MastCellAction

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.

[MastCellAction @MastCellAction]

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 https://t.co/cKXZdrtT9z

[MastCellAction @MastCellAction]

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 https://t.co/TRDgrAJzqT

[MastCellAction @MastCellAction]

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

[MastCellAction @MastCellAction]

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 https://t.co/TRDgrAJzqT

[MastCellAction @MastCellAction]

International Mast Cell Disease Awareness Month is here. Find out more here https://t.co/twjke0WHiY

#MCAS #mcasaware

[MastCellAction @MastCellAction]

❤️ 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!

[MastCellAction @MastCellAction]

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.

[MastCellAction @MastCellAction]

💥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

[MastCellAction @MastCellAction]

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.

[MastCellAction @MastCellAction]

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 https://t.co/vYG7MuZPoO

[MastCellAction @MastCellAction]

💜 We’ve designed a special edition t-shirt for International Mast Cell Disease Awareness Month. 25% of all profits will be donated to Mast Cell Action, directly supporting the MCAS community with resources, advocacy, and research
👉 Grab yours here: https://t.co/gdL9O2Kt7U

[MastCellAction @MastCellAction]

Imagine your body reacting to your own sweat, heat, or emotions.

For some with MCAS, even their own biology becomes a trigger.

[MastCellAction @MastCellAction]

Often, routines can help us to control MCAS - such as sleep, food and managing stress. It can take time to work out what works for each of us individually but can be well worth the effort!

[MastCellAction @MastCellAction]

🍝 Food and eating out can be a real challenge for people with MCAS with potential triggers in food and drink and also from surroundings.

#MCAS

[MastCellAction @MastCellAction]

❤️ We’re incredibly grateful to The Dyers Charitable Trust 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!

[MastCellAction @MastCellAction]

Check out our online events scheduled in May. We have MCAS friendly movement classes, sessions to boost wellbeing, information sessions and community events.

Find out more and book your place here https://t.co/NxeLHZgi49

[MastCellAction @MastCellAction]

We’re delighted to share the Mast Cell Action podcast, Let’s Talk MCAS with you!

Join us for our first ever episode, where our host Deborah Bircham, chats with Joy Mason, Mast Cell Action’s CEO.

Link to Spotify https://t.co/ZFDKWp1iTe
Link to Amazon https://t.co/csDMlVRzzO

[MastCellAction @MastCellAction]

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 https://t.co/vYG7MuZPoO

[MastCellAction @MastCellAction]

Many people with MCAS can spot the early signs looking back at their childhood and often the pieces can fall into place.

#MCAS #ChronicIllness

[MastCellAction @MastCellAction]

Check out our online events scheduled in May. We have MCAS friendly movement classes, sessions to boost wellbeing, information sessions and community events.

Find out more and book your place here https://t.co/NxeLHZgi49