Differences between Relapsing remitting MS and Progressive MS

A clinician discusses the differences between relapsing-remitting and progressive MS and the benefits of beginning MS treatment early.

[debbiedean]

This is the best description of relapsing and remitting MS that I've heard in 30 years.
Thank you

[CypeltResortAustralia]

Everytime I watch your videos, first thing I do is give them a thumbs up and like the video but then I walk around my house questioning why I put up with my stupid neurologist. All 3 of mine have never addressed those 5 mentioned areas!! THANKYOU FOR EDUCATING ALL OF US IN AUSTRALIA. I’m sending this link to them now!
🇦🇺 😍🙏😉💗

[Hannah-hqxs]

Thank you for this video, I'm 22 I was just diagnosed with relapsing MS three days ago so many things were missed by other blood works and doctors. I had numb and tingles for a month on a constant and this was my second time this year it had happened. I've had server vertigo last year and double vision and carpal tunnel but it was never put together to be diagnosed. 3 days ago I went to the ER and they got blood work done and rushed me to get a CT scan where I was told 30mins later they believed I had MS, then was rushed to see a neurologist next door and he said it would be beneficial to start steroids to battle my MS attack, I'm on my 2nd dose and the numbness has started to go away, ill be getting more blood work done, Xrays and RMI scan soon I am trying to be brave but it's been a lot of information within a day at the hospital it took them 6 hours when it had been going on for already a year and a bit although they've said I've caught it on time.

[Yaya-cltu]

I was diagnosed with MS 11 years ago, but because my MS was very mild, I was in denial that I had it. For years, I thought I was misdiagnosed. I took my medications sporadically and, during Covid stopped taking them for about 18 months. Recently, I started feeling numbness in both feet and two fingers on my dominant hand. I rushed to start taking treatment again, but I am nervous that I stayed in denial and relaxed with taking my meds for too long. I am taking prednisone for the numbness, but it isn't working at all. I am hoping the numbness will remit soon, but I will be certain to stay on my meds this time. No more bs denial; I have the disease.

[RickoColby]

Good comments so I figure I'll add for posterity ....
I am a male diagnosed w/ MS at 55. From NY living in SoCaL for past 12 yrs.
I had tingly hands and feet for a year and thought diabetes... Had a bad attack after a flight, when I got home and saw the Dr I got an MRI for ultimate MS diagnosis.
After one year... Dr unsure if RR or PP. Time will tell.
Taking full med right out of the gate (Rituximab and daily Gabapentin), I get flares but never get back to "baseline".
Just gotta fight the fight.~ Meds, Diet, exercise, no stress. I don't have a lot of strength or ability to work hard, cog fog, with a little bit of trbl walking.
I watch a lot of Dr Aaron Bolster on YT to learn. My neurologist (younger male) doesn't have a very good bed side manner. I think I have Primary MS but at a yr in it is hard to tell.

[joeleenwebb]

I´m 24. Doctors have told me for 6 years that I´m "fine and there´s nothing wrong with you" I did my research and figured that I might have MS....guess what... I do. I finally put my foot down and "demanded" for them to take me seriously. They really hated that I had the answer already ready lol

[ahc]

This video is so eye opening. Thank you. Makes me understand so much.

[julieb]

This woman is so giving the wrong impression about rrms . I had it for 20+ yrs before I became spms . Not once did I return to baseline after a relapse . Most people ( especially over time and repeated relapses) don’t go back to baseline . They are left with some disability or problem which never goes back to normal . This is why over time your disability worsens and problems increase . Like bladder weakness, worsening mobility, lack of finger dexterity and cognition problems . This woman over and over repeats how you go back to being a normal person between relapses which for nearly all ms’ers just isn’t true and gives an untrue picture to people newly diagnosed .

[KinEllKokabel]

Diagnosed this morning. MRI showed ‘lesions’. Dizziness. Staggering. Falling over. Impaired vision in right eye. Since end of summer 2019

[Rashy]

I’m almost certain I have RRMS. Everything is congruent with that specific type of MS. When I told my doctor my symptoms and mentioned that I think it could be RRMS he seemed to agree. I’m going for an MRI (don’t know when). I’m nervous but at least I’ll get an answer.

[henp]

I think of my disease primary progressive MS as a slope on a trend chart that never stops

[kenjohnson]

Very Informative, I learned a lot, I have PPMS and I was hoping that you would have mention that one medication out there to treat it, you never said.

[LisaDonaldson-mh]

Because I have RRMS
It's difficult to get the exact Diagnosis For RRMS.
Because it's so Random.😮
It's the Flare ups that is the best Time to get an MRI.
The lesions will show up..
However
To explain my condition to get
Support from my family...
I don't think they understand...
I have had depression anxiety and then alcohol use...
I no longer have a Self medication attitude towards alcohol.🎉
However..
I still wonder if my DRINKING triggered my RRMS.😢
So because of my alcohol abuse I don't feel like my family will understand this condition.

So Whenever I have a RRMS relapse...
EVERYONE thinks it's a Drinking Relapse 😢.
The best thing I can do for my own HEART and spirit..
Is
KNOW your Truth.

I'm so grateful for videos like this.
It's helps Ground me.
And know that I am NOT GOING THROUGH THIS ALONE ❤

[vondabyers]

Thank you for the info.. wonderful video

[funnydogs]

What about the attacks with confusion, inability to speak, hallucinations and such

[jeffbruner]

I have PPMS I'm 51 and in a wheelchair and can't use my left arm and losing my vision I'm on Mayzent and I like it better than Ocravis Infusion. What do you recommend

[TimeForElohim]

I was diagnosed with MS last week. It hasn't hit me yet lbs. 😶‍🌫️🙄

[crystalr]

is it possible to have no lesions on brain and spine mri and then later on they can eventually appear and have Ms?

[martinmatko]

What is the role of CCSVI Venous Hypertension and proper/improved Cerebrospinal Blood flow?? #CCSVI #BloodFlowMatters

TY DR

CCSVI is definitely one of the causes of MS.

The novelty for some years is that we are certain that, after studying at the La Sapienza University of Rome, there are 3 types of CCSVI:

* a 1 type with patients suffering from an obstacle to the endovacular venous discharge, i.e. due to congenital or acquired anomalies that restrict and block the drainage of the investigated veins (jugular, vertebral, azygos)

* a 2nd type with patients suffering from an extra-vascular venous obstruction, i.e. due to external compression of the vessel

* a 3 type with patients suffering from endo-vacular and extra-vascular venous obstruction

So to simplify we can say that there is a CCSVI of the "hydraulic" type (1 type), a CCSVI of the "mechanical" type (2 type) and a "mixed" CCSVI of the two previous types (3 type), the 2 and the 3 type represent about 85% of cases.

A patient with type 1 CCSVI will have a greater indication for angioplasty treatment, a patient with type 2 CCSVI will have a specific indication for specific physiotherapy decompressive treatment (RIMA Method), a patient with type 3 CCSVI it will have an indication for both an endo-vascular dilatation treatment and an extra-vascular decompression treatment.

The RIMA Method devised by Dr. Domenico Ricci of Bari is able to release compressed veins throughout their course, as shown by a publication of June 2015 after a one-year study (Internal jugular Venous Compressione Syndrome: hemodynamic outcomes after cervical vertebral decompression manipulations-Pubmed).

For information: Dr. Domenico Ricci cell.3393828399


MRI IN MS VASCULAR PATHOLOGY


This quantification of the disease pathology will help!


#CCSVI

Venous Hypertension

>microbleedings

>iron

>inflammation

>free radicals

>neurodegeneration

#multiplesclerosis


M.S. - Mystery Solved


Mysterious Autoimmunity

= CCSVI Neurodegeneration


M.S. - Mystery Solved


Mysterious Autoimmunity

= CCSVI Neurodegeneration


Keep in mind!

Also venous hypertension ➡️ impaired CSF absorption ➡️ reduced G Lymphatic drainage ➡️ interstitial peptides accumulation ➡️ NEURO INFLAMMATION #CCSVI


Eliminating cause of the Symptoms of so called Multiple Sclerosis will End MS. Apparently it is unquantifiable the length of time Symptom$ can be treated!

If you hadn't noticed


Who Knew??

#BloodFlowMatters

What is the role of proper/improved Blood flow? #CCSVI Apparently #BloodFlowMatters


Stroke common occurrence in Individuals diagnosed with Diabetes, unproven autoimmune THEORY so called MS


Supplying Oxygen and Nutrients to Cell in a Body. Blood Circulation through and including activity/exercise. Building Blocks of life, having made yourself what you are functioning today! #CCSVI


#Healthcare game changer when the cause

The doctor of the future will give no medicine, but will interest his patient in the care of the

human frame, in diet and in the cause and prevention of disease.

—THOMAS EDISON


Best possiblity easing/eliminating cause of SymptoMS!

You can relate!

If your veins are blocked they should be opened if you have SymptoMS or not!


MRI IN MS VASCULAR PATHOLOGY


Who Knew??

#BloodFlowMatters

What is the role of proper/improved Blood flow? #CCSVI Apparently #BloodFlowMatters


Stroke is a common occurrence in Individuals diagnosed with Diabetes Neurovascular Disease Multiple Sclerosis  is beingreferred 'slow Stroke'. What is the role of proper/improved Blood flow in both conditions as much CCSVI has been Scientifically confirmed a causative factor in Symptoms of so called MS!


Supplying Oxygen and Nutrients to every Cell in a Body. Blood Circulation through and including activity/exercise. Building Blocks of life, having made yourself what you are functioning today! #CCSVI


#Healthcare game changer when the cause of the Symptoms of Medical conditions are eliminated!


The doctor of the future will give no medicine, but will interest his patient in the care of the

human frame, in diet and in the cause and prevention of disease.

—THOMAS EDISON


Best possiblity easing/eliminating cause of SymptoMS!

You can relate!

If your veins are blocked they should be opened if you have SymptoMS or not!


A Vascular problem led to the crippling nightmare of Multiple Sclerosis

The real Multiple Sclerosis nightmare started at the point of NeuroDx

The disaster of diagnosis being made by general physical observation over time, .

Especially when Time is something you can’t afford #CCSVI


Multiple Sclerosis is strong and you often need help.

Make you be worthy of this help, don't stand in a corner complaining, do your part! 💪

#Symptoms often ease/DISAPPEAR

Facilitate Collaboration Neurovascular Disease Research! #CCSVI

FB Group: MSS

facebook.com/groups/4939355…!

[ragub]

My body does not go to a "baseline" after an attack. Disability increases after successive attacks. Dr says "So long you might have SPMS, but that does not affect your treatment"