Multiple Sclerosis: BUILDING the North American CCSVI Society Part 2
www.kvmr.org THE link for Wed. 2 at 1200 Pacific TIME This is a community radio show. The programme is called Rabble Rousing. John Fletcher will be hosting the show. Special thanks to Susan ThePennygirl (youtube user) Great news this week in CCSVI research. Canada and Italy have allocated several million dollars toward CCSVI research. A group of cardiovascular specialists from over 47 countries have UNAMIMOUSLY come to the consensus view that CCSVI comes before MS CCSVI is congenital (we are born with it). I have a radio interview scheduled on Feb 10th at 1200 noon PACIFIC TIME the radio show is Rabble Rousing with John Fletcher This is huge on getting CCSVI some public exposure. Please check out Joan Beal’s radio interview it has been posted on several CCSVI facebook spots. Also, I had alluded in this video about a link between FIBRIN and stress. FIBRIN is present in the blood and it causes blood to thicken or have higher viscosity. During times of stress it is proven that FIBRIN production increases. With chronic cerebrospinal insufficiency the veins that drain deoxygenated blood from the brain become narrowed. I have often wondered why my MS attacks have been during very stressful times in my life. Well….If under stress my blood thickens and it makes it that much harder to drain because of CCSVI. This makes a lot of sense. Thank you everyone for your continued support and for getting the word out and standing up for what is right. Together WE WILL. Mark
@eddysacat
I have done nothing.
You have allowed yourself to look for that light at the end of the tunnel.
YOU made the difference in yourself, I just gave you some info.
UR the coolest for your kind words.
Thank you,
Mark
@marykaygwinn
I doubt he even knows who I am.
I am a huge fan of his though and I am going to fight that the truth gets out and Dr. Zamboni is recognized for his heart, courage, and brilliance.
@auntoni51
God bless you right back.
Watch out for those brain farts they can happen at the most unfortunate times.
Wait a minute….I am thinking of the other farts. LOL
Keep fighting. Keep trying.
Keep your head up.
The journey is only beginning.
Take good care, sweet Ione,
Mark
Yes,Mark. The highest ratio of M.S. p.p is in the Shetland Isles of Scotland. They have the same hours of sun as the Arctic Circle, and its sea-boundedness, resulting in close community marriages, both make for a compounded genetic lack of vitamin D which could easily be the cause of high ccvis.
You are wise, dear lass.
I have seen vids for the “Shine on Scotland” campaign.
What you said makes perfect sense.
Intermarriage between clans with similar genetic make up etc…
You are very wise,
Have a good day.
Mark
Spot on as usual.
It was a big shock to hear on T.V, that anyone with near ancestors with or who themselves have names beginning Mc or Mac have a 40% more likely chance of having M.S. My family have the names on both sides.( But , living an outdoor life in countries with all year sun can change the expected pattern if you live there from your early teens!)
Awesome. This is great. I am glad you are having success. We will all make a difference. Keep Moving Strong!
Hey Folks,
Thanks to Mark
for doing this ! Help get the word out re: the broadcast by contacting your local MS support groups in your areas, I was able to reach 5 in surrounding counties today! And remember you can listen live via the web site.
If anyone can’t listen at time of air I will do my best to get studio copies out to you! just send me a note. Lets get the word out !!
Thanks to you all, susan
Mark,
I will be listening to your radio show. So amazing what is going on here.
There is a genetic link to MS. That and being born in the northern hemisphere and a lack of vitamin D. If we all have haywire veins or arteries leading from our brains, and this gets corrected. I am betting that our immune systems will quit attacking. For all of us with MS this will be like we are being reborn!!
Please folks consider Mexico,in N.A.CCSVI they have physicians that studied worked and trained in Europe,Canada,US etc. I had my son mrv tested Jan.12 for about 550 usd, this is a low cost option. sing me in Mark!
Dad 4 ms folks & son. Blessings! Rick.
Thank you Mark keep going
Good video, I like what your saying. Very positive and reassuring to know that WE are not letting the pharmaceutical companies bog us down. We know they have to get those billions. Why else would they be prescribing meds that were in the past used for epilepsy. It’s easy to make billions when the RandD is already done.
I just wish it could be next week. But we all know it will be a few years and that’s way better than decades
Keep up the good work and count me in!!!!!!!
I just wanted to say my mother just got her neck scanned and they didnt find any blocked arteries the only thing was that one of them was slightly thiner but the blood was still flowing they said. She’s on a big downer now she got all hyped up over this thing and was sure there was going to be somehting to it now i dunno either.
They should have been looking at the veins instead of the arteries.
Particularly the jugular and azygous.
The fact that nothing showed up should not defeat you.
If someone can do the exam according to Zamboni’s protocol, they will find something.
I cannot reiterate this enough.
Just to be able to spot these strictures takes training specific to the protcol established by Zamboni’s team.
Do not lose heart.
Mark
Mark, thanks so much for a balanced and positive commentary on this. *doing a victory dance for us* Here here as to what you are saying about the MS Society. Sick of conspiracy theories and Society bashing – CCSVI will prove itself if it warrants it right? Go well with your radio show and love ya mate. Kerri xo
I can’t wait to see all of us 500,000 MS zombies wake up and become vivacious again!!!!!!!
ME TOO!!!!
hey mark what is the time frame?testing and the help we all need from all of this we go though every day the stuff no one knows but use nomater what we tell its like we need help where we can get it.good idea bad idea see first then shot it down.try i do it its slow but i do it.they need to try so we can move.thanks for getting use out there with out you we would be ten steps back thanks man we need you. mike
Thanks Mark
Now what the MS-world needs is activism
@Regna: Arteries play no role in MS.
The blocked veins in the neck are related with so-called cerebral MS.
Spinal-MS is probably related with blocked veins in the spinal area. It isn’t researched as much as for CCSVI yet.
Progressive MS (20%) is said not to be cured by angioplasty.
Big question is who scanned your mother’s neck: it needs a specific training.
This is the best thing I have heard in a long time. I would like to start a chapter in the state I live in. I don’t know what to do to get it started or I don’t know if that is something that anyone would want to do. But either way this is great . Thank you for being real and true
How’s the US CCSVI organization coming along, we NEED to rally at the White house! Something BIG, to be noticed, videos/blogging are great but we need to demonstrate like Canada and the UK did. The US government is in our healtjcare system now, lets make some noise and demand our rights as AMERICAN citizens!!
@bbrfitz
It is actually going along quite well. It is formed and has status.
It is not the NA CCSVI Society as I had planned.
I was informed not long after this video that the administrator for CCSVI in MS has already got “the society” started so not to double work….
Anyway. Have a great day.
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