Real progress in ME/CFS research (part 2 of 2)

Please, everyone, get out your check book and send a check to the Whittemore Peterson Institute. Whatever you can afford - even $5. It adds up. To all the "Naysayers" on fibromyalgia and chronic fatigue: Your outdated opinions are going to be buried by the scientific evidence that will emerge from good research.

OMG! An effective institution devoted to CFIDS! Thank you so much for your work!

I think it`s very important that every ME/CFS sufferers, relatives and friends donate some money for this institute. $ 5 - 10 is not that much! (or $ 50 - 100)

Just google for "Whittemore Peterson Institute". You will find it! :-)

WPI is our HOPE!

I think it`s very important that every ME/CFS sufferers, relatives and friends donate som money for this institute. $ 5 - 10 is not that much!

Just google for "whittemore peterson institute" . You will find it! :-)

The Norwegian Arbeiderpartiet (akin to the UK Labour party) have today announced their new politics and "the change" of direction within medicine and particularly for ME sufferers: (from the Arbeiderpariet national partymeetings of 21. April 2009)

Thank you so much for posting this. Here in the UK we continue to have our devastating neurological illness viewed as psychological (with all government research funding going to psychiatrist), and look with hope to the Whittmore Peterson Insitute to prove that it is not.

Hi Bluebottle83: I know the horrible situation in UK. The homeland of "Wessely-School". It`s dobble tragic because a lot of european contries have adapt the NICE guidelines for ME. The same tragedy has happend in both US and Canada too. Wessely and his psyco-friends have failed all these years. It is an enormous political scandal and what a disgrace! It seems that Norway wants to go for a change and I really hope this will be a domino-effect for UK and the rest of the world! Thats my hope!

Things are not going to change here in France. When I asked my doctor if I also had Myalgic Encephalomyelitis, he "pretended"? he didn't know what I was talking about until I said CFS and he bluntly said that I had probably CFS as well but anyway there's no treatment for either Fibromyalgia or CFS, that the only treatment for me was.... psychotherapy...

leobalt wrote:
Whittemore, Peterson, Mikovits!
Thanks for your passion to speed up biomedical scientific research into ME!
Many hugs, kisses and flowers to you!

(Sorry leoblat, but your post was misunderstod as spam, by youtube.. And off course it was not! Therfore I post it again, for you)

Agree. God bless the WPI and Judy Mikovits.