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Try the Mediterranean diet, try Herb's like turmeric, ginger and Asian ginsing and speak to a chiropractor, Blessed Be.

Does the MS hug feel like a cramp in your legs but it’s around your ribs?

I am interested to know how you know that this is like wearing a ladies corset🤔😉

Love your videos!

Thank you for the many great videos! They explain our illness very well and show that you are not alone.

th-cam.com/video/EHVXJpDBcmU/w-d-xo.html In this video, Alan Macdonald, FCAP, A pathologist from Florida, and a well respected researcher goes over some impressive findings regarding Spinal Fluids of patients with Multiple Sclerosis. In particular, nematode worms observed under Dark Field microscopy, or even with the naked eye.

th-cam.com/video/EHVXJpDBcmU/w-d-xo.html In this video, Alan Macdonald, FCAP, A pathologist from Florida, and a well respected researcher goes over some impressive findings regarding Spinal Fluids of patients with Multiple Sclerosis. In particular, nematode worms observed under Dark Field microscopy, or even with the naked eye.

Can I ask I have these symptoms after covid do yours pass ?

Can you get this without ms

Thanks for that report. I really appreciate your honesty. May God bless you and keep you healthy.

Acupressure

missing you

I have this only on one side. Is that typical?

July 2020 the tightness was so bad I thought I was having a heart attack. Went to ER... Cardiologist, Gastroenterologist ( he found a small gallstone, but DOES NOT think my pain is related). Long story short (too late), I still have this pain almost every night. Like a belt is TIGHTLY wrapped around my bra line. NOTHING HELPS. Doctors & I haven't got a clue 😥

How are you ?

USA

What country is this please?

Thanks for the upload and transparency. You insight brings hope. I was diagnosed October 2019 and entirely taken aback. This condition is mysterious and a blow to the self-confidence. Pain is more than physical. To go from working and active to significantly challenged sucks. I'm curious to know if you've had success with, or heard of the Terry Wahls Protocol/ diet? She's a Dr. who went a wheelchair to walking by eating differently. What works for you besides medicines? Again, thanks for the post. Stay💪and🥗

I use ice to numb it!

That was a beautiful thing that your boys did.

Brave man

Great video, humour is what gets me through everyday.

Really a motivational person

Can this go away

Your Dad is only 63 ??!!.....Did he have you when he was 12 ?!

I think most people who live with pain understand pain the most/ I 100 percent agree family comes first no matter how bad you hurt

I appreciate you telling this so I want feel crazy when I tell my ms doctor 😃

I have this problem a whole lot like at night or in the mornings

I can't believe you didn't even lament about the Bruins! Glad the vids are back

Hey. How are you doing! Been a long time!

Good to see you back. Yes,I think some of us MS'ers are not taking this seriously. It can be lethal as they say it is 10 x more lethal than the flu and they are still attempting to figure out if is airborne. Everyone stay safe and healthy.

Thank you for posting this. This one helped answer some questions I had. I haven’t seen vids from you in a while, it’s good to see you doing well. .

Hi! I have been experiencing the exact symptoms for several months. I’ve been waiting to see a neurologist I see him the end of May. Everything you talked about related to me perfectly. I’d like to chat about it!

Hi, thought Id share my story. It started in Nov 18, I thought bugs were biting me whilst I was watching TV, but when I looked there was nothing there. It really freaked me out, as it only happened when I relaxed on an evening, this happened now and again for a couple of months, I'd have a few weeks off and then the symptoms would return. It was about May 19 that I remember walking around and my t shirt feeling odd, like my skin was sun burnt and I had the intense itching all over, my face, chest, back, legs and feet, groin and lower back. I went to the docs and they prescribed me antihistamine which I took for a month but it didn't help. I started getting the itching more often like something was running across my face, like being tickled with a feather. It was like pin pricks and sharp stabs and electric shocks. These symptoms got worse and worse until it was happening every day. I went to the docs and they said my nerves sounded like they were getting too excited, so I was prescribed Amitriptyline, I took 10mg then 20mg over a few months but got frustrated that they weren't helping and ended up going 30mg, and that seemed to work. It didn't take my symptoms of the itch and pain away completely but it reduced it by about 80% which was great. This lasted about 3 months because I ended up having a random flare up in Dec 19 which went eventual died back down. But I'd say for 3 to 4 months I was symptom free taking the medication. But it wasn't all was good, I started to notice I was getting extremely anxious in situations I normally wouldn't, like I was getting nervous and I couldn't look people in the eye. I realised it must be the meds. I reduced back down to 20mg and immediately I felt back to normal but my symptoms came back bad. I went back to the docs again and they said it was anxiety and prescribed me some anxiety meds but they said I had to get off Amitriptyline first. Over a few weeks I reduced down and experienced some pretty bad withdrawal symptoms as well as having the itchiness come back. After doing some research I knew I didn't have anxiety plus the tablets they wanted me to try would have no effect on my suspected nerve pain, so I went back to the docs. They kind of fobbed me off again and prescribed me Gabapentin. I researched the tablets and read some horror stories, so decided against it but the itchiness was intense. So again I went back to the docs and demanded I see a neurologist. Out of my own research I asked if I could try Nortriptyline which is similar to Amitriptyline but newer and slightly different make up. And that's where I am today, I await my appointment for the neurologist and until then I'll keep on the Nortripyline. I started on 10mg which worked at first but I'm currently going through a bad flare up and not even 20mg seems to be helping. Will be going up to 30mg soon and I hope it helps. I really hope I don't get the nasty paranoia side effect either. I will say this, some days are better than others, sometimes I can get distracted and mostly forget the itching is there but some days it's so intense its all I think about. Other symptoms cold hands and feet, forgetful when talking to people.

Lawrence here from Dinsmore Colony in Saskatchewan Sir those damn DRUGS I was in same situation my neurologist gave me another drug it's called Lemtrada it helped me

Never knew this was a symptom I have SPMS and I’ve been suffering from this on my scalp like bugs and my skin. I’m itching all night. I have been vaping CBD tonight and it’s helped. Now I’m itching all over again since I’ve stopped vaping and about to go to bed. Thx for your video!

Can you help me? Not me but my husband. He’s been diagnosed since 2010, refuses a wheelchair and all of his neurologist have told him he needs to be in a wheelchair. Who am I to say he needs to be in a wheelchair, when my sweet Hubster isn’t ready.

I don't have ms but I do have "nerve itches" and they are very aggravating

good luck

At what point (if ever) did you have lesions show up on MRI and did you have a lumbar puncture?

My nuero opthamologist was talking to me he thinks I have ms I have so many horrible symptoms but so far my mri of head and spine look ok and each day I get worse and worse I just had a spinal tap also after this if this comes out fine then I need to be referred to a neurologist its horrible all my symptoms all my symptoms r in my left side of my body I have dizziness swaying off balance numbness tingling burning pain in leg toes arm fingers I have double vision in my left eye I even have the same thing what they call an ms hug I have alot of back pain I'm so tired I wake up thruout the night with muscle spasms I also have urinary problems constipation I cant even take a shower without feeling off balance swaying tingling and forget that pedicure I got 2 weeks ago horrible I just hope I get the diagnosis its I have been tested for so many other things and they r all fine

nice job kids helping dad

are there ways u can quiet your immune system?

I have a stutter too... Hang in there... You got this

Me too. I hate it. Any tips? :’( I’m desperate. Any way... how you’re okay. :/

If youre 65 tho the govt foots most of the bill. If youre elderly or mentally handicapped in a care facility its free. Theres nothing fair about that when alot of us will never see those benefits. You must be VERY well off if you can afford that and still have a roof over your head, but what would happen if u cant provide, is it all free under disability?

Have you ever tried using a nasal spray? I have ms also and ever since the beginning I have had a problem with inflammation in my ears(so bad that not even a q-tip could fit at all and I become very dizzy when it is at its worst. This inflammation also diminished my ability to swallow efficiently but with the nasal spray it goes away completely(for as long as the medicine is working) I just wanted to give you a head up on that if you haven't tried that before.

As an amateur stand up comedian with MS, you and Richard Pryor are big inspirations for me. I'm probably one of just a VERY small group of comedians in Canada doing any circuit with MS. Hell, I wouldn't be surprised if I was the only one.

Welcome back, keep fighting

Good to see you again! As a fellow male with MS, it is incredible to have another guy's viewpoint on this. Been 10 years symptomatic, 3 years diagnosed, and over 2 years since last relapse. Have you tried Lemtrada? That stuff works WONDERS