yeah. If I actually clear the congested feeling where the spine meets the skull, it can sometimes settle at the base of the spine instead. Some kinda intracranial pressure nonsense? I never got deep into the spinal-structural stuff.
I'm not sure how to process or interpret this occurrence, but I'd love to hear your theories or any research you've come across touching on this symptom.
/end
#MECFS#PEM#pwME
I'm not sure if I've had it before, but didn't really notice amidst the cascade. This time it was v. clear since it was notably stronger than the upper one.
I lost 90% of walking again with this flare, but that's been a pretty regular feature the last few years.
#PEM
3/
I had a flare last week that came with a lot of mast cell stuff w/in 30 min of trigger.
At 1hr #PEM started hitting, and the base of skull feeling showed up, but I also got it around the bottom of T-spine/top of L-spine, and it was stronger than the C-spine feeling.
2/
Folkx that get #PEM:
You know that base-of-skull miserable feeling that can show up with PEM?
Have you ever had it show up in other parts of your spine, too?
1/
#MECFS#pwME#POTS#MCAS#NEISvoid
🧪 This paper says that the Covid virus uses histamine receptors to help it enter our cells, and that ordinary antihistamines can prevent mice from being infected. This seems exciting? But the only coverage I saw was on...Newsmax?? Someone tell me what I'm missing. journals.asm.org/doi/10.1128/...
UK: ‘Our lives are shattered’: Teachers’ legal fight for long Covid support.
"More than 100 teachers whose lives have been "shattered" by the virus claim they have been left with no support"
#COVID19UK#LongCOVID#Teachers
Source: archive.md/HcgeJ
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