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CCSVI explained

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Valentina

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Dec 9, 2009, 4:45:02 PM12/9/09
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Here is a video (actually four) in which a neurologist professor in
Rome, Salvetti, explain the CCSVI:
http://www.aism.it/index.aspx?codpage=video_salvetti_CSSVI

It is in Italian, but if you understand Spanish or French, maybe you can
try to follow it. The medical language is about the same everywhere. He
speaks slowly.

It very very very interesting since he didn't read just the medlines,
but the real studies.
This are some lines that I take while listening:

He explains that this kind of venous insufficiency is the same that
causes ulcers in the legs of older peolpe (my granpa is full of such
ulcers!). The difference is that our insufficiency is in the brain...

The procedure that Zamboni used is to test with ecography those who has
some degree of insufficiency and those who result positive were tested
with a venography which is a invasive examination, the only one who can
assert the insufficiency in vein likes azygos.

He explains also the difference between PPSM e RRSM with different
stenosys, since those with PPSM had the ssme pattern of stenosys.

The patients treated during a relaple recovered fully in just some days,
just like with Solumedrol!

Salvetti says that the work of Zamboni is impressive, but the iron
deposit are ery common in other diseases which do not provoke MS
lesions, so he thinks that there are also other factors, not only the
vascular one.

Very impressive, really!


--
Valentina, from Florence, Italy

ne...@millions.com

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Dec 10, 2009, 12:07:06 AM12/10/09
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Valentina, avete messo in evidenza un aspetto importante circa gran
parte della ricerca medica: i medici di pratica mai realmente leggono
la ricerca o leggono appena i sommari di ricerca?

Grazie, Valentina.

Sempre con repect.

Donn

Gabriella

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Dec 11, 2009, 7:00:38 AM12/11/09
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Ciao Valentina e ciao a tutti!
Oggi nel sito della Regione Emilia-Romagna ᅵ apparsa la convocazione della
commissione sanitᅵ e all'ordine del giorno c'ᅵ: Informativa dell'Assessorato
alle Politiche per la Salute su "Trattamento endovascolare nei pazienti
affetti da sclerosi multipla". Se riesco ad organizzarmi con i figli, provo
ad andare a sentire di cosa si tratta.
Gli interventi del dott. Zamboni fatti su malati di sm inviati dal dott.
Salvi, sono stati sospesi a causa di una lettera che ᅵ stata inviata lo
scorso settembre da un gruppo di neurologi bolognesi che chiedono chiarezza
al riguardo. Adesso la Regione Emilia-Romagna deve pronunciarsi. In assenza
di fondi ᅵ difficile che la sperimentazione e quindi gli interventi possano
proseguire.
Appena ho aggiornamenti li invio.
Ciao
Gabriella

Traduco con google, non conoscendo l'inglese abbastanza bene:

Hello Valentina and hello to all!
Today the site of the Emilia-Romagna has appeared the convening of the
Committee on Health and the agenda is: Informative Under the Same health
policies on "Endovascular treatment in patients with multiple sclerosis."
If I can arrange with children, I try to go to hear what it is.
Surgical operations of Dr. Zamboni made on MS patients sent by Dr. Salvi,
were suspended due to a letter that was sent last September by a group of
neurologists Bolognese seeking clarity in this regard. Now, the
Emilia-Romagna has to decide. In the absence of funds is difficult for the
trial and then operations to continue.
As soon as I send updates.
Hello
Gabriella

Prima di stampare, pensa all'ambiente ** Think about the environment
before printing


"Valentina" <vale...@TOGLIQUESTOduestrade.it> ha scritto nel messaggio
news:yTUTm.106344$9f6.1...@twister1.libero.it...

Valentina

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Dec 11, 2009, 8:07:08 AM12/11/09
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> Surgical operations of Dr. Zamboni made on MS patients sent by Dr. Salvi,
> were suspended due to a letter that was sent last September by a group of
> neurologists Bolognese seeking clarity in this regard. Now, the
> Emilia-Romagna has to decide. In the absence of funds is difficult for the
> trial and then operations to continue.

Hello Gabriella, how long!
Thank you for this news.

--
Valentina

Peter Black

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Dec 11, 2009, 12:26:44 PM12/11/09
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Please send whatever information you hear. All is not lost; however,
the National Multiple Sclerosis Society in North America is funding a
trial at university in Bufalo.

On Fri, 11 Dec 2009 12:00:38 GMT, "Gabriella" <spam...@libero.it>
wrote:

Gabriella Villari

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Dec 12, 2009, 7:23:20 AM12/12/09
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Il dott. Zamboni spiega le sue ricerche:

http://watch.ctv.ca/news/w5/the-liberation-treatment/#clip237617

http://watch.ctv.ca/news/w5/the-liberation-treatment/#clip237656

http://watch.ctv.ca/news/w5/the-liberation-treatment/#clip237746

Per ora ho visto questi tre video, forse ce ne sono altri nello stesso sito.
E' stupendo che un italiano abbia fatto un scoperta cos� ed � incredibile
che nel suo paese le ricerche siano state interrotte. Personalmente sono
molto fiduciosa sull'esito dell'inchiesta e credo che tutto si sbloccher�
presto.
Saluti a tutti
Gabriella from Bologna, Italy


traduco con Google:

Dr. Zamboni, talks about his research:

http://watch.ctv.ca/news/w5/the-liberation-treatment/#clip237617

http://watch.ctv.ca/news/w5/the-liberation-treatment/#clip237656

http://watch.ctv.ca/news/w5/the-liberation-treatment/#clip237746

For now I saw these three videos, perhaps there are others in the same site.
It's amazing that an Italian has made a discovery well and it is incredible
that in his country searches have been interrupted. Personally I am very
confident on the outcome of the investigation and believe that everything
will unlock soon.
Greetings to all
Gabriella from Bologna, Italy


"Valentina" <vale...@TOGLIQUESTOduestrade.it> ha scritto nel messaggio
news:yTUTm.106344$9f6.1...@twister1.libero.it...

Peter Black

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Dec 12, 2009, 11:01:24 AM12/12/09
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On Sat, 12 Dec 2009 12:23:20 GMT, "Gabriella Villari"
<gabriell...@TOGLIQUESTOlibero.it> wrote:

>It's amazing that an Italian has made a discovery well and it is incredible
>that in his country searches have been interrupted. Personally I am very
>confident on the outcome of the investigation and believe that everything
>will unlock soon.

I sincerely hope this is a worthwhile treatment for MS. Yet, I
remember the excitement I felt when similar results were presented for
HHV6 (Human Herpes Virus six) as the cause of MS. And I remember the
profound gut wrenching sadness I felt when it was learned that the
results could not be duplicated in other trials. We must wait.
Please, let this one be real.

BigArtie

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Dec 12, 2009, 5:36:51 PM12/12/09
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"Peter Black" <no...@none.us> wrote in message
news:s6e7i51fh413fcfca...@4ax.com...

Peter, Serious question, have you considered trying LDN?
What are you using now for your MS?


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