We have developed multiple resources to support people affected by MCAS and those caring for people with MCAS.
Some of our resources are for children and families, others are for adults. Use the tabs at the bottom of this page to find the right resources for you.
We are delighted that our reasonable adjustments support pack is finally ready! From knowing your rights, to informing your employer about MCAS or implementing policies and reasonable adjustments to support you in the workplace, we've got it covered! Download the full pack here.
Please do get in touch to let us know if the pack has helped you!
This work has been made possible by an award from Postcode Places Trust, a grant-giving charity funded entirely by players of People’s Postcode Lottery.
With thanks to Annisha Sidhu and Katya Kozary for making this project possible.
We are committed to making our resources accessible to everyone in our community. We understand that some individuals may experience electromagnetic sensitivity (EMF) or prefer hard copies of materials for various reasons.
If you prefer/require hard copies of materials, we are happy to provide alternative formats whenever possible. Please reach out to us here. We will do our utmost to assist you and ensure your experience is as comfortable as possible.
Our goal is to create an inclusive environment where everyone can fully engage with our content and discussions. If you have any questions or suggestions regarding accessibility, please don't hesitate to get in touch. Your feedback helps us continually improve our efforts to ensure that everyone feels welcome and supported.
After nearly 18 months of work, our Freedom Kit is finally ready to share!
This kit is a resource for families to use to share information with schools in order to help create a plan for children with MCAS in education settings. The kit has information about MCAS and spaces to record information about your child or the child you care for with MCAS to make it easier to share this with education and childcare settings.
We would love to hear your feedback about this resource.
Download the full pack here!
Our parent support leaflet has developed to help support parents and carers of children living with systemic mast cell activation and Mast Cell Activation Syndrome (MCAS).
It provides suggestions for how to care for your personal mental wellbeing whilst caring for someone with MCAS, and shares ideas and suggestions for how to communicate and support each other as a family.
In this leaflet, we hope to share ideas and suggestions that support a positive way of thinking and approaching a new way of family life, whilst accepting the challenges that may lay ahead.
Download our newly launched parent support leaflet here
We are delighted to have published a children's book, Casper the Chameleon. Written by our very own Director of Operations, Joy Mason.
Order your copy for free by emailing denise@mastcellaction.org.
We hope the following resources will be used in partnership with the book to support wellbeing in the MCAS community.
Read more about Casper and how to get your FREE copy here.
Our mission is to provide invaluable resources and support to individuals and families living with Mast Cell Activation Syndrome (MCAS). We understand the challenges and complexities that come with managing this condition, and we're dedicated to making a meaningful difference in the lives of those affected.
However, we can't do it alone.
As a non-profit organisation, we rely on the generosity and support of individuals like you, to continue our important work. Your contributions enable us to maintain and expand our range of resources, including educational materials, support groups, research initiatives, and more.
By donating, you're directly impacting the MCAS community, offering hope and assistance to those who need it most. Every contribution, no matter the size, makes a difference and is deeply appreciated. If you can, please donate here.
This leaflet documents some of the tests that may be used to diagnose MCAS and explains how to read the results.
This information guide about MCAS, and the additional needs a student with MCAS may have, can be shared with Disability Officers and other members of staff at universities.
This resource has been designed to provide general guidance and help students to access support as they approach further education at university.
This PDF combines our freedom kit, MCAS for teachers pack and letter for schools in one handy download.
The resource pack to help you to share vital information about your child's mast cell disorder with school and other care-givers.
This pack can be used to share information about MCAS with teachers and other care-givers.
Use this letter template along with the Freedom kit to share your child's needs with their school or childcare provider
A form designed to help you to plan the questions you would like to ask and symptoms you would like to discuss at medical appointments.
In the world of chronic illness, it's normal to have good and not-so-good days. But if you do too much on the good days, you can end up needing extra rest on the not-so-good days. It's like a seesaw that goes up and down.
When we feel worried or are in 'fight, flight or freeze' mode, our muscles can become tight without us even realising it. To help ourselves feel calmer, we can try focusing on each group of muscles in our body.
A short mindfulness practice for those feeling illness or discomfort
A PDF to support our session on mast cells and the mind by Deborah Bircham
When we are feeling worried or scared it can be tricky to find a way to feel better about the things that are bothering us. Download and complete this plan which you can follow when those worries feel overwhelming.
People with chronic illnesses like MCAS often have limited energy. In the spoon theory, by Christine Miserandino, this is represented as having 12 spoons per day. This can help to explain the impact of some everyday tasks on those living with chronic illness.
In the same way that a jigsaw is made up of lots of different pieces, each of us are madeup of lots of different parts too. This puzzle can help you to talk about MCAS being just one part of that puzzle.
An exercise to help children identify the things which make them feel good, those which don't and what helps them to feel better when things aren't going so well.
The ball of worries activity introduces children to a practical coping strategy to make thoughts and worries appear more manageable.
A leaflet designed to help support parents and carers of children living with systemic mast cell activation and MCAS. It provides suggestions for how to care for your personal wellbeing whilst caring for someone with MCAS, and shares ideas and suggestions for how to communicate and support each other as a family.
An exercise to help you find the activities that make you feel good and may help to improve your mood. Suitable for children and adults.
This worksheet helps you to estimate your personal stress levels and gives you an idea of your current wellbeing.
This is a quick and easy resource designed to help you, and those that care about you, to check-in with how you are doing.
This leaflet documents some of the tests that may be used to diagnose MCAS and explains how to read the results.
This is our full pack with multiple resources to support requesting reasonable adjustments in the workplace with MCAS.
This guide helps you to understand your rights and the support that could be put into place in your workplace to help you.
This guide for employers explains MCAS and the support that could be put into place in the workplace for those with MCAS.
This cheat sheet has top tips that might be helpful when creating an MCAS-friendly work place.
A workplace adjustments passport is a live record of all workplace adjustments agreed with your employer.
This template may be helpful when requesting reasonable adjustments from your employer.
This table may support you to break down the reasonable adjustments that could be made to support you in your workplace.
This letter may be useful if you need to challenge a refusal to implement reasonable adjustments in your workplace.
This template policy can be shared with your workplace to support the development and implementation of a reasonable adjustment policy.
This information guide about MCAS, and the additional needs a student with MCAS may have, can be shared with Disability Officers and other members of staff at universities.
This resource has been designed to provide general guidance and help students to access support as they approach further education at university.
A form designed to help you to plan the questions you would like to ask and symptoms you would like to discuss at medical appointments.
When we experience anxiety or stress, our muscles can tense up. Progressive muscle relaxation can help to alleviate this tension and promote a sense of calm.
In the world of chronic illness, it's entirely normal to experience both 'good' and 'bad' days. However, if you overexert yourself on the good days, it can lead to an overcompensation of rest on the bad days. Trying to find a smoother path with more balance to your ‘good’ and ‘bad’ days can help to stop the cycle.
A short mindfulness practice for those feeling illness or discomfort
A PDF to support our session on mast cells and the mind by Deborah Bircham
People with chronic illnesses like MCAS often have limited energy. In the spoon theory, by Christine Miserandino, this is represented as having 12 spoons per day. This can help to explain the impact of some everyday tasks on those living with chronic illness.
This worksheet helps you to estimate your personal stress levels and gives you an idea of your current wellbeing.
This is a quick and easy resource designed to help you, and those that care about you, to check-in with how you are doing.
You can use this blank recipe conversion page to note down any MCAS friendly changes you have made to your favourite recipe's.
This toolkit contains information about substances in food and in the environment that can affect mast cell activity or trigger MCAS symptoms. It also includes practical advice to help you understand and avoid these triggers, as needed.
This histamine bucket is a useful visual aid in trying to understand the impact of factors contributing to histamine levels.
SIGHI is an organisation that provides information about histamine-related disorders.
Blogs, books and recipes written by the low histamine chef (Yasmina Ykelenstam), a health journalist who has managed her own histamine intolerance for more than 10 years.
A medication timetable to log daily medications
A medication log blank which you can use to record medications, dosages and medication times in order to keep on track.
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Mast Cell Action relies entirely on the generosity of people like you. Please make a donation now and together we can make a difference to those affected by MCAS.