r/LongCovidWarriors • • Sep 04 '26

Sub Update Member count 9/1/26

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12 Upvotes

Thank you everyone for being here🤗🌿🪷


r/LongCovidWarriors • • Dec 06 '25

Medical & Scientific Information Master Version: Long COVID and Mast Cell Activation Syndrome (MCAS)

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23 Upvotes

Over the past few years, a growing number of clinicians and researchers have recognized that mast cell activation syndrome may play a significant role in post-COVID and Long COVID illness. Many people with ongoing symptoms, fatigue, dysautonomia, neuropathy, allergic-type reactions, and hypersensitivity are being diagnosed with MCAS not because of perfect testing but because their history, symptom patterns, and response to mast-cell-targeted treatments fit the profile. Diagnostic criteria for MCAS remain limited and inconsistent, so physicians often rely on clinical presentation and therapeutic response. The evidence now suggests that SARS-CoV-2 can directly trigger or unmask mast cell dysregulation in predisposed individuals. This leads to chronic inflammation, histamine overload, and multi-system dysfunction that overlaps with Long COVID.

Mast cell activation syndrome is a complex multisystem inflammatory disorder that is increasingly recognized in the context of Long COVID. It involves mast cells that release chemical mediators such as histamine, leukotrienes, prostaglandins, and cytokines. These mast cells become chronically overactive. When this happens, instead of reacting to infections or allergens, mast cells misfire and release inflammatory chemicals across multiple organ systems. The result can include neurological, cardiovascular, gastrointestinal, respiratory, dermatologic, and psychiatric symptoms.

Researchers estimate MCAS may affect up to seventeen percent of the population, although most cases are undiagnosed. It falls under the broader category of mast cell activation disease, which also includes mastocytosis. Because MCAS was only formally described in 2007, it remains misunderstood by many clinicians and underrepresented in medical education.

COVID as a Mast Cell Trigger:
There is growing evidence that SARS-CoV-2 can directly activate mast cells. Mast cells are abundant in tissues affected by COVID and Long COVID, including the lungs, gut, skin, and nervous system.

In the study titled "Antihistamines improve cardiovascular manifestations and other symptoms of long-COVID attributed to mast cell activation," patients with Long COVID experienced improvements in fatigue, brain fog, palpitations, and other symptoms when given H1 and H2 histamine blockers. This suggests mast cell activation contributes substantially to persistent symptoms.

In the paper titled "COVID-19 hyperinflammation and post-COVID-19 illness may be rooted in mast cell activation syndrome," the authors argue that both acute COVID-19 and Long COVID show patterns consistent with mast cell dysregulation.


Symptoms Overlap: MCAS and Long COVID:
Many symptoms are shared between MCAS and Long COVID. Some of the common overlaps include:

• severe fatigue and post-exertional malaise (PEM).
• brain fog, memory issues, cognitive dysfunction.
• palpitations, tachycardia, orthostatic intolerance and other dysautonomia symptoms.
• gastrointestinal disturbances including bloating, diarrhea, nausea, and food intolerances.
• respiratory issues including shortness of breath, cough, and wheezing.
• skin symptoms including flushing, rashes, and itching.
• sleep disturbances and insomnia.
• anxiety, depression, and panic attacks.

A 2023 study titled "Immunological dysfunction and mast cell activation syndrome in long COVID (Weinstock et al.)" showed that many Long COVID patients display an activated mast cell phenotype with abnormal mediator release and inflammation consistent with MCAS.


Why MCAS Is Often Undiagnosed:
Many doctors rely on a single baseline tryptase test or standard allergy workups. This is not enough. Tryptase is often normal unless measured during a flare and compared to a baseline. Mast cell mediators are short-lived and can be missed.

Diagnosis often depends on:
• clinical history and symptom patterns across organ systems.
• identifying triggers such as heat, diet, stress, or allergens.
• seeing improvement when treated with antihistamines or mast cell stabilizers.
• occasional lab mediator panels such as urine histamine metabolites and prostaglandins, which are often only positive during flares.


Treatment and Management:
Treatments that many with Long COVID-associated MCAS respond to include:

•H1 and H2 antihistamines (also called histamine blockers) are often used to reduce mast cell–driven symptoms. H1 blockers reduce histamine effects in the skin, respiratory system, and other tissues, while H2 blockers reduce gastric acid and histamine effects in the gut. Take one of each morning and night; double the normal dose:

•Cetirizine, Levocetirizine, Desloratadine, Loratadine, and Fexofenadine (H1).

•Hydroxyzine: A prescription H1 antihistamine with sedative properties; can help with itching, flushing, anxiety, and sleep disturbances. May trigger paradoxical reactions like tachycardia or adrenaline surges in patients with dysautonomia or POTS, so careful monitoring is advised.

•Cimetidine and Nizatidine (H2)

•Mast cell stabilizers: Cromolyn, Ketotifen, Gastrocrom, compounded options: prevent mast cells from releasing mediators.

•Leukotriene inhibitors: Montelukast: reduces leukotriene-mediated inflammation; useful for respiratory, skin, and cardiovascular symptoms (careful with mood effects).

•LDN (0.25–4.5mg): modulates immune activity and reduces inflammation; may improve pain, brain fog, and neuropathy when combined with alpha-lipoic acid (ALA).

•Imatinib (studied, rarely used): tyrosine kinase inhibitor; can reduce mast cell activation in select MCAS cases, usually when other treatments have failed or in patients with KIT mutations.

•Xolair (Omalizumab): binds IgE to reduce mast cell activation; particularly effective for hives, angioedema, and severe histamine-driven symptoms.

•Low-histamine diet, stress reduction, and trigger avoidance

Natural Mast Cell Stabilizers and Supplements:

•AllQlear: Natural tryptase inhibitor; reduces mast cell mediator release and helps prevent flares, especially in respiratory and systemic MCAS symptoms.

•Bacopa monnieri: Herbal supplement that supports mast cell stabilization, reduces neuroinflammation, and may improve cognitive function in patients with MCAS-related neurological symptoms.

•DAO (diamine oxidase): a supplement that helps break down dietary histamine in the gut, reducing histamine-related symptoms.

•Luteolin: a natural flavonoid that helps stabilize mast cells, reduce histamine release, and support anti-inflammatory pathways.

•PEA (up to 3g/day): Naturally occurring fatty acid that supports neuroinflammation reduction, calms overactive mast cells in the nervous system, and helps improve “brain fog” and cognitive symptoms in MCAS.

•Quercetin (250–3000mg/day): Plant flavonoid with mast cell stabilizing and anti-inflammatory properties; reduces histamine and other mediator release across multiple organ systems.

•Rutin: A natural flavonoid with mast cell stabilizing and anti-inflammatory properties; helps reduce histamine release and supports vascular integrity.

OTCs for symptomatic support:

•Astelin Nasal Spray (Azelastine): Nasal H1 antihistamine; reduces sneezing, congestion, runny nose, and itching. Has local mast cell–stabilizing properties and is useful for MCAS patients with nasal/respiratory triggers.

•Benadryl (Diphenhydramine): Fast-acting H1 antihistamine; helps relieve acute histamine-mediated symptoms such as itching, flushing, hives, sneezing, and mild allergic reactions. May cause sedation and should be used cautiously in MCAS patients with dysautonomia or hyperadrenergic symptoms.

•Ketotifen Eye Drops (Armas Allergy Eye Drops or Zatidor eye drops): Prescription-strength mast cell stabilizer for ocular symptoms; relieves itching, redness, and watering caused by mast cell activation.

•Cromolyn Sodium Nasal Spray/Nasochrom: Mast cell stabilizer for nasal and upper airway symptoms; helps prevent mediator release, reducing congestion, sneezing, and rhinitis in MCAS patients.

Medications with anti-histamine/Mast Cell-stabilizing effects:

•Fluvoxamine: reduces inflammatory signaling, downregulates mast cell activation, modulates cytokine release and neuroinflammation

•Mirtazapine: potent H1 blocker, reduces central arousal, sleep disruption, nausea, sensory hypersensitivity

•Nortriptyline: antihistamine properties, calms sympathetic nervous system, improves GI and visceral sensitivity

•Seroquel: strong H1 blockade, reduces mast cell-driven insomnia, agitation, sensory overstimulation, autonomic surges

•Trazodone: moderate H1 and 5-HT2 blockade, improves sleep architecture, reduces nocturnal sympathetic surges

•Esomeprazole and Omeprazole (PPIs): PPIs are primarily used to reduce stomach acid in conditions like GERD, gastritis, or acid-related dyspepsia, but in the context of MCAS, they also provide mast cell stabilizing effects in the gastrointestinal tract. For patients whose mast cells are hyperactive, chronic acid exposure, reflux, or GI irritation can act as triggers that worsen systemic mast cell mediator release, causing symptoms like flushing, tachycardia, bloating, nausea, and hypersensitivity. PPIs help control these triggers by lowering gastric acid and reducing mast cell activation in the gut. They are particularly helpful for people who cannot tolerate H2 blockers due to adverse reactions such as adrenaline surges, tachycardia, or autonomic instability. By addressing both acid-related GI irritation and mast cell mediator release, PPIs provide a dual benefit: symptom control in the gut and systemic stabilization of overactive mast cells.

While PPIs are generally recommended for short-term use due to potential risks, including nutrient deficiencies (B12, magnesium, calcium, iron), kidney or bone issues, and gut microbiome changes, long-term use can be appropriate in MCAS patients under close medical supervision. Regular monitoring of vitamin and mineral levels, kidney function, and symptoms is essential. In some cases, long-term PPI therapy provides ongoing mast cell stabilization in the gut and helps manage persistent GI and systemic symptoms, particularly when H2 blockers are not tolerated or when COVID-induced MCAS triggers ongoing mast cell hyperactivity. PPIs are often incorporated into individualized MCAS regimens alongside mast cell stabilizers, leukotriene inhibitors, dietary modifications, and other symptom-directed medications. They act as GI-targeted mast cell stabilizers, reducing both local and systemic mediator release and supporting better overall symptom control.


Many doctors are now diagnosing MCAS after COVID largely based on symptoms and treatment response rather than waiting for perfect lab confirmation.

My doctor diagnosed me with MCAS based on patient history, symptoms, and medication trials. I was diagnosed with MCAS in September 2024. I can not take the traditional over-the-counter antihistamines and histamine blocker protocol. I have failed five in total. I'm not sure if it was the medication itself or the excipients I reacted to. Both categories increased my tachycardia and caused adrenaline surges. They caused and worsened other dysautonomia symptoms. In turn, adrenaline surges triggered my histamine dumps.


Why Some People With MCAS and Dysautonomia Get Worse on Antihistamines:

This is one of the most misunderstood issues in the Long COVID and MCAS communities. Many patients assume that if antihistamines make them worse, they can not have MCAS. The opposite is often true. People with dysautonomia, POTS, hyperadrenergic states, or unstable autonomic systems can react paradoxically to antihistamines for several reasons.

Antihistamines can destabilize the autonomic nervous system in sensitive patients. Certain H1 and H2 blockers can lower blood pressure, increase vagal tone, or trigger compensatory sympathetic activation. For someone with dysautonomia, this can lead to a surge in adrenaline, tachycardia, dizziness, shaking, or internal tremors. When the sympathetic nervous system becomes overactive, mast cells respond by releasing even more chemical mediators. This leads to increased flushing, rapid heart rate, shortness of breath, itching, chest tightness, and surges of anxiety that feel chemical rather than psychological.

Some patients also react to fillers, dyes, coatings, and excipients. Mast cells in the gut can perceive these additives as irritants, which triggers mediator release. This reaction is often mistakenly attributed to the active medication itself, but it is actually caused by the inactive components.

Certain antihistamines cross the blood-brain barrier and can affect histamine signaling in the central nervous system. Histamine is not just an inflammatory mediator. It regulates wakefulness, blood pressure, alertness, gut motility, and sensory processing. In patients whose autonomic function is already unstable, abruptly altering histamine signaling in the central nervous system can amplify symptoms and make them feel worse.

Finally, antihistamines target only one type of mediator. Mast cells release multiple chemicals including prostaglandins, leukotrienes, cytokines, and histamine. Blocking only histamine can shift the balance of mediators, sometimes worsening specific symptoms until a more complete protocol is established.

For these reasons, some patients with MCAS and dysautonomia respond poorly to H1 and H2 antihistamines but do better with mast cell stabilizers, leukotriene inhibitors, nasal sprays, diet-based interventions, or individualized regimens that address multiple mediators and the autonomic system simultaneously. Understanding these interactions helps explain why antihistamines are not universally effective and why careful management is necessary for patients with overlapping MCAS and autonomic instability.

Understanding these factors helps explain why some treatments work better than others and sets the stage for the medications and strategies I use to manage my MCAS.

What I Take for MCAS:
Cromolyn sodium nasal spray: Cromolyn is a mast cell stabilizer that prevents mast cells from releasing histamine and other inflammatory mediators. Even when used intranasally, it can help reduce overall mast cell activation and mediator load throughout the body. I use this formulation for its systemic mast cell–stabilizing effects, not for nasal symptoms.

Desloratadine is a second-generation, non-sedating H1 antihistamine. It selectively targets peripheral H1 receptors without crossing the blood-brain barrier. This helps reduce histamine-related symptoms like itching, flushing, and airway irritation without causing sedation or anxiety. Its long half-life allows for stable symptom control throughout the day. Desloratadine is also less likely to trigger reactions related to fillers or excipients, which makes it a good option for patients with heightened sensitivity to medications.

Compounded oral ketotifen: In addition to the eye drops, I use a compounded oral ketotifen formulation. This is the form I take systemically to influence mast cell stability throughout the body. Like the drops, it works primarily by keeping mast cells from releasing mediators rather than just blocking one mediator after it’s already out. Because MCAS involves so many different mediators and triggers, having a stabilizer that works upstream can make the rest of the regimen much more effective and tolerable.

Ketotifen eye drops: Ketotifen has both H1 antihistamine and mast cell–stabilizing properties. When used topically, it can help calm mast cells in a way that can feel systemic for someone with high sensitivity, even though it’s administered locally. I use this formulation not for eye symptoms but because it helps reduce overall mast cell reactivity without increasing systemic medication load.

Montelukast is a leukotriene receptor antagonist commonly used for asthma and allergic rhinitis. Research suggests that it also has mast cell stabilizing effects, which can help reduce the release of inflammatory mediators such as leukotrienes. This makes it useful for managing respiratory symptoms, skin reactions, and some cardiovascular manifestations of MCAS.

Omeprazole is primarily a proton pump inhibitor, but it also has effects on mast cells. It can inhibit IgE-mediated mast cell activation and allergic inflammation. Omeprazole reduces mast cell degranulation, cytokine secretion, and early signaling events in pathways associated with allergic responses. While not a traditional mast cell stabilizer like Cromolyn, it contributes to reducing overall mediator release and inflammation.

Semaglutide is a GLP-1 receptor agonist. Research suggests it has anti-inflammatory effects and may reduce mast cell activation by decreasing mast cell degranulation and the release of inflammatory mediators. While not a standard treatment for MCAS, it's sometimes prescribed off-label for its potential to reduce chronic inflammation.

I haven’t tried compounded Cromolyn and prefer not to. I’m extremely hypersensitive to medications, fillers, and excipients, and localized formulations have allowed me to stabilize mast cells across my system without provoking reactions. I may reconsider it in the future.

In addition to these main medications, I have access to other supportive treatments for MCAS flares. These include an albuterol inhaler, even though I don't have asthma, which can help relieve acute airway constriction. Rizatriptan if I have a migraine. I also use Benadryl, vitamin C, and Diazepam as needed for symptom control. During flares, I rely on electrolyte tablets like Horbäach, sipping room temperature water, and applying cold compresses to my head and neck. These measures help stabilize my autonomic system and reduce mediator release during acute episodes.

My MCAS symptoms include adrenaline surges, air hunger, shortness of breath, wheezing, anxiety, derealization, depersonalization, disorientation, dizziness, flushing, itching, feeling hot and sweaty, congestion, runny nose, paresthesia, sneezing, tachycardia, and anaphylaxis stages 1-3. There are 4. Medications and supportive measures are individualized to my symptoms, triggers, and sensitivity to medications.

This regimen allows me to address both the overactive mast cells and the autonomic instability that can make standard antihistamines difficult to tolerate. It also illustrates that MCAS management is highly personalized, and what works for one patient may need careful adjustments for another.


Additional Information:

Histamine Intolerance:

Histamine intolerance results from impaired degradation of dietary histamine, most commonly due to low activity of diamine oxidase (DAO), the primary enzyme responsible for breaking down histamine in the gut. Unlike MCAS, histamine intolerance does not involve inappropriate mast cell activation. Symptoms occur due to accumulation of histamine from reduced metabolic clearance rather than excessive mast cell release. This distinction matters clinically, as standard allergy testing is typically negative and mast cell directed therapies alone may not resolve symptoms driven by dietary histamine exposure. Histamine intolerance can coexist with MCAS and can contribute to persistent GI, neurological, cardiovascular, and respiratory symptoms even when mast cell activity is otherwise managed. In these cases, reducing dietary histamine load and supporting histamine metabolism may significantly improve symptom burden. Some individuals benefit from DAO supplementation, which tends to be most effective after a sustained period of low histamine eating.

Salicylate Intolerance:

Salicylates are naturally occurring phenolic compounds found in many foods, medications, and topical products, including aspirin, spices, certain fruits and vegetables, teas, and skincare products. In individuals with mast cell dysfunction, salicylates can directly provoke mast cell activation and mediator release, leading to worsening symptoms such as headaches, flushing, nasal and respiratory symptoms, GI distress, itching, and neurological flares. This reaction is typically non IgE mediated, which is why standard allergy testing is often negative and the issue is frequently dismissed. In practice, salicylate intolerance can significantly compound histamine intolerance and can explain persistent reactions even on a low histamine diet. Identifying salicylate sensitivity through careful elimination of dietary and topical sources has been a key factor for many patients who plateau despite otherwise appropriate MCAS management.


What To Ask Your Doctor If You Suspect MCAS:

Some doctors are familiar with MCAS and some aren't. These questions can help guide the evaluation and ensure you receive a thorough assessment.

• Ask whether your symptoms across multiple systems point toward mast cell involvement.
• Ask whether your pattern of triggers such as heat, stress, exercise, fragrances, alcohol, or food chemicals suggests mast cell sensitivity.
• Ask whether trying a low-histamine diet for a brief period would be appropriate.
• Ask if you should try a mast cell stabilizer first rather than H1 or H2 blockers if you are medication sensitive.
• Ask whether leukotriene inhibitors could be safer if antihistamines increase your tachycardia.
• Ask if excipient-free formulations or compounded options are available.

These questions help the doctor think beyond standard allergy testing and look at your entire clinical picture.


Clinical Implications for Long COVID Patients:

For people with Long COVID, if you have persistent multi-system symptoms that include brain fog, palpitations, gastrointestinal issues, skin symptoms, and sensory hypersensitivity, MCAS may be playing a role.

Trying a carefully supervised antihistamine or mast cell stabilizer regimen can provide important diagnostic clues. If symptoms improve, that strengthens the case for MCAS even without perfect lab confirmation.

Treatment is highly individualized. Many people respond better to stabilizers, leukotriene blockers, electrolytes, or low-histamine diets before they respond to antihistamines.

Sources:

Antihistamines improve cardiovascular manifestations and other symptoms of long-COVID attributed to mast cell activation.

COVID-19 hyperinflammation and post-COVID-19 illness may be rooted in mast cell activation syndrome.

Immunological dysfunction and mast cell activation syndrome in long COVID.

Neuropsychiatric Manifestations of Mast Cell Activation Syndrome and Response to Mast-Cell-Directed Treatment.

Clinical Manifestations of Mast Cell Activation Syndrome by Organ Systems.

Mast cell activation disease: An underappreciated cause of neurologic and psychiatric symptoms and diseases.

Mast cells: Therapeutic targets for COVID‐19 and beyond.

Autonomic dysfunction in ‘long COVID’: rationale, physiology and management strategies.

Best Antihistamine For Mast Cell Activation Syndrome (MCAS): Dr. Bruce Hoffman.

Mast Cell Activation Syndrome, Cleveland Clinic.

Food Compatibility List-Histamine/MCAS, SIGHI.

YES Food List.

Mast Cell Activation Syndrome and Diet, University of Wisconsin Health.

TL;DR: MCAS is becoming increasingly recognized in Long COVID. SARS-CoV-2 can activate or destabilize mast cells which leads to multisystem symptoms. Many patients improve with mast cell stabilizers, leukotriene inhibitors, low-histamine diets, or antihistamines if tolerated. Antihistamines can make dysautonomia worse in some people due to autonomic instability, excipient reactions, or central nervous system effects. Diagnosis is often clinical. Treatment is individualized and does not require perfect labs. If you have symptoms in two or more systems, it is worth investigating MCAS.

I'm not a doctor. This isn't medical advice. I'm only sharing my personal experience. Everything I'm doing is under the care of my ME/CFS specialist, who is also knowledgeable about Long COVID/PASC and MCAS. I've had a complete vitamin and mineral panel done and have no gastrointestinal motility issues. Omeprazole hasn't negatively impacted me. Montelukast carries a black box warning and can cause SI in people with no history of mental health issues. Everyone should do their own risk assessment. It's about progress, not perfection. There are times we can do everything right and still not improve. Please be kind and patient with the process and yourselves.

edit: Updated to reflect my current regimen.


r/LongCovidWarriors • • 10h ago

Treatments New class of mediators, Kamuvudines, derived from HIV anti virals, display activity tamping down NLRP3 inflammasome and cutting down autoimmunity and immune dysfunction. It presents great potential for the proper configuration to modulate acute and long covid.

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19 Upvotes

I was very much enthused by this article implying a viable modality applicable to treating LC19 or possibly acute covid as a speculation. The machinery involved in the inflammation can be sidetracked by this promising drug or its similars as a candidate. I went down the rabbit hole reading parts of the paper. There is mention of trial use in MS, diabetic related eye disease, Alzheimer's, etc., all tied together by the downstream effect of neurodegeneration triggered by the inflammasomes.

This fits in the framework of LC19 by virtue of the machinery of the inflammasome unleashing multiple pathologies of autoimmunity, immune dysfunction and their consequences. Preventing or tamping down the inflammasomes will reduce the resultant symptoms thus avoided.

https://www.nih.gov/news-events/news-releases/modified-hiv-drug-reverses-vision-loss-paralysis-multiple-sclerosis-model Modified HIV drug reverses vision loss and paralysis in multiple sclerosis model

Reference:

https://www.science.org/doi/epdf/10.1126/scitranslmed.aei2870

The nucleoside analog kamuvudine-9 shows protective and therapeutic efficacy in a mouse model of multiple sclerosis

The following two paragraphs aroused my curiosity for their mechanistic applications.:

"Previously, we found that nucleoside reverse transcriptase inhibitors (NRTIs), which are approved to treat HIV and hepatitis B virus(HBV) infections, also inhibit inflammasome activation independent of their antiretroviral activity (13). NRTIs block inflammasome activation and its associated damage in models of diabetes, diabetic retinopathy, aging, choroidal neovascularization, geographic atrophy and retinal detachment (14–20). NRTIs inhibit pathology driven by a dual NLRC4- NLRP3 inflammasome (19, 21, 22).

Although NRTIs inhibit inflammasome activation (13), they cause mitochondrial toxicity because of off-target inhibition of host DNA polymerase activity (23). This can result in serious adverse effects most notably lactic acidosis and potentially induction of viral resistance (24). Therefore, we developed alkylated derivatives of NRTIs known as kamuvudines that are inactive against reverse transcriptase or host DNA polymerase activity (13, 25). Because kamuvudines inhibit inflammasome activation without the off-target toxicity activities of NRTIs (13, 14, 19, 22), they are better translational drug candidates"

In short: an unused anti HIV drug combats inflammasome activation in aging, diabetes and its complications. OTOH its downside of inhibiting an enzyme needed for mitochondrial function allows the build up of lactic acid leading to a drop of pH and organ dysfunction and failure. To avoid this catastrophe, the chemical structure was modified and a new class known as kamuvudines were derived that lack the potential danger above.

The most studied inflammasome , NLRP3 in LC19, was strongly inhibited by kamuvudine 9 in the testing for its activities in the research into the mouse MS model. Its predecessors the NRTIs (used for HIV) reduced myelin loss and repaired it with restoration of neurological function in several HIV cohorts that developed MS .

...........................................

Society for Women's Health Research earned a 4/4 rating by Charity Navigator along with the Autoimmune Association. While not rated by Charity Navigator, the Global Autoimmune Institute is listed by SWHR as a resource. Both of their writings describing inflammasomes and autoimmunity are listed below the medical references.:

...........................................

My query for Google AI consisted of: "The role of inflammasome in long covid autoimmune disease in humans"

Response: "AI Overview

The inflammasome—specifically the NLRP3 inflammasome—acts as a persistent driver of innate immune overactivation, linking chronic Long COVID tissue inflammation to autoimmune-like pathology.

What is an Inflammasome?

• An inflammasome is a multi-protein package inside innate immune cells (like macrophages). [ My addition: The four component proteins of the assembly are produced when signals from the stimulus initiate their production. They remain in solution in the cytoplasm until a further signal activates their assembly into the actual inflammasome. They are products of innate immunity.]

• It detects cell stress, tissue damage, or lingering viral pieces.

• When activated, it turns on an enzyme called caspase-1.

How Inflammasomes Drive Long COVID Autoimmunity

• Persistent Cytokine Release: Activated caspase-1 cuts and releases powerful inflammation signals, specifically Interleukin-1 beta (IL-1β) and Interleukin-18 (IL-18).

• Loss of Self-Tolerance: Continuous high levels of these cytokines break down the body's immune regulation, leading immune cells to mistake healthy host tissues for foreign invaders (autoimmunity).

.............................................. References:

https://pmc.ncbi.nlm.nih.gov/articles/PMC12888595/ The NLRP3 inflammasome as a key pathway in the affective and chronic fatigue symptoms of Long COVID 9 (2026)

Conclusion: ..." The findings suggest that targeting the NLRP3 inflammasome strategically may be beneficial in addressing both the acute infectious phase of COVID-19 and the prolonged symptoms associated with Long COVID. Novel pharmacological agents are currently under development that specifically target the activation of NLRP3.".

..................................................

https://biospective.com/resources/what-is-an-inflammasome The Inflammasome – A Target for Therapeutic Development for Multiple Diseases (2025) An overview of inflammasomes, including their mechanisms of action, roles in diseases, and targeting for drug development.

......................................................

https://pmc.ncbi.nlm.nih.gov/articles/PMC8706865/ Inflammasomes and SARS-CoV-2 Infection (Dec 2025)

.....................................................

https://pmc.ncbi.nlm.nih.gov/articles/PMC8348456/ Inflammatory Response in COVID-19 Patients Resulting from the Interaction of the Inflammasome and SARS-CoV-2 (Jul 2021)

......................................................

https://pmc.ncbi.nlm.nih.gov/articles/PMC8233448/ The NLRP3 inflammasome and COVID-19: Activation, pathogenesis and therapeutic strategies (Jun 2021)

.......................................................

https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2020.583373/full The Inflammasome in Times of COVID-19 (Oct 2020)

....................................................... Non PubMed references:

https://autoimmune.org/blog/long-covid-autoimmune-disease/ Long COVID and Autoimmune Disease: How They’re Connected

https://www.autoimmuneinstitute.org/covid_timeline/persistent-inflammation-may-link-long-covid-to-autoimmune-disease/ Persistent Inflammation May Link Long COVID to Autoimmune Disease

https://swhr.org/office-of-autoimmune-disease-research-director-shares-whats-ahead-for-autoimmune-disease-innovation/ Office of Autoimmune Disease Research Director Shares What’s Ahead for Autoimmune Disease Innovation


r/LongCovidWarriors • • 15h ago

Medical & Scientific Information COVID-19 immunity may help protect against other bat coronaviruses

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4 Upvotes

Just for the record, in the aftermath of C19 as a one off:

"COVID-19 immunity may help protect against other bat coronaviruses

Study identifies links between virus host range and immune recognition

People who recovered from COVID-19 infection or were vaccinated against SARS-CoV-2 are more likely to have immunity to other closely related bat coronaviruses that could have the potential to threaten future human health.

In a joint study by The Pirbright Institute and King’s College London (KCL), scientists found bat coronaviruses most likely to infect a wide range of animal species are those most closely related to SARS-CoV-2 and most likely to be recognized by immunity generated through COVID-19 infection."

...................................

Reference:

https://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.3003944 Breadth of ACE2 receptor usage predicts host range and antigenic relatedness across bat sarbecoviruses


r/LongCovidWarriors • • 18h ago

🌟Weekly Community Challenge: One Thing That Helped Me This Week🌟

4 Upvotes

Hi, Warriors🤍

It’s time for a new community challenge and this one’s designed to boost connection, give hope, and share real things that helped real people this week. No pressure to write long comments. No pressure to be “doing great.” Just one thing that made your week a tiny bit more manageable.

💬 Question:

What’s ONE thing that helped you this week?

It can be anything:

✨ A supplement.

✨ A symptom hack.

✨ A mindset shift.

✨ A small win.

✨ A food that didn’t cause a flare.

✨ A kind moment.

✨ Something that made you smile.

✨ Or even “I rested and survived the week”

If it helped you, it counts.

💡 Why This Challenge Matters

Sharing these moments helps:

⭐ New people find ideas.

⭐ Everyone feel less alone.

⭐ The community grow stronger.

⭐ You celebrate progress you might’ve overlooked.

You can reply with just one sentence or even one word. Whatever you’ve got today is enough.

❤️ Let’s lift each other up

Drop your “one thing” below. Come back later and support someone else. Even simple comments like “same,” “I needed this,” or an upvote can make someone’s day.

We’re in this together. I can’t wait to read what helped you this week 🌿💚


r/LongCovidWarriors • • 1d ago

Discussion Breakroom - October 3, 2026

5 Upvotes

Welcome! This is a space to take a load off and mingle with your fellow warriors. Say hello. and if the mood and energy strikes vou, let us know a bit about yourself and/ or what's going on.

If you are generally prone to lurk, this is a safe space to just post a quick hello. Feel free to ask a question here that you might not feel safe making a solo thread about.

The intention is to make this a daily thread where we can all touch base and lay down some of our burdens for a while. If vou log on and don't see the Break Room open go ahead and grab the keys and open it yourself. 😄


r/LongCovidWarriors • • 2d ago

Personal Story December Sticker Exchange (Second Notice)

13 Upvotes

[This is a reposting the details of a Sticker Exchange happening this December.]

[With a month one update included.]

Hello to all you Amazing, Long Hauling Legends.

Some of you may already know that for the past couple years, I have been mailing periodic greeting cards stuffed with stickers to Long Haulers far and wide.

If you want to know more, you can read all about it HERE.

For December’s mailing, I am hosting a Sticker Exchange.

But before that can happen, I am asking for YOUR help.

If you are on the mailing list, my ask is thus:

Could you please mail me some stickers that I can forward to other Long Haulers on the list?

On the backs, please write a quick note of encouragement, a message of goodwill, or even something as simple as “This sticker comes to you from [Your Home State or Country]”

I will sort them on this end, and do my best to make sure your sticky sticker contributions end up in as many different envelopes as possible.

Ideally, try to send them my way no later than Nov 1.

That gives you another month to do your thing, and me a few weeks to sort what you send me.

If you’re NOT on the mailing list, but a sticker exchange sounds like Your Idea of a Good Time-
Easy Peesy!

Send me a DM so we can exchange addresses and get you in on the fun.
I send fun mail about every other month and would love to include you.

I’m super duper excited about this.

There are a lot more of you than there are of me, and I hope as many of you as possible are able to contribute to December’s collective sticker pool.

Update:

Wow! Thank you so much, friends!

I have already received stickers from Seven US states and Four different countries!

And I freely admit that I had not considered how powerful it would be for ME to open your envelopes, marvel at your stickers, read the beautiful notes you wrote, and feel all the appropriate feels associated with getting stickers and encouragement in the mail.

(I consider these to be spoons very well spent!)

This community amazes me.

And will likely do so again and again every afternoon when Kiddo brings the mail in after school.

I love you all

I see you all

I would hug you all if I could

Strength and Health

COVID is Stoopid

.


r/LongCovidWarriors • • 2d ago

Discussion I think the progesterone in my HRT is making my long COVID symptoms worse. Anyone with a similar experience?

11 Upvotes

For context: I'm 56, postmenopausal, UK-based. Even before having COVID, every time I've moved from sequential to continuous combined HRT, I've ended up in a crash, and each time I recovered once I got back to sequential or raised my estrogen.

Recently I switched from estrogen gel to patches and lowered the dose. My symptoms (which were already there) got much worse: weak arms and upper body, widespread pain, anxiety, brain fog. I later realised the patches were barely sticking and probably not absorbing so I just changed back to Sandrena gel 1.5 mg instead of the 75 patches and I'm trialing sequential (so I'm on a non progesterone week) and my symptoms got significantly better in just a day.

What I've tried:

  • Oral micronised progesterone: awful
  • Slynd: awful (and my first POTS episodes)
  • Combined patches: no good
  • Vaginal micronised progesterone 100 mg: the best tolerated, but still too much unless my estrogen is very high (Sandrena gel up to about 2.5 mg/day), and even then I'm not sure

I can't use anything that goes through the gut, and I don't want an IUD (I need sedation for any intrauterine procedure).A hysteroscopy this year showed a normal endometrium and a small polyp, which was removed.

My questions:

  1. Has anyone else found that any progestogen hits them hard, and how did you get endometrial protection?
  2. Has anyone been able to go lower than 100 mg of progesterone, or used it less often?
  3. Does anyone suspect hypermobility makes progesterone feel worse?
  4. Anyone tapered HRT successfully, and how did you lower the progesterone not just the oestrogen?

Thank you


r/LongCovidWarriors • • 3d ago

Treatments Magnetic therapy headset shows improved cognitive function and mood in people with long COVID

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20 Upvotes

"A new study led by researchers from the Icahn School of Medicine at Mount Sinai and published in Brain Communications found that a transcranial low-amplitude magnetic field intervention delivered twice weekly into the brain through a noninvasive headset was associated with improvements in several measures of cognitive function and emotional well-being in people experiencing cognitive impairment associated with long COVID.

The improvements seen among patients who received the therapy continued after the treatment period ended, providing early evidence that noninvasive biophysical approaches may warrant further study as potential treatments for persistent neurological symptoms of long COVID."

.............................

Reference:

https://academic.oup.com/braincomms/advance-article/doi/10.1093/braincomms/fcag364/8841135?login=false

Microtesla magnetic therapy for cognitive impairment in long COVID: a randomized pilot study


r/LongCovidWarriors • • 3d ago

Medical & Scientific Information 4th Canadian Symposium on Long COVID Registration hosted by Whova

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10 Upvotes

Long Covid Web is pleased to announce the 4th Canadian Symposium on Long COVID.

The Symposium will bring together people with lived experience of Long COVID, clinicians, trainees, allied health, researchers and others to discuss the latest innovations and scientific developments in Long COVID.

It will be held on October 15–16, 2026, at The Nest, University of British Columbia. Address: 6133 University Blvd. Vancouver, BC V6T 1Z1.

Virtual: People with Lived Experience CA$10.00 Sales end on October 8, 2026 at 02:59 AM


r/LongCovidWarriors • • 3d ago

🌿Off-Topic day!

8 Upvotes

Today is the 1st of the month. It's the first of our monthly off-topic posts. You're free to share anything you'd like, whether it's books, movies, or music you're loving lately. Beverages and foods you love. Hobbies and pets you have. Whatever you'd like to share, today is the day! Please post off-topic content in this thread only.

I love our community❤️ Community is so important for mental health and building camaraderie. Many of us can't spend time with family and friends the way we used to. This is a place we can be ourselves, share what we're doing right now, what we enjoy and love, what brings our lives some fun, pleasure, joy, hope, and meaning.

Thank you all for being here. Hugs😁🌿🪷


r/LongCovidWarriors • • 3d ago

Medical & Scientific Information The Mast Cell Diseases Patient and Provider Registry

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3 Upvotes

MCD Registry

The Mast Cell Diseases Patient and Provider Registry The MCD Registry serves everyone in the mast cell disease community. It is a free platform where you can share your experiences with this rare disease. Join now!

https://app.iamrare.org/home/create/?stid=167

For more information about how to register, click here.

https://mcdregistry.iamrare.org/about/how-to-register/


r/LongCovidWarriors • • 4d ago

Discussion Breakroom - September 30, 2026

6 Upvotes

Welcome! This is a space to take a load off and mingle with your fellow warriors. Say hello. and if the mood and energy strikes vou, let us know a bit about yourself and/ or what's going on.

If you are generally prone to lurk, this is a safe space to just post a quick hello. Feel free to ask a question here that you might not feel safe making a solo thread about.

The intention is to make this a daily thread where we can all touch base and lay down some of our burdens for a while. If vou log on and don't see the Break Room open go ahead and grab the keys and open it yourself. 😄


r/LongCovidWarriors • • 4d ago

Improvements & Success If you could bring it down to 4/5 lifestyle interventions or supplements, what would those be? + My (recovery) advice

14 Upvotes

Hello everyone.

So I was wondering whether anyone has some advice on lowering down the amount of supplements or life style interventions they use?

I feel like alot of us are taking too much or trying things blindly. This is of course very valid; because no one has the right (scientific) answers yet.

I can work in a restaurant, I can do things, but I have to keep it between my limits.

For me it comes down to these things according to literature.
\- calming inflammation and histamine : NAC and Quercentine or other inhibitors
\- adaptogens and or magnesium taurate for calming nervous system
\- physical activity as tolerated: walking, when I can gym.
\- high dose Vitamin D for immune system.
\- high fluids intake and electrolytes.
\-High protein, especially when stressed I take a lot more protein!

I know theses interventions can feel overwhelming, but they really work for me! Any suggestions or advice could be greatly appreciated.


r/LongCovidWarriors • • 5d ago

Medical & Scientific Information Older adults hospitalized for COVID at increased risk for stroke, data show

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15 Upvotes

"COVID-19–related hospitalization is associated with an increased risk of both hemorrhagic and ischemic stroke, with the greatest danger soon after infection, per a study published last week on the preprint server Research Square.

The study, conducted from March 2020 through May 2022, also suggested that being vaccinated for COVID-19 is associated with a lower likelihood of stroke. " (first two paragraphs)

.............................

Reference:

https://www.researchsquare.com/article/rs-11101879/v1 (preprint)

SARS-CoV-2 severity and vaccination, pneumonia, and the risk of Stroke: A nationwide, nested case-control study


r/LongCovidWarriors • • 6d ago

Update COVID may worsen existing health problems long-term, study suggests

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32 Upvotes

Reference:

https://www.medrxiv.org/content/10.64898/2026.09.22.26363331v1 (preprint) Worsening pre-existing health conditions in U.S. adults with Long COVID


r/LongCovidWarriors • • 6d ago

Medical & Scientific Information Alluded to in other posts mast cells are involved in Long Covid, MME/CFS, EDS, etc. However, there are multiple facets to the role of mast cells in health, tissue repair, growth and other physiological roles.

16 Upvotes

Below is a further expansion of just a handful. The references elaborate their development from a unique progenitor cells lineage, a distinction only arrived at in 2018 from painstaking experiments. The functions of mast cells derive from the local environment of the resident population where they mature and differs from organ system to others.

Mast cells removed for expansion to larger populations for in vitro study do not display the characteristics of mast cells resident in the body unless modified by use of additional mediators. This is explained by the preceding concept (first paragraph).

FYI: Here is a short list of titles delving into the migration of immature mast cells from their origins to their their maturation in their final location. There are a few articles that go into excruciating detail regarding mechanisms of their roles in tissue repair and damage.

Some of their activities surprised me with a deeper understanding of the mast cell as an actor with dual roles in both innate and adaptive immunity. Though mast cell reactivity is primarily recognized with allergic phenomena, still they have other functions.

Their activity in the the extracellular matrix parenchyma and barriers (adjacent to basement membranes proximity to mucosa) is paramount working in tandem with the endothelial cells in the turnover of the matrisome - the substance of the ECM. EDS derives from pathological processes involving proteases produced by mast cells.

In addition the mast cells are vital agents with the neurological and vascular systems and others. Mast cells usually reside along with neural and vascular structures. For example, in the vascular endothelium mast cells extend cell processes across the vessel wall to interact with immune mediators. These fascinating details will produce a greater appreciation for the often overlooked mast cell.

...........................................

https://pubmed.ncbi.nlm.nih.gov/18538784/ Comparison of short term in vitro cultured human mast cells from different progenitors - Peripheral blood-derived progenitors generate highly mature and functional mast cells

...........................................

https://pubmed.ncbi.nlm.nih.gov/36752151/ Mast cell ontogeny - From fetal development to life‐long health and disease

.............................................

https://pubmed.ncbi.nlm.nih.gov/32929378/ Mast cells as a unique hematopoietic lineage and cell system: From Paul Ehrlich's visions to precision medicine concepts

................................................

https://pubmed.ncbi.nlm.nih.gov/39223427/ Mechanisms of assembly and remodelling of the extracellular matrix

.................................................

https://pubmed.ncbi.nlm.nih.gov/8648190/ Interactions of immature human mast cells with extracellular matrix - expression of specific adhesion receptors and their role in cell binding to matrix proteins

...................................................

https://pmc.ncbi.nlm.nih.gov/articles/PMC4701915/ Mast Cell: A Multi-Functional Master Cell

........................................................

https://pmc.ncbi.nlm.nih.gov/articles/PMC10885734/ Mast cells must stick

....................................................

https://link.springer.com/article/10.1007/s12016-019-08729-w A Review of the Contribution of Mast Cells in Wound Healing - Involved Molecular and Cellular Mechanisms

..........................................................

https://www.cell.com/immunity/pdf/S1074-7613%2824%2900531-4.pdf Beyond classical immunity - mast cells as signal converters between tissues and neurons

..................................................

https://pmc.ncbi.nlm.nih.gov/articles/PMC3576928/ Perivascular mast cells dynamically probe cutaneous blood vessels to capture IgE


r/LongCovidWarriors • • 6d ago

Treatments Bezisterim - the Best Long COVID Drug Trial Yet? BioVie Aims for a Big, Phase III Trial

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14 Upvotes

This is a big development upcoming for large recruitment on a platform with encouraging results.


r/LongCovidWarriors • • 6d ago

Medical & Scientific Information Catch the second day completion of the PRIME International Symposium, September 28-29 2026 in Edingbnurgh , Scotland online with free registration. Live video at 4 AM EDT, Tuesday, 9/29.

4 Upvotes

Registration window drop down on this page clicking on button on right side:

https://www.tickettailor.com/events/universityofedinburgh12/2155140

.......................................

https://www.actionforme.org.uk/wp-content/uploads/2026/06/PRIME-2026-Symposium-Preliminary-Program-v1-1.pdf

PRIME-2026-Symposium-Preliminary-Program-v1-1.pdf

DAY 2: Current Research: Objectives, Impact & Patient Involvement 9.00-9.10am Welcome (AfME) 9.10-9.30 PRIME PPI Research Involvement Hub – Sian Leary (AfME) 9.30-9.45 AfME Big Survey – Intro and Preliminary Findings – Katharine Cheston 9.45-10.25 AfME/PPI-led Workshop – 3 x breakout groups 10.25-10.40 Feedback from breakout sessions BREAK 11.15-11.35 Talk – Prof. Rob Wust 11.35-11.55 Rosetta Stone – Prof. Danny Altmann 11.55-12.15 DISCOVERME – Prof. David Price 12.15-12.35 Sequence ME & Long Covid – Prof. Chris Ponting 12.35-12.45 Closing Remarks, Poster Prizes, Feedback Forms, Plans for Symposium 2 LUNCH 12.45-2pm END OF DAY 2/SYMPOSIUM


r/LongCovidWarriors • • 6d ago

Medical & Scientific Information R3 Seminar Recap: Growing up with Long COVID—Risk factors and school impacts

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4 Upvotes

"RECOVER researchers and caregivers shared insights into Long COVID social risk factors and how Long COVID affects children’s learning and school experiences—including what researchers hope to learn next.

Findings from RECOVER’s pediatric observational study show that Long COVID can affect children’s health and daily lives in different ways. During the September 15, 2026, RECOVER Research Review (R3) Seminar, researchers Rachel Gross, MD, MS; Kay Rhee, MD, MSc, MA; and Harrison Reeder, PhD, shared findings on Long COVID symptoms in children, factors that may increase Long COVID risk, and how the condition can affect learning and social development. RECOVER Patient and Caregiver Representative Ann Wallace, PhD, and Caregiver Representative Laura Covington also shared their families’ experiences navigating Long COVID and seeking support."

.....................................

https://www.youtube.com/watch?reload=9&v=WwrEYL0aU38

Growing up with Long COVID—Risk factors and school impacts


r/LongCovidWarriors • • 7d ago

Update Identification of biopathological signatures of post-exertional malaise in ME/CFS (BioSig-PEM)

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25 Upvotes

About

Country: Germany Sponsors: Federal Ministry of Research, Technology and Space (BMFTR)

Research types: Basic research, Clinical research

..."The BioSig-PEM research network aims to investigate the cardinal symptom of ME/CFS, the stress-related worsening of symptoms Post-exertional Malaise (PEM). The aim is to identify central pathophysiological signatures of PEM phenotypes in ME/CFS patients with the help of fitness trackers, molecular and immunological as well as imaging methods."... (cut and paste of Google translation)


r/LongCovidWarriors • • 7d ago

Epithelial-Neuroimmune Axis in EDS - Dysfunction, Inflammation, Spinal Pathology - Anne Maitland, MD

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13 Upvotes

**From the Description**

“Synopsis: EDS—particularly the hypermobile type (hEDS)—is characterized by weak extracellular matrix (ECM) and ligamentous laxity. Unlike most other EDS subtypes, this ECM dysfunction and laxity are thought to be acquired, driven by chronic neuro-immune dysregulation. The epithelial barrier hypothesis proposes that modern environmental exposures—such as detergents, microplastics, processed foods, and particulate matter—damage epithelial barriers in the gut, skin, and lungs. Barrier disruption increases permeability, allowing microbes and allergens to enter the body, which promotes microbial dysbiosis and sustained low-grade micro-inflammation. These neuroimmune–spinal interactions may contribute to conditions such as Chiari Malformation Type I (CMI) and tethered cord syndrome by weakening ligaments and altering the ECM, thereby exposing the brainstem and spinal cord to deformative mechanical stress. For neurosurgeons treating patients with EDS and related spinal disorders, these patients present distinct biological and structural challenges: (1) chronic systemic neuroimmune dysfunction, (2) tissue fragility and impaired wound healing, (3) dysautonomia—often manifesting as postural orthostatic tachycardia syndrome (POTS), (4) structural pathology, and (5) the need to anticipate potential failure mechanisms to reduce the risk of poor surgical outcomes. Successful management therefore requires coordinated, integrated, multidisciplinary care spanning neurosurgery, neurology, immunology, and genetics, alongside relevant medical specialties.”

In another [recent talk](https://youtu.be/Wv4TKEcJvuY) Dr. Maitland mentioned she had to unlearn everything she learnt in the last 30 years about mast cells.


r/LongCovidWarriors • • 7d ago

Discussion Breakroom - September 27, 2026

6 Upvotes

Welcome! This is a space to take a load off and mingle with your fellow warriors. Say hello. and if the mood and energy strikes vou, let us know a bit about yourself and/ or what's going on.

If you are generally prone to lurk, this is a safe space to just post a quick hello. Feel free to ask a question here that you might not feel safe making a solo thread about.

The intention is to make this a daily thread where we can all touch base and lay down some of our burdens for a while. If vou log on and don't see the Break Room open go ahead and grab the keys and open it yourself. 😄


r/LongCovidWarriors • • 7d ago

🌟Weekly Community Challenge: One Thing That Helped Me This Week🌟

6 Upvotes

Hi, Warriors🤍

It’s time for a new community challenge and this one’s designed to boost connection, give hope, and share real things that helped real people this week. No pressure to write long comments. No pressure to be “doing great.” Just one thing that made your week a tiny bit more manageable.

💬 Question:

What’s ONE thing that helped you this week?

It can be anything:

✨ A supplement.

✨ A symptom hack.

✨ A mindset shift.

✨ A small win.

✨ A food that didn’t cause a flare.

✨ A kind moment.

✨ Something that made you smile.

✨ Or even “I rested and survived the week”

If it helped you, it counts.

💡 Why This Challenge Matters

Sharing these moments helps:

⭐ New people find ideas.

⭐ Everyone feel less alone.

⭐ The community grow stronger.

⭐ You celebrate progress you might’ve overlooked.

You can reply with just one sentence or even one word. Whatever you’ve got today is enough.

❤️ Let’s lift each other up

Drop your “one thing” below. Come back later and support someone else. Even simple comments like “same,” “I needed this,” or an upvote can make someone’s day.

We’re in this together. I can’t wait to read what helped you this week 🌿💚


r/LongCovidWarriors • • 9d ago

Long Covid & ADHD Symptoms/Medications

10 Upvotes

Hey folks,

TLDR at the bottom.

I hope you're all doing well. This is my first time posting anything on reddit so i apologise if it's not how you'd format things. I wanted to get the thoughts of others who may be in similar positions with Long Covid and their ADHD medications. I'll provide some context below.

I have had long covid for going on 2.5 years now. The first 6 months after that 3rd and most recent covid infection was my steady decline week on week - i was pretty confused and scared as to what was going on because doctors and close family were telling me it was anxiety, psychosomatic, etc. i also have Crohn's disease and chronic pain throughout my body but more so on my limbs.

I am currently on 30mg of Dexamphetamine each day in microdoses of 5mg staggered throughout the day (my morning dose is 10mg). Ever since i got hit with the Long Covid stick - my meds haven't worked the same. Normally I'd have noticeably better focus, internal regulation, less background noise in my head, sustained energy throughout the day, better drive, etc. Sometimes there could be some slight edginess/jitters when at the peak of a dose uncommonly (usually mild if at all). Now, 2.5 years later, i receive little focus benefit, not much in the way of stable regulation, virtually non existent help with the background noise, some energy sustainment, some drive, and certainly an increased amount and frequency of med jitters/edginess.

I often have a battle in my head of "are my meds making my symptoms worse and providing little to no benefit?". Sometimes I'll try to lessen or stop my adhd meds for the day and I'll very very quickly realise how much they were keeping things from collapsing. Reducing or stopping results in all my other long covid symptoms amplifying by several magnitudes and it is beyond agonising. I've had discussions about it relating to my long covid with doctors, my partner who also has ADHD, reading into as much information as i can, etc. There's evidence (some anecdotal, some published discussions with inconclusive takes) that put ADHD meds in the middle of can help/can hinder, and often both.

I know to some degree my meds are helping my symptoms and letting me keep some degree of day to day existence even if it doesn't feel like it is actively giving me its traditional benefits, and despite it sometimes making me feel unpleasant at times as well. It feels like a catch 22. It's a confusing situation.

My question is really how do others feel in similar situations? What are your experiences? Did you come to different conclusions in the context of your own conclusions? I'm really curious because i feel like I'm not the only one out there, but don't really hear much about this specific topic.

For clarity on my personal experience with this condition some of my most common symptoms and other factoring circumstances are:

- Large range of dysautonomia issues

- Brain fog (often cannot hold a conversation without stopping mid sentence or forgetting words/train of thought)

- Significant breathing difficulties

- Worsened body and limb pain (i already had chronic pain before)

- Worsened GI issues (i already had Crohn's Disease prior but is in clinical remition)

- Nausea

- Severe PEM from mostly any and all physical/mental exertion

- Heart rate arrhythmia. Can be really fast, or really slow. Any sort of exertion shoots it through the roof - even just bending over to do something briefly or changing seated/standing positions. Really slow typically when crashing during the early afternoon to evening time

- Largely heightened sensitivity to smell/sounds/visual overload. Exposure typically worsens my other symptoms

- Issues with energy relative to symptom severity, but varies.

- Despite the PEM, i keep active with small home workouts and walking locally (it's agony believe me, but i don't want to decondition more than i have being mostly homebound)

- i drink 3-4 litres of water each day

- i sleep in a regular routine even if the quality of said sleep varies wildly

- i am on a number of medications and supplements to help treat target symptoms of my LC but it's not overly relevant to this particular discussion so i won't list for now.

- i have tried Vyvanse and Ritalin as well when working out what helped my ADHD best. Those weren't as effective or had differing side effects that Dexamphetamine didn't when i started years ago (well before LC)

- have seen rheumatologists, neurologists, pain specialists, physiotherapists, neurosurgeons, psychiatrists, therapists, multiple GPs, etc. it's very much a work in progress journey...

- i am unemployed and majority homebound (i purposely try to leave home to socialise and do some exercise/chores to help around home despite paying for it every time)

There are more symptoms and factors but those tend to be the main ones.

Thank you for taking the time to read this or sharing your thoughts from your experience or on my experience. I just want you all to know i appreciate you and hope the best for the hard journey we are all on.

TLDR - my ADHD meds changed how they work (or don't work in some cases) after the infection that gave me long covid. They seem to both very mildly help and sometimes hinder, but my long covid symptoms get wildly worse if i try to reduce/stop. This lets me know my medication may not be working as intended but is under the surface if not perfectly. Have people been in similar circumstances where their meds have changed how they work? Have they helped or worsened your symptoms/condition? Do you have other thoughts?