CCSVI could bring hope to many Multiple Sclerosis patients

[MsCSimmonds]

Weirdly, when I started getting noticeable, frequent symptoms, namely creepy sensations in my legs and pins and needles in feet and hands. My thoughts of what could be going wrong went to a circulation problem as I have always suffered from really cold hands and put it down to that. I have finally been diagnosed with MS, strange how that comes as a relief, I am on Tysabri but am very interested in this research. I think my initial instincts about what was happening to me, were good. Fight MS

[robert80taylor]

We have been keeping patients hospitalized for a week to 10 days as a matter of safety and monitoring them for symptoms. Nobody who has the liberation therapy gets discharged earlier than that. During that time we do daily Doppler Ultrasounds, blood work and blood pressure monitoring among other testing. For more information Log on to ccsviclinic.ca OR Call on: +1 (404) 461-9560.

[robert80taylor]

This has been the safe practice standard that we have adopted and this post-procedure monitoring over 10 days is the subject of our recent study as it relates to CCSVI for MS patients.” For more information Log on to ccsviclinic.ca OR Call on: +1 (404) 461-9560.

[CCSVIROMANIA]

A new CCSVI clinic it is available in Bucharest, Doctors team from Bucharest are certified by DR.ZAMBONI in Ferrara and by Dr. Simka in Poland to perform the CCSVI treatment/procedures.

The price of the treatment INCLUDING Travel Expenses(flight ticket,accomodation,transfers,­all exams,angioplasty) is 8200 USD for USA/CANADA patients and for europe patients 5100 Euro Incl. Travel expenses.

[daddyschlong14]

So happy for that man at the end

[beanloveschristy]

omg,, deep breath

[TheRantingCabbie]

I once knew someone with MS. They told me about this discovery about the veins being narrowed. So why has there been skepticism? I don't suppose it's the almighty dollar talking? You know, like the drug companies profiting from you being sick instead of cured.

[derekdadey1]

Get screened in the US. Call CCSVI Clinic (404)461-9560 to schedule your pre- and post procedure screening today in Fargo, ND or email us at apply@ccsviclinic.ca. Find out more at ccsviclinic.ca

[Makzimia]

I am amazed to hear about this. My younger brother has lived with MS for 16 yrs. I told him stuff like this was around, but he has given up hope. I have tried to get a song used, I wrote for him, by the MS society, and I would gladly give all proceeds from it's sale to help funding for MS research like this. If you want more support for this and other research it costs time and money. Love and dedication will win a lot of these battles of life. The song is called Through faded eyes.

Tony

[sebasortiz]

Thanks for sharing this amazing video, my only brother is 22 years old, and he's been diagnosed with MS only a month ago. I have read a lot about MS and they say it happens mostly in the north of USA, Canada, and Europe. And I just wanted to add for the record that my brother is from and lives in Colombia south america. Anyways after reading many articles and watching several videos, this is the one that's giving me hope. I hope neurologist open their minds and support Zamboni in this research

[MultipleSclerosisMan]

This is such a moving and hopeful video. So many of us are so ill with this horrible disease. I pray that this is not another false dawn for us. I know that CCSVI treatment does not work for everyone nor indeed does everyone with MS have CCSVI but if it works to liberate some people then this is truly wonderful.

[twilightsamurai]

The big question is how long will it take for the medical community to take notice.



[guitarobsessed85]

@twilightsamurai They already have. The Nationaly MS society has given money for clinical trials.

[MyManindra]

wonderful,it means MS doctors were in dark themselves

[sploggon]

The UK Multiple Sclerosis Society have gone hysterical! their so-called experts would loose ££££.. support the msrc instead people.

[hcim71]

Thank you for posting this video, as well as the one where you legs show a terrible rapid tremor. I have the same rapid tremor, only it's internal (feels exactly like I see yours doing). And, I get virtually no deep sleep. I suffer horribly with virtually no restorative sleep. If they could fix this neurological problem, then I could finally sleep. Thank you so much for posting this video, as well as the other one with your legs.

[percykirby]

I pray so, my attack frequent and drop like bombs. I need this

[s12n]

it has worked for several people here in Kuwait .. fingers crossed for the rest .. they are waiting for 10 procedures to be done before going VERY public.

[xdarthduckiex]

Thank you very much for sharing this with us! :)

I'm very hopeful that this will pan out and turn out to be correct. * crosses fingers *

[dmplaura]

Isn't it wonderful? Message me if you want some info (links) where you can contact the Buffalo study. :)