It’s illustrates vain blocks in CCSVI associated to multiple sclerosis, and relate diagnosis and treatment.
Tag: ccsvi, multiple sclerosis, paolo zamboni, ZamboniDottor T. Il divulgatore scientifico
It’s illustrates vain blocks in CCSVI associated to multiple sclerosis, and relate diagnosis and treatment.
Tag: ccsvi, multiple sclerosis, paolo zamboni, Zamboni
Call the National Multiple Sclerosis Society @ 1-800-344-4867 and tell them to put you on the interested party list and TELL OUR DOCTORS TO START SENDING THEIR PATIENTS FOR AN MRV AND AT LEAST START CHECKING FOR CCSVI! Please pass this along! They are taking names and numbers and stories!
Thank you for your work and for giving us hope! and may you get all the funding you need to give us more! hope
Bless you
Thank you Dr. Zamboni! Don’t let them harness you at the university. You’ve gotten the word out, now we will pick up the political torch. Make sure you apply for all the research grants -MSCanada needs you! We’ll gladly fund your research, just open up a portal like some universities have done re:cancer research. We collectively have the $. What we don’t have is lots of time. We are young mothers & fathers; we are still are making are mark on this world; we can and WILL see this through!
Thank you so much Dr. Zamboni!
You have regain the hope for thousands of MS patients! including myself!
God bless you
Please join my new Facebook group M.S. (Millions Strong to raise awareness of C.C.S.V.I.). I have RRMS, and I feel hopeful for the first time in years. My group provides links to valuable resources to learn about new surgical procedures for people who suffer from M.S. – Patricia
Caffeine gives problems to some 10-20% of users for individual differences. It is the most common cause to psychological problems, chronic pain and many brain related issues today. Caffeine sells about 80% of all psyche medications.
Thank you AGAIN Dr. Zamboni . I hope you can train more doctors so we can all have this procedure.
with a few more doctors like zamboni there would be cures for aids and cancer and all sorts of other diseases …the only trouble is they all get snuffed out by the drug companies politicians and backs…they are all in it together scratching eachothers backs and letting us die….STAND UP AND FIGHT FOR WHATS YOURS……YOUR LIFE
AND THANK YOU DR ZAMBONI YOU ARE A HERO
Thank you for the suggestion of the video, but for me CCSVI it is only hope for a procedure that will make my life better. I hope that Dr. Zamboni will get the necessary funds to move from hope to action. Here in the United States I need to finish my paper work for Health Reform. Where will that coverage will fit on this procedure?
My brother has MS.Drug companies know they will lose BILLIONS and BILLIONS of dollars if Zamboni’s treatment works., and Governments get a big piece of the pie.That being said: how many doctors across North America(including the ones that did the study in Buffalo) are “paid off” by the drug companies to shoot down this amazing discovery or to give false trail results????They are doing it already,but are very careful so it doesn’t look too obvious.
I wish the liberation treatment was available to all,sadly,health care will not cover the testing or surgery..The drug companies know they will lose billions in MS drug revenues if this proves to be true.They are already paying off doctors across the US and Canada to shoot down Zamboni’s amazing discovery . The doctors and specialists are very cautious as NOT to make it look too obvious.
For Ken – here’s hoping on the 24th you’re sorted!! And all the other Ken’s out there!!
Thank you Dr. Zamboni. There is no way to fully express my thanks for your dedication. I hope to get your procedure in the next year. After I do, I’m going to start a fund for another person to get the procedure done.
@Brontegrrrl Dr. Zamboni should win a Nobel Prize for each Doctor that said he’s crazy.
Great video Paolo, we would like to include it also in Medting.com for the medical community to be aware of it. So it would be great if you added or give us your permission to upload.
Great video Paolo, we would like to include it also in Medting.com for the medical community to be aware of it. So it would be great if you added or give us your permission to upload.
my sister did treatment and it did not help her at all
‘THERE IS NO AUToiMMUNE DISEASE CALLED MS. IT IS A VASCULAR DISEASE. THE SCIENCE IS FINALLY HERE – NEUROS – YOU ARE ALLL WET WITH EGG ON YOUR FACES. YOU AE A DISGRACE .
This is an amazing discovery Dr. Zamboni. I am a vascular sonographer and would like to learn how to perform this study and would like to do research on it. If this holds to be at least 70% true then vascular sonographers need to learn how to perform this study. I don’t know where you are located but would love to learn how to perform this study from you and teach it so that sonographers around the world can perform it. Please contact me at RDMS1363@aol.com
Dr. Zamboni, i have read it is the jugular and azygos veins. Are there any other veins involved? could you please send me your University’s Vascular US dept. protocol to RDMS1363@aol.com. I am extremely interested in this and would like to help MS patients. If more sonographers learned how to do this, than more hospitals would incorporate this into the protocol when doing ALL MS patients. This is a major breakthrough and people need to be trained here in the US
CCSVI Diagnostics and Treatment at ccsvi-bg dot com
Call CCSVI Clinic; (404)461-9560 to schedule your screening today in Fargo, ND or email us at apply@ccsviclinic.ca. Yes, get screened within the US. No waiting….find out more at ccsviclinic.ca
I was diagnosed with MS back in 1983.Recently I came across ccsviclinic.ca. They are screening in Fargo, ND. Called (404)461-9560 and spoke to Nurse Lisa. Their Liberation Package includes pre-op video consultation with their doctors, flight costs, visas, accommodation within their hospital premises. The treatment includes stent, medications, reports & post-op followup for next 6 mths. Email:apply@ccsviclinic.ca. Getting liberated mid-October. Thankful to CCSVI Clinic for making this happen!
I have M.E./CFS and this is sounding very familiar with ccsvi. Researchers are now doing a study on the XMRV retrovirus they’ve discovered which is showing up in M.E./CFS patients. Currently I am part of the XMRV study. I’m wondering if we need to look into this area to see if there is a link between these two illnesses. I have many of the symptoms similar to the early stages of M.S., but have not been diagnosed with it, however I fall under the criteria of M.E. Is there a link between them?