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#31 | |||
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Elder
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Trish, really good questions...makes me think that this might be more complex than having my neck veins expanded...
I was wondering, if you have blocked carotid arteries, would you also tend to have blocked jugulars?
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Instant Karma's gonna get you-gonna knock you right in the head...John Lennon |
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#32 | |||
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Grand Magnate
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Trish, I though your questions were good too. I have lesions in both my brain and spinal cord so I was also thinking that this answer seems too simple. Also people are often dx with MS at a fairly young age. It just seems to go against conventional wisdom that they would have these type of blockages at a young age. But I guess it is possible. I am definitley looking forward to hearing more about this treatment in the future.
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#33 | |||
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Magnate
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Quote:
"...Zamboni found blockages not only in the veins in the neck directly beneath the brain -- the jugular veins --but in a central drainage vein, the azygos vein, which flushes blood down from the brain along the spine. Blockages here, he found were associated with the most severe form of MS, primary progressive, in which patients rapidly deteriorate. For this form of MS, there currently is no effective treatment..." From the link Laura supplied, with thanks to her! http://www.ctv.ca/servlet/ArticleNew...1121?s_name=W5
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I know the sound the river makes, by dawn, by night, by day. But can it stay me through tomorrows that find me far away? . I have this mental picture in my mind of you all, shaking bones and bells and charms, muttering prayers and voodoo curses, dancing around in a circle of salt, with leetle glasses and tiny bottles of cheer in the middle...myyyyyy friends! diagnosed 09/03/2004 scheduled to start Tysabri 03/05 Tysabri withdrawn from market 02/28/05 Copaxone 05/05-12/06 Tysabri returned to market 06/05/06 Found a new neuro 04/07 Tysabri 05/25/07-present Medical Marijuana legally 12/03/09 . Negative for JC virus antibodies! . I'm doing alright and making good grades, The future's so bright, I gotta wear shades! . |
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"Thanks for this!" says: | AfterMyNap (02-06-2010), barb02 (11-22-2009), dmplaura (11-22-2009), SallyC (11-22-2009), tkrik (11-23-2009) |
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#34 | |||
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Grand Magnate
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Some related info. Looking, non-invasive I think. A study looking for volunteers.
Michelle Andrews Project Coordinator Buffalo General Hospital Buffalo Neuroimaging Analysis Center 100 High Street Buffalo, NY 14203 CTEVD Study <ctevd@bnac.net> YI: I think this just looking in Bufflo.
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Kicker PPMS, DXed 2002 Queen of Maryland Wise Elder no matter what my count is. |
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#35 | |||
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Magnate
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Quote:
Imagine THAT inbox.... ![]() I too thought about spinal lesions, and it's a good question. Personally I think that the FACT there are blockages (which imo, doesn't matter as far as the age question is concerned) is a part of the bigger picture of the disease, BUT... I feel that the blockages COULD be the key to providing a better quality of life for many of us, and possibly stopping the process that's already existent. It's entirely possible that once the blockage starts, it gets worse over time gradually, resulting in the disease process we've known in the brain, optic nerve and spinal chord for so long now. If bad stuff's being left behind in the brain, as the program describes, due to the draining being restricted due to the narrowing, it's only logical that our immune system would POOF fly into action, and be confused possibly? .. leading to the attack on myelin. Of course I'm completely hypothesizing but wow.. the more I think about this one...
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2004 to present - Trigeminal Neuralgia 2007 to present - Burning Mouth Syndrome March 2008 - Multiple Sclerosis DX 05/2008 - Relapse 05/2008 to 02/2009 - Copaxone 10/2011 - Relapse - Optic Neuritis developed 9/2012 - Relapse - Balance issues 1 sided 8/2012 - Erythema Nodosum - diagnosed 10/2012, reaction to Topiramate (Topamax) April 7/14 - Raynaud's Syndrome DX |
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#36 | ||
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Junior Member
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Quote:
Also check out this link which says: Quote:
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"Thanks for this!" says: | AfterMyNap (02-06-2010), barb02 (11-22-2009), dmplaura (11-22-2009), gonnamakeit (11-22-2009), Riverwild (11-24-2009), SallyC (11-22-2009), tkrik (11-23-2009) |
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#37 | |||
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In Remembrance
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I think I'll e-mail this to my Doc/PCP and see what he thinks. I'll call in the morning..
![]() Maybe we should all have our jugular veins and the azygos veins checked for blockages, Huh???
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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#38 | |||
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Grand Magnate
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Quote:
This "story" actually goes back to the 70's, where a Dr Schelling made a discovery: Quote:
http://www.ms-info.net/ms_040504.pdf He also has a great website where you can view how Dawson Fingers are formed: http://www.ms-info.net/evo/msmanu/984.htm I believe that this "backjet" influence the formation of our "multiple plaques" disease, absolutely, but still wonder what the underlying problem is that causes our veins to do this in the first place. As was explained in the W5 show, it seems as though twenty-some % had further vein complications after the angioplasty surgery ... so is something else causing this "mechanical failure", which results in multiple plaques in our CNS? Anyway, it finally feel like they are on the right track to me ... Cherie
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I am not a Neurologist, Physician, Nurse, or Hairdresser ... but I have learned that it is not such a great idea to give oneself a haircut after three margaritas
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"Thanks for this!" says: | AfterMyNap (02-06-2010), dmplaura (11-23-2009), gonnamakeit (11-23-2009), Lady (11-27-2009), notasperfectasyou (11-22-2009), Riverwild (11-25-2009), SallyC (11-22-2009), tkrik (11-23-2009) |
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#39 | |||
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Member
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If you want more info on this all - check out www.thisisms.com they have an entire board/forum dedicated to this and people who have done it. They do it at Stanford (in CA).
They also have extensive information regarding the treatment on that site. ~Keri |
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#40 | |||
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Wise Elder
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Thanks everyone for all the links and info. I read through some links and will be reading through the others. As many of you know, my brother spent 20+ years as a researcher for neurological disease - MS included. I plan on sharing this information with him and seeing what he thinks about it all. I am sure with all his work/books (and he has lots) he has heard of this but I am not sure.
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The theory does make sense to me but I agree with you that the underlying problem is still a mystery. Something has to be causing and we are then back to the same questions - what caused this malfunction within our bodies. We are then back to the chicken and the egg question. It would be interesting to see the results of anyone in the study that was directly related to an MS patient in the study. It is interesting that for some families MS appears to be "hereditary" while in other families there is no direct link to it being hereditary. Case in point, I am the only one in my family that had/has it for the past 4 generations. Others on here have other family members who have it as well. Again, are these 2 different types of MS? Is one CCSVI an inherited condition and the other is completely different? I am very hopeful that this will be a start in a new direction for all of us MSers. Again, I think of this in terms of strokes or TIAs or brain injuries and the effects of such both short term and long term. |
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"Thanks for this!" says: | dmplaura (11-23-2009), gonnamakeit (11-23-2009), Lady (11-27-2009), Riverwild (11-25-2009), SallyC (11-23-2009) |
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Ccsvi | Multiple Sclerosis |