Comments for CCSVI Screening for Multiple Sclerosis http://ccsvi-multiple-sclerosis.com Tracking doctors who will screen for CCSVI (chronic cerebrospinal venous insufficiency) in MS patients Sat, 09 Jul 2011 02:07:13 +0000 hourly 1 http://wordpress.org/?v=3.2.1 Comment on News coverage on CCSVI in the US by Medical Books http://ccsvi-multiple-sclerosis.com/2009/12/news-coverage-on-ccsvi-in-the-us/comment-page-1/#comment-35 Medical Books Sat, 09 Jul 2011 02:07:13 +0000 http://ccsvi-multiple-sclerosis.com/?p=46#comment-35 cool posting cool posting

]]> Comment on News coverage on CCSVI in the US by Petite Tops http://ccsvi-multiple-sclerosis.com/2009/12/news-coverage-on-ccsvi-in-the-us/comment-page-1/#comment-34 Petite Tops Fri, 28 Jan 2011 12:53:54 +0000 http://ccsvi-multiple-sclerosis.com/?p=46#comment-34 ;,~ I am really thankful to this topic because it really gives up to date information `;' ;,~ I am really thankful to this topic because it really gives up to date information `;’

]]> Comment on An email response from Dr. Tomasz Ludyga’s office by jessica forester http://ccsvi-multiple-sclerosis.com/2010/01/an-email-response-from-dr-tomasz-ludygas-office/comment-page-1/#comment-33 jessica forester Tue, 30 Nov 2010 15:59:22 +0000 http://ccsvi-multiple-sclerosis.com/?p=52#comment-33 The CCSVI Liberation Treatment could be the cure but fact remains that the rate of re-occlusion is stuck at 50% and MS patients being treated in the European and Asian countries end up suffering as they did, 3 months ago. While Big Pharmaceutical Corporations and governments in the US and Canada are coming up with new ideas to stop any advancements to the CCSVI theory (Like the superbugs, etc.), millions continue to travel to countries like India and Poland to get this simple procedure and no valuable data is recorded to support the CCSVI theory. Unless we get our position strong enough to support the CCSVI Theory, we will never be able to beat the Pharma Corporations or start the treatment here and many will keep suffering and dying even after having the procedure done. I lost my elder brother last month because of a blood clot in his stent. He got liberated 5 months ago in Poland. We need to prove to the government that this works. Non-profit organizations like the CCSVI Clinic http://www.ccsviclinic.ca/ are tirelessly working to develop safer protocols with teams of world renowned surgeons even though they are feeling the negative pressure from you know who. This Atlanta based Organization has started Clinical Trials for CCSVI and we need to support these groups because they are our only hope to fight for the truth. Without the valuable data that they are collecting offshore, the procedures will not be allowed here, in our own countries. The CCSVI Liberation Treatment could be the cure but fact remains that the rate of re-occlusion is stuck at 50% and MS patients being treated in the European and Asian countries end up suffering as they did, 3 months ago. While Big Pharmaceutical Corporations and governments in the US and Canada are coming up with new ideas to stop any advancements to the CCSVI theory (Like the superbugs, etc.), millions continue to travel to countries like India and Poland to get this simple procedure and no valuable data is recorded to support the CCSVI theory. Unless we get our position strong enough to support the CCSVI Theory, we will never be able to beat the Pharma Corporations or start the treatment here and many will keep suffering and dying even after having the procedure done. I lost my elder brother last month because of a blood clot in his stent. He got liberated 5 months ago in Poland. We need to prove to the government that this works. Non-profit organizations like the CCSVI Clinic http://www.ccsviclinic.ca/ are tirelessly working to develop safer protocols with teams of world renowned surgeons even though they are feeling the negative pressure from you know who. This Atlanta based Organization has started Clinical Trials for CCSVI and we need to support these groups because they are our only hope to fight for the truth. Without the valuable data that they are collecting offshore, the procedures will not be allowed here, in our own countries.

]]> Comment on Clinic specifically for CCSVI by Maryellen Utsey http://ccsvi-multiple-sclerosis.com/2010/03/clinic-specifically-for-ccsvi/comment-page-1/#comment-32 Maryellen Utsey Sun, 26 Sep 2010 07:16:03 +0000 http://ccsvi-multiple-sclerosis.com/?p=64#comment-32 I am fascinated with the idea of the liberation treatment to treat multiple sclerosis. From what data I can acquire about doctors that provide treatment, I can only find one nebulous list repeated on a dozen websites. Is there a more preferable way to find treatment, per say in North America. There are places that offer Liberation Treatment for the United States that no one knows about, such as <a href="http://www.liberation-treatment-now.com" rel="nofollow">Liberation Treatment Now</A> I am fascinated with the idea of the liberation treatment to treat multiple sclerosis. From what data I can acquire about doctors that provide treatment, I can only find one nebulous list repeated on a dozen websites. Is there a more preferable way to find treatment, per say in North America. There are places that offer Liberation Treatment for the United States that no one knows about, such as Liberation Treatment Now

]]> Comment on News coverage on CCSVI in the US by Roy Mcgivern http://ccsvi-multiple-sclerosis.com/2009/12/news-coverage-on-ccsvi-in-the-us/comment-page-1/#comment-29 Roy Mcgivern Thu, 23 Sep 2010 21:27:03 +0000 http://ccsvi-multiple-sclerosis.com/?p=46#comment-29 I found this post helpful but I am interested in reading more about the liberation treatment. Do you know of any good articles like this one about <a href="http://liberation-treatment-now.com/ccsvi" rel="nofollow">CCSVI Liberation Treatment</A> that goes into detail about what would qualify a patient for treatment? I found this post helpful but I am interested in reading more about the liberation treatment. Do you know of any good articles like this one about CCSVI Liberation Treatment that goes into detail about what would qualify a patient for treatment?

]]> Comment on An email response from Dr. Tomasz Ludyga’s office by Roosevelt Maccutcheon http://ccsvi-multiple-sclerosis.com/2010/01/an-email-response-from-dr-tomasz-ludygas-office/comment-page-1/#comment-28 Roosevelt Maccutcheon Sun, 05 Sep 2010 19:53:00 +0000 http://ccsvi-multiple-sclerosis.com/?p=52#comment-28 I have read over a couple of your posts and I had been wanting to know if you wanted to swap webpage links? I am often seeking to swap links with websites on comparable themes! I look forward to hearing back from you before long. I have read over a couple of your posts and I had been wanting to know if you wanted to swap webpage links? I am often seeking to swap links with websites on comparable themes! I look forward to hearing back from you before long.

]]> Comment on Clinic specifically for CCSVI by Philip W Chao MD http://ccsvi-multiple-sclerosis.com/2010/03/clinic-specifically-for-ccsvi/comment-page-1/#comment-27 Philip W Chao MD Tue, 10 Aug 2010 17:45:41 +0000 http://ccsvi-multiple-sclerosis.com/?p=64#comment-27 I was listening to the lecture on youtube today - see - the CCSVI facebook page for the link Dr. Mark Haacke was showing examples and he mentioned my old mentor Dr. Salvatore Sclafani. If memory serves Sal is the chief of radiology at Kings County Hospital in Brooklyn NY his address is 450 Clarkson Ave Brooklyn NY 11203 I do not have his phone but I am sure you can call Kings County Hospital and get it Sal is a very talented interventional radiologist and I am sure you would do well to call him. As for the diagnostic part - I am a double fellowship trained neuroradiologist and body MRI specialist in Newark DE we have the CCSVI pulse sequences programmed into our scanner in Newark DE it is an 18 channel Espree - the worlds least claustrophobic 1.5T scanner. You can contact us at 1-302-838-7800 Philip W Chao MD I was listening to the lecture on youtube today -
see – the CCSVI facebook page for the link

Dr. Mark Haacke was showing examples and he mentioned my old mentor Dr. Salvatore Sclafani.

If memory serves Sal is the chief of radiology at Kings County Hospital in Brooklyn NY

his address is 450 Clarkson Ave
Brooklyn NY 11203

I do not have his phone but I am sure you can call Kings County Hospital and get it

Sal is a very talented interventional radiologist and I am sure you would do well to call him.

As for the diagnostic part – I am a double fellowship trained neuroradiologist and body MRI specialist in Newark DE

we have the CCSVI pulse sequences programmed into our scanner in Newark DE

it is an 18 channel Espree – the worlds least claustrophobic 1.5T scanner.

You can contact us at 1-302-838-7800

Philip W Chao MD

]]> Comment on Clinic specifically for CCSVI by nina Karapetian http://ccsvi-multiple-sclerosis.com/2010/03/clinic-specifically-for-ccsvi/comment-page-1/#comment-26 nina Karapetian Fri, 23 Jul 2010 12:28:32 +0000 http://ccsvi-multiple-sclerosis.com/?p=64#comment-26 Please help me - i need somewhere, any country, that does the liberation procedure (preferably not too far from England!) Thankyou in advance Nina Please help me – i need somewhere, any country, that does the liberation procedure
(preferably not too far from England!)
Thankyou in advance
Nina

]]> Comment on An email response from Dr. Tomasz Ludyga’s office by victor halls http://ccsvi-multiple-sclerosis.com/2010/01/an-email-response-from-dr-tomasz-ludygas-office/comment-page-1/#comment-24 victor halls Sun, 06 Jun 2010 16:58:43 +0000 http://ccsvi-multiple-sclerosis.com/?p=52#comment-24 Hi my name is victor halls i was diagnoised with ms about 10 yearsago but iam sure have been suffering with in for at less 8 years before that,i was working up untill 4 years ago as a roofer, but of lately my legs just wont work,as well as other symton.i heard of this treament about two years been looking for some where to get it done,there is nobody in the u.k as yet.if possiable i would like to come to poland to get it done. Hi my name is victor halls i was diagnoised with ms about 10 yearsago
but iam sure have been suffering with in for at less 8 years before that,i was working up untill 4 years ago as a roofer, but of lately my legs just wont work,as well as other symton.i heard of this treament about two years been looking for some where to get it done,there is nobody in the u.k as yet.if possiable i would like to come to poland to get it done.

]]> Comment on Contact by Media Blackout on cure for MS « Utah Alternative Conservative http://ccsvi-multiple-sclerosis.com/contact/comment-page-1/#comment-23 Media Blackout on cure for MS « Utah Alternative Conservative Sat, 22 May 2010 14:33:59 +0000 http://ccsvi-multiple-sclerosis.com/?page_id=21#comment-23 [...] who speaks Polish to contact EuroMedic for me.  If you speak Polish and can help out, please contact me. Share and [...] [...] who speaks Polish to contact EuroMedic for me.  If you speak Polish and can help out, please contact me. Share and [...]

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