Real Life Stories: Living with Mast Cell Activation Syndrome | Finding Your Range Podcast Episode 7
Want to learn more about living with EDS and Mast Cell Activation Syndrome? Take a listen to this episode to hear a real life story.
After a lifetime of symptoms, Keeya Steel was diagnosed with mast cell activation syndrome in 2015. Soon after, in effort to cope with the disease, Keeya created Hell's Bells and Mast Cells, a blog and collection of memes raising awareness about chronic illness and disability through humour. Like many MCAS patients, Keeya also struggles with dysautonomia and EDS, completing what she calls her "three-ring circus." Keeya lives in Minneapolis, Minnesota with her two poodles, Quixote and Sancho. Keeya recently finished filming for a documentary on mast cell activation syndrome.
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I am very grateful for my fellow Zebra Philip Quigley, a musician from Leyland in Lancashire UK, who wrote the music for this video and just for this channel. Thank you. I am delighted to have my own theme tune.
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The information provided in this video is not designed to replace medical advice or be used as a replacement. Please ask your medical practitioner if you have particular queries on your health.
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