Hello blogger friends and readers of way,
with this post, now back in the exclusive Mario, a new virtual friend who asked me a favor and spread the experience that they may be of help to those who, like him, is under the same conditions. And what could be better than this blog, dormant for almost a year to disclose, first of all, the experience of Mario and then to raise it in the most noble? Nothing at all, I think. Therefore, the forerunner of my subsequent publications, in here, I give him the post of Mario, also because it is not the first time that a public appeal from a serious illness. And if the last time, despite the efforts of virtual us bloggers, they failed to achieve anything now that we have real hope, it seems right to help Mario to give the maximum spread his heartfelt speech.
What follows, therefore, is a post that he wrote for another site. At the end, you will find his e-mail, so that those who need can contact him directly, without going through me first you do in certain situations, the better.
Happy reading and good luck.
CCSVI liberation from multiple sclerosis
Chronic Venous Insufficiency cerebrospinal
It 'just that the meaning of CCSVI or an acronym that gives hope to millions of people around the world.
chronic venous insufficiency of the brain, this is, as it is called in America, the''big idea''.
How many of my friends on this site know, I am affected in 2003 by a particularly insidious and highly debilitating disease with which you can definitely survive and that usually causes death, but makes it difficult for the quality of life .... Sclerosis Multipla.
The name alone makes one shudder the most, including myself when, following a hospitalization, I was diagnosed. Emotional impact is strong enough, I assure you, however, that from that moment the way we see things is deeply changed.
MS therapies or palliative virtually nil. Fortunately, the kind of progression that struck me was not that sudden and abrupt, so that, until now, I lead a mostly normal life.
I did 4 years of therapy with interferon, which I assure you to be a powerful drug, without the slightest advantage, until on the Internet in 2008 with studies carried out later in 2009, a vascular surgeon Italian had the big idea.
Paolo Zamboni is the name of the person who is giving hope to all of us ..
Prof.chirurgo vascular c / o University of Ferrara, assisted by Dr. Fabrizio Salvi, a neurologist c / o the Bellaria Hospital in Bologna.
COS'è LA CCSVI
Zamboni su studi effettuati inizialmente sulla moglie, affetta anch'essa da tale patologia, si accorse che da un esame ecocolordoppler, qualcosa non funzionava a dovere nella circolazione venosa della consorte, e da qui iniziò, insieme al Dott. Salvi, uno studio più approfondito della questione.
I due praticamente si accorsero che, nei pazienti affetti da sclerosi multipla, erano presenti delle stenosi, ossia dei restringimenti, a carico delle vene extracraniche giugulari ed a carico di una vena extravertebrale chiamata azygos, che provocherebbero una stasi del sangue a livello soprattutto celebrale, con conseguente accumulo di ferro nell'encefalo and hence chronic inflammation in the brain and spinal cord arising famous plates.
The accumulation of iron, it would be just the same composition of the blood, especially red blood cells, where the cell is made up of its iron.
In 2009 began the first trial, where they were subjected to Doppler ultrasound 65 MS patients with results nothing short of amazing:
100% of the patients had CCSVI.
course were also checked people with MS, where the problems were equal to zero or slightly more ...
The news was echoed internationally, especially among vascular surgeons from around the world, who decided includes for the first time in 2009 CCSVI in the category of congenital venous malformations and the research moved and spread out like wildfire, both in Canada and America, all with stunning results.
These patients were then practiced intervanto of''liberation'', a term used by us sclera, which is a dilated angioplasty, which for the first time was going to affect the veins and arteries. And it is here that the situation is failing to take off, because we wish to intervene in places where it had never occurred before.
intervanto In practice consists of making an intravenous injection, the femoral vein and the left groin from here through a Cater, sailed by an interventional radiologist, to get the points that are narrowing, inflating a balloon, return the vein to its natural opening, thus allowing the blood again, to resume its journey.
The testimonies of those who have already performed in the testing phase, the''liberation'', are exciting in that it already after the operation, almost all had regression of the disease leading to visual and improved quality of life .
All this could then add a nice chelation therapy, ie removal of heavy metals from the body, such as aluminum, iron, mercury and lead are also closely Related to CCSVI. Personally I already
from April I left all of interferon-based therapies, chelation therapy only to follow and wait for a service that I hope to do or this month or next.
I already had a Doppler ultrasound where I too was diagnosed with CCSVI the right jugular and by analyzing the urine have been found to have values \u200b\u200bof heavy metals in the body, for almost five times over the limit, and from there, I started chelation therapy that allows me to dispose of in the meantime.
PERSONAL CONSIDERATIONS
I sincerely hope that this month the ethics committees of Health to give the go ahead to start the angioplasties and still there are many obstructions.
I say this with a note of controversy, because in my view has not been given due publicity to the discovery, but some service on a variety of Tg and Medicine 33, saw nothing.
I say only that a box of interferon, which I did, well fornitami from 'ASL, for one month of therapy, costs 1700 Euro ... multiplied by the MS patients in the world and you will see that figure it will come out.
Apart from that this theory also completely subvert the medical definition of MS, which has always been regarded as an autoimmune disease of the body.
This is merely a problem of''disruption''and hydraulic enough, that would solve only a simple angioplasty.
INFORMATION AND SPECIALIZED
Almost in every region or fortunately, there appears a center pe CCSVI cmq below the most important: * A National Association
CCSVI - Onlus Bologna with the Presidency headed by Nicoletta Mantovani, Pavarotti's wife, also suffering from MS
http://www.ccsvi-sm.org/
* Two Center''Good''c / o Hospital Bellaria Bologna
http://ilbene.assisla.it/HOME.htm
* Three''SMuovilavita Foundation Onlus Vicenza''
http://www.smuovilavita.it/
* Four facebook just open and try CCSVI and opens up the world as well as numerous videos on youtube ... just to give you one, I'll give this a conference When both the CCSVI Zamboni that Salvi
http://www.youtube.com/watch?v=9nIVaSRt8eE
I hope to be helpful and not to have bored. Sorry
of heart, but I'm not a doctor, so I did not come easy way to express myself in a certain time limit or even address the topic but now I think I learn so much.
I ask only a great courtesy which is to disclose the topic with family and friends, now MS is unfortunately everywhere and I'm sure each of you know someone who is affected.
FOR ANY CLARIFICATION FEEL FREE TO CONTACT
I leave just expressing my great desire that I am sure will become a reality, which is to be able to tell my kids one day:''I was sick of
Multiple Sclerosis Society.''
My email is marcabi2001@yahoo.it
THANKS MARIO. BEST WISHES TO YOU AND ALL THOSE THAT YOU READ E AVRANNO BISOGNO.
