfort quite often 2023 having chest pains for 2 weeks and i work out and eat Healthy but i went to hospital Oct 6 did full test found nothing wrong with my heart i mentioned about the MS and then the dr said oh this could be the ms hug the crazy thing the pain went away the next day then in March of 24 it started again went back to the hospital same thing hearts ok im almost done since i moved in july i had a bad summer with this MS heart like attacks been very lazy i think my Ms is getting worse and theres no CURE TY FOR LISTENING TO ME IF YOU READ ALL OF THIS

Well done mate - I HAVE MS BUT MS DOESN'T HAVE ME

Eighteen years ago, I was officially diagnosed with RRMS at the age of 24(I am now 42). Just to mention, my original MS Neurologist expressed to me that he believed that my MS symptoms began at the age of 19 which I believe began at the age of 17(out of no where I began to feel as if I could not get enough sleep, and my energy was lacking. I was sent to a sleep doctor at this time who told me that I had sleep apnea. Then this doctor was ran out of town because he was lying to his patients about having sleep apnea. That’s why I look at the age of 17, and there’s a few other reasons. I always tell anyone that I’ve been blessed in having MS yet that doesn’t mean that it has always easy. I fight and stay strong(always). Much love, BRO!

Thanks Liam 😊

When I get the MS hugs, they are extremely severe. Quite possibly the most excruciating thing I’ve ever experienced, I even scream and sob in discomfort.

I am trying to do the same. I like watching your videos. Keep it up.

Got diagnosed at 16 that was 2021 and the way I found out was worst then blunt im trying to understand but at times it gets hard

In the same boat dude shit sucks but keep your head up. I like to think were both lucky. If we were born earlier in time, there aren't too many effective treatments out there, so it's like a death sentence. The future is bright

You are so professional in your videos! Thank you for sharing and take care

Thank you Liam for taking your time for helping myself and anyone else with Ms, unfortunately my neurologist doesn't think I need any treatment such as DMTs, he's obviously a psychic, and believes I'm fine without anything. Let's hope he's right😊

Getting it badly at night into legs and arms. A low voltage , say, 30 volts just buzzing and creeping me out. Also having a problem with bicep Neurologist doesn’t seemed to impressed with symptoms though. He’s not really impressed with MS as I believe his main gig is Alzheimer’s. Getting a new one but damn if it isn’t hard to find one in Mt.

Turn to THE ALPHA AND OMEGA count you BLESSING all I want to do is go to work

Is seb okay?

Thanks for doing this!

Definitely feel like i could use one of those. Walking is pretty hard for me on a daily basis

I was diagnosed in April 2023, I was told i have 5/6 lesions on my brain, I've never been given a spine MRI, I had a lumber puncher, which was positive for oliglocanal bands. Ive had optic neuritis twice, once in each eye. My neurologist has never offered me any treatment. Apparently i just have to get worse. Its a scary prospect. Fingers crossed for myself and everyone else who is suffering with any form of Ms

I hope one day ❤ we all celebrate cure 🎉

Looks so cool! How did you find it?

Hi Hope you’re doing well Your content is amazing 😊