That software engineer is Chris Schlechty — a fellow member of the Muscular Dystrophy Association’s National Community Advisory Committee. We talk about home automation, on-demand services, apps, self-driving cars, smart devices, and Seattle’s microbrews. Check…
Jivana Heyman — registered yoga therapist and teacher — talks about the origin of the Accessible Yoga organization and the upcoming conferences in New York and San Francisco. Want to know what Accessible yoga is…
Tis the season to talk romance and who better to hear from than our disability community sexpert, Dr. Danielle Sheypuk? Danielle — a licensed psychologist in New York City — discusses dating, sex, society, and…
October is National Disability Awareness Month. What does it mean to be disabled? A dictionary definition says it’s having a physical or mental condition that limits movements, senses, or activities. Does it coincide with the…
Service dogs can be a best friend for someone with a chronic health condition. In this podcast episode Hazel Weiss, diagnosed with Multiple Sclerosis in 1989, talks about her experiences with first Hams and now…
Retired Navy Lieutenant Laura Root — diagnosed with myotonic dystrophy type 2 (DM2) — talks about her current work with wounded warriors as a Level 3 Shooting Coach and mentor.
Diagnosed with MS as a teenager, Michael Muir spreads his “fun is therapeutic” philosophy while making the horse ranch experience accessible to everyone. To learn more about Michael’s organization visit the Access Adventure website. If you’d…
Declaring oneself disabled doesn’t have to be all bad. Once you accept having limited abilities and turn your focus on what you can still do – which is often a lot – you might be…
Recently my partner and I went on a road trip to visit a friend in Southern California. This friend – I’ll call her Debbie – was the first friend I made with a similar neuromuscular…