CCSVI AND MS IN EUROPE
CCSVI AND MS IN EUROPE
I read all messages about the CCSVI and the places where the treatment is possible; is there some body who know about some hospitals in Spain or France that begin to treat MS' patients.Thank you so much for your help.
INONU
my daughter ms'patient since 2001
Hi,
The neurologists at National Health System in Spain don't seem to be much interested in CCSVI. I have also contacted the National MS Society, but their answer is that they do not recommend the liberation procedure, not even the testing (unbelievable).
My sister has an appointment with Dr.Simka in Poland to get a doppler and a MRV.
The neurologists at National Health System in Spain don't seem to be much interested in CCSVI. I have also contacted the National MS Society, but their answer is that they do not recommend the liberation procedure, not even the testing (unbelievable).
My sister has an appointment with Dr.Simka in Poland to get a doppler and a MRV.
HELLO from germany
hello girls,
i follow the discusions and the infos in the ccsvi board since beginning...well, the vistis to poland increase in the last months enormous and the therapy gets more and more expensive...some 100 people are still on the "waiting list" of dr simka...i myself have no interest, my ms iss constant since some years.
two german universities are also active...frankfurt and jena, but only diagnosis, no op s...
whats going on in france, i don t know...may they wait also on results out of the now running buffalo study?
R in germany nick "günni"
i follow the discusions and the infos in the ccsvi board since beginning...well, the vistis to poland increase in the last months enormous and the therapy gets more and more expensive...some 100 people are still on the "waiting list" of dr simka...i myself have no interest, my ms iss constant since some years.
two german universities are also active...frankfurt and jena, but only diagnosis, no op s...
whats going on in france, i don t know...may they wait also on results out of the now running buffalo study?
R in germany nick "günni"
My spanish is bad
http://www.esclerosismultiple.com/pdfs/2009/CCSVI FELEM 22 12 09.pdf
But it is something about ccsvi....
And France:
http://www.lfsep.com/article_actualite. ... rubrique=1
Rob
http://www.esclerosismultiple.com/pdfs/2009/CCSVI FELEM 22 12 09.pdf
But it is something about ccsvi....
And France:
http://www.lfsep.com/article_actualite. ... rubrique=1
Rob
- Algis
- Family Elder
- Posts: 829
- Joined: Sat Nov 21, 2009 3:00 pm
- Location: XinYi District, Taipei City, , Taiwan
It is roughly the same as others CCSVI presentations. Last paragraph about "Shall I get tested for CCSVI"? says like all the others:
"No; except you are in study to explore this prospect. It is right now not proven nor there is evident relation between venous abnormalities and MS."
Maybe someone has the courage/time to translate all of the document.
"No; except you are in study to explore this prospect. It is right now not proven nor there is evident relation between venous abnormalities and MS."
Maybe someone has the courage/time to translate all of the document.
- thisisalex
- Family Elder
- Posts: 218
- Joined: Wed Dec 02, 2009 3:00 pm
- Location: Hungary
- Contact:
INONU,
here you can read about doctors is Europe
http://liberation-treatment.com/liberat ... nt/doctors
there is also an ultrasound clinic, only for diagnosis in Slovenia
Http://www.mc-sinigoj.si
alex
here you can read about doctors is Europe
http://liberation-treatment.com/liberat ... nt/doctors
there is also an ultrasound clinic, only for diagnosis in Slovenia
Http://www.mc-sinigoj.si
alex
- i cannot read what they wrote in slovenia...no alex...thisisalex wrote:INONU,
here you can read about doctors is Europe
http://liberation-treatment.com/liberat ... nt/doctors
there is also an ultrasound clinic, only for diagnosis in Slovenia
Http://www.mc-sinigoj.si
alex
"our big european problem"
are the so much different languages...not so many people trust themself, to "write" in english and make mistakes
R
Re: CCSVI AND MS IN EUROPE
Hello INONU,INONU wrote:
I read all messages about the CCSVI and the places where the treatment is possible; is there some body who know about some hospitals in Spain or France that begin to treat MS' patients.Thank you so much for your help.
INONU
this might interest you:
http://csvi-ms.net/forum_fr/viewtopic.php?f=2&t=8
http://csvi-ms.net/forum_fr/viewtopic.php?f=2&t=11#p45
Bonne chance!
Ana
Would anyone have a contact in Belgium?
I have a first doppler exam result from Poland: left jugular vein occlusion by pathologic valve.
Since have social security/med care in Belgium would be good to know who could contact for an MRV-follow-up. I will also ask my generalist there, but if already got a name of a helpful doctor (angiography?) or hospital that would be great.
Thanks
Steffi
I have a first doppler exam result from Poland: left jugular vein occlusion by pathologic valve.
Since have social security/med care in Belgium would be good to know who could contact for an MRV-follow-up. I will also ask my generalist there, but if already got a name of a helpful doctor (angiography?) or hospital that would be great.
Thanks
Steffi
Sorry, was posted twice
Last edited by Zeureka on Sun Jan 24, 2010 11:50 am, edited 1 time in total.
- thisisalex
- Family Elder
- Posts: 218
- Joined: Wed Dec 02, 2009 3:00 pm
- Location: Hungary
- Contact:
but there is an american solution to our european problem... google translaterobin50 wrote:
i cannot read what they wrote in slovenia...
"our big european problem"
http://translate.google.com/translate?j ... l=de&tl=en
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