CCSVI skeptics
It was wasn't it? the new findings in the SWI method appear to be ready to offer brand new looks at what is happening in MS lesions when using that information in light of the CCSVI model.Cheer that was an interesting explanation to Ken's question.
Cheer commented in her Bologna notes that Dr Haacke said that nothing in the CCSVI model is in conflict with the work he has done. I felt that this comment was very exciting. A search on google scholar for "haacke swi multiple sclerosis" gives a quick look at the kind of research this man has been doing. It means a lot that his work is in harmony with CCSVI.
Paper from 2005
paper from 2000
recent paper
I'm not offering medical advice, I am just a patient too! Talk to your doctor about what is best for you...
http://www.thisisms.com/ftopic-7318-0.html This is my regimen thread
http://www.ccsvibook.com Read my book published by McFarland Health topics
http://www.thisisms.com/ftopic-7318-0.html This is my regimen thread
http://www.ccsvibook.com Read my book published by McFarland Health topics
- notasperfectasyou
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Thanks everyone, and esp Marie and Cheer. I will go through Cheer's post, will take a while. But, I can work google pretty good. I'm something of a ccsvi lurker/spectator right now. You probrably noticed I'm really posting a lot about abx now, but that's not a reflection of any less interest in ccsvi. Honestly, I think it's good to keep it at arms length right now. But, you all know I care very deeply for all of you and hope and pray that this is "IT". So, next week I'll google up from Cheer's post and work on it in the obsessive approach I take to things. I'll check BT later and see if anyone made it over there. Thanks, Ken
It would be really nice to be able to put links in here
If I have included a bad link, google the word "Scholar", click link for "Google Scholar". Search for the name of the paper and author in Google Scholar.
If I have included a bad link, google the word "Scholar", click link for "Google Scholar". Search for the name of the paper and author in Google Scholar.
Ken,
abx helped me somewhat though I progressed on them, but your Kim is getting really good help from that quarter it seems. If I was you, I'd be doing the same thing; waiting to see and going with what works.
I am really happy for you guys that abx are working for her. I think you are smart to keep this in your back pocket ....it'll be there when you need it...........
abx helped me somewhat though I progressed on them, but your Kim is getting really good help from that quarter it seems. If I was you, I'd be doing the same thing; waiting to see and going with what works.
I am really happy for you guys that abx are working for her. I think you are smart to keep this in your back pocket ....it'll be there when you need it...........

I'm not offering medical advice, I am just a patient too! Talk to your doctor about what is best for you...
http://www.thisisms.com/ftopic-7318-0.html This is my regimen thread
http://www.ccsvibook.com Read my book published by McFarland Health topics
http://www.thisisms.com/ftopic-7318-0.html This is my regimen thread
http://www.ccsvibook.com Read my book published by McFarland Health topics
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- whyRwehere
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- cheerleader
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just wanted to say that any questions from skeptics are always more than welcome! They help us all banter around the science behind CCSVI. Since the conference, I feel more adept at explaining the variety of connections of prior MS research. Dr. Haacke has a cool take on it....none of this new research trashes the old, it all fits, and CCSVI puts it together.
As far as "tone"....yeah, MS can change a personality. I used to take Jeff's snapping at me personally, until he explained that sometimes he just couldn't take another minute without lying down and being silent. It wasn't me...it was the world. When he got his MS diagnosis, I better understood. When I saw what has been happening to his beautiful brain, I really understood, and I forgive him. But even caretakers need to vent now and then, right why??? I think we've all let loose on here, and we've all worked it out. Kinda like family.
cheer
As far as "tone"....yeah, MS can change a personality. I used to take Jeff's snapping at me personally, until he explained that sometimes he just couldn't take another minute without lying down and being silent. It wasn't me...it was the world. When he got his MS diagnosis, I better understood. When I saw what has been happening to his beautiful brain, I really understood, and I forgive him. But even caretakers need to vent now and then, right why??? I think we've all let loose on here, and we've all worked it out. Kinda like family.
cheer
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
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- CureOrBust
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I have a question, which I have yet to see discussed explicitly in a paper thus far; which has proven in the past, NOT to show that it never actually happened. I personally have a single trigger for a relapse, that being a cold/flu. When I always remind my neuro, he always responds with "that's quite common for people with MS". So, if its common, where's the medical explanation? Huh? huh?
When I think about it personally, it's hard to explain how easily I have adopted this idea, without a real personal understanding / explanation for my relapses.
My guess is that the cold / flu somehow makes the tight junctions of the BBB more susceptible to damage OR an activated immune system goes a little more crazy with the collateral damage. But I would like to read something from someone who actually knows what they are talking about, knowing its all theory for now.
When I think about it personally, it's hard to explain how easily I have adopted this idea, without a real personal understanding / explanation for my relapses.
My guess is that the cold / flu somehow makes the tight junctions of the BBB more susceptible to damage OR an activated immune system goes a little more crazy with the collateral damage. But I would like to read something from someone who actually knows what they are talking about, knowing its all theory for now.
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Dr. Zamboni talked about it briefly, Cure. He mentioned bacteria and viruses as being "endothelial disrupters" which can cause an exacerbation of stenosis by creating vasoconstriction. It will be in his paper next month in Vascular Surgery. That's always been my take on it, since the endo paper I wrote last year. I never really looked at it from the autoimmune viewpoint....but maybe others have a different take on it.
cheer
cheer
Husband dx RRMS 3/07
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
dx dual jugular vein stenosis (CCSVI) 4/09
http://ccsviinms.blogspot.com
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Hi.
There is significantly lower oxygen pressure in high altitudes, which makes oxygen absorption more and more difficult for the blood. This is the reason that people living on high mountains are so red. Their body produces more blood to overcome this lack of oxygen and absorb as much as possible.
sou
There is significantly lower oxygen pressure in high altitudes, which makes oxygen absorption more and more difficult for the blood. This is the reason that people living on high mountains are so red. Their body produces more blood to overcome this lack of oxygen and absorb as much as possible.
sou
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Hi, there were 2 papers presented at ECTRIMS. I saw it in the programme.BBE wrote: It was said that after the Bologna Conference there will be a presentation held at ECTRIMS. Why didn`t they mention CCSVI at ECTRIMS?
Erika
Aug. 7, 09 Doppler Ultras. in Poland, left Jugul. valve problem, RRMS since 1996, now SPMS,
- Nov.3,09: one stent in the left jug. vein in Katowice, Poland, LDN, never on DMDs
- Jan. 19, 11: control venography in Katowice - negative but I feel worse
- Nov.3,09: one stent in the left jug. vein in Katowice, Poland, LDN, never on DMDs
- Jan. 19, 11: control venography in Katowice - negative but I feel worse