After I finally got diagnosed I tried for 2 years to try to get back to reasonable/consistent level of functioning in my job. A lot of adjustments were made. Nothing of value other than ticking a box came from the CFS clinic PACE light course during that time. People will persist in trying for...
Apologies for an extremely basic question. We know there are issues with misdiagnosis in both including people as ME/CFS but also taking years for people to get an MECFS diagnosis. It seems anecdotally that some people with MS first get diagnosed with MECFS then after a few years get MS...
Agree it should be all focused on the study and definitely Chris did a good job of bringing it back on topic. The journalist feeble attempt to spice it up with a bit of populist controversy but Chris didn’t bite. :thumbup:
Well maybe that’s the difference @Rosie as I have moderate/mild ME so have some ok days and can go out only in crash/flare up I spend most of my time in bed
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