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Episode 7: Online Dating with a Spinal Cord Injury
In Episode #7 of Life After Paralysis, Tiffiny Carlson interviews two quadriplegics about the travails of online dating after their injuries. She interviews Rob Cella from Thunder Bay, Ontario and Brook McCall from Portland, Oregon. Listen here To learn more about SPINALpedia.com, visit: https://spinalpedia.com/about To listen to past episodes, visit https://podcasts.apple.com/us/podcast/spinalpedia-theres-life-after-paralysis-show/id1460418405
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Life After Paralysis Podcast Episode #3: Adaptive Camping
In Episode #3 of Tiffiny’s podcast for SPINALpedia Life After Paralysis, we chat about the in’s and out’s of adaptive camping, with all-terrain chairs, cots vs. transferring to the ground, tents and accessible lean-to’s and more discussed. Three avid campers on wheels also join in – Greg Niedzielski, Jason Thurston and Ty Hockett. Run-time is 43 minutes. Listen here or listen in the player below.
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Listen in: Chatting with Bob from Quad Podcast
It’s not very often I get a chance to talk about anything with another quad for so long. It was fun! Bob is in his 50’s, from Chicago, and has been paralyzed even longer than me. He is the host of the Quad Podcast (you should definitely check it out). Listen in as we talk about, well, everything. Link
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Tiffiny’s Newest Podcast, Life After Paralysis for SPINALpedia
My newest podcast episode is out. This month I hosted a roundtable discussion on ableism with three amazing guests – Kelly Giannattasio Narowski, Froy D La Peña and Tim Abrahamson. Please take a listen if you’re so inclined. Listen here
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Podcast Episode #9: Quadriplegic Technology
Episode #9, Quadriplegic Technology, of my podcast True Wheelchair Life: SCI Life Uncovered is live! Listen in as my three awesome guests Eric Anderson, Mark E Felling and Ian Mackay share the technology they use in their day-to-day lives, including how Siri saved one of their lives. Listen here
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1/28/12: The small and sassy blogger, Jane Hash
In episode #82 of No Free Rides, Tiffiny is joined by Jane Hash, a fun-loving woman with Osetogenesis Imperfecta who hosts her own podcast and is making a documentary about her one-of-a-kind life.