Does anyone know if this research by Dr Passie got off the ground and was concluded and what the results were?

Ellick.

Yes, the work is "off the ground" and is in progress.

When this first round is concluded, there will be a full report submitted for peer review.

Clusterbusters is very much involved with this project. I will keep you all up to date with any news, when it can be released.

Bobw
(who should have taken German in high school instead of French ;-(

Yes thanks for the link to the article v/v. Sorry forgot my manners.

I wrote to Dr Passie and asked if I could take part in the research. He agreed but I would have had to gone and lived in Germanyfor 6 months.

Like most people who work for a living I can't afford to take 6 months off.

Maybe a charity fund could be set up for people to take part in research. I'm not thinking of me, more like chronics in the 40s age group and younger.

And thanks from the heart to you Bob for keeping the most successful treatment so far by a long way out there for all to find.

Ellick.

Thanks for that Bob. I will set about raising some money in my area. It may take some time. I guess awareness stuff will need to be first as not many people know about CH.
I have some links to fundraisers but they tend to be administered by right wing kind of people who would have all their stereotype images ratified at the thought of clusterbusters. I can see their faces getting red at the very thought !

Ellick.