et al found two distinct immunotypes of ME/CFS based on the cerebrospinal fluid analysis. Great collaboration with
@MBVanElzakker
@microbeminded2
and the BragĂŠe clinic in Sweden. (1/)
***
Prof. Akiko Iwasaki
@VirusesImmunity
¡
May 16
While we do not know why some people with ME/CFS have elevated MMPs and cytokines, our data suggest potentially distinct drivers of disease that manifest in similar clinical phenotypes. Future studies are needed to probe therapeutic pathways suitable for these clusters. (4/)
There is some research that suggests menstruation is a detoxing process, to keep the body in a state of preparedness for pregnancy. Itâs interesting that FM affects women at an age when their period is ceasing.
I looked at the Slay News article linked from Italy regarding the spike protein neurological damage.
I could only see the abstract (too cheap to support the journal by buying the full text!) but they appear to state that Covid infection caused more damage than the shots. This has been common throughout the plandemic. Access to the full dataset often shows that the conclusions don't correspond to the data.
Thank you for the exposition of the fibromyalgia research. We had lectures on diagnosis 35 years ago but treatment was never very successful or satisfying. Maybe understanding the underlying chemistry will promote more useful treatments.
Follow The Science: Why Peter Marks Was Asked To Leave The FDA
... Thanks to Dr. Marksâ terrible decisions, we are left with a drug that has no proven benefit and that just killed a young patient, a vaccine that is not completely safe is being administered to children that have no significant risk of harm from the underlying infection, and an overburdened healthcare system that had to pay billions for another unproven, harmful therapy. Advocates for Dr. Marks claim that he has acted to help patients with life-threatening conditions which have no alternative treatments. But in reality, he catered to industry and hurt patients.
Has this area of healthcare progressed since the Middle Ages? They will be putting people on trial for witchcraft next:
"Long Covid patients feel dismissed and unsupported by healthcare providers
People living with Long Covid often feel dismissed, disbelieved and unsupported by their healthcare providers, according to a new study from the University of Surrey.
The study, which was published in the Journal of Health Psychology, looked at how patients with Long Covid experience their illness. The study found that many patients feel they have to prove their illness is physical to be taken seriously and, as a result, often reject psychological support, fearing it implies their symptoms are "all in the mind".
We found that the problem isn't people with Long Covid refusing help â it's about the deep need for people to be believed. When a patient feels dismissed, offering psychological support instead of medical care can be misconstrued as insulting.""
Just had a scary health crisis with my 16 yr old daughter (unvaxxed). January got random very high pulse. Soon it accompanied every activity she did, oftentimes spiking to 160 or 170 even if she was walking, or just sitting and doing nothing. She had real difficulty climbing stairs. Went to the GP and the cardiologist- they said, disautonomia , a variant of POTS. They seriously donât know how to treat it, they only know how to prescribe pills. So we were told to use compression socks and do more exercise and electrolytes and a lot of water. My daughter presented with weird red patches under her eyes, apparently, the nerves donât fire in the arteries properly and the blood pools in legs and other areas, unable to properly push blood to the brain, so you feel dizzy. I was actually going to reach out to you for help- but miraculously, the crazy system I put her under seems to be working. (Can I just say that they both tried to put her on antidepressants and nothing else? One wanted SSRIs the other talked about the older style antidepressants, having weaned my son off of those- no thank you!!!) I also want to say that since this diagnosis we have encountered 3 other young women with exactly the same diagnosis, this is seriously rampant right now, the symptoms are vague and itâs probably a large bucket of slightly different diagnosisâs but what do I know.
I gave my daughter:
The compression socks, an exercise bike in her room, required daily walks, preferably in sun.
For supplements, vitamin d with k2, she gets a magnesium malate every night (per your article), for mood L-tryptophan and 5-HTP, I threw in riboflavin (B2), L-Glutamine for leaky gut and selenium in case she had a undiagnosed thyroid issue (which they refused to really test). She is now about 95% better. Itâs an incredible transformation.
Still struggling with my son with celiac, though, he has incredible air and now Iâm researching SIBO. Ugh.
Miss you on X. I canât believe they have already enforced the Data act in the UK and thatâs how they censored you. Itâs terrible. I tried sending you a new study that Kevin McKernan shared yesterday about spike in the arteries 17 months later and in 48% stroke victims.
Thank you for sharing this. I also know of a few cases. This isn't medical advice and I'm not a doctor, but tachycardia has been linked to spike-induced vagus nerve damage:
Vagus nerve inflammation contributes to dysautonomia in COVID-19
Have a look at <herv-k102.substack.com> for Nov., 2024. The article gives a statistical assessment of the occurrence of spike protein shedding-related conditions.
Your daughter's POTS looks quite likely to fit the hypothesis. If you can find a physician who can think about this you might find potential treatment.
Spike detox protocols may also be useful. We couldn't get ivermectin when our daughter was forced to take her Covid shots by her employer, but we did use a month of artemisinin.
My friend did not see one multidisciplinary team member on her path to a diagnosis of MND until the last 5 weeks of her life. Her GPs were the gatekeepers who stopped her from entering into that pathway, she was told firmly by each different GP (there were many) a multitude of different causes and it went from an exercise injury to ME/CFS to vitamin deficiency to age related then she was told it was possibly depression, all of the diagnoses was guesswork, not one GP consulted with the other to discuss her case or initiate investigation.
In the end we had to plead with a temporary GP to allow her to be seen by an emergency doctor in hospital, they did so very reluctantly. In reality dealing with the GP can often be an exercise in futility. Once it was recognised in hospital that she was ill the multidisciplinary team took over but this only happened in the last weeks of her life. It is tragic that nothing is learned from any of this which leaves the system free to repeat this mistreatment time after time. In the UK they speak fine words about what should happen with multidisciplinary teams, protocols, flowcharts and investigations but they are just words typed onto paper when the reality is often very late referral at the ground level leading to undocumented misery especially if you are 65yrs or older.
Sabine shared her related investigations:
Possible autoimmune mechanisms through COVID modRNA products
Another underlying basic damage mechanism
https://drbine.substack.com/p/mogliche-autoimmunmechanismen-durch
New paper just published:
Prof. Akiko Iwasaki
@VirusesImmunity
Published today! Victoria Bastos, @KerrieGreene_
et al found two distinct immunotypes of ME/CFS based on the cerebrospinal fluid analysis. Great collaboration with
@MBVanElzakker
@microbeminded2
and the BragĂŠe clinic in Sweden. (1/)
***
Prof. Akiko Iwasaki
@VirusesImmunity
¡
May 16
While we do not know why some people with ME/CFS have elevated MMPs and cytokines, our data suggest potentially distinct drivers of disease that manifest in similar clinical phenotypes. Future studies are needed to probe therapeutic pathways suitable for these clusters. (4/)
https://x.com/VirusesImmunity/status/1923407742183575965
***
Cerebrospinal fluid immune phenotyping reveals distinct immunotypes of myalgic encephalomyelitis/chronic fatigue syndrome
15 May 2025
https://academic.oup.com/jimmunol/advance-article/doi/10.1093/jimmun/vkaf087/8133211?login=false
There is some research that suggests menstruation is a detoxing process, to keep the body in a state of preparedness for pregnancy. Itâs interesting that FM affects women at an age when their period is ceasing.
I looked at the Slay News article linked from Italy regarding the spike protein neurological damage.
I could only see the abstract (too cheap to support the journal by buying the full text!) but they appear to state that Covid infection caused more damage than the shots. This has been common throughout the plandemic. Access to the full dataset often shows that the conclusions don't correspond to the data.
Thank you for the exposition of the fibromyalgia research. We had lectures on diagnosis 35 years ago but treatment was never very successful or satisfying. Maybe understanding the underlying chemistry will promote more useful treatments.
đ
Follow The Science: Why Peter Marks Was Asked To Leave The FDA
... Thanks to Dr. Marksâ terrible decisions, we are left with a drug that has no proven benefit and that just killed a young patient, a vaccine that is not completely safe is being administered to children that have no significant risk of harm from the underlying infection, and an overburdened healthcare system that had to pay billions for another unproven, harmful therapy. Advocates for Dr. Marks claim that he has acted to help patients with life-threatening conditions which have no alternative treatments. But in reality, he catered to industry and hurt patients.
https://realclearwire.com/articles/2025/04/01/follow_the_science_why_peter_marks_was_asked_to_leave_the_fda_1101329.html
Has this area of healthcare progressed since the Middle Ages? They will be putting people on trial for witchcraft next:
"Long Covid patients feel dismissed and unsupported by healthcare providers
People living with Long Covid often feel dismissed, disbelieved and unsupported by their healthcare providers, according to a new study from the University of Surrey.
The study, which was published in the Journal of Health Psychology, looked at how patients with Long Covid experience their illness. The study found that many patients feel they have to prove their illness is physical to be taken seriously and, as a result, often reject psychological support, fearing it implies their symptoms are "all in the mind".
We found that the problem isn't people with Long Covid refusing help â it's about the deep need for people to be believed. When a patient feels dismissed, offering psychological support instead of medical care can be misconstrued as insulting.""
More:
https://www.msn.com/en-gb/health/other/long-covid-patients-feel-dismissed-and-unsupported-by-healthcare-providers/ar-AA1BOdO4
Just had a scary health crisis with my 16 yr old daughter (unvaxxed). January got random very high pulse. Soon it accompanied every activity she did, oftentimes spiking to 160 or 170 even if she was walking, or just sitting and doing nothing. She had real difficulty climbing stairs. Went to the GP and the cardiologist- they said, disautonomia , a variant of POTS. They seriously donât know how to treat it, they only know how to prescribe pills. So we were told to use compression socks and do more exercise and electrolytes and a lot of water. My daughter presented with weird red patches under her eyes, apparently, the nerves donât fire in the arteries properly and the blood pools in legs and other areas, unable to properly push blood to the brain, so you feel dizzy. I was actually going to reach out to you for help- but miraculously, the crazy system I put her under seems to be working. (Can I just say that they both tried to put her on antidepressants and nothing else? One wanted SSRIs the other talked about the older style antidepressants, having weaned my son off of those- no thank you!!!) I also want to say that since this diagnosis we have encountered 3 other young women with exactly the same diagnosis, this is seriously rampant right now, the symptoms are vague and itâs probably a large bucket of slightly different diagnosisâs but what do I know.
I gave my daughter:
The compression socks, an exercise bike in her room, required daily walks, preferably in sun.
For supplements, vitamin d with k2, she gets a magnesium malate every night (per your article), for mood L-tryptophan and 5-HTP, I threw in riboflavin (B2), L-Glutamine for leaky gut and selenium in case she had a undiagnosed thyroid issue (which they refused to really test). She is now about 95% better. Itâs an incredible transformation.
Still struggling with my son with celiac, though, he has incredible air and now Iâm researching SIBO. Ugh.
Miss you on X. I canât believe they have already enforced the Data act in the UK and thatâs how they censored you. Itâs terrible. I tried sending you a new study that Kevin McKernan shared yesterday about spike in the arteries 17 months later and in 48% stroke victims.
Look at HPV vax implication in POTS. Rampant. And HPV was the precursor to Covid vax.
Very scary. Iâm very happy she didnât get the HPV vax either.
Thank you for sharing this. I also know of a few cases. This isn't medical advice and I'm not a doctor, but tachycardia has been linked to spike-induced vagus nerve damage:
Vagus nerve inflammation contributes to dysautonomia in COVID-19
https://pmc.ncbi.nlm.nih.gov/articles/PMC10412500/
Gut-brain axis > Kefir, prebiotics, probiotics, Mg etc
Also, anti depressants would only harm the gut-brain axis. So naturally, thatâs what they push on everyone.
Have a look at <herv-k102.substack.com> for Nov., 2024. The article gives a statistical assessment of the occurrence of spike protein shedding-related conditions.
Your daughter's POTS looks quite likely to fit the hypothesis. If you can find a physician who can think about this you might find potential treatment.
Spike detox protocols may also be useful. We couldn't get ivermectin when our daughter was forced to take her Covid shots by her employer, but we did use a month of artemisinin.
This is great info- thank you so much!
My friend did not see one multidisciplinary team member on her path to a diagnosis of MND until the last 5 weeks of her life. Her GPs were the gatekeepers who stopped her from entering into that pathway, she was told firmly by each different GP (there were many) a multitude of different causes and it went from an exercise injury to ME/CFS to vitamin deficiency to age related then she was told it was possibly depression, all of the diagnoses was guesswork, not one GP consulted with the other to discuss her case or initiate investigation.
In the end we had to plead with a temporary GP to allow her to be seen by an emergency doctor in hospital, they did so very reluctantly. In reality dealing with the GP can often be an exercise in futility. Once it was recognised in hospital that she was ill the multidisciplinary team took over but this only happened in the last weeks of her life. It is tragic that nothing is learned from any of this which leaves the system free to repeat this mistreatment time after time. In the UK they speak fine words about what should happen with multidisciplinary teams, protocols, flowcharts and investigations but they are just words typed onto paper when the reality is often very late referral at the ground level leading to undocumented misery especially if you are 65yrs or older.
Thank you for sharing this shockingly bad, but all too familiar story.
How it should work, Vs reality.
It's "free at the point of care", but what care?
Bioweapon
its just poisioning