ME/CFS News
@mecfsnews.bsky.social
News, interesting information and commentary on ME/CFS.
May 12 is ME/CFS Awareness Day. Speak with other people about ME/CFS today. Reject invisibility and stigma, build awarenesss and support.
May 12, 2024 at 9:23 AM
May 12 is ME/CFS Awareness Day. Speak with other people about ME/CFS today. Reject invisibility and stigma, build awarenesss and support.
PrecisionLife, Action for ME, and the MRC Human Genetics Unit have been awarded an Advancing Precision Medicine grant by Innovate UK to improve diagnosis & treatment of ME/CFS and Long Covid. precisionlife.com/news-and-eve...
December 15, 2023 at 4:33 PM
PrecisionLife, Action for ME, and the MRC Human Genetics Unit have been awarded an Advancing Precision Medicine grant by Innovate UK to improve diagnosis & treatment of ME/CFS and Long Covid. precisionlife.com/news-and-eve...
DecodeME study needs more participants with ME/CFS in the UK. The more, the better. The recruitment will end in two weeks.
If you have been sent a spit kit but did not return it, please return it now.
Sign up here www.decodeme.org.uk/portal/
If you have been sent a spit kit but did not return it, please return it now.
Sign up here www.decodeme.org.uk/portal/
November 1, 2023 at 9:36 AM
DecodeME study needs more participants with ME/CFS in the UK. The more, the better. The recruitment will end in two weeks.
If you have been sent a spit kit but did not return it, please return it now.
Sign up here www.decodeme.org.uk/portal/
If you have been sent a spit kit but did not return it, please return it now.
Sign up here www.decodeme.org.uk/portal/
Tomorrow the next ME/CFS Research Roadmap webinar will take place. The topic is metabolism in ME/CFS.
It's open to the public and attendees can participate in Q&A sessions. Register here event.roseliassociates.com/me-cfs-resea...
It's open to the public and attendees can participate in Q&A sessions. Register here event.roseliassociates.com/me-cfs-resea...
October 25, 2023 at 4:27 PM
Tomorrow the next ME/CFS Research Roadmap webinar will take place. The topic is metabolism in ME/CFS.
It's open to the public and attendees can participate in Q&A sessions. Register here event.roseliassociates.com/me-cfs-resea...
It's open to the public and attendees can participate in Q&A sessions. Register here event.roseliassociates.com/me-cfs-resea...
Today the PolyBio research foundation will host a webinar on infection-associated chronic diseases. ME/CFS and Long Covid will be discussed.
It's open to the public. Join here polybio.org/polybio-fall...
It's open to the public. Join here polybio.org/polybio-fall...
October 20, 2023 at 7:11 AM
Today the PolyBio research foundation will host a webinar on infection-associated chronic diseases. ME/CFS and Long Covid will be discussed.
It's open to the public. Join here polybio.org/polybio-fall...
It's open to the public. Join here polybio.org/polybio-fall...
People With Long COVID and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Exhibit Similarly Impaired Vascular Function
www.amjmed.com/article/S000...
www.amjmed.com/article/S000...
October 12, 2023 at 10:58 AM
People With Long COVID and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Exhibit Similarly Impaired Vascular Function
www.amjmed.com/article/S000...
www.amjmed.com/article/S000...
The next ME/CFS Research Roadmap webinar will take place on October 19, 2023. This webinar will be about the immune system. Attendees can participate in Q&A sessions.
More details here event.roseliassociates.com/me-cfs-resea...
The previous webinar of the series was great.
More details here event.roseliassociates.com/me-cfs-resea...
The previous webinar of the series was great.
September 30, 2023 at 6:24 AM
The next ME/CFS Research Roadmap webinar will take place on October 19, 2023. This webinar will be about the immune system. Attendees can participate in Q&A sessions.
More details here event.roseliassociates.com/me-cfs-resea...
The previous webinar of the series was great.
More details here event.roseliassociates.com/me-cfs-resea...
The previous webinar of the series was great.
ME Action Network has created a website for the MillionsMissing.org movement.
There have been 16 MillionsMissing demonstrations since 2016, in hundreds of cities across the world. It is a global movement calling for justice for people with ME/CFS.
There have been 16 MillionsMissing demonstrations since 2016, in hundreds of cities across the world. It is a global movement calling for justice for people with ME/CFS.
September 27, 2023 at 5:58 AM
ME Action Network has created a website for the MillionsMissing.org movement.
There have been 16 MillionsMissing demonstrations since 2016, in hundreds of cities across the world. It is a global movement calling for justice for people with ME/CFS.
There have been 16 MillionsMissing demonstrations since 2016, in hundreds of cities across the world. It is a global movement calling for justice for people with ME/CFS.
Important: if you live in the UK are have been diagnosed with ME/CFS, then please participate in the DecodeME study.
More participants are needed to increase the confidence we can have in the findings.
www.decodeme.org.uk/portal/
More participants are needed to increase the confidence we can have in the findings.
www.decodeme.org.uk/portal/
September 19, 2023 at 1:15 PM
Important: if you live in the UK are have been diagnosed with ME/CFS, then please participate in the DecodeME study.
More participants are needed to increase the confidence we can have in the findings.
www.decodeme.org.uk/portal/
More participants are needed to increase the confidence we can have in the findings.
www.decodeme.org.uk/portal/
The German government is investing 15 million euros in ME/CFS research for the next three years. They emphasize the importance of research into ME/CFS since this is also the most debilitating and complex form of Long Covid.
x.com/BMBF_Bund/st...
x.com/BMBF_Bund/st...
September 12, 2023 at 11:43 AM
The German government is investing 15 million euros in ME/CFS research for the next three years. They emphasize the importance of research into ME/CFS since this is also the most debilitating and complex form of Long Covid.
x.com/BMBF_Bund/st...
x.com/BMBF_Bund/st...