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Latest posts tagged with #mcas on Bluesky

Posts tagged #mcas

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Lipedema: What It Is, What You Can Do About It Do you have lumps and bumps or symmetrical pockets of fat on your legs?  What about your arms, hips, abdomen, or buttocks?&nb…

If you've got it...there's hope.

#BlogPost #ChronicIllness #ChronicPain #EDS #MCAS #POTS #HolisticHealth #Lipedema 💕 #Wellness

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Everything I read said LDN is low risk and easy to stop, but akathesia insomnia worsened my already-very-low #ME baseline for many months. I understand all meds and supplements have risks and we don't know how to tell who will react most negatively etc (especially in a population with #MCAS) 3/4

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tomu nejde utect. Clovek musi sakra zodpovedne rozhodovat o kazdem jidle. Vylouceni ze socialnich interakci kvuli #MCAS a #EDS je dalsi vec. Uz pres 10 let musim byt extremne opatrna v jidle a rozhodne nejen v jidle. To neni volba, nebo fnukani, tohle jsou me utrzky kazdodenniho zivota. #delamcomuzu

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Narocny vyber jidla resim denne, prakticky u kazdeho jidla. Tech omezeni je mnoho. Od reakci kvuli #MCAS, pres gastro potize vlivem #EDS, ktere zahrnuji cely zazivaci trakt. Prubeh jidla zaroven vyrazne komplikuji blokady, subluxace a skriple nervy. Musim byt opatrna, protoze pripadne zvraceni

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Amy Scoggins’ ‘The Caretaker And The Warrior’: Advocating for Ehlers-Danlos Syndrome After her teen daughter was diagnosed with Hypermobile Ehlers-Danlos Syndrome (EDS), American painter Amy Scoggins decided to use her platform to raise awareness of the rare inherited disease. She…

"After her teen daughter was diagnosed with Hypermobile Ehlers-Danlos Syndrome (EDS), American painter Amy Scoggins decided to use her platform to raise awareness..."

#Artist #Art #ChronicIllness #ChronicPain #EDS #hEDS #MCAS #SelfCare
💕 #Wellness

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Traveling With Hope: An Interview With Nicola of Earth Balance Tai Chi ***** Have you ever tried tai chi or qigong? So many of us get asked if we’ve tried yoga (to the point where some of us want to scream when we hear that word) but it seems to me that Chinese …

Tai chi & qigong for people with #EhlersDanlosSyndrome? Yes, indeedy.

#BlogPost #ChronicIllness #ChronicPain #EDS #MCAS #POTS #HolisticHealth #TaiChi #QiGong 💕 #Wellness

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I use to feel shame as I got sicker and relied more on the internet for finding community.

That is totally gone now.

People who don’t have Long Covid will never understand what going through this is like.

Social media is a lifeline for every part of this disease.

#longcovid #mecfs #pots #mcas

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Intuitive Eating vs. Mindful Eating–Which Is Better For You? (Some Tips For Folks With EDS, MCAS, &/or POTS) Have you ever thought about the difference between mindful eating and intuitive eating?  They are not the same thing, but both can be helpful approaches to nutrition when a person lives with E…

How about both?

#BlogPost #GutHealth #Nutrition #Diet #Microbiome #EDS #hEDS #MCAS #POTS #HolisticHealth #SelfCare #HappyGutHappyLife 💕 #Wellness

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Specialty areas graphic
What I treat most often...

#ChronicPain #AcuteInjury #GutHealth #EDS #MCAS #CosmeticAcupuncture #Skincare #ScarRevision #MensHealth #PreventiveCare 💕 #Wellness

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Self-Care For Folks With Hypermobile Ehlers-Danlos Syndrome (Yes, You Do Deserve It) Self-care when you live with a complex disorder like EDS (especially if you have the usual add-ons like MCAS or POTS) is crucial&#…

It's not selfish.

#BlogPost #EDS #hEDS #MCAS #POTS #HolisticHealth #SelfCare 💕 #Wellness

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The under-the-radar disease Venus Williams, Halsey and Solange Knowles all have in common The disease, which impacts around 4 million Americans, has disrupted the lives of some of the biggest names in sports and music.

Did you know about these people and their chronic illnesses?

#EDS #MCAS #POTS #ChronicIllness #Representation #HolisticHealth 💕 #Wellness

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Health coaching, Edu-coaching, Consultation: The Which and Why and When for People with Ehlers-Danlos Syndrome Working with a health coach can be one of the most affirming, valuable, inspiring things you can do when you decide that yes, it i…

Which resonates most for you?

#BlogPost #HealthCoach #EduCoach #Consultations #ChronicIllness #ChronicPain #EDS #hEDS #MCAS #HolisticHealth 💕 #Wellness

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Mittwoch was anderes/falsches im Essen. Folge Nierenschmerzen, Muskelschwäche, totaler Horror. Letztes Jahr hielt das ein halbes Jahr an! Passiert immer mal, meist so um Ostern herum oder so. Grauenvoll! Einmal was Falsches gegessen halbes Jahr Horror. Hab nur 1 Niere😭😭😭 #MEcfs vermutlich auch #MCAS

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#LiegendDemo #mecfs #cureME #fightME #demonstration #longcovid #Postcovid #Postvac #PAIS #MCAS #POTS #Dysautonomie #EDS #CCI #SFN #FQAD #disability #Ostern #Danke

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Community Voices: Dominique McGinn "Living with pain, skin injuries, and cEDS." My name is Dominique McGinn, I am a Primary School teacher from Scotland. I am 25 years old and was diagnosed with classical Ehlers-Danlos syndrome (cEDS) at age 3. My dad and younger brother also…

It's worldwide and everyone has their own experience with it.

#Scotland #ChronicIllness #ChronicPain #EDS #MCAS #POTS #HolisticHealth
💕 #Wellness

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Traveling With Hope: An Interview With Nicola of Earth Balance Tai Chi ***** Have you ever tried tai chi or qigong? So many of us get asked if we’ve tried yoga (to the point where some of us want to scream when we hear that word) but it seems to me that Chinese …

A wonderful resource for anyone with #EhlersDanlosSyndrome or any other complex condition.

#BlogPost #ChronicIllness #ChronicPain #EDS #MCAS #POTS #HolisticHealth #TaiChi 💕 #Wellness

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In Kreis Kleve, we, a group of parents, are connected by the sheer force of our children having #LongCovid. I have never met Rosa, but the window to her #MECFS and #MCAS prison is imprinted in my brain. Taped off. Dark. Burried.

Here is here story (in German) & that of Kathi.

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Ehlers Danlos Syndrome and Men: Three Key Issues Men and their experiences living with hypermobile Ehlers Danlos syndrome is a whole topic…one that doesn’t get nearly enough attention in my opinion.  When you look online for info…

Guys have #EhlersDanlosSyndrome too, you know.

#BlogPost #MensHealth #GuysWithEDS #ChronicPain #ChronicIllness #EDS #hEDS #MCAS #POTS #HolisticHealth 💕 #Wellness

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On a whim, I picked up some frozen haskap berries at the Italian Centre the last time we were in the city. Tonight I made a crisp with them and WOW do I feel good. Researching haskaps tells me they have extremely high levels of C3Gs, good vit C and antimicrobial properties.
#mcas #chronicillness

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Only a Canary alkemy published a post on Ko-fi

Kofi post about a short #horror based on having #MCAS

ko-fi.com/post/Only-a-...

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We all have our specialty areas, too. Here are mine.

#ChronicPain #AcuteInjury #GutHealth #EDS #MCAS #CosmeticAcupuncture #Skincare #ScarRevision #MensHealth #PreventiveCare 💕 #Wellness

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Self-Care For Folks With Hypermobile Ehlers-Danlos Syndrome (Yes, You Do Deserve It) Self-care when you live with a complex disorder like EDS (especially if you have the usual add-ons like MCAS or POTS) is crucial&#…

Nope. Definitely not selfish.

#BlogPost #ChronicIllness #ChronicPain #EDS #hEDS #MCAS #POTS #HolisticHealth #Acupuncture #TuiNa #SelfCare 💕 #Wellness

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Intuitive Eating vs. Mindful Eating–Which Is Better For You? (Some Tips For Folks With EDS, MCAS, &/or POTS) Have you ever thought about the difference between mindful eating and intuitive eating?  They are not the same thing, but both can be helpful approaches to nutrition when a person lives with E…

Why not both?

#BlogPost #EDS #hEDS #MCAS #POTS #HolisticHealth #GutHealth #Mindful #Intuitive 💕 #Wellness

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Friends, I'm consulting the hive mind here, and actively want your feedback. If you have #MCAS and/or #gastroparesis would you be willing to share your symptoms and/or what process led to you getting diagnosed? V

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Will your doc recognize it’s from #Covid? Probably not. But you’ll get care. If you go in w/ #MECFS you’ll be shown the door. There is also so much comorbidity of ME w/ #POTS #MCAS #EDS etc that even if you have one of these & don’t have ME, learning about it could still help you to answers. 2/

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Cheyanne Perry — Living a Full Life with Deadly Allergies. “It’s in My Blood” is a series that feature people with chronic illnesses, and also their passions and talents.

Cheyanne Perry — Living a Full Life with Deadly Allergies. “It’s in My Blood” is a series that feature people with chronic illnesses, and also their passions and talents.

"The goal of this #blog series is to highlight aspects of #identity that are separate from illness; however, #writing is especially helpful in compensating for the #isolation my illness causes.": buff.ly/q48CzG0

Featuring: hospitalprncss
#ChronicPain #MCAS #ChronicLife #allergies

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How Chinese Medicine Treats hEDS (Where to Begin) Acupuncture and other modalities of Chinese medicine can be an excellent resource for people with complex disorders, EDS and the c…

How does Chinese medicine treat EDS?

#BlogPost #EDS #hEDS #MCAS #POTS #HolisticHealth #SelfCare #Strategies
💕 #Wellness

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Does anyone on my feed have any experience with #MCAS? The more I'm reading about histamine in foods & the symptoms of MCAS, the more the pieces fit. But it's overwhelming & no 2 articles seem to say the same thing so I'm beyond confused & more than a little desperate. I don't know where to begin.

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Gonna go back to physical therapy again too I'm glad about that. And another allergist referral for MCAS/MCS stuff.

Don't know if it will help or not. Any of #MCAS friends have any luck with any medicines that have helped?

Thought about trying Zyflo but it's bad for your liver.

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I would like to find other people on here that deal with MCAS in their own lives. I don’t spend very much time talking about it but it would be nice to know other people going through the same thing I am on a physical level.

#MCAS

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