{"id":561,"date":"2010-07-11T16:19:08","date_gmt":"2010-07-11T16:19:08","guid":{"rendered":"http:\/\/viscontitoscoalda.com\/?p=561"},"modified":"2010-07-11T16:19:08","modified_gmt":"2010-07-11T16:19:08","slug":"speranza-o-no-per-la-cura-della-sclerosi-multipla","status":"publish","type":"post","link":"https:\/\/viscontitoscoalda.com\/index.php\/2010\/07\/11\/speranza-o-no-per-la-cura-della-sclerosi-multipla\/","title":{"rendered":"Speranza o no per la cura della Sclerosi Multipla?"},"content":{"rendered":"

una cosa mi lascia solo perplessa sulla sperimentazione sulla CCSVI:<\/span><\/p>\n

si tratteranno pazienti con vero “intervento” e altri con finto intervento: quindi sedati, aperti e trattati sotto “farsa” per capire quanto ci sia un effetto placebo o meno…??<\/span><\/p>\n

SPERANZA PER CHI SOFFRE DI SM?? o una falsa speranza a favore di….<\/a><\/span><\/p>\n

National Post \u00b7 Thursday, Jun. 17, 2010<\/span><\/p>\n

\n
\n

In Canada, Dr. Sandy McDonald (Barrie Vascular Imaging) has personally funded the testing of over 200 MS sufferers using the equipment and testing protocols pioneered by Dr. Paolo Zamboni. The results he has obtained are amazing.<\/span><\/p>\n

The testing for chronic cerebrospinal venous insufficiency (CCSVI) poses no risk to patients and the treatment, balloon angioplasty, is well known and low risk. It is not experimental and has been used around the world since 1973. The only people in Canada who are denied testing and treatment for CCSVI venous malformations are those individuals who have been diagnosed with MS.<\/span><\/p>\n

So why are MS sufferers discriminated against? I think the answer lies in the fact that there are two groups in the controversy over Dr. Zamboni’s “liberation” treatment: those who live off MS and those who live with it. The latter group funds the former group in what is a $6-billion a year MS industry. If a treatment is found for the latter group, what would be left for the group that lives off MS?<\/span><\/p>\n

MS suffers know the difference between real hope and false hope. Delaying tactics will not deter MS sufferers nor will it silence them.<\/span><\/p>\n

Linda Hume-Sastre, Ottawa.<\/span><\/p>\n<\/div>\n<\/div>\n

Read more: http:\/\/www.nationalpost.com\/Hope%20those%20with%20false%20hope\/3163985\/story.html#ixzz0tITcxrGN<\/a><\/span><\/p>\n

Grazie a Luca, che lo ha trovato e inserito in questo forum:<\/span><\/p>\n

una falsa speranza??<\/a><\/span><\/p>\n

“In Canada la Dr. Sandy McDonald ha personalmente testato pi\u00f9 di 200 pazienti sofferenti di sm con il protocollo e l’equipaggiamento usati per primi dal Dr. Paolo Zamboni. I risultati ottenuti sono stupefacenti.
\nI test diagnostici per la CCSVI non sono rischiosi per i pazienti e il suo trattamento, l’angioplastica con palloncino, \u00e8 ben conosciuto e a basso rischio. Non si tratta di una cura sperimentale essendo usata in tutto il mondo sin dal 1973.
\nLe sole persone per\u00f2 in Canata a cui \u00e8 negato questa diagnostica e relativo trattamento per la CCSVI sono le persone con sm.
\nPerch\u00e9 tale discriminazione? Ritengo la risposta risieda nei fatti: ci sono due gruppi in questa controversia, quelli che vivono DI sm e quelli che vivono CON la sm. Il primo gruppo si trova nell’industria per la sm e fattura 6 miliardi di dollari l’anno. Se viene trovata una cura, cosa rester\u00e0 a chi vive in questa industria?
\nChi soffre di sm conosce la differenza tra vera speranza e falsa speranza. E le varie strategie ritardanti non intaccheranno la loro determinazione n\u00e9 li ridurranno al silenzio.<\/span><\/span><\/span><\/span><\/p>\n

Linda Hume-Sastre, Ottawa.<\/span><\/p>\n


\n<\/span><\/p>\n

————————–<\/span><\/p>\n

Only one thing leaves me puzzled on trial on CCSVI:<\/em><\/p>\n

treating patients with true “intervention” and others with fake intervention: so sedated, open and dealt with under “farce” to understand how there is a placebo effect or not …??<\/em><\/p>\n

SPERANZA PER CHI SOFFRE DI SM?? o una falsa speranza a favore di….<\/em><\/p>\n

National Post \u00b7 Thursday, Jun. 17, 2010<\/em><\/p>\n

In Canada, Dr. Sandy McDonald (Barrie Vascular Imaging) has personally funded the testing of over 200 MS sufferers using the equipment and testing protocols pioneered by Dr. Paolo Zamboni. The results he has obtained are amazing.<\/em><\/p>\n

The testing for chronic cerebrospinal venous insufficiency (CCSVI) poses no risk to patients and the treatment, balloon angioplasty, is well known and low risk. It is not experimental and has been used around the world since 1973. The only people in Canada who are denied testing and treatment for CCSVI venous malformations are those individuals who have been diagnosed with MS.<\/em><\/p>\n

So why are MS sufferers discriminated against? I think the answer lies in the fact that there are two groups in the controversy over Dr. Zamboni’s “liberation” treatment: those who live off MS and those who live with it. The latter group funds the former group in what is a $6-billion a year MS industry. If a treatment is found for the latter group, what would be left for the group that lives off MS?<\/em><\/p>\n

MS suffers know the difference between real hope and false hope. Delaying tactics will not deter MS sufferers nor will it silence them.<\/em><\/p>\n

Linda Hume-Sastre, Ottawa.<\/em><\/p>\n

Read more: http:\/\/www.nationalpost.com\/Hope%20those%20with%20false%20hope\/3163985\/story.html#ixzz0tITcxrGN<\/em><\/p>\n

——————————————————–<\/em><\/p>\n

Une seule chose me laisse perplexe sur le proc\u00e8s sur CCSVI:<\/em><\/p>\n

le traitement des patients avec une v\u00e9ritable \u00abintervention\u00bb et d’autres avec l’intervention de faux: si s\u00e9dation, ouverte et trait\u00e9e aux termes “farce” de comprendre comment il ya un effet placebo ou non …??<\/em><\/p>\n

Espoir pour les malades de la SEP? ou d’un faux espoir en faveur de la ….<\/em><\/p>\n

SPERANZA PER CHI SOFFRE DI SM?? o una falsa speranza a favore di….<\/em><\/p>\n

National Post \u00b7 Thursday, Jun. 17, 2010<\/em><\/p>\n

In Canada, Dr. Sandy McDonald (Barrie Vascular Imaging) has personally funded the testing of over 200 MS sufferers using the equipment and testing protocols pioneered by Dr. Paolo Zamboni. The results he has obtained are amazing.<\/em><\/p>\n

The testing for chronic cerebrospinal venous insufficiency (CCSVI) poses no risk to patients and the treatment, balloon angioplasty, is well known and low risk. It is not experimental and has been used around the world since 1973. The only people in Canada who are denied testing and treatment for CCSVI venous malformations are those individuals who have been diagnosed with MS.<\/em><\/p>\n

So why are MS sufferers discriminated against? I think the answer lies in the fact that there are two groups in the controversy over Dr. Zamboni’s “liberation” treatment: those who live off MS and those who live with it. The latter group funds the former group in what is a $6-billion a year MS industry. If a treatment is found for the latter group, what would be left for the group that lives off MS?<\/em><\/p>\n

MS suffers know the difference between real hope and false hope. Delaying tactics will not deter MS sufferers nor will it silence them.<\/em><\/p>\n

Linda Hume-Sastre, Ottawa.<\/em><\/p>\n

Read more: http:\/\/www.nationalpost.com\/Hope%20those%20with%20false%20hope\/3163985\/story.html#ixzz0tITcxrGN
\nMerci \u00e0 Luca, qui a trouv\u00e9 et ajout\u00e9 \u00e0 la tribune:<\/em><\/p>\n

un faux espoir?<\/em><\/p>\n

\u00abLe Canada Dr Sandy McDonald a personnellement test\u00e9 plus de 200 patients atteints de SEP avec le protocole et le mat\u00e9riel utilis\u00e9 pour la premi\u00e8re fois par le Dr Paolo Zamboni. Les r\u00e9sultats sont \u00e9tonnants.
\ntests de diagnostic pour CCSVI ne sont pas \u00e0 risque pour les patients et de son traitement, l’angioplastie par ballonnet, est bien connu, \u00e0 faible risque. Ce n’est pas un traitement exp\u00e9rimental utilis\u00e9 dans le monde entier depuis 1973.
\nLes seules personnes dans Canata mais se voient refuser ce diagnostic et un traitement efficace pour les personnes atteintes de SP sont CCSVI.
\nPourquoi cette discrimination? Je crois que la r\u00e9ponse r\u00e9side dans les faits: il ya deux groupes dans ce cas, ceux qui vivent sur le SM, et ceux qui vivent avec la SP. Un groupe est pour l’industrie n. facture et 6 milliards de dollars par an. Si elle a trouv\u00e9 un rem\u00e8de, ce que les personnes vivant dans cette industrie?
\nmalades MS conna\u00eetre la diff\u00e9rence entre la v\u00e9ritable esp\u00e9rance et de faux espoirs. Et les retardateurs de diverses strat\u00e9gies de ne pas affecter la d\u00e9termination ou de les r\u00e9duire au silence.<\/em><\/p>\n

Linda Hume-Sastre, Ottawa.<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"

una cosa mi lascia solo perplessa sulla sperimentazione sulla CCSVI: si tratteranno pazienti con vero “intervento” e altri con finto intervento: quindi sedati, aperti e trattati sotto “farsa” per capire quanto ci sia un effetto placebo o meno…?? SPERANZA PER CHI SOFFRE DI SM?? o una falsa speranza a favore di…. National Post \u00b7 Thursday, … Continua a leggere Speranza o no per la cura della Sclerosi Multipla?<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[18],"tags":[88,269,287],"class_list":["post-561","post","type-post","status-publish","format-standard","hentry","category-i-miei-libri","tag-ccsvi","tag-rischio","tag-sclerosi-multipla"],"_links":{"self":[{"href":"https:\/\/viscontitoscoalda.com\/index.php\/wp-json\/wp\/v2\/posts\/561","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/viscontitoscoalda.com\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/viscontitoscoalda.com\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/viscontitoscoalda.com\/index.php\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/viscontitoscoalda.com\/index.php\/wp-json\/wp\/v2\/comments?post=561"}],"version-history":[{"count":0,"href":"https:\/\/viscontitoscoalda.com\/index.php\/wp-json\/wp\/v2\/posts\/561\/revisions"}],"wp:attachment":[{"href":"https:\/\/viscontitoscoalda.com\/index.php\/wp-json\/wp\/v2\/media?parent=561"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/viscontitoscoalda.com\/index.php\/wp-json\/wp\/v2\/categories?post=561"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/viscontitoscoalda.com\/index.php\/wp-json\/wp\/v2\/tags?post=561"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}