3 Mums 1 Mission ARFID.
Join three dedicated mums on a mission to raise awareness about Avoidant/Restrictive Food Intake Disorder (ARFID). Through heartfelt conversations, expert insights, and real-life stories, we aim to break the stigma surrounding ARFID and provide support for families navigating this challenging journey. Tune in for honest discussions, practical tips, and a sense of community as we advocate for understanding and compassion.
Who are we?
Jo
@eff_and_arfid
Hi, I'm Jo. I live in Hampshire with my husband and our two daughters, Lily and Ethel.
Ethel was diagnosed with ARFID in August 2024 after years of concerns around her eating. From just 18 months old, she showed very little interest in food, only accepting dry, crunchy snacks and refusing cooked meals.
Our journey to diagnosis and support wasn't easy. Despite repeatedly asking for help, we were met with a lack of understanding and a "watch and wait" approach, leaving us feeling isolated and unsure where to turn. Alongside ARFID, Ethel is awaiting an autism assessment, and everyday experiences such as school lunches, playdates and birthday parties can bring additional challenges.
Like so many families, our hope is to raise awareness, improve understanding and help ensure that no one has to face this journey alone.
Michelle
@arfidlifeuk
Hi, I'm Michelle, and I live in Essex with my husband, Andy, our daughter, Millie, and our son, Arlo, who was diagnosed with ARFID in 2023.
Our journey began during weaning, when it became clear that Arlo's relationship with food was different. Textures, strong smells, and anything wet or slimy felt overwhelming to him. After years of searching for answers, navigating the postcode lottery, and hearing there were no services or that he was "too young," we finally received an ARFID diagnosis.
Although the journey has been challenging, it also led me to discover my voice. Through sharing our lived experience, I'm passionate about raising awareness, supporting other families, and helping create a future where no one has to fight so hard to be understood.
Sarah
@sarah_arfid_advocate
Hi, I'm Sarah, and I live in Hertfordshire with my husband, our teenage son, and our daughter, Grace.
Grace developed late-onset ARFID following increasing anxiety around food and gastrointestinal symptoms. Although she had always been a fantastic eater, her food intake gradually became more restricted, and despite numerous investigations, we were repeatedly told there was nothing physically wrong. After being discharged from services and months without the support we desperately needed, Grace's health deteriorated to the point where she required hospital admission and NG tube feeding. She was later diagnosed with ARFID, alongside her autism diagnosis.
Like many families, our journey was filled with uncertainty, frustration and a lack of understanding. Today, I'm passionate about raising awareness and helping other families know they are not alone.
Do you have a story to tell and want to help raise awareness?
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We're looking for inspiring guests to join our podcast and share their experiences. If you have a story that could make a difference, we'd love to hear from you.
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Contact us today at 3mums1missionarfid@gmail.com to be considered as a potential guest on our podcast.