All Episodes
Two Disabled Dudes — 307 episodes
300 - Season Finale: 300 Episodes Rooted in Connection
299 - Building Hope From Broken Systems
298 - Invisible Illness, Unbreakable Bond: Part 2
297 - Invisible Illness, Unbreakable Bond: Part 1
296 - Support That Meets You Where You Are
295 - Pushing Harder Isn’t Always the Answer
294 - Finding Your People Without Losing Yourself
293 - Rare Disease Day: This is What Advocacy Looks Like
292 - The Hidden System Behind Rare Disease Treatments
291 - Taking on the World’s Longest Stairway
290 - Don’t Suffer Twice
289 - Re-release: From Dad to Advocate to CEO
288 - Choosing to Smile Even When it's Hard
287 - The Fine Line Between Hope and Denial
286 - Grateful. Angry. Both.
285 - Knowing When to Stop: Disability, Limits, and Letting Go
284 - What Achievement Asks Of Us
283 - Disability Advocacy in Work and Travel
282 - Adapt the Plan, Not the Dream
281 - Pixels With Purpose - Ben Forred
280 - Is Accessibility Really About Access… or Attitude?
279 - 2DD LIVE: The Power of Owning Your Disability
278 - Mic Trouble, a Gift Card, and Streaking on a Cruise Ship
277 - Season Finale - Gratitude, Growth, and Dog Poop DNA
276 - World Domination…With a Twist of Kindness
275 - A Soft Blanket and a Bold Mission
274 - When Compassion Leads the Play: Inside Uplifting Athletes
273 - Letting Go of One Dream to Discover a Thousand More
272 - Bridging Worlds: Empowering Patients and Transforming Trials
271 - Rae of Hope: The Power of Inclusion
270 - RDD 2025 with Jett Foundation: "Disability Doesn’t Define Us!"
269 - Red Pandas, Wheelchairs, and the Courage to Say “This Sucks”
268 - Energy Management: How Not to Become a Pile of Poop by 6 PM
267 - Life After Diagnosis: The Power of Humor, Resilience, and Letting Go
266 - Spreading the Word, Saving Lives: Key Insights from ACD
265 - Holding Onto Hope Without Letting Go of Today
264 - A Mother's Journey with CTNNB1 Syndrome and her Family's Path to Inclusivity
263 - The Surprising Truth About Independence
262 - Do Our Resolutions Reveal Our Age?
261 - Season 13 Begins: Travel, Community, & Vacation Prep
260 - Our Perceptions of Disability Were Wrong
259 - If Sean & Kyle Won The Election
258 - Navigating Setbacks: 4 Tips for Gaining Momentum
257 - Journey to the World's Highest Road, Part 2
256 - Journey to the World’s Highest Road, Part 1
255 - Season Finale - We’re Riding the World’s Highest Road
254 - From Dad to Advocate to CEO: John Crowley's Continued Commitment
253 - Uplifting Athletes: Harnessing the Power of Sport for Rare Diseases
252 - NFL Plans Crushed, His Response Changes Lives
251 - From Canes to Canines: Linda's Path to Mobility
250 - Thriving with Duchenne - Rare Disease Day with Jett Foundation
249 - 20 Years in the Making: REATA's Story of Skyclarys
248 - Everyone Holds a Piece w/ FARA CEO, Jen Farmer
247 - Tenacity and the Power of Persistence
246 - Empowering Accessibility, One Review at a Time
245 - Settle or Soar? Embracing Uncertainty
244 - Change & Consistency with Progressive Disease
243 - EveryCure and the Power of Collaboration w/ Dr. David Fajgenbaum
242 - Dave Lynch: 27 Years, 700+ Patients, and the First Treatment
241 - Feeling Helpless? Here Are 4 Ways To Help
240 - Adapting to Life's Curveballs
239 - Season Premier - Are You a Doer or a Talker?
238 - Season Finale - The Dynamics of Friendship
237 - The Vital Role of Caregivers in Rare Disease Advocacy
236 - A Mom's Perspective on Devastation and Gratitude
235 - Addressing the Epidemic of Wheelchair Damage by Airlines
234 - World Duchenne Awareness Day - Jett Foundation
233 - Should Disability Heighten Our Sense of Responsibility?
232 - Can Rare Disease Create Heroes?
231 - Speak Up, Stand Out: Silence is Not Advocacy
230 - Navigating Mental Illness: Parent Stories
229 - Exercise and Motivation: Challenges of Disability
228 - Podcasting Insights and Reflections
227 - Pushing Boundaries: A Blind Athlete's Story
226 - Navigating Disability & Long-term Relationships
225 - From Preterm to Pediatrician: Tyler's Triumph with CP
224 - The Power of the Patient Voice - BIO International
223 - Attitudes Can Change - Let's Talk Debra
222 - Is Technology Good or Bad? Yes.
221 -Disability & Fun Can Coexist
220 - Season Finale - How Much is Too Much?
219 - Physical Therapy Goals with Dr. Gretchen Hawley
218 - Accessibility: Inconvenient or Impossible?
217 - Are Disabled Students Forgotten On University Campuses?
216 - The Emotional Response To Research
215 - Birthday Parties Can Be Tough with Guest Host: Effie Parks
214 - Inspiration Porn - Are We Part of the Problem?
213 - Why is Government so HARD?
212 - Wheelchairs: If You Help, This is For You
211 - Thriving with Duchenne, RDD 2023
210 - Death and Sex - Buckle Up!
209 - How A Mom Launched The First Drug Approval in FA
208 - Is There a Wrong Way?
207 - Asking For Help: Pride vs. Practicality
206 - Why Authenticity Matters at Home & Work
205 - Finally, A Dating App For People With Disability
204 - What If Kindness Isn't The Answer?
203 - Reason vs Excuse: It's Up To You
202 - Addressing Independence and Accessibility with Rare Disease
201 - How Does Positivity Become Toxic?
200 - State of the Podcast and A Few Favorite Moments
199 - RAVE: A Principle Everyone Ought to Consider
198 - What's Your CanDo Story?
197 - Looking for the Pause Button on Friedreich's Ataxia
196 - Two Disabled Slackers
195 - Leveraging Crypto for Rare Disease - Vibe Bio CEO, Alok Tayi
194 - Taking It Personally May Hold You Back
193 - Accessibility Matters, Air Travel Is Not Exempt
192 - Life's Short, Live With Intention
191 - A Mother Who Never Stops
190 - Our Reactions Determine Our Outcomes
189 - LIVE at Chan Zuckerberg Initiative Rare As One
188 - Dealing With Disability Among Friends
187 - Life Lessons From the Bike Trail
S8 - Catching Up with The Dudes
185 - Season Finale - Nothing Stays the Same
184 - Thriving With Duchenne - Jett Foundation
183 - Doing The Right Thing with James Mackay, CEO Aristea Tx
182 - Comparing Ted Lasso to Reality with Heidi Behr, LCSW
181 - Every Person Matters with Tom Hamilton
180 - The Not So Dark Side with Amy Grover
179 - Keep Your Eye On The Ball
178 - Man Turning Into Stone - Joe Sooch
177 - The only thing to fear is...
176 - Rare Disease Symptoms - The Devil You Know
175 - Making Noise About Hemophilia
174 - The Dudes with Squirmy and Grubs
173 - Don't be Weird - Ennis Rook Bashe
172 - Rare Disease is Complicated but There's Reason for Hope
171 - What if Everyone Is Disabled?
170 - What's Your Strategy?
169 - Season Finale - NO REGERTS!
168 - 2DD Forum: CureDuchenne FUTURES Conference 2021
167 - Peace of Mind with Mobility Roadside Assistance
166 - Ultra Rare Drugs at No Cost to the Patient - Stan Crooke
165 - Coaching for Rare and Chronic Conditions - Denise Archilla
164 - Mental Health: Why Talking About the Tough Stuff Takes the Weight off
163 - Actor, Producer, Person - Patrick James Lynch
162 - Superheroes With Once Upon a Gene
161 - Men's Mental Health in Rare Disease With David Ross
160 - Money Talks With the Dudes
159 - Patient Pioneers in Gene Therapy with AVROBIO
158 - 2DD Forum With The Marfan Foundation
157 - Letters to the Younger 2DDs
156 - Using Technology to Improve Accessibility
155 - How We Describe the Challenges of Disability
154 - SMA Awareness with Nick Sinagra
153 - NTSAD Annual Family Conference
152 - How Do You Use Your Influence?
151 - Season Premier: Pandemic Observations
150 - Drugs, Turning 40 & The Future
149 - An Elvis Presley Tribute Artist with Autism
148 - Why Sean Hates His Gym
147 - DD pt5: My view: Patients Get Medicine at Lowest Cost Possible - Tim Walbert
146 - DD pt4: Why Sean Baumstark Is Banned From Clinical Trials
145 - DD pt3: Pre-clinical & Tacos
144 - DD pt2: Do Good and...with John Crowley
143 - DD pt1: Half a BILLION Dollars!?
142 - Rare Disease in India
141 - Rude or Cooperative?
140 - A Sister's Perspective on Bullying
139 - Where The Hell Are The Instructions?
138 - We Only Have One Life to Live
137 - Rare Disease Day Special with Psychologist Dr. Al Freedman
136 - When It Hits The Fan - Part 1
136 - When it Hits The Fan - Part 2
135 - Goals Don't Accomplish Themselves
134 - Our Wants vs. Our Don't Wants
133 - Season 5 Premiere - What do You Want out of Life?
132 - 2DD Forum with the XLH Network
131 - 2DD Forum at Ultragenyx Rare Family Day
130 - Season 4 Finale - More 2DD Grievances
129 - She Created What She Needed - Effie Parks
128 - Addressing Rare Disease Mental Health - Psychologist Al Freedman
127 - Does Disability Force Premature Decisions?
126 - I'm Fine, Thanks - Chris Doveton
125 - "I know you're drunk, buddy"
124 - Walk in My Shoes - A Journey With Cystinosis
123 - Why Do We Keep Our True Selves Hidden?
122 - Red Tape is Easier With Help
121 - How to Join the rideATAXIA Global Challenge
120 - What is Alport Syndrome? - Kevin Schnurr
119 - Are You Messy Like Kyle or Neat Like Sean?
118 - How We Can Serve the Community Through Google's Project Euphonia - Bob MacDonald
117 - What does Team Gleason have in Common with Google?
Bonus Conversation With Friends!
116 - What would you change about yourself if you could?
115 - Leading the VEDS Movement - Katie Wright
114 - Don't Judge a Dude by his Wheelchair
113 - How do we Define Each Other?
112 - Season Finale - Different Reactions to Coronavirus
111 - Copiing in Times of Uncertainty with Team Amicus
110 - How Rare Diseases Impact Carriers - Taylor Kane
109 - Hawk's Eye View on Duchenne MD - Hawken Miller
108 - #QuarantineLife
107 - Patient focused Drug Development - James Valentine
106 - No Arms, no Legs, no Problem - Gabe Adams
105 - The Dudes Vent
104 - His Brain Injury Created a New Mindset
103 - Giving Back After Spinal Cord Injury
102 - Four Tips for Making Decisions
101 - Funding Research One Cookie at a Time
100 - Jeremy Cowart
099 - The Scarcity Mindset
098 - The Pharma/Patient Relationship - Opportunities to Improve - Andra Stratton
097 - A life of Ehlers Danlos Advocacy - Lara Bloom
096 - Owning up to your shortcomings
095 - Season 2 Finale - Are you Determined or Stubborn?
094 - 2DD Update on 2019 Goals
093 - Online Dating for People With a Disability
092 - Why Humor is Essential with Dr. David Fajgenbaum
091 - Chasing Our Cure with Dr. David Fajgenbaum
090 - LIVE at the 2019 Global Genes RARE Patient Advocacy Summit
089 - Creating Community for Young Adults with Our Odyssey
088
087 - Conquering White Mountain
086 - How to Gain Control Over Life - Kipp Wesslen
085 - Beyond the Finish With the Pease Brothers
084 - How to Stop Limiting Yourself
083 - Reasons to Push Your Limits
082 - What are you proud of? - Muffy Ritz
081 - Be Yourself - LIVE at Amicus Therapeutics
080 - Accountability is the key to getting stuff done (GSD)
079 - Cindy Kolbe Interview
078 - South Dakota
077 - Thriving Blind with Kristin Smedley
076 - Our Moms
075 - The Relationship Between the Patient and the Scientist
074 - Jeff Bell Part 2 - Adversity to Advocacy
073 - Jeff Bell Part 1 - Adversity 2 Advocacy
072 - Reasons Versus Excuses
071 - Photos from the first part of 2019
070 - Rob Long
069 - Things We Like
James Miller | Lifeology
067 - He's an Athlete No Matter the Circumstance - Glenn Hartrick
066 - Death March for Ataxia with Mike De Rosa
064 Official - Hasan Banks
065 - Can of Worms
Grievances with the Dudes
062 - Only You Have the Power to Destroy Your Life - Gabriel Cordell
061 - Just Do It!
060 - Mind Games and Disability
Two Dudes' Goals for 2019
058 - 2018 Year Review
057 - The Nomadic Dreamer
056b - Australia Researcher Q&A
056a - AUS Intro Story
Exploring Life Transitions with Kyle and Sean
054 - Travis Flores
053 - Nutrition with Shana and Donna
052 - Surviving Sepsis Unshattered with Carol Decker
051 - PR with Heather Burgett
050.Kyle - Sean Interviews Kyle
050.Sean - Kyle Interviews Sean
049 - Little Levi & Miracle Flights
048 - Rare Disease Advocate Luke Rosen, KIF1A.org
047 - Barry Rice, Cycle Ataxia
046 - A conversation With the Dudes
045 - sick Chick Shira Strongin
044 - Francisco Sanchez - A Doctor With SCI Paying it Forward
043 - Nic Noviki - Easterseals Disability Film Challenge
042 - On Being Savage with Les Ballard
041 - Spring Cleaning of the Mind
040 - Breaking the Paralyzed Paradigm, with Arash Bayatmakou
How to Ward Off Decrepitude
038 - Ilana Jacqueline
037 - RDW Panel For The Ataxian
036 Patient engagement live at Reata
LIVE at Reata Pharmaceuticals
Katie Stevens President, Dyskeratosis Congenita Outreach (DCO)
033 - Steps to Bust Your Funk
032 Behind The Scenes
031 - Anniversary Episode! Listener Appreciation
030 - 000 Rerun
029 - Wonderful and Different with Paul Avery
028 2DD Challenge Check-in
Episode 027
026 - Self Discipline
025 - Leadership with Drew Dudley
024 - The Parent Perspective with Tom Hamilton
023 Patrick Lawrence & CAF
023 - Challenged Athletes Foundation
023 - The Psychology of Disability with Dr. Dan Gotlieb
021 - rideATAXIA Europe, Le Peloton de l'Espoir
020 - LIVE at Horizon Pharma
019 - Dr. David Fajgenbaum - Conquering Castleman Disease
018 - Breaking Your Chains w/ Rudy Garcia-Tolson
017 -Roger Crawford
KHTK Interview
016 - Nutrition with Dr. Liz Applegate
Race Across America - Team FARA
RAAM Crew Chief Mike Bryant (Kyle's Dad)
013 - Kyle & Sean's #1 Advice
012 - Matt Fritsch - The Spinal Cord Injury (SCI) Community
011 - Ron Bartek Part 2 - Collaboration: We're All In This Together
010 - Adaptive Equipment Grants - The Ataxian Athlete Initiative
009 - Ron Bartek, Co-Founder and President, FARA
008 - Paul Melmeyer of the National Organization for Rare Disorders
007 - Max Bronstein
006 - Nicole Boice
005 - Focus on Rare Disease Day with Special Guests: Nicole Boice, Max Bronstein, and Paul Melmeyer
004 – Travel Gone Wild – How to conquer apprehension during travel with a disability.
003 - Travel and Mobility
002 - Self Image
001 - Life Is About How We React
000 - Welcome to the Two Disabled Dudes Podcast