We exist to promote progress in the awareness, diagnosis and treatment of Mast Cell Activation Syndrome and to provide support to people affected by MCAS.
Joined June 2016
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Join us on Monday 29th June from 7-8pm for an informative and engaging Q&A session with Chloe Hall and Alison Holloway, two leading dietitians and experts on Mast Cell Activation Syndrome (MCAS). Find out more and book your place ow.ly/fVsh50Z5xYz
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“Hard days don’t erase the progress I’ve already made.”
Symptoms can fluctuate, but every step you’ve taken still counts.
#MCASMantras
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Today we celebrate #GlobalWellnessDay – a day to honour our health and well-being. Today is the perfect reminder to prioritise your mind, body, and spirit. Take time for self-care, connect with nature, and embrace wellness. How are you looking after yourself today? 💙 #MCAS
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Join us on Monday 22nd June from 7-8:30pm for a session on Mindful Movement for Illness hosted by Deborah Bircham from Live Well with Chronic Illness. JFind out more and book your place here ow.ly/SPBy50Z5yjB
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💥Exciting things are happening every month for the MCAS community! Join our online events and be part of something special. Sign up for our newsletter now and make sure you’re always in the know—don’t miss out!
#MCAS #MCASAware #MCASEvents #MastCellAction
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🦸Being an MCAS Hero isn’t about big gestures.
It’s about quietly showing up, month after month, so others don’t feel alone. Our MCAS Heroes are part of the heart of Mast Cell Action.
Become an MCAS Hero today, find out more mastcellaction.org/mcas-hero…
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❤️ We’re incredibly grateful to The Hospital Saturday Fund for their recent donation to support those with MCAS. Your generosity helps our MCAS community feel recognised, heard, and supported. Thank you for making a real difference!
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Join us on Tuesday 9th June from 5:45-6:45pm for our monthly Virtual Self-Massage sessions hosted by Ellen from Flexback. Find out more and book your place mastcellaction.beaconforms.c…
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Join us on Monday 29th June from 7-8pm for an informative and engaging Q&A session with Chloe Hall and Alison Holloway, two leading dietitians and experts on Mast Cell Activation Syndrome (MCAS). Find out more and book your place ow.ly/fVsh50Z5xYz
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😎With holiday season approaching, we wanted to remind you about our handy guide to travelling with MCAS. It’s full of tips and resources for managing MCAS on the go, wherever you go. Download the resource here ow.ly/kXe250Z5xL0
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Join us on Monday 22nd June from 7-8:30pm for a session on Mindful Movement for Illness hosted by Deborah Bircham from Live Well with Chronic Illness. JFind out more and book your place here ow.ly/SPBy50Z5yjB
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Join us on Tuesday 9th June from 5:45-6:45pm for our monthly Virtual Self-Massage sessions hosted by Ellen from Flexback. Find out more and book your place mastcellaction.beaconforms.c…
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The chemicals and scents in everyday products can cause dangerous reactions for some people with MCAS.
#MCAS #MastCellActivationSyndrome #ChronicIllness #InvisibleIllness #AllergyAwareness #ChemicalSensitivity #DisabilityAwareness #HealthAwareness #MastCellAction
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Join us on Tuesday 9th June from 5:45-6:45pm for our monthly Virtual Self-Massage sessions hosted by Ellen from Flexback. Find out more and book your place mastcellaction.beaconforms.c…
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International Mast Cell Disease Awareness Month is here. Find out more here mastcellaction.org/internati…
#MCAS #mcasaware
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❤️ We’re incredibly grateful to The Hospital Saturday Fund for their recent donation to support those with MCAS. Your generosity helps our MCAS community feel recognised, heard, and supported. Thank you for making a real difference!
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When someone says “but you don’t look ill”… and you smile, because explaining would take more energy than you have. What they don’t see: the symptoms you manage quietly, the calculations behind every plan the strength it takes just to get through the day.
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💥Exciting things are happening every month for the MCAS community! Join our online events and be part of something special. Sign up for our newsletter now and make sure you’re always in the know—don’t miss out!
#MCAS #MCASAware #MCASEvents #MastCellAction
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Many people with MCAS have to advocate for themselves as there is still limited awareness among professionals. Our work at Mast Cell Action is trying to change this.
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We’d love to stay in touch with you. We send out a short, informative newsletter every fortnight. It covers the latest updates from Mast Cell Action, MCAS news and info about upcoming events, services and support.
Sign up here mastcellaction.org/become-a-…
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