https://meassociation.org.uk/2023/11/the-me-association-writes-to-the-president-of-the-royal-college-of-psychiatrists-regarding-their-website-information-on-me-cfs/
The ME Association writes to the president of the Royal College of Psychiatrists regarding their website information on ME/CFS
Yes it will be. https://meassociation.org.uk/wp-content/uploads/2020Health-Counting-the-Cost-Sept-2017.pdf
The IoM report claimed 17-24 billion dollars in USA
https://www.cdc.gov/me-cfs/about/index.html#:~:text=An estimated 836,000 to 2.5,medical bills and lost incomes.
:thumbup: 10k is definitely achievable. Great help if members who have social media presence, especially folks with blogs and some followers, can share the link regularly every couple of weeks or so
@Perrier I think most patients have tried LDN is overstating things significantly. I only know of one person. I haven’t tried it and I suspect a fair number here haven’t either.
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.