Chronische Cerebro-Spinale Veneuze Insufficiëntie :: Toon onderwerp - Ashton Embry's Samenvatting

Summary

The recent scientific results on CCSVI and MS from both the University of Buffalo and Georgetown University have essentially left very little doubt that CCSVI is a causal factor in MS in the majority of, but not all, cases.
Furthermore, persons with MS with more disability are much more likely to also be affected by CCSVI and thus there is little question that CCSVI accelerates the MS disease progression.

Given the above, every person with MS should be tested for CCSVI. If CCSVI is detected, it should be treated as soon as possible. Persons with MS do not have the luxury to wait five to ten years for research to prove what is reasonably well established at present.
Nutritional strategies which counter CCSVI, BBB breakdown and autoimmune reactions are essential both before and after CCSVI treatment.

Nutritional strategies which counter CCSVI, BBB breakdown and autoimmune reactions are essential both before and after CCSVI treatment.

Ik durf het bijna niet te vragen... kan iemand (of iemanden) een vertaling maken :-)

I recently read your opinion piece on CCSVI which was made available online in Annals of Neurology (Khan et al, 2010) last week. I see it as part of “MS Wars: Part II – The Medical Empire Strikes Back”.

The only part of the article I found distasteful was your advice for persons with MS to not get tested for CCSVI for at least 5-10 years (while further research is being done).

The advice in your opinion piece of not to get treated for CCSVI for at least 5 -10 years from now is both irresponsible and dangerous. And this brings us to the topic of the serious lack of objectivity of such advice.

One big problem with you saying not to get treated for CCSVI is that almost all of you are closely aligned with the pharmaceutical industry and thus have a major conflict of interest when you offer such advice.

In summary, your Point of View is completely out of date and your advice regarding CCSVI testing and treatment is totally compromised and of no value.
It is also potentially very harmful for persons with MS. Five to ten years is a very long time to have to wait for testing and treatment of CCSVI and such a long time represents a huge amount of lost brain (Time is Brain).
I can only suggest you try hard to take a patient-centred, evidence-based approach and do everything you can to make testing and treatment of CCSVI available as soon as possible.

Voor degene die munitie willen voor een dialoog met specialisten is het verstandig het hele artikel te lezen...

Auteur:	Gast [ za 20 feb 2010, 20:07 ]
Berichttitel:	Ashton Embry's Samenvatting - Feb 2010
Ashton Embry laat weer van zich horen in Ashton-style: CCSVI and MS: Integrating New Data to Help Guide Actions Citaat: Summary The recent scientific results on CCSVI and MS from both the University of Buffalo and Georgetown University have essentially left very little doubt that CCSVI is a causal factor in MS in the majority of, but not all, cases. Furthermore, persons with MS with more disability are much more likely to also be affected by CCSVI and thus there is little question that CCSVI accelerates the MS disease progression. Given the above, every person with MS should be tested for CCSVI. If CCSVI is detected, it should be treated as soon as possible. Persons with MS do not have the luxury to wait five to ten years for research to prove what is reasonably well established at present. Nutritional strategies which counter CCSVI, BBB breakdown and autoimmune reactions are essential both before and after CCSVI treatment.

Auteur:	sankol [ za 20 feb 2010, 21:09 ]
Berichttitel:	Re: Ashton Embry's Samenvatting - Feb 2010
Een heel duidelijk en logisch verhaal, jammer dat sommige dit inzicht missen!

Auteur:	linda [ zo 21 feb 2010, 11:17 ]
Berichttitel:	Re: Ashton Embry's Samenvatting - Feb 2010
Citaat: Nutritional strategies which counter CCSVI, BBB breakdown and autoimmune reactions are essential both before and after CCSVI treatment. dat denk ik ook maar je kan alles ook oplossen met alleen voeding,volgens mij. [voorbeelden genoeg Hetty de Roo,Therry Wahls,MacDougall etc.] liberation is leuk maar voeding does the trick also . tenminste als voeding je ding is natuurlijk.

Auteur:	alphons [ zo 21 feb 2010, 20:14 ]
Berichttitel:	Re: Ashton Embry's Samenvatting - Feb 2010
Ik durf het bijna niet te vragen... kan iemand (of iemanden) een vertaling maken

Auteur:	linda [ zo 21 feb 2010, 20:24 ]
Berichttitel:	Re: Ashton Embry's Samenvatting - Feb 2010
tuuk Alphons, count me in. misschien melde zich nog een paar vertalers dan kun jij de te vertalen stof misschien verdelen??

Chronische Cerebro-Spinale Veneuze Insufficiëntie https://www.ccsvi.nl/forum/

Ashton Embry's Samenvatting - Feb 2010 https://www.ccsvi.nl/forum/viewtopic.php?f=24&t=232	Pagina 1 van 4

Auteur:	Esme [ zo 21 feb 2010, 20:28 ]
Berichttitel:	Re: Ashton Embry's Samenvatting - Feb 2010
alphons schreef: Ik durf het bijna niet te vragen... kan iemand (of iemanden) een vertaling maken Ja hoor, no problemo, ich spreche jede Sprache Wilt u alleen de samenvatting of het hele stuk?

Auteur:	Gast [ zo 21 feb 2010, 20:42 ]
Berichttitel:	Re: Ashton Embry's Samenvatting - Feb 2010
The recent scientific results on CCSVI and MS from both the University of Buffalo and Georgetown University have essentially left very little doubt that CCSVI is a causal factor in MS in the majority of, but not all, cases. Uit de laatste wetenschappelijk onderzoeken met betrekking tot CCSVI en MS van zowel de Universiteit van Buffalo als Georgetown, blijkt dat er heel weinig twijfel bestaat over het gegeven dat CCSVI een oorzakelijk factor is voor MS. Furthermore, persons with MS with more disability are much more likely to also be affected by CCSVI and thus there is little question that CCSVI accelerates the MS disease progression. Daarnaast is het zeer waarschijnlijk dat mensen met MS, die erg achteruit zijn gegaan, ook zeer waarschijnlijk aangedaan (?) zijn door CCSVI, waardoor er weinig twijfel bestaat dat CCSVI de progressie van MS bespoedigt. Gezien bovenstaande, zou iedere persoon met MS getest moeten worden op CCSVI. Indien CCSVI is ontdekt, zou er zo snel mogelijk behandeld moeten worden. Mensen met MS hebben niet de luxe vijf of tien jaar te wachten op onderzoeksresultaten die zouden bewijzen wat op dit moment redelijk duidelijk is. Given the above, every person with MS should be tested for CCSVI. If CCSVI is detected, it should be treated as soon as possible. Persons with MS do not have the luxury to wait five to ten years for research to prove what is reasonably well established at present. Nutritional strategies which counter CCSVI, BBB breakdown and autoimmune reactions are essential both before and after CCSVI treatment.

Auteur:	Gast [ do 25 feb 2010, 14:39 ]
Berichttitel:	Re: Ashton Embry's Samenvatting - Feb 2010
Artikeltje "An Open Letter to the Authors of CCSVI and MS" van Ashton Embry: Citaat: I recently read your opinion piece on CCSVI which was made available online in Annals of Neurology (Khan et al, 2010) last week. I see it as part of “MS Wars: Part II – The Medical Empire Strikes Back”. Citaat: The only part of the article I found distasteful was your advice for persons with MS to not get tested for CCSVI for at least 5-10 years (while further research is being done). Citaat: The advice in your opinion piece of not to get treated for CCSVI for at least 5 -10 years from now is both irresponsible and dangerous. And this brings us to the topic of the serious lack of objectivity of such advice. One big problem with you saying not to get treated for CCSVI is that almost all of you are closely aligned with the pharmaceutical industry and thus have a major conflict of interest when you offer such advice. Citaat: In summary, your Point of View is completely out of date and your advice regarding CCSVI testing and treatment is totally compromised and of no value. It is also potentially very harmful for persons with MS. Five to ten years is a very long time to have to wait for testing and treatment of CCSVI and such a long time represents a huge amount of lost brain (Time is Brain). I can only suggest you try hard to take a patient-centred, evidence-based approach and do everything you can to make testing and treatment of CCSVI available as soon as possible. Voor degene die munitie willen voor een dialoog met specialisten is het verstandig het hele artikel te lezen...

Auteur:	linda [ do 25 feb 2010, 14:53 ]
Berichttitel:	Re: Ashton Embry's Samenvatting - Feb 2010
Citaat: Voor degene die munitie willen voor een dialoog met specialisten is het verstandig het hele artikel te lezen... an garde !!!

Auteur:	Nanda [ do 25 feb 2010, 14:59 ]
Berichttitel:	Re: Ashton Embry's Samenvatting - Feb 2010
Time is Brain !! Het allerbeste argument!

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