Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged at the end of 2019 and caused the devastating global pandemic of coronavirus disease 2019 (COVID-19), in part because of its ability to effectively suppress host cell responses1,2,3. In rare cases, viral proteins dampen...
I missed that there is a conference programme posted on the site. It would be good to get someone from @PhysiosforME or likewise to attend, and report back if possible.
BACME has a new and updated website: https://bacme.info/. It's an improvement on the old one, and includes some new content (but nothing of note).
They are also advertising their November 2022 conference: https://bacme.info/event/bacme-2022-conference/. Non-BACME members can attend, but it's a...
I'm wondering if anyone has recent experience of the Liverpool ME/CFS service, particularly since the new NICE guideline was published?
The webpages look like they are under development, so I can't see what they offer and if it's remotely worthwhile persuing a referral...
Other confusion is arising due to enrollees not realising that registering their interest last year is not the same as signing up. I don't think this was made particularly clear, as I was confused when I landed on the Decode sign-up page last week. If you see other patients saying they haven't...
I have been seeing a lot of frustration from people who don't meet the criteria for spit sample collection. I'm sure the team at Decode are aware of this. I'm wondering if this has the potential to become an issue over the next week or two, and even going forward...
I don't think that's a good...
I think this probably refers to some work Peter White (F-ME) was doing looking at other (non-ME) charities and how they raise funds and invest. If you search recent minutes you might find exactly what it refers to.
I suspect trying to get MEA to do anything radically different is a lost cause!
There are a few threads on heart rate monitoring and wearables in this sub-form: https://www.s4me.info/forums/monitoring-and-pacing.222/ . This thread might be better there.
Mod note: thread has now been merged, but other threads in this subforum do have useful information.
Agree. Was quite shocked to see this. Oversimplisitc, and wrong. If you've developed ME/CFS after SARS-Cov-2 then by definition you have long covid, so for these patients there's only one illness (and it has two names).
Thanks @Adrian . Have you got any further persuading them that they need a dedicated website or webpage for comms? I saw on the most recent Forward-ME meeting minutes that FME discussed PAG's 'objection' to ME/CFS Delivery Plan comms going through FME (which I also don't think is a good idea)...
I'm under the care of an NHS rheumatologist, rather than an ME clinic or something of that nature.
I'm still not entirely sure of his opinion of ME/CFS. He's a rheumatologist so I guess he primarily sees people with arthritis and other autoimmune diseases. He did mention GET once (and I...
It might *help* prevent, but most people don't do any sort of significant rest/convalescence and don't develop ME/CFS, which would suggest there are more powerful factors at play—ones that we might have little control over, such as genes and our microbiome.
Hi @Andy
This group, the Attitudes and Education Working Group, is one of three groups in the government's ME/CFS Delivery Plan. The other groups are the (UKCRC) Research working group and the Living With ME working group. There is also a Task and Finish Group which will oversee the project and...
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to our use of cookies.