I avoided the neuroinflammation by hitting my FSM machine hard.
My parents, on the other hand, now have lung scarring and non-essential tremor. The tremor was so apparent the nurses commented on it suddenly developing when my father was in the hospital. He also now has POTS.
None of us can get rid of the BPPV.
In terms of statistical evidence for vitamins, you’re only looking at 43% improvement and 57% sufficiency. In comparison, sotrovimab has been shown to improve outcomes in 80% of patients. Even ivermectin has better results than what you linked me here.
One study looking at orthostatic issues post COVID infection in millions of patients.
Small case study of six patients who were never hospitalized but developed dysautonomia.
Another study looking at POTS and tachycardia.
More than 50% left with symptoms in post-acute phase after several months.
Dysautonomia is happening more than it’s being reported in the MSM; its prevalence is being discussed on forums for medical professionals. I only know this because my PCP has discussed the developments of treatment and disease research with me extensively over the past couple of months. Her whole family got COVID in early autumn; her husband had a stroke from it about a month later, and she has multiple long haulers she’s treating, both vaccinated and unvaccinated. Hence why she’s been researching autonomic dysfunction so extensively.
For the record, though, there’s a god awful website claiming everything under the sun is a symptom of PACS and long haul COVID dysautonomia. That is BS, full stop. But tachycardia, heart murmurs, POTS, etc. are issues from the disease itself as well as the neuroinflammation it leaves behind. Hence why you lose your sense of smell—it attacks the nerve cells of the olfactory bulb. Anosmia doesn’t seem to happen with Omicron, so hopefully it has settled down on the neurological attack front.
I’m an econometrician by trade. I understand statistical analysis and inference. I didn’t want to get into the nitty-gritty in my original post as I am stuck posting from my phone until I reset my password, so I gave a personal example. Big woop.
I avoided the neuroinflammation by hitting my FSM machine hard.
My parents, on the other hand, now have lung scarring and non-essential tremor. The tremor was so apparent the nurses commented on it suddenly developing when my father was in the hospital. He also now has POTS.
None of us can get rid of the BPPV.
In terms of statistical evidence for vitamins, you’re only looking at 43% improvement and 57% sufficiency. In comparison, sotrovimab has been shown to improve outcomes in 80% of patients. Even ivermectin has better results than what you linked me here.
One study looking at orthostatic issues post COVID infection in millions of patients.
Small case study of six patients who were never hospitalized but developed dysautonomia.
Another study looking at POTS and tachycardia.
Dysautonomia is happening more than it’s being reported in the MSM; its prevalence is being discussed on forums for medical professionals. I only know this because my PCP has discussed the developments of treatment and disease research with me extensively over the past couple of months. Her whole family got COVID in early autumn; her husband had a stroke from it about a month later, and she has multiple long haulers she’s treating, both vaccinated and unvaccinated. Hence why she’s been researching autonomic dysfunction so extensively.
I’m an econometrician by trade. I understand statistical analysis and inference. I didn’t want to get into the nitty-gritty in my original post as I am stuck posting from my phone until I reset my password, so I gave a personal example. Big woop.