What have you done to raise funds for Mast Cell Action? 

A French bulldog festival event. 10% of all ticket sales are donated to Mast Cell Action. 

How is the challenge going so far? 

We completed it and sold 500 tickets! 

What is your link to Mast Cell Activation Syndrome? Can you share a brief history of your story with us? 

Since late 2019, I have been living with chronic pain, rashes, swelling, gastrointestinal problems, and many other debilitating symptoms. Along the way, I’ve been diagnosed with fibromyalgia, Functional Neurological Disorder (FND), vestibular migraines, Complex PTSD (CPTSD), and osteoarthritis. Finally, in late 2024, I received a diagnosis of Mast Cell Activation Syndrome (MCAS). 

Navigating the unpredictable symptoms of MCAS while balancing my roles as a mother and a student has been an immense challenge. Despite the physical and emotional toll of the condition, I persevered and recently completed my Master’s degree in Criminal Psychology. 

Throughout my journey, I’ve faced many obstacles that come with managing a chronic illness, especially in trying to balance family, studies, and personal well-being. This experience has inspired me to raise awareness about MCAS and its impact on sufferers, who often deal not only with physical and psychological challenges but also with a lack of understanding from the wider community. 

As part of my mission to create more awareness and support for those with MCAS, I ran the New Forest Frenchie Fest, a festival celebrating all things French Bulldog! Through this event, I aim to raise funds and spread the word about MCAS, using proceeds from ticket sales to support those living with the condition. 

Why did you choose Mast Cell Action? What impact has Mast Cell Action had for you? 

Mast Cell Action gave me a lifeline when I was at my lowest and the weekly zoom sessions and support from the charity and other sufferers has been invaluable, inspiring me to launch a petition earlier this year and fundraise in the hope of creating more awareness and support. I have made friends and connections through Mast Cell Action, who have allowed me to share my struggles and not feel so alone. 

What did you enjoy most about your fundraising experience?  

It was lovely to see so many French bulldogs and their owners all in one place having a pawty! I felt a real sense of achievement from organising my own festival.  

What would you say to other people considering doing a fundraiser for Mast Cell Action? 

Go for it!! There are so many ways you can channel your hobby or passion in to a rewarding fundraising experience.  

What message would you like to share with the MCAS community? 

Believe in yourself and don’t ever give up! Together we are stronger!