Page 2 of 5

Re: Lyme disease foundations and associations in Europe

Posted: Tue 5 Feb 2008 22:23
by Martian
These aren't all foundations and associations, right? And what is what?

I think normally each country has no more than one Lyme foundation and association. I was thinking about listing those if they exist in a country, and a few other important sites if they exist. I don't intend to list as many as 16 links for one country, that's way too much IMO.

Re: Lyme disease foundations and associations in Europe

Posted: Wed 6 Feb 2008 1:10
by cave76
YIPPEE---- Yvonne is back. :)

Now that 'the American ladies' (of which I am one of the most disruptive ) have settled down a bit, maybe we'll get LE back to science.

However, it's ALWAYS fun in LymeCafe and Dysfunctional (Nope, make that Unconventional) Protocols. :D :D

Where's my :bonk: ?????

Re: Lyme disease foundations and associations in Europe

Posted: Wed 6 Feb 2008 10:57
by Yvonne
Martian wrote:These aren't all foundations and associations, right? And what is what?

I think normally each country has no more than one Lyme foundation and association. I was thinking about listing those if they exist in a country, and a few other important sites if they exist. I don't intend to list as many as 16 links for one country, that's way too much IMO.
Ok, I understand. In Germany there are more than one Lyme foundation and association.
I thought that the links I post were important.
And to select what is what costs something more time .
So you can delete what I post and when I can I will post it later once more.

Re: Lyme disease foundations and associations in Europe

Posted: Wed 6 Feb 2008 11:36
by minitails2
Yeah Yvonne,
Is there anyway of finding out if there is an organization in France near Mulhouse in the Alsace area. It's about 30 K north of Basel Swit. and about 100 K south of Strasbourg? My S.O./boyfriend Chris lived there for a year on a fellowship and his old boss has had lyme. Chris was hoping to send him some information about where to get more information because he's worried his friend might still be sick. Thanks.

Glad to see you back. :)

Re: Lyme disease foundations and associations in Europe

Posted: Thu 7 Feb 2008 12:32
by Yvonne
I don't know Minitails. But perhaps you can ask NellyP who also is a member of this forum and so far as I know she is from France.

Re: Lyme disease foundations and associations in Europe

Posted: Sat 9 Feb 2008 10:14
by Yvonne

Re: Lyme disease foundations and associations in Europe

Posted: Sat 9 Feb 2008 15:45
by cave76
The English version is "under construction". Is that also true of the Hungarian version?

Just wondering.

Re: Lyme disease foundations and associations in Europe

Posted: Sat 9 Feb 2008 16:48
by Yvonne
Partial.You can read 2 Pdf's from it.

They write that they soon prepare the last version.

Re: Lyme disease foundations and associations in Europe

Posted: Sun 2 Mar 2008 12:16
by Yvonne
Slide Show

Bózsik, Béla pál, MD and therapeutic Workgroup, Lyme Borreliosis Foundation Hungary :

http://www.lymenet.hu/dolgok/_THERAPY.ppt#1

Re: Lyme disease foundations and associations in Europe

Posted: Sun 2 Mar 2008 16:08
by cave76
I've heard of him and he's a not too frequent poster on a list that used to be more populated with docs and researchers--- still good but not quite as. :( I always enjoyed reading his posts.

I think he's retired? And I also think he was the ONLY 'international' ILADS doctor. Not sure of that last bit of information.