Please, Help Prof. Zamboni official trials
Please, Help Prof. Zamboni official trials
http://www.ccsvi-sm.org/?q=node%2F717
It is a found-rising campain organised by the italian CCSVI-MS association. As someone of you may know, Prof. Zamboni left the trial sponsored by AISM-FISM (italian MS-Society) because they didn't want to use the right protocol and there was a seroius risk to have wrong results.
Now Prof. Zamboni can have his own trials officially supported by the University of Ferrara. But he needs funds to start the trials.
Please, donate to help Prof. Zamboni demonstrate the correlation CCSVI-MS!!
It is a found-rising campain organised by the italian CCSVI-MS association. As someone of you may know, Prof. Zamboni left the trial sponsored by AISM-FISM (italian MS-Society) because they didn't want to use the right protocol and there was a seroius risk to have wrong results.
Now Prof. Zamboni can have his own trials officially supported by the University of Ferrara. But he needs funds to start the trials.
Please, donate to help Prof. Zamboni demonstrate the correlation CCSVI-MS!!
re: donations for Dr Zamboni's clinical trials
Hi Mattia,
Thank you for posting this link!
Would it be possible to have a Paypal link added to the website so that people can make a donation easily from a computer?
I would like to donate, but I don't know how to do this using a bank account number from another country.
If anyone else knows how to do this, please let me know.
Thank you,
Mary Ann
Thank you for posting this link!
Would it be possible to have a Paypal link added to the website so that people can make a donation easily from a computer?
I would like to donate, but I don't know how to do this using a bank account number from another country.
If anyone else knows how to do this, please let me know.
Thank you,
Mary Ann
DX 6-09 RRMS, now SPMS
Hallo
I'm back on these pages to say that it is now possible to donate for the research of Prof. Zamboni using Paypal.
Here's the link to the site of the italian CCSVI-MS association where is possible to donate: http://bravedreams.ccsvi-sm.org/en
Pleas, help Prof. Zamboni, help the research to proof the correlation between CCSVI and MS!!!
Thank you
Mattia
I'm back on these pages to say that it is now possible to donate for the research of Prof. Zamboni using Paypal.
Here's the link to the site of the italian CCSVI-MS association where is possible to donate: http://bravedreams.ccsvi-sm.org/en
Pleas, help Prof. Zamboni, help the research to proof the correlation between CCSVI and MS!!!
Thank you
Mattia
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Hi, i'm assuming this is another link you can use to donate using paypal.
http://www.ccsvi-sm.org/
It is. Donation made!!
Bob
http://www.ccsvi-sm.org/
It is. Donation made!!
Bob
Thank you to those who have made a donation.
We're still far away from the target.
Here can be found detail about the trials and the related costs: http://bravedreams.ccsvi-sm.org/en/clinical-trial
And here the onéline list of the donors with the reached amount: http://bravedreams.ccsvi-sm.org/en/clinical-trial
Please support Prof. Zamboni!
http://bravedreams.ccsvi-sm.org/en/dona ... -donations
Mattia
We're still far away from the target.
Here can be found detail about the trials and the related costs: http://bravedreams.ccsvi-sm.org/en/clinical-trial
And here the onéline list of the donors with the reached amount: http://bravedreams.ccsvi-sm.org/en/clinical-trial
Please support Prof. Zamboni!
http://bravedreams.ccsvi-sm.org/en/dona ... -donations
Mattia
- secondopinion
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asking questions first
If there is a project looking for financial support and its proposed mechanism of action is in clear contradiction with evidence based and generally accepted medical knowledge, then one has to ask first, maybe this is just a project for profit only?
I am not against innovative and aggressive new treatments, but in case of MS I would better think for aggressive immunosupressive/immunomodulatory treatment, like rituximab (which has been shown to be effective even for progressive disease, in subsets of younger people) or similar and first-line, not for "rescuing" patients whose brain tissue is unfortunately already too much destructed beyond the line of repair.
I am not against innovative and aggressive new treatments, but in case of MS I would better think for aggressive immunosupressive/immunomodulatory treatment, like rituximab (which has been shown to be effective even for progressive disease, in subsets of younger people) or similar and first-line, not for "rescuing" patients whose brain tissue is unfortunately already too much destructed beyond the line of repair.
As I understand it, CCSVI is not in contradiction with the previous immune/autoimmune theory, it dovetails nicely with it. There was always the missing piece of the puzzle for why the immune reaction begins in MS and how the leukocytes get into the CNS when the blood brain barrier should keep them out in large numbers. CCSVI may be a promoter of the condition of MS as it is already understood. With the very high association with MS that has been shown and the possible effect on blood flow to the organs most affected in MS (brain and spine), I consider it very much worth supporting research into CCSVI.
- 1eye
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more fools and the mean of spirit disguised as 'skeptic's
I was going to post, that maybe this is just another posting by some anonymous troll, but as usual I have to stick in my $0.02 and point out that dying persons are people too and deserve rescue. The CCSVI procedure has much evidence behind it. It also has been known to be used to rescue the dying, and damaged people.
I find it heartless to refer to anyone as "destructed" (sound like Malden?) 'beyond repair'. Of course it is common for ego-rich overly self-inflated would-be doctors to play at being God, but to describe a human being that way is something that, if God existed, He would never do, even if He were playing at being human. That is a game a completely moral being would find too dangerous, as it would risk behaving like the person who sent that posting.
Of course you can try drugs, even mabs, as a last resort, which one would hope would not be necessary, after attempting the obvious Liberation procedure.
If there is a project looking for financial support and its proposed mechanism of action is in dispute by the mean-minded, perhaps donating to it might be one of the best possible ways to allocate scarce money, since the human race might profit greatly by putting these fools in their places, and silencing them forever?
They would probably not be quiet, not knowing even what is good for themselves. It is better, as Lisa Simpson is fond of saying, to remain silent and be thought a fool, than to speak up and remove all doubt. Or, as the chef in the restaurant I used to work at used to say: "It's better to shut up and people think you're stupid, than to open your mouth and prove it."
I find it heartless to refer to anyone as "destructed" (sound like Malden?) 'beyond repair'. Of course it is common for ego-rich overly self-inflated would-be doctors to play at being God, but to describe a human being that way is something that, if God existed, He would never do, even if He were playing at being human. That is a game a completely moral being would find too dangerous, as it would risk behaving like the person who sent that posting.
Of course you can try drugs, even mabs, as a last resort, which one would hope would not be necessary, after attempting the obvious Liberation procedure.
If there is a project looking for financial support and its proposed mechanism of action is in dispute by the mean-minded, perhaps donating to it might be one of the best possible ways to allocate scarce money, since the human race might profit greatly by putting these fools in their places, and silencing them forever?
They would probably not be quiet, not knowing even what is good for themselves. It is better, as Lisa Simpson is fond of saying, to remain silent and be thought a fool, than to speak up and remove all doubt. Or, as the chef in the restaurant I used to work at used to say: "It's better to shut up and people think you're stupid, than to open your mouth and prove it."
This unit of entertainment not brought to you by FREMULON.
Not a doctor.
"I'm still here, how 'bout that? I may have lost my lunchbox, but I'm still here." John Cowan Hartford (December 30, 1937 – June 4, 2001)
Not a doctor.
"I'm still here, how 'bout that? I may have lost my lunchbox, but I'm still here." John Cowan Hartford (December 30, 1937 – June 4, 2001)
- 1eye
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- Location: Kanata, Ontario, Canada
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You have just pointed out why it is a dangerous things to do to an 'MS' patient, to give them Tysabri. Its mechanism of action is to prevent leukocytes from crossing the blood-brain barrier, when it has been breached by some unknown mechanism, or, as we now know, by CCSVI. If they are prevented from entering the CNS compartment, when normally at least they, could cross into it, they are prevented from keeping PML (and who knows what other pathogens?) in check. The auto-immune hypothesis has been proven by this drug to be a deadly 'theory'. Other drugs somehow induce leukemia, though one could speculate that a condition involving angiogenesis might have something to do with that as well (do they cause leukemia in healthy controls?).Cece wrote:As I understand it, CCSVI is not in contradiction with the previous immune/autoimmune theory, it dovetails nicely with it. There was always the missing piece of the puzzle for why the immune reaction begins in MS and how the leukocytes get into the CNS when the blood brain barrier should keep them out in large numbers. CCSVI may be a promoter of the condition of MS as it is already understood. With the very high association with MS that has been shown and the possible effect on blood flow to the organs most affected in MS (brain and spine), I consider it very much worth supporting research into CCSVI.
If, as we now know, there is no auto-immune condition causing hyper-immunity, some 'MS' patients might have *hypo*-immunity, and be prime targets for PML. Especially those who have had immune modification by Interferon or chemotherapy, or even steroids.
This unit of entertainment not brought to you by FREMULON.
Not a doctor.
"I'm still here, how 'bout that? I may have lost my lunchbox, but I'm still here." John Cowan Hartford (December 30, 1937 – June 4, 2001)
Not a doctor.
"I'm still here, how 'bout that? I may have lost my lunchbox, but I'm still here." John Cowan Hartford (December 30, 1937 – June 4, 2001)
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