Real Life Stories: Living with Mast Cell Activation Syndrome | Finding Your Range Podcast Episode 7

Finding Your Range Podcast : Hypermobility and Chronic Pain Uncovered with Jeannie Di Bon

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.