Why so little ME/CFS research from France and Germany?

[Hip]

Great interview, Mike.

Interesting that they are already using rituximab in France in certain specific cases of ME/CFS.

 

[*GG*]

Hi all

Here's my interview with Marie from ASFC (Association française du Syndrome de Fatigue Chronique) about what it's like for ME patients in France.

http://www.mikeseumarathons.eu/france.html

The two French ME facebook support groups I'm aware of have posted some nice messages and donated to Invest In ME this week for their biomedical projects.

Feel free to share/circulate

Mike

I hit the link above, Tried to share this on Facebook, but did not see a Button. FYI Are there links to Pages for Facebook group?

Thank you for your efforts!

GG

 

[Mike Harley]

I hit the link above, Tried to share this on Facebook, but did not see a Button. FYI Are there links to Pages for Facebook group?

Thank you for your efforts!

GG

Hi

Yep sure, I'm at www.facebook.com/mikeseumarathons

Feel free to share

 

[frederic83]

Interesting that they are already using rituximab in France in certain specific cases of ME/CFS.

It is not really for treating the CFS, but in known autoimmune disease. Some people have CFS and one or more autoimmune diseases. No way I could get Rituximab in France. And I think this treatment is not suggested that much.