This continues the Guardian articles already posted in the The pain that can't be seen special feature: Wednesday's link:
The pain that can't be seen
‘I felt betrayed’: how Covid research could help patients living with chronic fatigue syndrome
People with ME/CFS face debilitating symptoms but often feel dismissed by doctors. The focus on long Covid could help change that
by Christina Frangou
theguardian.com/australia-n...
Tuesday's link:
healthunlocked.com/thyroidu...
Monday's link:
Just a comment:
I have seen several calls for long Covid clinics (and research, etc.) across the media, and across the world. Not for one moment denying the need. But let us make sure they do not get implemented as long Covid-only clinics.
I have a horrible premonition that if someone is referred, or self-refers, the first question is likely to be about when they started to feel fatigued. And if that is before, say, November 2019, it can't possibly be related to Covid-19 so goodbye. The clinics might say, truthfully, that their funding is for long Covid sufferers. But if the issues and/or treatments are the same, they need to be established for and open to all who need them.
Beginning Levothyroxine (Dose?)
Covid 19 and Guidance for Hashimoto’s patients 
Frontiers in Endocrinology paper: 'Higher Prevalence of “Low T3 Syndrome” in Patients With Chronic Fatigue Syndrome' advocates T3 trials
