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    Maria Gjerpe TEDx talk on the MEandYOU crowdfunding for the Norwegian rituximab trial

    I saw Maria on TV in a makeover TV programme some years ago. I didn´t know about her and her history at that time, so it was amazing to see her. She looked radiant, energetic and was a very postive person. Trinny and Susannah from the UK were in Norway and picked up Maria in the street. She told...
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    What is the course of your ME/CFS?

    Looking back at 24 years of having ME, diagnosed after 20 years, I´ve gone from being homebound to almost being well when I not longer have been exposed to some of the factors that Naviaux presented as causing the Cell Danger Response; amalgam/mercury, mold and infections like Lyme and Yersinia...
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    Pirate paper website Sci-Hub dealt another blow by US courts

    In memory of Aaron Swartz, who gave his life to free access to research articles and other documents behind paywalls https://en.wikipedia.org/wiki/Aaron_Swartz
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    Question concerning XMRV

    I believe this study also contributed to the "death" of the claim that XMRV is related to ME/CFS. "We found no significant increases in seroreactivity to XMRV antigens among blood donors and ME/CFS patients". Clin Vaccine Immunol. 2012 Sep;19(9):1399-410. doi: 10.1128/CVI.00391-12. Epub 2012...
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    Clinicians guide for ME/CFS by IOM, recommended by Dr. M. Hanson

    I couldn´t find any post about this, although there might be. Dr. Maureen Hanson has highlighted a report and Clinicians Guide for ME/CFS, published by IOM. She did that during her talk in Malmoe, Sweden, October, 17. See 1:10:47. Here is the Clinicians guide. She heard from patients who...
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    Wessely gets touchy feely

    Here is an interview with SW that I find interesting, although also challenging to read. http://www.bmj.com/content/347/bmj.f6803.long
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    Wessely gets touchy feely

    Hi @Andy , photo deleted. I guess I´m still too upset from a GP´s visit in my home, me on the sofa, some months ago. Before she even asked me about my story and actual condition, she claimed that CBT and GET would be good for me. It´s not only in the UK...
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    Wessely gets touchy feely

    Hmmm. The tweets replying to that one are worth reading as well as other links from SW´s tweets. Edit: photo and related text deleted
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    Will The UK Establishment Finally Stop Denying The Reality Of ME? Huff Post

    Great :thumbsup:. Shouldn´t this be announced in a separate thread as it´s a bit OT here? Too good to be missed by interested people.
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    UK ME/CFS Biobank hosting Unrest screening with livestreamed Q&A after, Thurs 2nd Nov

    I´m watching it now... https://panopto.lshtm.ac.uk/Panopto/Pages/Viewer.aspx?id=3f756fa1-4190-454f-83a5-71a1063508bd
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    Thyroid, autoimmune thyroiditis, Hashimoto's

    I think Dr. Jeffrey Dach has written very good articles on Hashimoto´s here. I was diagnosed with autoimmune thyroiditis /Hashimoto´s 23 years ago, and I wished that I had had those articles at that time. He is clearly very knowledgeable and experienced re Hashimoto´s.
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    Invest in ME ...Highlighting Issues With the PACE Trial.../David Tuller 2017

    Pre-conference Dinner Analysis Highlighting Issues With the PACE Trial http://www.investinme.org/IIMER-Newslet-main-1710-01.shtml
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    Ramsey award program - 5 research groups awarded

    http://go.solvecfs.org/webmail/192652/47628203/a0e396f30e624026a094c53cd974b2c0431bbec3aee7ebdea9f777a6ba844cd6 Congratulations to the research groups getting grants for further studies! Announcing the 2017 SMCI Ramsay Award Program Results October 31, 2017 The Solve ME/CFS Initiative is...
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    Videos from RME Sweden conference, Malmo, 19 Oct 2017 - Maureen Hanson, Jo Cambridge

    Anomalous microbiome and metabolic profiling in ME/CFS-patients Prof Maureen Hanson, Cornell University, USA From 1:10:47 ME/CFS and the immune system. Where are we now? Geraldine (Jo) Cambridge, PhD, Dep. Medicine, University College, London From 5:33
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