I am a Christian, Conservative Southern Lady; 26+ yrs married. I Love Nature. ME/CFS & LC
Any tweets are of my opinion and are not intended as medical advice.
@zufrieden275 I have moments where I attempt to process all the bad, but it becomes to much. So I lay it down. I don’t forget, or fall asleep, but Gods feet is where a lot of my troubles land.
BREAKING:
78-year-old pastor Clive Johnston has been convicted in Ireland for publicly reading the Bible verse John 3:16
The judge claims abortion-minded women could be influenced to choose life for their unborn babies.
He made no direct mention of abortion.
Pray for him 🙏
I am continuing to deal with the effects of #LC and #MECFS. I too, have noticed having these crescent shapes that are crimson red and very noticeable. Thanks for sharing.😃
If you have Long Covid or MECFS, Most of you will have these Crimson Crescents which is a sign of Chronic Immune Activation. #LongCovid#pwME#POTS#Dysautonomia#pwLC
Thank You Dr. Gustavo for posting this information. It is very insightful for all and helps those of us trying to do research. Sharing important information such as this can lead to answering many questions and offers hope to all who are affected.
We reaffirm that
THE MAIN AND MOST FREQUENT CAUSE OF
CHRONIC FATIGUE SYNDROME/MYALGIC ENCEPHALOMYELITIS (ME/CFS)
IS PERSISTENT ZOONOTIC INFECTIONS.
https://t.co/XKl7nhXeGC
There are other less frequent causes,
but persistent infections with Babesia, Bartonella, Borrelia (BBB), and Mycoplasma are the most frequent cause of ME/CFS in patients from Europe, North America, Australia, Russia, and South Africa.
There should no longer be any doubt about this.
The four infections mentioned can be detected using a basic test that is over 100 years old: the PERIPHERAL BLOOD SMEAR (PBS).
It is inexpensive and only requires a drop of blood, which is spread on a glass slide for observation under a light microscope.
It is important that the visualization be performed by an experienced professional.
This is an examination that should be performed on all patients with ME/CFS.
We also recommend it for all patients with any chronic illness who have neuropsychiatric symptoms, including children.
After the PBS, the patient should undergo serological and PCR tests for the specific detection of pathogens. However, it is important to keep in mind that serological tests can produce false negatives.
As with medications, because it is an inexpensive test, the use of the PBS is minimized in favor of more expensive tests.
Regarding funding, grants, and financial support for research studies, these should focus on treatments against the etiological agents, which are the root cause of the symptoms. However, after more than 30 years of research without progress, this is unlikely to happen. As some researchers have already stated, only studies that go around in circles without solving the problem are funded, since there are enough contributions and grants for about 30 more years of research.
Regarding treatment, on page 4 of the report we published, we mention the drugs and supplements included in current treatment protocols.
However, the practical problem is that these drugs are not patented and are not expensive, so large pharmaceutical companies, other institutions, and research groups are unlikely to support their use. On the contrary, the use of low-cost drugs is criticized and attacked as a major threat to their revenue. This has already been seen during the COVID pandemic: safe medications, widely used, including in young children, suddenly became unsafe, and yet institutions and paid media outlets warned against their use.
Patients in Europe and North America would have to seek out doctors experienced in treating persistent infections caused by Babesia, Bartonella, Borrelia (BBB), and Mycoplasma. Unfortunately, these infections are still considered rare in medical schools, so doctors practically graduate without any knowledge of them.
Thank You Dr. Gustavo. Your assessment valuble. I've been trying to give credence to this for a long time. To patients and medical professionals. The root cause is a vital component to getting positive answers. Unfortunately, this is not what is being addressed. Thank You for all your professional input. It's greatly appreciated ❤️
Case Report:
A FEMALE PATIENT, WHO HAS BEEN ILL FOR 40 YEARS AND IS BEDRIDDEN.
At age 11, she suffered tick bites, which subsequently caused great weakness, severe fatigue, and other persistent symptoms.
Her primary diagnosis is ME/CFS (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome).
She has also been diagnosed with:
· Postural orthostatic tachycardia syndrome (POTS), Dysautonomia.
· Low cortisol and adrenal insufficiency.
· Persistent digestive problems and gastrointestinal dysbiosis.
· Food and chemical allergies and intolerances.
· Hypersensitivities (to light and noise).
Of all the diagnoses mentioned, none are Etiological Diagnoses.
These are all diagnoses that refer to the consequences of the lesions caused by the etiological agents and the body's responses to these agents.
The causative agents are different from the human body itself, they are primarily microorganisms, toxins, and allergens.
THE FOLLOWING WERE IDENTIFIED IN THE BLOOD SMEAR:
· BABESIA (Parasite).
· BARTONELLA (Bacteria).
· MICROSPORIDIA (Opportunistic Fungus).
THESE ARE ETIOLOGICAL DIAGNOSES.
I am certain that the diagnosis of Chronic Fatigue Syndrome is incomplete; it is a mistake to rely solely on this diagnosis based on symptoms, as it fails to address the root causes.
Universities should teach how to make Etiological Diagnoses and Treatments.
Funded research has not achieved significant progress.
If a chronic illness affects multiple systems (musculoskeletal, brain, heart, intestines, adrenal glands, etc.), the presence of hematogens should be investigated. A peripheral blood smear is essential.
In this case, the patient has spent practically her entire life bedridden. This basic and inexpensive test has never been performed.
Regarding materials, the blood smear only requires 3 to 4 glass slides, which are then sent to an experienced physician for examination using an optical microscope.
We have reported several similar cases; see details in the following publications:
https://t.co/XKl7nhXeGC
https://t.co/pKpBVwq3a7
The Historical Importance of the 1934 Los Angeles County Hospital Outbreak and beyond
"The 1934 Los Angeles County General Hospital outbreak is one of the most fascinating and little-known medical events in American history — and also one of the most covered-up by institutional authorities for decades. It’s a foundational episode in understanding the origins of certain chronic, poorly understood illnesses such as Myalgic Encephalomyelitis (ME), often misbranded later under the trivializing term chronic fatigue syndrome (CFS)."
Continued👇👇👇
https://t.co/B01uz0TUi4
Schools should have EXACTLY ONE FLAG flying out front and in the classroom, THE AMERICAN FLAG.
Period.
No rainbow flags, no foreign flags, no activist banners… just Old Glory waving high!
One Nation. One Flag. One Pledge.
😱 I AM ABSOLUTELY SHOCKED — JAW ON THE FLOOR after watching this video dropped TODAY (May 9, 2026).
How is this not front-page news everywhere?!
DNA scientist Dr. David J. Speicher drops bombshells on Joe Rogan re: clear FRAUD in the mRNA shots that could blow up their liability protection.
They safety-tested one version made WITHOUT DNA plasmids… then injected millions with a completely different product loaded with massive untested DNA contamination, including the SV40 promoter (known carcinogen).
Kevin McKernan’s sequencing of real injected vials confirmed plasmids everywhere. This explains the turbo cancer explosion.
They lied saying genome integration was “impossible.”
Criminal!
Full video transcript:
“Because of the fact that it’s classified as a vaccine, they don’t have to worry about being sued?”
“Well, they do. They do. The immunity from liability is dependent on there having been no fraud and there clearly was fraud.”
[continuing with the rest of the transcript as before…]
This is the smoking gun — Process 1 vs Process 2, residual DNA with SV40, turbo cancers. They KNEW. When does accountability hit?! Repost if you’re furious. We demand the truth! 🤯💉🔥
Posted May 9, 2026 — Video via @thehealthb0t — Watch & share the full clip
I hopped over to James' Instagram and cried so much for him last night.
And I just keep getting angry because many people with severe ME/CFS seem to have hypermobility which means
1.) Treatment-resistant mast cell involvement requiring monoclonal antibodies (Xolair) to stop mast cell mediators from continuing to inflame/damage the brain and spine, and other drugs that block mast cell/mast cell mediator neuroinflammation (Celebrex, Qulipta, antihistamines, etc.)
2.) Doxy and/or methylene blue to lower collagen-degrading enzymes --the matrix metalloproteinases (MMPs)---to help to restore extracellular matrix
3.) Specialized lympathic drainage (@PerrinTechnique) to support clearance of toxin build-up in the body
4.) Advanced microscopy/live blood analyses and/or cerebral spinal fluid extraction and analyses to look for the underlying infection(s) triggering this illness because the immune system isn't able to mount an antibody response WHICH DOES NOT MEAN IT IS NOT PRESENT --and treat the infection!!!
5.) Advanced spine and vascular imaging to detect CCI, AAI, Chiari formation, tethered cord, CSF leaks, vascular compression syndromes, etc. GI motility testing
I am a health systems administrator with hEDS and ME/CFS who figured this out in about 6 months, and I have A LOT of questions for physicians who can't seem to treat patients at all.
If I didn't currently work in Medicaid long term services and supports and was back writing business plans for hospitals, I would design the world's best clinic for this.
BREAKING: We did it.
We have formally filed a Citizen’s Petition to the
@FDA
demanding that HCQ and Ivermectin be made available over the counter.
This isn’t just about medication—it’s about your fundamental right to medical freedom.
We will not let the medical industrial complex dictate what you can and cannot access.
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