A massive new peer-reviewed review (161 studies, 2+ million patients) makes it clear.
COVID-19 isn’t just a respiratory infection.
It’s a multi-system disease leaving lasting scars on lungs, heart, brain, kidneys, and more.🧵
Among hospitalized patients the numbers are stark.
Lungs - 78% affected
Heart - 32%
Nervous system - 43%
Kidneys - 28%
Months later, 10-35% still live with organ dysfunction.
Why? The virus triggers:
a cytokine storm (immune system fire),
endothelial injury (blood vessels damaged),
micro-clots that choke tiny capillaries.
In hospital wards we’ve seen it all.
Lungs scarred, oxygen capacity never the same.
Hearts inflamed, misfiring into arrhythmias.
Brains hit with strokes, encephalitis, or lingering brain fog.
Kidneys failing, some never recovering.
Immune systems knocked off balance, even turning against the body.
Variants changed the picture but not the playbook.
Delta hit harder in the lungs.
Omicron shifted to upper airways, with less loss of smell/taste.
But the core mechanisms - vascular injury, inflammation, clotting - remain.
But what about those who never set foot in a hospital?
This is where the story often gets dismissed.
No oxygen, no ICU, you’re fine.
Except - many aren’t.
The data on mild cases is harder to pin down - studies use different definitions, follow people for different lengths of time.
That’s why this review doesn’t give hard percentages for non-hospitalized patients.
Still, the evidence is consistent:
Even after mild COVID, people report and show measurable changes.
Lungs - lingering breathlessness, chronic cough, exercise intolerance, even post-COVID asthma.
Heart - chest pain, palpitations, POTS-like dysautonomia.
Brain - brain fog, memory lapses, persistent loss of smell/taste, neuropathy.
Kidneys - subtle declines in function (protein in urine, lower eGFR).
Gut & liver - IBS-like symptoms, altered gut microbiome, sometimes persistent enzyme elevation.
Immune & hormones - crushing fatigue, new autoantibodies, disrupted menstrual cycles, lowered testosterone.
Mental health - anxiety, depression, PTSD, insomnia, slowed cognition.
The difference isn’t whether damage exists.
The difference is how it shows up.
Hospitalized - dramatic, organ failure, visible on scans.
Mild cases - quieter, widespread dysregulation that chips away at quality of life.
The authors conclusion is blunt -
COVID-19 is a multi-system infection with silent aftermaths.
It requires long-term monitoring, multi-disciplinary care, and targeted therapies.
This was never just the flu.
Ochilov at al., Silent Invasion: COVID-19’s Hidden Damage to Human Organs 2025. mdpi.com/2673-8112/5/9/…
The cost isn’t just human.
Ongoing disability, reduced productivity, long-term medical care - COVID’s hidden damage is already reshaping healthcare systems and economies.
The price tag will echo for decades. @szupraha @ZdravkoOnline
None of this was inevitable.
With stronger public health response - better prevention, ventilation, vacc strategies - we could have reduced both the human and economic toll.
Ignoring COVID’s long shadow only compounds the loss.
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One mystery of Long COVID - why immune cells get stuck in a harmful, inflammatory mode.
A new study shows the switch is metabolic - and a single checkpoint can decide whether Th17 cells protect or drive disease.🧵
In both children and adults with Long COVID, we see immune cells stuck in a harmful mode.
Among them - Th17 cells, which can either protect us or drive chronic inflammation.
A new study in Science Signaling, 2025 uncovers why these cells flip - and what keeps them locked in the pathogenic state.
Th17 cells have two faces -
non-pathogenic (protective, balanced),
pathogenic (autoimmune, chronic inflammation).
The critical switch? Cellular metabolism.
“Up to 5 million people worldwide may be walking around with hidden heart damage after COVID - their hearts silently struggling months or even years later.”
Estimate from the European Society of Cardiology (2025).
The first spotlight.🧵
Europe’s leading cardiology authority has issued official guidance on COVID’s cardiovascular impact.
Published in the European Journal of Preventive Cardiology.
This is the real manual for what to do - a long-awaited step that gives hope change is possible.
Because until now, patients were left in the dark.
No clear communication of risk
No instructions for doctors.
No pathway for care.
COVID was treated as over once the infection passed.
Children after mild or ordinary COVID-19 show measurable brain changes. Some improve, others persist.
This is a peer-reviewed MRI study in Brain and Behavior, 2025.
MRI data in children are still scarce - every study counts.🧵
Importantly, all cases were mild-to-moderate - no severe illness - yet measurable brain changes were still detected.
Study design
26 children (8-12 yrs) after COVID-19 vs 26 healthy controls
MRI analyzed at the group level - consistent differences between groups.
This means - we can’t say exactly X kids had changes but as a group, post-COVID children showed significant alterations compared to controls
Children don’t just bounce back after COVID.
A Bavarian study shows deep neurocognitive and emotional impacts in kids & teens - fatigue, loss of motivation, attention problems, mood disorders.
What they found🧵
85 children, ages 2-17 (avg 12.5, 61% girls). All had confirmed COVID and symptoms lasting ≥4 weeks.
They underwent multidisciplinary exams - psychiatry, neurology, cardiology, pulmonology, gastro + neuropsychological testing.
Most common symptoms.
fatigue (82%)
loss of motivation (73%)
attention/concentration problems (72%)!
low mood (53%)
anxiety (32%)
post-exertional malaise (70%)!
Not just stress.
SARS-CoV-2 can turn our own defenders into traitors.
A study in Sci Transl Med, 2025 shows the virus drives neutrophils into PMN-MDSCs cells that don’t fight, but suppress T cells.🧵
Instead of attacking the virus, these neutrophils hit the brakes on adaptive immunity.
T cells divide less, signal less.
The immune response collapses from within - right when it should be gaining strength.
And this is not just correlation.
Simply exposing neutrophils to SARS-CoV-2 in vitro was enough to reprogram them.
Contact with viral particles or proteins alone triggered the shift into PMN-MDSCs.
The virus can actively manipulate immunity from the start - not just passively ride the inflammation.
New study: SARS-CoV-2 doesn’t just lower white cell counts - it reshapes the T-cell landscape. Both the numbers and the quality of T-cells drop, especially in older and severely ill patients. And this has consequences. 🧵
Acute COVID-19 = a blow to T-cells. Patients had markedly lower absolute numbers of T-lymphocytes (CD4+, CD8+, naive and memory) compared to healthy controls. Classic lymphopenia - COVID cuts into the immune arsenal from the start. The immune system starts the fight with half its arsenal already gone.
Severity mirrors depth of the crash. The sickest patients had the lowest lymphocyte counts, especially CD8+ and naive T-cells. The steeper the disease, the deeper the T-cell depletion.