DecodeME study for Brits with ME/CFS

They’ll do genetic testing on samples that’s similar to 23andMe. (Genome wide association study.) It’ll look for known variations in genes and try to find patterns among people who develop ME/CFS and people who don’t.

Their survey may be relevant to the vax-injured community because it’s pretty well designed. We might also want to ask them about the vax injured- our symptoms overlap heavily with ME/CFS and we can mess with these studies if we end up in the control group.

CC: @Ccukcvfam