Thank you for sharing. I am living in Virginia. It's legal with a prescription. Over 2 years was consuming canibus, tried smoking it but that's very inflammatory, gummies and tincture were the best for me. My calves stopped spasticity at night and got longer sleeping time. My Nuroligist stopped writing me a prescription and wanted me to try oral baclifin 10mg. The first week was ok sleep but now it has reduced to 2-3 hrs. And now I'm afraid he will up the baclifin dose. I'm not pleased with that result. And my spasms haven't fully returned, but my calves have started to eake a bit at night, making my sleeping less.

All support from ms brother to another, I'm glad u can walk like along walk , i hope get my health back someday too

Found out I had MS on my 30th birthday this year, symptoms I have is numbness in the finger tips, fatigue, vertigo, and at the same time numbness and weakness on my right leg, getting out of bed and my spine feels weak and walking feels off. My doctors appointments are taking so long for every appointment that’s given which causing a worrisome and depression because I don’t know how to go about this.

Look into lion's mane mushroom as well.

Try the Mediterranean diet, use Herb's like turmeric, ginger and Asian ginseng and speak to a chiropractor.

Going through the diagnosis now. I have Lharametes syndrome however it's spelled LOL. But yes, I get the wobbles with hot showers, lose feeling in fingers, and eye sight. Had multiple MRIs not an MS specialist. So difficult 😢 yes lessions on my MRI imaging.

Thanks for making this video - my wife was diagnosed with RRMS two years ago and seems to have ADHD symptoms showing up - maybe another thing the disease has taken from her. It’s frustrating and scary - but it’s very helpful to see there are others experiencing the same thing out there.

💪🏾feel better Liam, I know the feeling after the Ocrevus infusion… totally drained. Wishing you all the best ❤

Good video expect for the toxic positivity part of don't worry people with MS can lead normal lives Please remove that part as it putting advice. Good 60swc video otherwise

Hope you enjoy the videos ☺️

Ive had ms for 14 years. When i bend my neck i get electric shocks down from the bottom of my back to my toes. Through my legs.

Thank you for sharing. I'm a dad of two litle girls 2-4 years old. I'm in the middle of a long search of what the hell is wrong with me.. Today I have an appointment with a neurologist. Are mri for ms diagnose with contrast fluids? I had lots of mri due to other health issues.. but last time I had a 🧠 scan it was without fluid and just got send away and told me I don't see anything wrong. Now my list of symptoms is a mile long and I'm afraid not being taken seriously..

I’ve both. The distractions from pins and needles, over heating, right foot doesn’t act like mine…. Yeah, then ADHD dxd before MS. It’s fatigue on freeze tags?

Being a parent when you have MS is tough - but we're tougher!! 🤙🏻 🧡

I hope you fine bro, have it since 19 im 27. I just got a wake up call and your the first one i saw. Im not watching the whole Video. But i wanted to say stay strong and focused🤙

Love your openness. I have worries and many issues with my MS. I’ve been diagnosed for 9 years, originally with RRMS, but in 2020 I was diagnosed with SPMS. I get really upset as I’m only 47 and still want to be sexually active m regardless of having SPMS, but I’ve not had oral sex from my long term boyfriend for 9 years. I don’t think he realises that I loved him going down on me, but MS has caused many issues, as I can’t abduct (open my legs) which causes problems in the bedroom! I have bad planking as well with my leg. He’s also not interested in sex, nor foreplay. I just want to be stimulated! He appears to have gone off any sexual interaction with me. He has post thrombotic syndrome so I know he has leg issues with standing and trusting me. But along with that I also poor core issues now, so I can’t cowgirl him, which used to be a very climatic experience, but he’s not given any suggestions for us, as I feel unfulfilled 😢! Do you have any suggestions to help me/us. He now knows that I masturbate, but no questions regarding that neither. I feel my condition has really taken over and I just want him!!

My wife had her first full dose 3 days ago and feels very unwell 😢we don't know if it's normal either

Thanks

🧡💪🏽

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 KZbin, 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

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 😊