Help Jeff Johnson raise money to find a cure for Multiple Sclerosis. Visit his fund raising home page at nationalMSsociety website and add /goto/jeffjohnson to the URL
that is nationalMSsociety AND dot org AND /goto/jeffjohnson
There are vain blocks and there are vein blocks.. Am sure this procedure is to remove vein blocks, not vain blocks. I have MS. Suppose it is from vein blocks..
Dr.Avneesh Gupte, the Neurosurgeon at Noble Hospital performing the procedure has been encouraged by results in Cerebral Palsy patients as well. “We are fortunate to be able to offer the treatment because not every hospital is able to perform these types of transplants.You must have the specialized medical equipment and specially trained doctors and nurses”. Log on to ccsviclinic.ca for more information.
Other recent MS patients who have had Autologous Stem Cell Transplantation (ASCT), or stem cell therapy have posted videos and comments on YouTube v=jFQr2eqm3Cg. Log on to ccsviclinic. ca for more information.
A universal benefit reported by every patient has been the recovery of bladder control. Most MS patients have various bladder control symptoms that include urinary urgency, incontinence, nocturia, or urinary hesitancy as a result of the disruption of electrical impulses from the brain to the nerves and muscles that are involved in emptying the bladder (pudenal nerve, urethral sphincter, detrusor muscle). Log on to ccsviclinic. ca for more information.
A group of Canadian patients just back from Noble have reported similar results. “I can actually see what I thought were long-dead muscles forming in my feet” said Larry Vermeersch of Kenora, Ontario. “My balance is back and I’m walking without a cane. I’m a pretty hard guy to convince, but getting these two procedures together has made me a believer. I’m looking forward to the physio ahead because I can feel everything coming back.” Log on to ccsviclinic. ca for more information.
“I feel I am completely cured” says Ms. Gianopoulos, “my symptoms have disappeared and I have a recovery of many functions, notably my balance and my muscle strength is all coming (back). Even after six months, I feel like there are good changes happening almost every day. Before, my biggest fear was that the changes wouldn’t (hold). I don’t even worry about having a relapse anymore”. Log on to ccsviclinic. ca for more information.
After 6 months of offering stem cell therapy in combination with the venous angioplasty liberation procedure, patients of CCSVI Clinic have reported excellent health outcomes. Ms. Kasma Gianopoulos of Athens Greece, who was diagnosed with the Relapsing/Remitting form of MS in 1997 called the combination of treatments a “cure”. Log on to ccsviclinic. ca for more information.
Can anyone please tell me why is this so "contriversial?" If a vein is blocked what is so contriversial about unblocking it? They cant say its because the surgery is dangerous or the risk are too high because open heart surgery and brain surgery is dangerous too and has high risk.
@mrsardath Unblocking the veins (if any blockage exists) isn't the controversial part. The controversial part is that Dr. Zamboni's results haven't been corroborated by other MS researchers. It certainly is possible that a small percentage of MS cases is correlated with CCSVI, but it looks like that may be those cases may be in the very small minority
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.
CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
Dear Dr..I am Dx with Primary M.S and Male 32 yrs...I irst came down in 2003 but became scared of the change and tryed to forget it. In 2008 I finally admitted to myself and got my Dx....could CCSVI work in Primany?
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?
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!
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
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
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
'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 .
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.
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.
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.
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.
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?
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
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
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!
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!
i have a question. when we suppose, that the hypothesis of prof. zamboni ist true, why do medicaments like glatirameracetat oder interferone helps? (or why cortisone helps?) has anyone an idea?
This comment has received too many negative votesshow
This kind of blockage may be caused by muscle spasticity, as in my case. The spasms were caused by chronic poisoning by caffeine dependence. I stopped my caffeine use in Feb -08, and was on my feet without walking stick in a week, and now I'm almost complitely cured from more than 20 years of debilitating symptoms, that put me on pension for disability in my prime years. I stopped poisoning my body, didn't need any meds or operations, seems like a sweet deal to me.
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.
Dr Zamboni ur an ANGEL and this couldnt have come at a better time.....both my feet feel like if I had 2 x 350lbs muscle guys squishing them non-stop 24/7 that or cement boots on!!! Auguri Bello!!!
YES I AGREE, DR ZAMBONI NEEDS TO WIN THE NOBLE PRICE!!!
I 100% agree with both comments and was thinking the exact same thing. My gut says he will win the Nobel prize in Medicine...it just might take a while!
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Help Jeff Johnson raise money to find a cure for Multiple Sclerosis. Visit his fund raising home page at nationalMSsociety website and add /goto/jeffjohnson to the URL
that is nationalMSsociety AND dot org AND /goto/jeffjohnson
Ekorn999 2 months ago
There are vain blocks and there are vein blocks.. Am sure this procedure is to remove vein blocks, not vain blocks. I have MS. Suppose it is from vein blocks..
2ndSamuel710 5 months ago
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Dr.Avneesh Gupte, the Neurosurgeon at Noble Hospital performing the procedure has been encouraged by results in Cerebral Palsy patients as well. “We are fortunate to be able to offer the treatment because not every hospital is able to perform these types of transplants.You must have the specialized medical equipment and specially trained doctors and nurses”. Log on to ccsviclinic.ca for more information.
Jessica1963Forester 6 months ago
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Other recent MS patients who have had Autologous Stem Cell Transplantation (ASCT), or stem cell therapy have posted videos and comments on YouTube v=jFQr2eqm3Cg. Log on to ccsviclinic. ca for more information.
Jessica1963Forester 6 months ago
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A universal benefit reported by every patient has been the recovery of bladder control. Most MS patients have various bladder control symptoms that include urinary urgency, incontinence, nocturia, or urinary hesitancy as a result of the disruption of electrical impulses from the brain to the nerves and muscles that are involved in emptying the bladder (pudenal nerve, urethral sphincter, detrusor muscle). Log on to ccsviclinic. ca for more information.
Jessica1963Forester 6 months ago
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A group of Canadian patients just back from Noble have reported similar results. “I can actually see what I thought were long-dead muscles forming in my feet” said Larry Vermeersch of Kenora, Ontario. “My balance is back and I’m walking without a cane. I’m a pretty hard guy to convince, but getting these two procedures together has made me a believer. I’m looking forward to the physio ahead because I can feel everything coming back.” Log on to ccsviclinic. ca for more information.
Jessica1963Forester 6 months ago
“I feel I am completely cured” says Ms. Gianopoulos, “my symptoms have disappeared and I have a recovery of many functions, notably my balance and my muscle strength is all coming (back). Even after six months, I feel like there are good changes happening almost every day. Before, my biggest fear was that the changes wouldn’t (hold). I don’t even worry about having a relapse anymore”. Log on to ccsviclinic. ca for more information.
Jessica1963Forester 6 months ago
After 6 months of offering stem cell therapy in combination with the venous angioplasty liberation procedure, patients of CCSVI Clinic have reported excellent health outcomes. Ms. Kasma Gianopoulos of Athens Greece, who was diagnosed with the Relapsing/Remitting form of MS in 1997 called the combination of treatments a “cure”. Log on to ccsviclinic. ca for more information.
Jessica1963Forester 6 months ago
Can anyone please tell me why is this so "contriversial?" If a vein is blocked what is so contriversial about unblocking it? They cant say its because the surgery is dangerous or the risk are too high because open heart surgery and brain surgery is dangerous too and has high risk.
mrsardath 8 months ago
@mrsardath Unblocking the veins (if any blockage exists) isn't the controversial part. The controversial part is that Dr. Zamboni's results haven't been corroborated by other MS researchers. It certainly is possible that a small percentage of MS cases is correlated with CCSVI, but it looks like that may be those cases may be in the very small minority
NeuroJoe 5 months ago in playlist BIOL481
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.
CCSVIROMANIA 8 months ago
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CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
Gregmills007 10 months ago
This has been flagged as spam show
CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
Gregmills007 10 months ago
Dear Dr..I am Dx with Primary M.S and Male 32 yrs...I irst came down in 2003 but became scared of the change and tryed to forget it. In 2008 I finally admitted to myself and got my Dx....could CCSVI work in Primany?
SEL500 11 months ago
Frequently Asked Questions about CCSVI in Bulgaria ccsvibg.com
CCSVIBG 11 months ago
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?
BondGirl070 1 year ago
This has been flagged as spam show
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!
rebecawatson57 1 year ago
Comment removed
derekdadey1 1 year ago
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
derekdadey1 1 year ago
Comment removed
derekdadey1 1 year ago
CCSVI Diagnostics and Treatment at ccsvi-bg dot com
CCSVIBG 1 year ago
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
AudreyRDMS 1 year ago
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
AudreyRDMS 1 year ago
'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 .
MrLeooreo 1 year ago
my sister did treatment and it did not help her at all
MrPerrinjames 1 year ago
This has been flagged as spam show
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.
mcgirc 1 year ago
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.
mcgirc 1 year ago
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.
spunkyrigpa 1 year ago
For Ken - here's hoping on the 24th you're sorted!! And all the other Ken's out there!!
naders71 1 year ago
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.
kodiak1966 1 year ago 2
This has been flagged as spam show
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.
kodiak1966 1 year ago
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?
ecurra19 1 year ago 2
AND THANK YOU DR ZAMBONI YOU ARE A HERO
spark23ca 1 year ago 3
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
spark23ca 1 year ago
Thank you AGAIN Dr. Zamboni . I hope you can train more doctors so we can all have this procedure.
Vivianne766 2 years ago
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
MillionsStrong4MS 2 years ago
Thank you so much Dr. Zamboni!
You have regain the hope for thousands of MS patients! including myself!
God bless you
obada9x 2 years ago
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!
msclinicaltrialsinfo 2 years ago
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
gekiryudojo 2 years ago 7
This has been flagged as spam show
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!
9gabbycats 2 years ago
hello all,
i have a question. when we suppose, that the hypothesis of prof. zamboni ist true, why do medicaments like glatirameracetat oder interferone helps? (or why cortisone helps?) has anyone an idea?
Glysity 2 years ago
This comment has received too many negative votes show
This kind of blockage may be caused by muscle spasticity, as in my case. The spasms were caused by chronic poisoning by caffeine dependence. I stopped my caffeine use in Feb -08, and was on my feet without walking stick in a week, and now I'm almost complitely cured from more than 20 years of debilitating symptoms, that put me on pension for disability in my prime years. I stopped poisoning my body, didn't need any meds or operations, seems like a sweet deal to me.
moonshinener 2 years ago
I drink much more coffee as my wife does, and I have no MS (!?!)
Anyway, if quitting caffeine worked well in your case, I find this very positive.
Zzozze 2 years ago
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.
moonshinener 2 years ago
Dr Zamboni ur an ANGEL and this couldnt have come at a better time.....both my feet feel like if I had 2 x 350lbs muscle guys squishing them non-stop 24/7 that or cement boots on!!! Auguri Bello!!!
YES I AGREE, DR ZAMBONI NEEDS TO WIN THE NOBLE PRICE!!!
SpaceSurfR 2 years ago 3
I 100% agree with both comments and was thinking the exact same thing. My gut says he will win the Nobel prize in Medicine...it just might take a while!
canadarobin 2 years ago 3
An incredible discovery. Dr. Zamboni should win the Nobel prize.
Brontegrrrl 2 years ago 13
@Brontegrrrl Dr. Zamboni should win a Nobel Prize for each Doctor that said he's crazy.
scifiak 1 year ago 2
This is one of the most exciting discoveries , since the development of insulin for diabetes.
yangbob 2 years ago 4