#anaphylaxis — Public Fediverse posts
Live and recent posts from across the Fediverse tagged #anaphylaxis, aggregated by home.social.
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Fatal delays in epipen treatment for food anaphylaxis in children, finds research
Fatal delays in administering life-saving adrenaline autoinjector (EpiPen) for food anaphylaxis, a severe and rapid allergic reaction, is…
#NewsBeep #News #Health #Adrenaline #allergy #anaphylaxis #AU #Australia #Breathing #CardiacArrest #Children #Emergencymedicine #food #foodallergy #Heart #Hospital #medicine #mortality #research
https://www.newsbeep.com/au/635505/ -
Fatal delays in epipen treatment for food anaphylaxis in children, finds research
Fatal delays in administering life-saving adrenaline autoinjector (EpiPen) for food anaphylaxis, a severe and rapid allergic reaction, is…
#NewsBeep #News #Health #Adrenaline #allergy #anaphylaxis #AU #Australia #Breathing #CardiacArrest #Children #Emergencymedicine #food #foodallergy #Heart #Hospital #medicine #mortality #research
https://www.newsbeep.com/au/635505/ -
Safety review links herb in popular cold and flu supplements with life-threatening anaphylaxis
A herb found in popular cold and flu supplements in Australia has officially been linked with life-threatening anaphylaxis.…
#NewsBeep #News #Health #allergy #anaphylaxis #andrographispaniculata #armaforce #AU #Australia #BioCeuticals #coldandflusupplement #medicine #TGA #TherapeuticGoodsAdministration
https://www.newsbeep.com/au/596650/ -
Safety review links herb in popular cold and flu supplements with life-threatening anaphylaxis
A herb found in popular cold and flu supplements in Australia has officially been linked with life-threatening anaphylaxis.…
#NewsBeep #News #Health #allergy #anaphylaxis #andrographispaniculata #armaforce #AU #Australia #BioCeuticals #coldandflusupplement #medicine #TGA #TherapeuticGoodsAdministration
https://www.newsbeep.com/au/596650/ -
Microbial metabolism of food allergens determines the severity of IgE-mediated #anaphylaxis.
#Microbiota degrade peanut #allergens, lowering IgE binding & anaphylaxis, revealing a pathway to reduce reactions.
https://davidojcius.blogspot.com/2026/03/microbial-metabolism-of-food-allergens.html #allergy #peanut
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ALK receives positive CHMP opinion for EURneffy 1 mg
ALK-Abello has secured a positive recommendation to extend the marketing authorisation for EURneffy. The opinion covers the 1 mg dose, complementing the 2 mg version approved by the EC in August 2024 for anaphylaxis in patients weighing 30 kg or more. EVP of R&D Henriette Mersebach notes this supports the company pediatric focus for respiratory allergy.
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recent review -
IgE and non-IgE-mediated pathways in anaphylaxis [2025]
https://pubmed.ncbi.nlm.nih.gov/40802080/ -
Why was it so hard to figure out the cause of death was anaphylactic shock?
https://www.youtube.com/post/UgkxCTbilYTQnuuyEtHEF07YgWW4vRnmYjXI
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Why was it so hard to figure out the cause of death was anaphylactic shock?
https://www.youtube.com/post/UgkxCTbilYTQnuuyEtHEF07YgWW4vRnmYjXI
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Why was it so hard to figure out the cause of death was anaphylactic shock?
https://www.youtube.com/post/UgkxCTbilYTQnuuyEtHEF07YgWW4vRnmYjXI
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Why was it so hard to figure out the cause of death was anaphylactic shock?
https://www.youtube.com/post/UgkxCTbilYTQnuuyEtHEF07YgWW4vRnmYjXI
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https://www.europesays.com/ie/166345/ Long-term study shows peanut patch treatment builds tolerance in toddlers #allergy #anaphylaxis #Asthma #children #Efficacy #Éire #food #Health #IE #ImmuneSystem #Immunology #immunotherapy #Ireland #PeanutAllergy #Placebo #Protein #Research #skin
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neffy® (epinephrine nasal spray) Approved in Japan as the First and Only Needle-Free Emergency Treatment of Allergic Reactions (anaphylaxis)
ARS Pharmaceuticals, Inc. nef…
#Japan #JP #JapanNews #allergicreactions #anaphylaxis #ARSPharma #emergencytreatment #epinephrine #Japanesepatients #nasalspray #neffy #news #pharmaceuticals
https://www.alojapan.com/1373297/neffy-epinephrine-nasal-spray-approved-in-japan-as-the-first-and-only-needle-free-emergency-treatment-of-allergic-reactions-anaphylaxis/ -
neffy® (epinephrine nasal spray) Approved in Japan as the First and Only Needle-Free Emergency Treatment of Allergic Reactions (anaphylaxis)
ARS Pharmaceuticals, Inc. nef…
#Japan #JP #JapanNews #allergicreactions #anaphylaxis #ARSPharma #emergencytreatment #epinephrine #Japanesepatients #nasalspray #neffy #news #pharmaceuticals
https://www.alojapan.com/1373297/neffy-epinephrine-nasal-spray-approved-in-japan-as-the-first-and-only-needle-free-emergency-treatment-of-allergic-reactions-anaphylaxis/ -
https://www.alojapan.com/1373297/neffy-epinephrine-nasal-spray-approved-in-japan-as-the-first-and-only-needle-free-emergency-treatment-of-allergic-reactions-anaphylaxis/ neffy® (epinephrine nasal spray) Approved in Japan as the First and Only Needle-Free Emergency Treatment of Allergic Reactions (anaphylaxis) #AllergicReactions #anaphylaxis #ARSPharma #EmergencyTreatment #epinephrine #Japan #JapanNews #JapanesePatients #NasalSpray #neffy #news #pharmaceuticals ARS Pharmaceuticals, Inc. neffy 1 mg and 2 mg doses approved by Japanese regulators neffy offers a new delivery method for epinephrine in Japan for adu
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https://www.alojapan.com/1373297/neffy-epinephrine-nasal-spray-approved-in-japan-as-the-first-and-only-needle-free-emergency-treatment-of-allergic-reactions-anaphylaxis/ neffy® (epinephrine nasal spray) Approved in Japan as the First and Only Needle-Free Emergency Treatment of Allergic Reactions (anaphylaxis) #AllergicReactions #anaphylaxis #ARSPharma #EmergencyTreatment #epinephrine #Japan #JapanNews #JapanesePatients #NasalSpray #neffy #news #pharmaceuticals ARS Pharmaceuticals, Inc. neffy 1 mg and 2 mg doses approved by Japanese regulators neffy offers a new delivery method for epinephrine in Japan for adu
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Real-World Evidence Supports Clinical Effectiveness of neffy® (epinephrine nasal spray) in Patients Experiencing Anaphylaxis
ARS Pharmaceuticals, Inc. Findings accepted for publication in the official journal of the American College of Allergy, Asthma…
#NewsBeep #News #Medication #allergicreactions #anaphylaxis #anaphylaxissymptoms #CA #Canada #clinicaleffectiveness #epinephrineinjection #foodchallenge #Health #Healthcareprovider #neffy #treatmentoutcomes
https://www.newsbeep.com/ca/130871/ -
https://www.europesays.com/uk/409252/ Real-World Evidence Supports Clinical Effectiveness of neffy® (epinephrine nasal spray) in Patients Experiencing Anaphylaxis #AllergicReactions #anaphylaxis #AnaphylaxisSymptoms #ClinicalEffectiveness #EpinephrineInjection #FoodChallenge #Health #HealthcareProvider #Medication #neffy #TreatmentOutcomes #UK #UnitedKingdom
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Real-World Evidence Supports Clinical Effectiveness of neffy® (epinephrine nasal spray) in Patients Experiencing Anaphylaxis
ARS Pharmaceuticals, Inc. Findings accepted for publication in the official journal of the American College of Allergy, Asthma…
#NewsBeep #News #Medication #allergicreactions #anaphylaxis #anaphylaxissymptoms #AU #Australia #clinicaleffectiveness #epinephrineinjection #foodchallenge #Health #Healthcareprovider #neffy #treatmentoutcomes
https://www.newsbeep.com/au/129018/ -
2025-8-9 Is this MCAS anaphylaxis, anxiety, or anaphylaxis from anxiety?
I almost didn’t want to share this one, because I’m in a bit of a nervous state, and I was worried about the people who think people with Long Covid are psychological malingerers, etc. When I had to leave work, and filed for US Social Security Disability, I kept my Generalized Anxiety Disorder out of my initial application, afraid of getting the dreaded “just anxiety,” dismissal that many complex chronic illness kin are familiar with. (I was later told this was a bad move, and to definitely include all mental health and neurodivergence things, which I did for the ongoing process.)
Even as I’m having less anaphylaxis risk, it’s taking time to recover psychologically. I told my therapist how I felt like I backslid over a decade in mental health work overnight from the first recent anaphylaxis episode. She kindly said that while I might feel as scared and threatened as I often did back then, that the trigger was different. I was not feeling that anxious about an email, I was feeling that way about a literal life and death situation, one which I still don’t fully understand the triggers of.
A decade ago, de-stigmatizing mental healthcare was really important to me too. Now, I’m especially aware of how much these issues intersect, so heck yeah, publishing the medical art about anxiety.
Lastly, I wanted to include few examples of the ways in which these issues intersect. These are absolutely the tip of the iceberg.
- Mast Cell Activation Snydrome (often MCAS for space, in my art) can trigger so, so many pyschological symptoms. Mast Attack has a great overview of the topic, and while I haven’t been able to read the study fully because of the severe brain fog, Prevalence and treatment response of neuropsychiatric disorders in mast cell activation syndrome caught my eye.
- Anaphylaxis, or near anaphylaxis, has many symptoms in common with anxiety, from chest tightness to clammy skin, and “a feeling of impending doom”. While MCAS is not allergies, All Things Allergies has an easy intro to anxiety & anaphylaxis, and here’s a study The impact of anaphylaxis on the quality of life and mental health of adults.
- Ehlers-Danlos Syndrome co-occurs with many mental health issues, and I really appreciate how this article lists suspected mechanisms, misattributions, and related factors.
- Postural Orthostatic Tachycardia Syndrome, or POTS, is a form of autonomic dysfuntction (when things your body normally does automatically stop behaving normally), and is a part of my Long Covid. It involves a high heart rate, and often symptoms like room spinning or lightheadedness, trembling or shaking, shortness of breath, and poor bloodflow. POTS is often misdiagnosed as anxiety, and The Disabled Ginger wrote about it here.
Theories that diseases are caused by mental states and can be cured by will power are always an index of how much is not understood about the physical terrain of a disease.
Moreover, there is a peculiarly modern predilection for psychological explanations of a disease, as of everything else. Psychologizing seems to provide control over the experiences and events (like grave illnesses) over which people have in fact little or no control. Psychological understanding undermines the ‘reality’ of a disease. That reality has to be explained.
Susan Sontag, illness as metaphor (New York: Farrar, Straus and Giroux, 1977), p. 55.
p.s. mental health is physical health and physical health is mental health. you got a literal brain in your body and all of your body is involved in everything that you do. please take care of yourselves and each other. <3
https://www.illmarks.com/2025-8-9-is-this-mcas-anaphylaxis/
#allergy #anaphylaxis #anxiety #art #autoimmune #bodyHorror #bodyMapping #chronicIllness #gad #generalizedAnxiety #immune #longCovid #longcovid #mastCell #mastCellActivationSyndrome #mastCellDisease #mastcell #mcas #medart #medblog #medicalArt #medwriting #mentalHealth #MillionsMissing #pwLC #pwme #SciArt #sciblog #sciwriting #symptom
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2025-8-9 Is this MCAS anaphylaxis, anxiety, or anaphylaxis from anxiety?
I almost didn’t want to share this one, because I’m in a bit of a nervous state, and I was worried about the people who think people with Long Covid are psychological malingerers, etc. When I had to leave work, and filed for US Social Security Disability, I kept my Generalized Anxiety Disorder out of my initial application, afraid of getting the dreaded “just anxiety,” dismissal that many complex chronic illness kin are familiar with. (I was later told this was a bad move, and to definitely include all mental health and neurodivergence things, which I did for the ongoing process.)
Even as I’m having less anaphylaxis risk, it’s taking time to recover psychologically. I told my therapist how I felt like I backslid over a decade in mental health work overnight from the first recent anaphylaxis episode. She kindly said that while I might feel as scared and threatened as I often did back then, that the trigger was different. I was not feeling that anxious about an email, I was feeling that way about a literal life and death situation, one which I still don’t fully understand the triggers of.
A decade ago, de-stigmatizing mental healthcare was really important to me too. Now, I’m especially aware of how much these issues intersect, so heck yeah, publishing the medical art about anxiety.
Lastly, I wanted to include few examples of the ways in which these issues intersect. These are absolutely the tip of the iceberg.
- Mast Cell Activation Snydrome (often MCAS for space, in my art) can trigger so, so many pyschological symptoms. Mast Attack has a great overview of the topic, and while I haven’t been able to read the study fully because of the severe brain fog, Prevalence and treatment response of neuropsychiatric disorders in mast cell activation syndrome caught my eye.
- Anaphylaxis, or near anaphylaxis, has many symptoms in common with anxiety, from chest tightness to clammy skin, and “a feeling of impending doom”. While MCAS is not allergies, All Things Allergies has an easy intro to anxiety & anaphylaxis, and here’s a study The impact of anaphylaxis on the quality of life and mental health of adults.
- Ehlers-Danlos Syndrome co-occurs with many mental health issues, and I really appreciate how this article lists suspected mechanisms, misattributions, and related factors.
- Postural Orthostatic Tachycardia Syndrome, or POTS, is a form of autonomic dysfuntction (when things your body normally does automatically stop behaving normally), and is a part of my Long Covid. It involves a high heart rate, and often symptoms like room spinning or lightheadedness, trembling or shaking, shortness of breath, and poor bloodflow. POTS is often misdiagnosed as anxiety, and The Disabled Ginger wrote about it here.
Theories that diseases are caused by mental states and can be cured by will power are always an index of how much is not understood about the physical terrain of a disease.
Moreover, there is a peculiarly modern predilection for psychological explanations of a disease, as of everything else. Psychologizing seems to provide control over the experiences and events (like grave illnesses) over which people have in fact little or no control. Psychological understanding undermines the ‘reality’ of a disease. That reality has to be explained.
Susan Sontag, illness as metaphor (New York: Farrar, Straus and Giroux, 1977), p. 55.
p.s. mental health is physical health and physical health is mental health. you got a literal brain in your body and all of your body is involved in everything that you do. please take care of yourselves and each other. <3
https://www.illmarks.com/2025-8-9-is-this-mcas-anaphylaxis/
#allergy #anaphylaxis #anxiety #art #autoimmune #bodyHorror #bodyMapping #chronicIllness #gad #generalizedAnxiety #immune #longCovid #longcovid #mastCell #mastCellActivationSyndrome #mastCellDisease #mastcell #mcas #medart #medblog #medicalArt #medwriting #mentalHealth #MillionsMissing #pwLC #pwme #SciArt #sciblog #sciwriting #symptom
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2025-8-9 Is this MCAS anaphylaxis, anxiety, or anaphylaxis from anxiety?
I almost didn’t want to share this one, because I’m in a bit of a nervous state, and I was worried about the people who think people with Long Covid are psychological malingerers, etc. When I had to leave work, and filed for US Social Security Disability, I kept my Generalized Anxiety Disorder out of my initial application, afraid of getting the dreaded “just anxiety,” dismissal that many complex chronic illness kin are familiar with. (I was later told this was a bad move, and to definitely include all mental health and neurodivergence things, which I did for the ongoing process.)
Even as I’m having less anaphylaxis risk, it’s taking time to recover psychologically. I told my therapist how I felt like I backslid over a decade in mental health work overnight from the first recent anaphylaxis episode. She kindly said that while I might feel as scared and threatened as I often did back then, that the trigger was different. I was not feeling that anxious about an email, I was feeling that way about a literal life and death situation, one which I still don’t fully understand the triggers of.
A decade ago, de-stigmatizing mental healthcare was really important to me too. Now, I’m especially aware of how much these issues intersect, so heck yeah, publishing the medical art about anxiety.
Lastly, I wanted to include few examples of the ways in which these issues intersect. These are absolutely the tip of the iceberg.
- Mast Cell Activation Snydrome (often MCAS for space, in my art) can trigger so, so many pyschological symptoms. Mast Attack has a great overview of the topic, and while I haven’t been able to read the study fully because of the severe brain fog, Prevalence and treatment response of neuropsychiatric disorders in mast cell activation syndrome caught my eye.
- Anaphylaxis, or near anaphylaxis, has many symptoms in common with anxiety, from chest tightness to clammy skin, and “a feeling of impending doom”. While MCAS is not allergies, All Things Allergies has an easy intro to anxiety & anaphylaxis, and here’s a study The impact of anaphylaxis on the quality of life and mental health of adults.
- Ehlers-Danlos Syndrome co-occurs with many mental health issues, and I really appreciate how this article lists suspected mechanisms, misattributions, and related factors.
- Postural Orthostatic Tachycardia Syndrome, or POTS, is a form of autonomic dysfuntction (when things your body normally does automatically stop behaving normally), and is a part of my Long Covid. It involves a high heart rate, and often symptoms like room spinning or lightheadedness, trembling or shaking, shortness of breath, and poor bloodflow. POTS is often misdiagnosed as anxiety, and The Disabled Ginger wrote about it here.
Theories that diseases are caused by mental states and can be cured by will power are always an index of how much is not understood about the physical terrain of a disease.
Moreover, there is a peculiarly modern predilection for psychological explanations of a disease, as of everything else. Psychologizing seems to provide control over the experiences and events (like grave illnesses) over which people have in fact little or no control. Psychological understanding undermines the ‘reality’ of a disease. That reality has to be explained.
Susan Sontag, illness as metaphor (New York: Farrar, Straus and Giroux, 1977), p. 55.
p.s. mental health is physical health and physical health is mental health. you got a literal brain in your body and all of your body is involved in everything that you do. please take care of yourselves and each other. <3
https://www.illmarks.com/2025-8-9-is-this-mcas-anaphylaxis/
#allergy #anaphylaxis #anxiety #art #autoimmune #bodyHorror #bodyMapping #chronicIllness #gad #generalizedAnxiety #immune #longCovid #longcovid #mastCell #mastCellActivationSyndrome #mastCellDisease #mastcell #mcas #medart #medblog #medicalArt #medwriting #mentalHealth #MillionsMissing #pwLC #pwme #SciArt #sciblog #sciwriting #symptom
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2025-8-9 Is this MCAS anaphylaxis, anxiety, or anaphylaxis from anxiety?
I almost didn’t want to share this one, because I’m in a bit of a nervous state, and I was worried about the people who think people with Long Covid are psychological malingerers, etc. When I had to leave work, and filed for US Social Security Disability, I kept my Generalized Anxiety Disorder out of my initial application, afraid of getting the dreaded “just anxiety,” dismissal that many complex chronic illness kin are familiar with. (I was later told this was a bad move, and to definitely include all mental health and neurodivergence things, which I did for the ongoing process.)
Even as I’m having less anaphylaxis risk, it’s taking time to recover psychologically. I told my therapist how I felt like I backslid over a decade in mental health work overnight from the first recent anaphylaxis episode. She kindly said that while I might feel as scared and threatened as I often did back then, that the trigger was different. I was not feeling that anxious about an email, I was feeling that way about a literal life and death situation, one which I still don’t fully understand the triggers of.
A decade ago, de-stigmatizing mental healthcare was really important to me too. Now, I’m especially aware of how much these issues intersect, so heck yeah, publishing the medical art about anxiety.
Lastly, I wanted to include few examples of the ways in which these issues intersect. These are absolutely the tip of the iceberg.
- Mast Cell Activation Snydrome (often MCAS for space, in my art) can trigger so, so many pyschological symptoms. Mast Attack has a great overview of the topic, and while I haven’t been able to read the study fully because of the severe brain fog, Prevalence and treatment response of neuropsychiatric disorders in mast cell activation syndrome caught my eye.
- Anaphylaxis, or near anaphylaxis, has many symptoms in common with anxiety, from chest tightness to clammy skin, and “a feeling of impending doom”. While MCAS is not allergies, All Things Allergies has an easy intro to anxiety & anaphylaxis, and here’s a study The impact of anaphylaxis on the quality of life and mental health of adults.
- Ehlers-Danlos Syndrome co-occurs with many mental health issues, and I really appreciate how this article lists suspected mechanisms, misattributions, and related factors.
- Postural Orthostatic Tachycardia Syndrome, or POTS, is a form of autonomic dysfuntction (when things your body normally does automatically stop behaving normally), and is a part of my Long Covid. It involves a high heart rate, and often symptoms like room spinning or lightheadedness, trembling or shaking, shortness of breath, and poor bloodflow. POTS is often misdiagnosed as anxiety, and The Disabled Ginger wrote about it here.
Theories that diseases are caused by mental states and can be cured by will power are always an index of how much is not understood about the physical terrain of a disease.
Moreover, there is a peculiarly modern predilection for psychological explanations of a disease, as of everything else. Psychologizing seems to provide control over the experiences and events (like grave illnesses) over which people have in fact little or no control. Psychological understanding undermines the ‘reality’ of a disease. That reality has to be explained.
Susan Sontag, illness as metaphor (New York: Farrar, Straus and Giroux, 1977), p. 55.
p.s. mental health is physical health and physical health is mental health. you got a literal brain in your body and all of your body is involved in everything that you do. please take care of yourselves and each other. <3
https://www.illmarks.com/2025-8-9-is-this-mcas-anaphylaxis/
#allergy #anaphylaxis #anxiety #art #autoimmune #bodyHorror #bodyMapping #chronicIllness #gad #generalizedAnxiety #immune #longCovid #longcovid #mastCell #mastCellActivationSyndrome #mastCellDisease #mastcell #mcas #medart #medblog #medicalArt #medwriting #mentalHealth #MillionsMissing #pwLC #pwme #SciArt #sciblog #sciwriting #symptom
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2025-8-9 Is this MCAS anaphylaxis, anxiety, or anaphylaxis from anxiety?
I almost didn’t want to share this one, because I’m in a bit of a nervous state, and I was worried about the people who think people with Long Covid are psychological malingerers, etc. When I had to leave work, and filed for US Social Security Disability, I kept my Generalized Anxiety Disorder out of my initial application, afraid of getting the dreaded “just anxiety,” dismissal that many complex chronic illness kin are familiar with. (I was later told this was a bad move, and to definitely include all mental health and neurodivergence things, which I did for the ongoing process.)
Even as I’m having less anaphylaxis risk, it’s taking time to recover psychologically. I told my therapist how I felt like I backslid over a decade in mental health work overnight from the first recent anaphylaxis episode. She kindly said that while I might feel as scared and threatened as I often did back then, that the trigger was different. I was not feeling that anxious about an email, I was feeling that way about a literal life and death situation, one which I still don’t fully understand the triggers of.
A decade ago, de-stigmatizing mental healthcare was really important to me too. Now, I’m especially aware of how much these issues intersect, so heck yeah, publishing the medical art about anxiety.
Lastly, I wanted to include few examples of the ways in which these issues intersect. These are absolutely the tip of the iceberg.
- Mast Cell Activation Snydrome (often MCAS for space, in my art) can trigger so, so many pyschological symptoms. Mast Attack has a great overview of the topic, and while I haven’t been able to read the study fully because of the severe brain fog, Prevalence and treatment response of neuropsychiatric disorders in mast cell activation syndrome caught my eye.
- Anaphylaxis, or near anaphylaxis, has many symptoms in common with anxiety, from chest tightness to clammy skin, and “a feeling of impending doom”. While MCAS is not allergies, All Things Allergies has an easy intro to anxiety & anaphylaxis, and here’s a study The impact of anaphylaxis on the quality of life and mental health of adults.
- Ehlers-Danlos Syndrome co-occurs with many mental health issues, and I really appreciate how this article lists suspected mechanisms, misattributions, and related factors.
- Postural Orthostatic Tachycardia Syndrome, or POTS, is a form of autonomic dysfuntction (when things your body normally does automatically stop behaving normally), and is a part of my Long Covid. It involves a high heart rate, and often symptoms like room spinning or lightheadedness, trembling or shaking, shortness of breath, and poor bloodflow. POTS is often misdiagnosed as anxiety, and The Disabled Ginger wrote about it here.
Theories that diseases are caused by mental states and can be cured by will power are always an index of how much is not understood about the physical terrain of a disease.
Moreover, there is a peculiarly modern predilection for psychological explanations of a disease, as of everything else. Psychologizing seems to provide control over the experiences and events (like grave illnesses) over which people have in fact little or no control. Psychological understanding undermines the ‘reality’ of a disease. That reality has to be explained.
Susan Sontag, illness as metaphor (New York: Farrar, Straus and Giroux, 1977), p. 55.
p.s. mental health is physical health and physical health is mental health. you got a literal brain in your body and all of your body is involved in everything that you do. please take care of yourselves and each other. <3
https://www.illmarks.com/2025-8-9-is-this-mcas-anaphylaxis/
#allergy #anaphylaxis #anxiety #art #autoimmune #bodyHorror #bodyMapping #chronicIllness #gad #generalizedAnxiety #immune #longCovid #longcovid #mastCell #mastCellActivationSyndrome #mastCellDisease #mastcell #mcas #medart #medblog #medicalArt #medwriting #mentalHealth #MillionsMissing #pwLC #pwme #SciArt #sciblog #sciwriting #symptom
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FYI, Asian needle ants (Brachyponera chinensis) are in the Philadelphia area. Their painful sting can induce anaphylaxis, so be careful. If you find them please submit pic to iNaturalist so Michael Skvarla (Penn State) can come collect samples for confirmation. #ants #stinging #stinger #inaturalist #invasive #insects #anaphylaxis #delco #philadelphia #pennsylvania #hymenoptera https://share.inquirer.com/OTb0j7
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FYI, Asian needle ants (Brachyponera chinensis) are in the Philadelphia area. Their painful sting can induce anaphylaxis, so be careful. If you find them please submit pic to iNaturalist so Michael Skvarla (Penn State) can come collect samples for confirmation. #ants #stinging #stinger #inaturalist #invasive #insects #anaphylaxis #delco #philadelphia #pennsylvania #hymenoptera https://share.inquirer.com/OTb0j7
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FYI, Asian needle ants (Brachyponera chinensis) are in the Philadelphia area. Their painful sting can induce anaphylaxis, so be careful. If you find them please submit pic to iNaturalist so Michael Skvarla (Penn State) can come collect samples for confirmation. #ants #stinging #stinger #inaturalist #invasive #insects #anaphylaxis #delco #philadelphia #pennsylvania #hymenoptera https://share.inquirer.com/OTb0j7
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FYI, Asian needle ants (Brachyponera chinensis) are in the Philadelphia area. Their painful sting can induce anaphylaxis, so be careful. If you find them please submit pic to iNaturalist so Michael Skvarla (Penn State) can come collect samples for confirmation. #ants #stinging #stinger #inaturalist #invasive #insects #anaphylaxis #delco #philadelphia #pennsylvania #hymenoptera https://share.inquirer.com/OTb0j7
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FYI, Asian needle ants (Brachyponera chinensis) are in the Philadelphia area. Their painful sting can induce anaphylaxis, so be careful. If you find them please submit pic to iNaturalist so Michael Skvarla (Penn State) can come collect samples for confirmation. #ants #stinging #stinger #inaturalist #invasive #insects #anaphylaxis #delco #philadelphia #pennsylvania #hymenoptera https://share.inquirer.com/OTb0j7
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https://www.europesays.com/uk/278948/ MHRA Approves UK’s First Nasal Spray for Anaphylaxis #AdverseEffects #ALK #ALKTyrosineKinaseReceptor #allergens #allergy #anaphylaxis #AnaplasticLymphomaKinase #CD246 #child #childhood #Children #ClinicalResearch #ClusterOfDifferentiation246 #Europe #European #ExerciseInducedAnaphylaxis #Health #kids #Medication #Otolaryngology;ENTSpecialty;ENTSpeciality #Pediatrics #SideEffects #SportsMedicine #UK #UKSiteContent;UnitedKingdomSiteContent #UnitedKingdom
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A bee uprising provoked by Asian murder hornets with humans as incidental victims:
https://apnews.com/article/france-bees-attack-8c24d5919db13eac5b817c91daf1e7ab
#bees #anaphylaxis -
Recent events in polo-playing billionaire bee-swallowing deaths:
https://www.vice.com/en/article/billionaire-dies-after-swallowing-a-bee-during-polo-match/
#billionaires #bees #polo #death #anaphylaxis -
Hand me my Epipen... I'm goin' in.
250 [little finger to my mouth] MILLION pissed off and disoriented bees.
I can't even imagine the crash site cleanup. Perhaps Casa Bonita could send an emergency shipment of Sopapillas?
"Warning after millions of bees escape overturned truck in US"
-
Adrenaline Nasal Spray for Treatment of Anaphylaxis in Children
The indication for adrenaline nasal spray Neffy has been expanded (by the US FDA) to include children four years of age and older who weigh 15 to...........
#AdrenalineNasalSpray #Allergy #Anaphylaxis #NasalSpray
SCIEU Team -
Adrenaline Nasal Spray for Treatment of Anaphylaxis in Children
The indication for adrenaline nasal spray Neffy has been expanded (by the US FDA) to include children four years of age and older who weigh 15 to...........
#AdrenalineNasalSpray #Allergy #Anaphylaxis #NasalSpray
SCIEU Team -
Adrenaline Nasal Spray for Treatment of Anaphylaxis in Children
The indication for adrenaline nasal spray Neffy has been expanded (by the US FDA) to include children four years of age and older who weigh 15 to...........
#AdrenalineNasalSpray #Allergy #Anaphylaxis #NasalSpray
SCIEU Team -
Adrenaline Nasal Spray for Treatment of Anaphylaxis in Children
The indication for adrenaline nasal spray Neffy has been expanded (by the US FDA) to include children four years of age and older who weigh 15 to...........
#AdrenalineNasalSpray #Allergy #Anaphylaxis #NasalSpray
SCIEU Team -
Key recommendations from the Emergency treatment of peri-operative anaphylaxis: Resuscitation Council UK algorithm for anaesthetists
-
When I was first diagnosed with MCAS I thought “a condition I can control!”
I genuinely believed that since there were clear & obvious triggers - I could put in the work, overhaul my life and be free of attacks.
When a patient plans - mast cells laugh.
I threw myself into research trying to learn how to adopt a low histamine diet, clean my air and change my body care and cleaning products.
I (falsely) assumed that if I made enough changes - sacrificed HARD enough - I wouldn’t have to deal with flare ups.
It was exhausting. Many of the changes DID help. A low histamine diet, cleaner air, a proper med and supplement schedule and non toxic cleaning products all helped to reduce my overall “bucket” so that my symptoms were less severe.
The problem was - I continued having attacks. From minor attacks to full blown anaphylaxis - no matter how much work I put in the attacks didn’t stop.
It was incredibly frustrating - and I began tracking everything I ate, used or did in an effort to find patterns.
In the end I realized that sometimes - there are no answers. “Putting in the work” doesn’t guarantee you won’t have attacks.
It’s a help - and we should do whatever we can to minimize our symptoms - but chronic illness (and especially MCAS) doesn’t care about your plans.
I had to learn to let go. Constantly blaming myself, over analyzing every situation and trying to nail down exact triggers was exhausting me.
It wasn’t helping my physical health and was destroying my mental health
At a certain point - we have to accept that chronic illness can be wildly unpredictable - and flares are NOT our fault.
Setbacks happen - and the best thing you can do is give yourself grace and remember that the pain WILL pass.
This applies to Covid as well. I see far too many people who are covid cautious being blamed for their infections. Being grilled as to what their exact precautions were as people try and exploit a perceived weakness somewhere.
This isn’t helping.
If you’re masking and doing everything you can do to avoid covid - you’re doing a great job. If you got infected anyways - that’s the fault of our institutions and governments who’ve allowed the virus to run rampant and encouraged people NOT to take precautions
Just like we have to let go of trying to find every possible trigger for our chronic illness - we have to let go of the blame when people get infected with Covid.
Blame, shame and guilt aren’t helping anyone - and they aren’t good for your health.
To be clear - “letting go” doesn’t have to mean giving up. It doesn’t mean you stop trying to improve your health or stop mitigating for COVID.
It simply means you stop fighting the reality that you’re sick. You lean IN to the conditions and try and find ways to accommodate
It’s a difficult thing to do. I’m still having to work at it every single day. But it’s worth making the effort.
Society, HCWs and even friends & family can be cruel to those with chronic illness - we don’t need to be cruel to ourselves.
Which brings me to my third and final article in my series on living with MCAS - Learning to Let Go.
This post explains how I learned to be kinder & gentler with myself and accept that setbacks WILL happen and they’re not my fault:
https://www.disabledginger.com/p/learning-to-let-go-how-to-accept
1/2
#CovidIsAirborne #CovidCautious #CovidIsNotOver #CleanAir #WearaMask #Disability #LongCovid #Ableism #Denial #CleanAir #Pandemic #PublicHealth #InfectionControl #Eugenics #SafeHealthcare #N95 #Respirators #MasksWork #MaskUp #Spoonie #Discrimination #Dysautonomia #mecfs #pots #mcas #communitycare #wearamask #chronicillness #keepmasksinhealthcare #MaskBans #NoMaskBans #MastCellActivationSyndrome #mastcells #histamine #lowhistaminediet #mastocytosis #anaphylaxis
-
When I was first diagnosed with MCAS I thought “a condition I can control!”
I genuinely believed that since there were clear & obvious triggers - I could put in the work, overhaul my life and be free of attacks.
When a patient plans - mast cells laugh.
I threw myself into research trying to learn how to adopt a low histamine diet, clean my air and change my body care and cleaning products.
I (falsely) assumed that if I made enough changes - sacrificed HARD enough - I wouldn’t have to deal with flare ups.
It was exhausting. Many of the changes DID help. A low histamine diet, cleaner air, a proper med and supplement schedule and non toxic cleaning products all helped to reduce my overall “bucket” so that my symptoms were less severe.
The problem was - I continued having attacks. From minor attacks to full blown anaphylaxis - no matter how much work I put in the attacks didn’t stop.
It was incredibly frustrating - and I began tracking everything I ate, used or did in an effort to find patterns.
In the end I realized that sometimes - there are no answers. “Putting in the work” doesn’t guarantee you won’t have attacks.
It’s a help - and we should do whatever we can to minimize our symptoms - but chronic illness (and especially MCAS) doesn’t care about your plans.
I had to learn to let go. Constantly blaming myself, over analyzing every situation and trying to nail down exact triggers was exhausting me.
It wasn’t helping my physical health and was destroying my mental health
At a certain point - we have to accept that chronic illness can be wildly unpredictable - and flares are NOT our fault.
Setbacks happen - and the best thing you can do is give yourself grace and remember that the pain WILL pass.
This applies to Covid as well. I see far too many people who are covid cautious being blamed for their infections. Being grilled as to what their exact precautions were as people try and exploit a perceived weakness somewhere.
This isn’t helping.
If you’re masking and doing everything you can do to avoid covid - you’re doing a great job. If you got infected anyways - that’s the fault of our institutions and governments who’ve allowed the virus to run rampant and encouraged people NOT to take precautions
Just like we have to let go of trying to find every possible trigger for our chronic illness - we have to let go of the blame when people get infected with Covid.
Blame, shame and guilt aren’t helping anyone - and they aren’t good for your health.
To be clear - “letting go” doesn’t have to mean giving up. It doesn’t mean you stop trying to improve your health or stop mitigating for COVID.
It simply means you stop fighting the reality that you’re sick. You lean IN to the conditions and try and find ways to accommodate
It’s a difficult thing to do. I’m still having to work at it every single day. But it’s worth making the effort.
Society, HCWs and even friends & family can be cruel to those with chronic illness - we don’t need to be cruel to ourselves.
Which brings me to my third and final article in my series on living with MCAS - Learning to Let Go.
This post explains how I learned to be kinder & gentler with myself and accept that setbacks WILL happen and they’re not my fault:
https://www.disabledginger.com/p/learning-to-let-go-how-to-accept
1/2
#CovidIsAirborne #CovidCautious #CovidIsNotOver #CleanAir #WearaMask #Disability #LongCovid #Ableism #Denial #CleanAir #Pandemic #PublicHealth #InfectionControl #Eugenics #SafeHealthcare #N95 #Respirators #MasksWork #MaskUp #Spoonie #Discrimination #Dysautonomia #mecfs #pots #mcas #communitycare #wearamask #chronicillness #keepmasksinhealthcare #MaskBans #NoMaskBans #MastCellActivationSyndrome #mastcells #histamine #lowhistaminediet #mastocytosis #anaphylaxis
-
When I was first diagnosed with MCAS I thought “a condition I can control!”
I genuinely believed that since there were clear & obvious triggers - I could put in the work, overhaul my life and be free of attacks.
When a patient plans - mast cells laugh.
I threw myself into research trying to learn how to adopt a low histamine diet, clean my air and change my body care and cleaning products.
I (falsely) assumed that if I made enough changes - sacrificed HARD enough - I wouldn’t have to deal with flare ups.
It was exhausting. Many of the changes DID help. A low histamine diet, cleaner air, a proper med and supplement schedule and non toxic cleaning products all helped to reduce my overall “bucket” so that my symptoms were less severe.
The problem was - I continued having attacks. From minor attacks to full blown anaphylaxis - no matter how much work I put in the attacks didn’t stop.
It was incredibly frustrating - and I began tracking everything I ate, used or did in an effort to find patterns.
In the end I realized that sometimes - there are no answers. “Putting in the work” doesn’t guarantee you won’t have attacks.
It’s a help - and we should do whatever we can to minimize our symptoms - but chronic illness (and especially MCAS) doesn’t care about your plans.
I had to learn to let go. Constantly blaming myself, over analyzing every situation and trying to nail down exact triggers was exhausting me.
It wasn’t helping my physical health and was destroying my mental health
At a certain point - we have to accept that chronic illness can be wildly unpredictable - and flares are NOT our fault.
Setbacks happen - and the best thing you can do is give yourself grace and remember that the pain WILL pass.
This applies to Covid as well. I see far too many people who are covid cautious being blamed for their infections. Being grilled as to what their exact precautions were as people try and exploit a perceived weakness somewhere.
This isn’t helping.
If you’re masking and doing everything you can do to avoid covid - you’re doing a great job. If you got infected anyways - that’s the fault of our institutions and governments who’ve allowed the virus to run rampant and encouraged people NOT to take precautions
Just like we have to let go of trying to find every possible trigger for our chronic illness - we have to let go of the blame when people get infected with Covid.
Blame, shame and guilt aren’t helping anyone - and they aren’t good for your health.
To be clear - “letting go” doesn’t have to mean giving up. It doesn’t mean you stop trying to improve your health or stop mitigating for COVID.
It simply means you stop fighting the reality that you’re sick. You lean IN to the conditions and try and find ways to accommodate
It’s a difficult thing to do. I’m still having to work at it every single day. But it’s worth making the effort.
Society, HCWs and even friends & family can be cruel to those with chronic illness - we don’t need to be cruel to ourselves.
Which brings me to my third and final article in my series on living with MCAS - Learning to Let Go.
This post explains how I learned to be kinder & gentler with myself and accept that setbacks WILL happen and they’re not my fault:
https://www.disabledginger.com/p/learning-to-let-go-how-to-accept
1/2
#CovidIsAirborne #CovidCautious #CovidIsNotOver #CleanAir #WearaMask #Disability #LongCovid #Ableism #Denial #CleanAir #Pandemic #PublicHealth #InfectionControl #Eugenics #SafeHealthcare #N95 #Respirators #MasksWork #MaskUp #Spoonie #Discrimination #Dysautonomia #mecfs #pots #mcas #communitycare #wearamask #chronicillness #keepmasksinhealthcare #MaskBans #NoMaskBans #MastCellActivationSyndrome #mastcells #histamine #lowhistaminediet #mastocytosis #anaphylaxis
-
When I was first diagnosed with MCAS I thought “a condition I can control!”
I genuinely believed that since there were clear & obvious triggers - I could put in the work, overhaul my life and be free of attacks.
When a patient plans - mast cells laugh.
I threw myself into research trying to learn how to adopt a low histamine diet, clean my air and change my body care and cleaning products.
I (falsely) assumed that if I made enough changes - sacrificed HARD enough - I wouldn’t have to deal with flare ups.
It was exhausting. Many of the changes DID help. A low histamine diet, cleaner air, a proper med and supplement schedule and non toxic cleaning products all helped to reduce my overall “bucket” so that my symptoms were less severe.
The problem was - I continued having attacks. From minor attacks to full blown anaphylaxis - no matter how much work I put in the attacks didn’t stop.
It was incredibly frustrating - and I began tracking everything I ate, used or did in an effort to find patterns.
In the end I realized that sometimes - there are no answers. “Putting in the work” doesn’t guarantee you won’t have attacks.
It’s a help - and we should do whatever we can to minimize our symptoms - but chronic illness (and especially MCAS) doesn’t care about your plans.
I had to learn to let go. Constantly blaming myself, over analyzing every situation and trying to nail down exact triggers was exhausting me.
It wasn’t helping my physical health and was destroying my mental health
At a certain point - we have to accept that chronic illness can be wildly unpredictable - and flares are NOT our fault.
Setbacks happen - and the best thing you can do is give yourself grace and remember that the pain WILL pass.
This applies to Covid as well. I see far too many people who are covid cautious being blamed for their infections. Being grilled as to what their exact precautions were as people try and exploit a perceived weakness somewhere.
This isn’t helping.
If you’re masking and doing everything you can do to avoid covid - you’re doing a great job. If you got infected anyways - that’s the fault of our institutions and governments who’ve allowed the virus to run rampant and encouraged people NOT to take precautions
Just like we have to let go of trying to find every possible trigger for our chronic illness - we have to let go of the blame when people get infected with Covid.
Blame, shame and guilt aren’t helping anyone - and they aren’t good for your health.
To be clear - “letting go” doesn’t have to mean giving up. It doesn’t mean you stop trying to improve your health or stop mitigating for COVID.
It simply means you stop fighting the reality that you’re sick. You lean IN to the conditions and try and find ways to accommodate
It’s a difficult thing to do. I’m still having to work at it every single day. But it’s worth making the effort.
Society, HCWs and even friends & family can be cruel to those with chronic illness - we don’t need to be cruel to ourselves.
Which brings me to my third and final article in my series on living with MCAS - Learning to Let Go.
This post explains how I learned to be kinder & gentler with myself and accept that setbacks WILL happen and they’re not my fault:
https://www.disabledginger.com/p/learning-to-let-go-how-to-accept
1/2
#CovidIsAirborne #CovidCautious #CovidIsNotOver #CleanAir #WearaMask #Disability #LongCovid #Ableism #Denial #CleanAir #Pandemic #PublicHealth #InfectionControl #Eugenics #SafeHealthcare #N95 #Respirators #MasksWork #MaskUp #Spoonie #Discrimination #Dysautonomia #mecfs #pots #mcas #communitycare #wearamask #chronicillness #keepmasksinhealthcare #MaskBans #NoMaskBans #MastCellActivationSyndrome #mastcells #histamine #lowhistaminediet #mastocytosis #anaphylaxis
-
When I was first diagnosed with MCAS I thought “a condition I can control!”
I genuinely believed that since there were clear & obvious triggers - I could put in the work, overhaul my life and be free of attacks.
When a patient plans - mast cells laugh.
I threw myself into research trying to learn how to adopt a low histamine diet, clean my air and change my body care and cleaning products.
I (falsely) assumed that if I made enough changes - sacrificed HARD enough - I wouldn’t have to deal with flare ups.
It was exhausting. Many of the changes DID help. A low histamine diet, cleaner air, a proper med and supplement schedule and non toxic cleaning products all helped to reduce my overall “bucket” so that my symptoms were less severe.
The problem was - I continued having attacks. From minor attacks to full blown anaphylaxis - no matter how much work I put in the attacks didn’t stop.
It was incredibly frustrating - and I began tracking everything I ate, used or did in an effort to find patterns.
In the end I realized that sometimes - there are no answers. “Putting in the work” doesn’t guarantee you won’t have attacks.
It’s a help - and we should do whatever we can to minimize our symptoms - but chronic illness (and especially MCAS) doesn’t care about your plans.
I had to learn to let go. Constantly blaming myself, over analyzing every situation and trying to nail down exact triggers was exhausting me.
It wasn’t helping my physical health and was destroying my mental health
At a certain point - we have to accept that chronic illness can be wildly unpredictable - and flares are NOT our fault.
Setbacks happen - and the best thing you can do is give yourself grace and remember that the pain WILL pass.
This applies to Covid as well. I see far too many people who are covid cautious being blamed for their infections. Being grilled as to what their exact precautions were as people try and exploit a perceived weakness somewhere.
This isn’t helping.
If you’re masking and doing everything you can do to avoid covid - you’re doing a great job. If you got infected anyways - that’s the fault of our institutions and governments who’ve allowed the virus to run rampant and encouraged people NOT to take precautions
Just like we have to let go of trying to find every possible trigger for our chronic illness - we have to let go of the blame when people get infected with Covid.
Blame, shame and guilt aren’t helping anyone - and they aren’t good for your health.
To be clear - “letting go” doesn’t have to mean giving up. It doesn’t mean you stop trying to improve your health or stop mitigating for COVID.
It simply means you stop fighting the reality that you’re sick. You lean IN to the conditions and try and find ways to accommodate
It’s a difficult thing to do. I’m still having to work at it every single day. But it’s worth making the effort.
Society, HCWs and even friends & family can be cruel to those with chronic illness - we don’t need to be cruel to ourselves.
Which brings me to my third and final article in my series on living with MCAS - Learning to Let Go.
This post explains how I learned to be kinder & gentler with myself and accept that setbacks WILL happen and they’re not my fault:
https://www.disabledginger.com/p/learning-to-let-go-how-to-accept
1/2
#CovidIsAirborne #CovidCautious #CovidIsNotOver #CleanAir #WearaMask #Disability #LongCovid #Ableism #Denial #CleanAir #Pandemic #PublicHealth #InfectionControl #Eugenics #SafeHealthcare #N95 #Respirators #MasksWork #MaskUp #Spoonie #Discrimination #Dysautonomia #mecfs #pots #mcas #communitycare #wearamask #chronicillness #keepmasksinhealthcare #MaskBans #NoMaskBans #MastCellActivationSyndrome #mastcells #histamine #lowhistaminediet #mastocytosis #anaphylaxis
-
Epinephrine (or Adrenaline) Nasal Spray for Treatment of Anaphylaxis
Neffy (epinephrine nasal spray) has been approved by the FDA for the emergency treatment of Type I allergic reactions including life-threatening...........
#Adrenaline #Allergy #Anaphylaxis #Epinephrine #FDA #NasalSpray #Neffy
SCIEU Team -
Epinephrine (or Adrenaline) Nasal Spray for Treatment of Anaphylaxis
Neffy (epinephrine nasal spray) has been approved by the FDA for the emergency treatment of Type I allergic reactions including life-threatening...........
#Adrenaline #Allergy #Anaphylaxis #Epinephrine #FDA #NasalSpray #Neffy
SCIEU Team -
Epinephrine (or Adrenaline) Nasal Spray for Treatment of Anaphylaxis
Neffy (epinephrine nasal spray) has been approved by the FDA for the emergency treatment of Type I allergic reactions including life-threatening...........
#Adrenaline #Allergy #Anaphylaxis #Epinephrine #FDA #NasalSpray #Neffy
SCIEU Team -
Epinephrine (or Adrenaline) Nasal Spray for Treatment of Anaphylaxis
Neffy (epinephrine nasal spray) has been approved by the FDA for the emergency treatment of Type I allergic reactions including life-threatening...........
#Adrenaline #Allergy #Anaphylaxis #Epinephrine #FDA #NasalSpray #Neffy
SCIEU Team -
Epinephrine (or Adrenaline) Nasal Spray for Treatment of Anaphylaxis
Neffy (epinephrine nasal spray) has been approved by the FDA for the emergency treatment of Type I allergic reactions including life-threatening...........
#Adrenaline #Allergy #Anaphylaxis #Epinephrine #FDA #NasalSpray #Neffy
SCIEU Team