Podcast appearances and mentions of Kyle Bryant

ONCE UPON A GENE - EPISODE 100 A Rare Collection- Because of You with Kyle Bryant, Jennifer Siedman, Liz Morris, and Ashley Fortney Point There's power in storytelling- for the listener and the storyteller. A Rare Collection is a monthly series featuring people from the rare disease community, sharing a story with a common theme. Kyle Bryant, Jennifer Sideman, Liz Morris, and Ashley Fortney Point share stories of rare disease. EPISODE HIGHLIGHTS Kyle Bryant, Living with Friedreich's Ataxia Kyle was diagnosed with Friedreich's Ataxia at age 17. It's a disease that affects balance and coordination and has symptoms of scoliosis, vision loss, hearing loss and life-shortening heart complications. At the time he was diagnosed, he ignored that his future would be much different than what he'd imagined. After a few years, he wanted to take a cross-country bike ride. Kyle reads a page from his book about how he convinced his parents to join him. Jennifer Siedman, Mother to Ben Jennifer loved a little boy with a rare disease called Sanfilippo Syndrome. That boy graced this Earth for 17 years with a big lion roar of a laugh and a gentle heart. He loved farms, tractors, baseball and chocolate donuts. His quiet determination convinced a researcher to pursue a treatment and because of it, there are other children today with Sanfilippo Syndrome who's future might look different than his. Jennifer knows who she is today because she was Ben's mother. Jennifer shares a story of her mother-in-law who, through her own determination, modeled the skills she would need to be the best mother and advocate she could be to Ben.  Liz Morris, Mother to Colson The Pacific Northwest is abundantly beautiful. Seattle's true appeal is in it's wild spaces. Carkeek Park in northern Seattle is one of Liz's favorites with organic healing powers she needs. Trails lead through the lush woods, there's an expansive shoreline with built-in driftwood seating and open green hills overlooking the sea and mountains. Liz and her husband sat on the beach at Carkeek Park on a hazy August evening in 2016 and talked of their future. They talked of the future they wanted for their future child, which Liz was six months pregnant with. Colson was born in October 2016. He was impacted by mitochondrial disease, a genetic disorder that compromised his body's ability to turn food into energy. Liz shares a story of living with enough. Ashley Fortney, Mother to Davis In 2014, Ashley welcomed her son Davis into the world after a difficult pregnancy filled with many hospitalizations and much worry. From the start, the doctors thought there might be something different about Davis. Davis was diagnosed with Koolen-de Vries syndrome at age 7, but he's continued to grow, learn and prove that nothing can stop him. Ashley shares all the ways that Davis has helped the family grow and find support from others in the community and all the ways he makes the world a better place. TUNE INTO THE ONCE UPON A GENE PODCAST ⁠Spotify⁠ ⁠https://open.spotify.com/show/5Htr9lt5vXGG3ac6enxLQ7⁠ ⁠Apple Podcasts⁠ ⁠https://podcasts.apple.com/us/podcast/once-upon-a-gene/id1485249347⁠ ⁠Stitcher⁠ ⁠https://www.stitcher.com/podcast/once-upon-a-gene⁠ ⁠Overcast⁠ ⁠https://overcast.fm/itunes1485249347/once-upon-a-gene⁠ CONNECT WITH EFFIE PARKS ⁠Website⁠ ⁠https://effieparks.com/⁠ ⁠Twitter⁠ ⁠https://twitter.com/OnceUponAGene⁠ ⁠Instagram⁠ ⁠https://www.instagram.com/onceuponagene.podcast/?hl=en⁠ ⁠Built Ford Tough Facebook Group⁠ ⁠https://www.facebook.com/groups/1877643259173346/

About the Guest(s): Dr. Kyle Bryant is a respected chiropractor and expert in functional extremity adjusting, currently operating in Kennewick, Washington. He is a Certified Chiropractic Extremities Practitioner (CCEP) with extensive experience in integrating low-level laser therapy into chiropractic treatments. After beginning his chiropractic journey in Ireland, where he served as a team chiropractor for a traveling sports team, Dr. Bryant further honed his skills in Spokane, Washington. He has recently launched Functional Extremities Chiropractor (FEC), a robust training program for professionals aiming to specialize in extremity and joint care. Episode Summary: Join Dr. Chad Woolner and Dr. Andrew Wells in this enlightening episode of the Laser Light Show as they explore the intersection of chiropractic care and low-level laser therapy with special guest Dr. Kyle Bryant. Known for his expertise in functional extremity adjusting, Dr. Bryant shares insights about his newly launched program and the unique integration of laser therapy in his practice, ICE (Integrative Chiropractic and Extremities). Dr. Bryant discusses how his foundational experiences with sports injuries led to a passion for chiropractic care, particularly extremity adjustments. Through his Functional Extremities Chiropractor program, he aims to educate practitioners on handling extremity and joint issues effectively. The discussion highlights the complementarity of low-level laser therapy with chiropractic treatments, showcasing how these modalities can expedite patient recovery and enhance treatment outcomes. By stacking therapies like chiropractic adjustments and laser treatments, practitioners can offer comprehensive care that improves patient satisfaction and increases clinical efficacy. Key Takeaways: Dr. Bryant has launched the Functional Extremities Chiropractor program, designed to educate practitioners on effective extremity adjustments. Integration of low-level laser therapy with chiropractic adjustments can significantly expedite recovery and enhance treatment outcomes. The FEC system helps identify proprioceptive deficiencies in patients, allowing tailored treatments to improve joint function and alleviate pain. Laser therapy provides a non-invasive method to restore function and mitigate symptoms, benefiting a wide range of patient conditions. The combination of techniques and the systematic approach in Dr. Bryant's practice maximizes the physiological benefits for patients. Notable Quotes: "The FEC system helps chiropractors gain confidence by understanding how the biomechanical side of extremities influences the spine and vice versa." "Lasering the brain in conjunction with an extremity issue can help restore function as opposed to merely alleviating pain." "One of the biggest takeaways from chiropractic care combined with laser therapy is that there's only an upside potential." "With lasers, you can expand your ability to help a wider range of conditions walking through your door." "The goal is to find the source of issues, not only to relieve pain but to restore functionality." Resources: Functional Extremities Chiropractor Program: functionalextremitieschiropractor.com Clinic: Integrative Chiropractic and Extremities (ICE) Mentioned Practitioners: Dr. Trevor Berry, Dr. Brandon Brock, Dr. Kurt Gehr, Dr. Kristin Heischetter, Dr. Rob Silverman, Dr. Dan Murphy. Functional Health Mastery Delve into this episode to uncover a wealth of approaches on how low-level laser therapy can revolutionize extremity care in chiropractic practice and stay tuned for more enlightening content from the Laser Light Show.

ONCE UPON A GENE - EPISODE 205 Mastering the Art of the Supermarket Answer When Someone Asks, How Are You with Jennifer Siedman Jennifer Siedman is a relatable, rare mom who has a lot of experience with rare disease. She is the Director of Community Engagement at the Courageous Parents Network and joins us to share her approachable strategies for engaging with friends and acquaintances as a rare parent or caregiver. EPISODE HIGHLIGHTS What is the supermarket answer and what is the origin of it? The questions we get out at the supermarket are often simple and common— like "How are you?", "How is your child?", "How can I help?" or "Do you want to grab dinner?". I would get a barrage of questions and comments from people I bumped into at the store and I would have to think each time how I would answer. It felt complicated and I created a strategy to help, called the supermarket answer. It's a mental list that I would go through in my head to determine if someone wanted and could handle the truth, or if they just wanted the supermarket answer. We live a life others find difficult to connect with and it makes us feel disconnected to give the supermarket response and state that everything is great when it's not. I found that because I became comfortable in the process of evaluating what someone was looking for in their question and, more importantly, comfortable with determining what I needed in that moment, I started asking people what answer they were looking for. What is the strategy checklist? Ask yourself: What am I up for emotionally? What is the other person up for emotionally? What truth do you feel like telling in that moment? Do you need to share a trial or triumph? Are there situations where you feel more inclined to answer an honest and thorough answer over a supermarket answer? If I go to a party where there are few people that would relate to my life, I often feel myself aligned with sharing only the supermarket answer. On the other hand, I find that I almost never give the supermarket answer when I'm within my disease organization or with other parents that understand me and they're able to receive my emotional baggage the same way I can receive theirs. What is your advice for parents who are struggling to share their story? It's your story to tell however you want to tell it and it will evolve over time. Owning it and knowing you can tell little truths or big truths, depending on the day, can be very empowering and make answering those uncomfortable questions more comfortable. Understanding your own capacity to hold your vulnerability will help you embrace your story and know when it's the right moment to let big truths out. LINKS AND RESOURCES MENTIONED ONCE UPON A GENE - Episode 114 - The Bravery of the Brokenhearted - A Big Brothers Perspective on Grief From the Loss of a Sibling with Sanfilippo Syndrome with Noah Siedman https://effieparks.com/podcast/episode-114-noah-siedman ONCE UPON A GENE - Episode 109 - A Rare Collection - What I Know For Sure with Noah Siedman, Grayson Skibington and Nash Hawkins https://effieparks.com/podcast/episode-109-what-i-know-for-sure ONCE UPON A GENE - Episode 100 - A Rare Collection- Because of You with Kyle Bryant, Jennifer Siedman, Liz Morris and Ashley Fortney Point https://effieparks.com/podcast/episode-100-rare-collection-because-of-you Courageous Parents Network https://courageousparentsnetwork.org/ Dante Labs https://us.dantelabs.com/ CONNECT WITH JENNIFER Email jennifer@courageosparentsnetwork.org jennifer@courageosparentsnetwork.org CONNECT WITH EFFIE PARKS Website https://effieparks.com/ Twitter https://twitter.com/OnceUponAGene Instagram https://www.instagram.com/onceuponagene.podcast/?hl=en Built Ford Tough Facebook Group https ://www.facebook.com/groups/1877643259173346/

Born in 1989 Ukraine with extensive physical challenges, missing bones and parts of limbs, muscle,s and organ tissue due to in-utero radiation poisoning from the Chernobyl nuclear disaster, Oksana Masters was left to fend for herself in an orphanage. The world was stacked against her, and the conditions in the three orphanages she endured were, as she described, truly brutal. But, she refused to give up.Then, at age 7, she'd find herself adopted by a single, American mom, whose own years-long journey to bring Oksana home is its own astonishing story. The simple fact that she survived is remarkable. But, she didn't just survive, once in her home, enduring multiple additional surgeries and amputations, her indomitable spirit refused to let anyone tell her what she could or could not do. And, nearly a decade later, she'd end up stunning not just her mom, and the local community, but the entire world, becoming the United States' most decorated winter Paralympic or Olympic athlete, taking home seventeen medals in four different sports. She has since been featured everywhere from Sports Illustrated to The New York Times and has written a powerful memoir, The Hard Parts: A Memoir of Courage and Triumph, that recounts her astonishing journey from the shadow of Chernobyl to the world's biggest stages. In today's deeply moving and inspiring conversation, you'll discover:How an unwavering spirit can conquer the most daunting physical challenges.The power of love, support, and perseverance in overcoming trauma and adversity.The importance of embracing your unique differences and using them to your advantage.What it takes to excel in not just one, but four different sports on the world stage.The life-changing impact of a single decision to never give up.And so much more.Join us as we explore the extraordinary life of Oksana Masters, and learn how she turned her greatest challenges into her most exceptional victories. How she became unstoppable, and showed the world what was possible. You can find Oksana at: Website | InstagramIf you LOVED this episode you'll also love the conversations we had with Kyle Bryant about how to transform challenges into action.Check out our offerings & partners: My New Book SparkedMy New Podcast SPARKED. To submit your “moment & question” for consideration to be on the show go to sparketype.com/submit. Visit Our Sponsor Page For Great Resources & Discount Codes Hosted on Acast. See acast.com/privacy for more information.

What happens when a couple of guys who spent time at a traditional public accounting firm get together over a few beers to discuss what frustrates them about their jobs? How about the birth of a new-breed CPA firm, Market Street Partners, that has been recognized in recent years by Accounting Today, Inside Public Accounting and the Chattanooga Times as one of the fastest growing and best CPA firms in the country to work for. Listen to see how Kyle Bryant has built one of today's leading CPA firms by focusing on people and exceptional client service.  

Kyle Bryant, Founder of Titus Land Holdings, joins us to discuss how we went from attorney to real estate investor, his firm's land investing strategies, what his team looks like, and much more. Connect with Kyle on Twitter @tkyle and at https://www.tituslandholdings.com/ To join the DJE Investor list visit https://www.djetexas.com/access For multifamily mentoring visit https://www.ApartmentEducators.com

Kyle Bryant is the Managing Partner of Market Street Partners in Chattanooga, Tennessee. Kyle oversees the firm's operations and has provided assurance, tax, and business consulting services for over a decade. In this episode, Kyle and Stuart discuss the rapid growth of Chattanooga, what attracts businesses to invest in the region, and what the projections are for the future. As a manager of the largest transaction in Chattanooga's history, Kyle is a top-tier professional in his city and gives an insight into how accounting is developing the Tennessee market.Together they discuss: The story behind Market Street Partners (01:00) Kyle's journey as a private CPA (2:30) Kyles work at the Lamp Post Group (3:30) Serving a new group of clients in Chattanooga (4:30) The size and profile of Market Street Partners (5:30) Local and remote employees at Market Street Partners (07:30) The competitive landscape in Chattanooga (08:30) Market Street Partners' mission (9:50) What retirement looks like for Kyle (11:00) Market Street Partners' media strategy (12:45) Why accountants are reluctant to delve into business development and sales (14:20) Chattanooga's local economy and development (16:15) What types of businesses come to the South East (18:30) The shortage of young accounting professionals (19:30) What Kyle does outside of work (21:10) Market Street Partners' tech stack (21:40) The game plan for the near future (23:30)

Patrick and Amy are joined by three of the most prolific and committed rare disease podcasters out there: Effie Parks from Once Upon A Gene, Kyle Bryant from Two Disabled Dudes, and Bo Bigelow from Stronger Every Day. Those three titans behind the mic join us for a candid discussion about patient centricity, we touch on some recent news, FLOW's Jessica Lauren Richmond is back with the latest installment of The Well.   Show Notes: Subscribe to: Once Upon a Gene 2DD Stronger Everyday   Recent novel therapy news:   CSL Behring gene therapy makes comeback after hold for FDA priority review   BioMarin delays planned FDA filing for hemophilia gene therapy   FDA Grants Breakthrough Therapy Designation to BIVV001 for Hemophilia A Treatment   Presenting Sponsor: Takeda. Visit bleedingdisorders.com to learn more.   The Bloodstream Podcast is brought to you in part by a new campaign from CSL Behring called Portraits of Progress. To learn more, check out www.PortraitsofProgress.com    Subscribe to BloodStream Podcast   Connect with BloodStream Media: BloodStreamMedia.com BloodStream on Facebook  BloodStream on Twitter

Kyle Bryant worked for a small CPA firm out of college focused mostly on audits but eventually left to work with Access America Transport and the Lamp Post Group. There he discovered a passion for helping small businesses. Kyle felt like his career elevated quickly when he spent 18 months working on the Access America Transportation sale to Coyote Logistics in 2014. This was the largest transaction in Chattanooga's history and gave him the experience and confidence to help many more startups through the fundraising and transaction process.

Kyle Bryant worked for a small CPA firm out of college focused mostly on audits but eventually left to work with Access America Transport and the Lamp Post Group. There he discovered a passion for helping small businesses. Kyle felt like his career elevated quickly when he spent 18 months working on the Access America Transportation sale to Coyote Logistics in 2014. This was the largest transaction in Chattanooga's history and gave him the experience and confidence to help many more startups through the fundraising and transaction process.

Over the last two years, parents of public school kids across America woke up and had the time to pull back the curtain and actually see what was going on in their kids' classrooms.  Many of these parents knew something was 'off'.  The more they dug into these issues, the uglier things were.  Sleeping parents finally decided to get involved, took action, demanded accountability from their local schools and their boards and have now stepped up to bring conservative, common-sense values back to public education.  Daryn and Randy interview conservative school board candidate, Kyle Bryant from the Liberty Public School District in Liberty, MissouriKeep up with Kyle at bryantforlps53.com  https://www.facebook.com/bryantforlps53-------------------------------------SUPPORT OUR SPONSORS FOR THIS SHOWGet accurate, honest and true news by reading The Epoch Times.   Visit: www.IReadEpoch.comEnter promo code GRIT and get your first month for just $1.-------------------------------------STAY IN THE LOOP AND UP TO DATEVisit Website https://patriotswithgrit.com/Help Support Patriots With Grit https://patriotswithgrit.com/donate/Recommend Patriots To Interview https://patriotswithgrit.com/recommend/Grab Some Fun Merch https://patriotswithgrit.com/shop/-------------------------------------SUBSCRIBE TO PODCASThttps://podcasts.apple.com/us/podcast/patriots-with-grit/id1615813244-------------------------------------HANG OUT WITH US ON THESE SOCIAL MEDIA PLATFORMSRUMBLE: https://rumble.com/c/c-1011237YOUTUBE: https://youtube.com/channel/UCPq8tmHN8_Mn1M_wHs8xYiQFACEBOOK Page: https://www.facebook.com/patriotswithgritCLOUT HUB: https://app.clouthub.com/#/users/u/PatriotsWithGrit/postsTELEGRAM: https://t.me/PatriotsWithGritLINKS TO ALL SOCIAL MEDIA: http://patriotswithgrit.com/links/-------------------------------------

Learn how movement plays a significant role in our total body health. Our special guest, Dr. Kyle Bryant, a chiropractor and owner of Integrated Chiropractic and Extremities Clinic explains how functional movement and posture can help avoid injury. Steve White, Pacific Clinic's Executive Director, also explains how a simple exercise can show a direct correlation to life expectancy.  

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On this episode we learn about land investing and what it takes to be successful in the world of unknowns that come with it. Today's guests Clint Turner and Kyle Bryant tell us their stories about careers investing in land. We talk about everything from wholesaling to creating passive income with no money down. Tim Stone, Ian Cushing, and Nick Galbreath had the honor of hosting this wisdom filled episode.

This week, we talk to patient advocate and FA ambassador for the Friedreich's ataxia Research Alliance, Kyle Bryant, about the importance of getting involved in rare disease communities. To learn more about Friedreich's ataxia, visit curefa.org. Listen to Kyle's podcast, Two Disabled Dudes, at twodisableddudes.com.

Today on the Dads with Daughters Podcast I spoke with Jay Armstrong, a father of three who is fighting a rare, degenerative brain disease while working to be the best dad he can be. We talk about fatherhood, living with this disease, but also about the legacy that he is working to leave for his kids. As a part of this legacy, we talk about the new book he just released this month, Bedtime Stories for the Living.  About the Book If you live with a rare life altering disease, you spend a lot of time in your head. It's hard to put the thoughts into words. In Bedtime Stories for the Living, Jay Armstrong accurately articulates the thoughts of any person living with a rare disease or anyone simply struggling to overcome their challenges.” Kyle Bryant, spokesperson for the Friedreich's Ataxia Research Alliance and host of the Two Disabled Dudes podcast. A regular dad. A rare brain disease. A chance to live forever. A cell phone's ring interrupts the silence as Jay Armstrong sits in his high school classroom preparing for the year ahead. Something about the ring makes his stomach drop. It's his doctor. The words, “diffuse cerebellar atrophy, a rare, degenerative brain disease” float through the speaker. All of Jay's youthful dreams of being a writer rush back, flooding the twenty years he has spent teaching students how to appreciate novels, memoirs, and poetry. The care he put into teaching them how to write with clarity, insight, and humor, and how to dance at the prom. The bedtime stories he never told his children spin in his imagination. It will all die when he dies. Bedtime Stories for the Living is an episodic memoir in which Jay shows his children how to accept their limitations and find joy. The collection of tender, witty stories about fatherhood, persevering despite illness, and pursuing your dreams, demonstrates how love gives us the strength to face heartache with bravery, humor, and grace. If you've enjoyed today's episode of the Dads With Daughters podcast we invite you to check out the Fatherhood Insider. The Fatherhood Insider is the essential resource for any dad that wants to be the best dad that he can be. We know that no child comes with an instruction manual and most are figuring it out as they go along. The Fatherhood Insider is full of valuable resources and information that will up your game on fatherhood. Through our extensive course library, an interactive forum, step-by-step roadmaps, and more you will engage and learn with experts but more importantly with dads like you. So check it out today!

In this episode, I interview Dr. Bryant but as I call him “DR KYLE”.We discuss what chiropractic care is and what is is NOT. Doctor Kyle explains how his practice is a little different than most traditional chiropractic clinics. Doctor Kyle focuses more on ‘TOTAL body health and looking at the root causes of peoples aches and pains when they come to him. As a Extremities certified chiropractor, he looks also at injuries and trauma that may result in patients chronic pain.Additionally, Dr. Kyle has a good understanding of chronic illnesses and how they too can have a better results with a full body adjustment.There is a misconception that chiropractors are ‘cracking spines and necks'. We discuss the myth around that and what is really going on when you hear a cracking soundThe other modalities that Dr Kyle incorporates in his practice are extra special. He also offers physical therapy techniques, laser, and vibrational therapy.Dr. Kyle believes that total health starts with the spine but the connection extends thru out the body starting from the brain.BIO: Dr. Kyle Bryant is a chiropractor who is the descendant of multiple Tri-citian generations. He attended Kamiakin high school and graduated in 2003. After playing collegiate soccer and earning his bachelor's degree from Gonzaga in 2007, he went on to begin his chiropractic education at the University of Western States in Portland, OR. After graduating in 2012 he moved abroad with his wife, Desiree, to Ireland to begin the first experience of his professional career. After a year over-seas, the Bryants decided it was time to become a little more settled to begin a family and further develop Dr. Kyle's career – which landed them in Spokane, WA. After 3 unforgettable years with treating patients and receiving a certification in extremity injuries, the Bryants again felt it was time to move due to their growing family – but this time back to home.Integrative Chiropractic and Extremities and Dr Kyle represent the ONLY active CCEP (certified chiropractic extremities practitioner) within a 100 mile radius, which allows him to incorporate arm and leg injuries into spinal dysfunction injuries. The certification required an additional year of study and requires an exceptional knowledge in biomechanics of the extremity joints and injuries that can result as a consequence of their dysfunction.“I enjoy working with patients and families of all ages who participate in a wide range of activities from weekend warriors, to musicians, to elite athletes. My approach is holistically focused within a chiropractic-wellness paradigm – I believe the body is self-healing and we must learn how to tap into these abilities if we are to understand solutions to our health. This perspective allows me to focus on finding medical answers through preventative health and function. Another unique component of my treatment philosophy is rooted in the CCEP knowledge of extremities and overall mechanics of body movement. I welcome any patient striving to better themselves and improve their health!”In his personal life, Dr. Kyle is married to his wonderful wife, Desiree and has three kiddos . He enjoys being a dad, spending time with his family and friends, staying active, and of course – playing soccer!Find Doctor Kyle at ICE Clinic in Kennewick, WA Call: 509-820-3828 or online at: www.iceclinics.comYou can find Tavia @ IG #healthcoachtaviaOr www.sweetcoachtavia.com

In this episode, I interview Dr. Bryant but as I call him “DR KYLE”.We discuss what chiropractic care is and what is is NOT. Doctor Kyle explains how his practice is a little different than most traditional chiropractic clinics. Doctor Kyle focuses more on ‘TOTAL body health and looking at the root causes of peoples aches and pains when they come to him. As a Extremities certified chiropractor, he looks also at injuries and trauma that may result in patients chronic pain.Additionally, Dr. Kyle has a good understanding of chronic illnesses and how they too can have a better results with a full body adjustment.There is a misconception that chiropractors are ‘cracking spines and necks'. We discuss the myth around that and what is really going on when you hear a cracking soundThe other modalities that Dr Kyle incorporates in his practice are extra special. He also offers physical therapy techniques, laser, and vibrational therapy.Dr. Kyle believes that total health starts with the spine but the connection extends thru out the body starting from the brain.BIO: Dr. Kyle Bryant is a chiropractor who is the descendant of multiple Tri-citian generations. He attended Kamiakin high school and graduated in 2003. After playing collegiate soccer and earning his bachelor's degree from Gonzaga in 2007, he went on to begin his chiropractic education at the University of Western States in Portland, OR. After graduating in 2012 he moved abroad with his wife, Desiree, to Ireland to begin the first experience of his professional career. After a year over-seas, the Bryants decided it was time to become a little more settled to begin a family and further develop Dr. Kyle's career – which landed them in Spokane, WA. After 3 unforgettable years with treating patients and receiving a certification in extremity injuries, the Bryants again felt it was time to move due to their growing family – but this time back to home.Integrative Chiropractic and Extremities and Dr Kyle represent the ONLY active CCEP (certified chiropractic extremities practitioner) within a 100 mile radius, which allows him to incorporate arm and leg injuries into spinal dysfunction injuries. The certification required an additional year of study and requires an exceptional knowledge in biomechanics of the extremity joints and injuries that can result as a consequence of their dysfunction.“I enjoy working with patients and families of all ages who participate in a wide range of activities from weekend warriors, to musicians, to elite athletes. My approach is holistically focused within a chiropractic-wellness paradigm – I believe the body is self-healing and we must learn how to tap into these abilities if we are to understand solutions to our health. This perspective allows me to focus on finding medical answers through preventative health and function. Another unique component of my treatment philosophy is rooted in the CCEP knowledge of extremities and overall mechanics of body movement. I welcome any patient striving to better themselves and improve their health!”In his personal life, Dr. Kyle is married to his wonderful wife, Desiree and has three kiddos . He enjoys being a dad, spending time with his family and friends, staying active, and of course – playing soccer!Find Doctor Kyle at ICE Clinic in Kennewick, WA Call: 509-820-3828 or online at: www.iceclinics.comYou can find Tavia @ IG #healthcoachtaviaOr www.sweetcoachtavia.comThe Sweet Life Coaching Podcast https://businessinnovatorsradio.com/the-sweet-life-coaching-podcast/Source: https://businessinnovatorsradio.com/ep-26-chiropractic-care-and-chronic-illness-its-more-than-you-think-with-dr-kyle-bryant-dc-coach-tavia-morse-salvadalena

ONCE UPON A GENE - EPISODE 100 A Rare Collection- Because of You with Kyle Bryant, Jennifer Siedman, Liz Morris, and Ashley Fortney Point There's power in storytelling- for the listener and the storyteller. A Rare Collection is a monthly series featuring people from the rare disease community, sharing a story with a common theme. Kyle Bryant, Jennifer Sideman, Liz Morris, and Ashley Fortney Point share stories of rare disease. EPISODE HIGHLIGHTS Kyle Bryant, Living with Friedreich's Ataxia Kyle was diagnosed with Friedreich's Ataxia at age 17. It's a disease that affects balance and coordination and has symptoms of scoliosis, vision loss, hearing loss and life-shortening heart complications. At the time he was diagnosed, he ignored that his future would be much different than what he'd imagined. After a few years, he wanted to take a cross-country bike ride. Kyle reads a page from his book about how he convinced his parents to join him. Jennifer Siedman, Mother to Ben Jennifer loved a little boy with a rare disease called Sanfilippo Syndrome. That boy graced this Earth for 17 years with a big lion roar of a laugh and a gentle heart. He loved farms, tractors, baseball and chocolate donuts. His quiet determination convinced a researcher to pursue a treatment and because of it, there are other children today with Sanfilippo Syndrome who's future might look different than his. Jennifer knows who she is today because she was Ben's mother. Jennifer shares a story of her mother-in-law who, through her own determination, modeled the skills she would need to be the best mother and advocate she could be to Ben.  Liz Morris, Mother to Colson The Pacific Northwest is abundantly beautiful. Seattle's true appeal is in it's wild spaces. Carkeek Park in northern Seattle is one of Liz's favorites with organic healing powers she needs. Trails lead through the lush woods, there's an expansive shoreline with built-in driftwood seating and open green hills overlooking the sea and mountains. Liz and her husband sat on the beach at Carkeek Park on a hazy August evening in 2016 and talked of their future. They talked of the future they wanted for their future child, which Liz was six months pregnant with. Colson was born in October 2016. He was impacted by mitochondrial disease, a genetic disorder that compromised his body's ability to turn food into energy. Liz shares a story of living with enough. Ashley Fortney, Mother to Davis In 2014, Ashley welcomed her son Davis into the world after a difficult pregnancy filled with many hospitalizations and much worry. From the start, the doctors thought there might be something different about Davis. Davis was diagnosed with Koolen-de Vries syndrome at age 7, but he's continued to grow, learn and prove that nothing can stop him. Ashley shares all the ways that Davis has helped the family grow and find support from others in the community and all the ways he makes the world a better place. TUNE INTO THE ONCE UPON A GENE PODCAST Spotify https://open.spotify.com/show/5Htr9lt5vXGG3ac6enxLQ7 Apple Podcasts https://podcasts.apple.com/us/podcast/once-upon-a-gene/id1485249347 Stitcher https://www.stitcher.com/podcast/once-upon-a-gene Overcast https://overcast.fm/itunes1485249347/once-upon-a-gene CONNECT WITH EFFIE PARKS Website https://effieparks.com/ Twitter https://twitter.com/OnceUponAGene Instagram https://www.instagram.com/onceuponagene.podcast/?hl=en Built Ford Tough Facebook Group https://www.facebook.com/groups/1877643259173346/

In the last of our Emerging Researchers Series, I speak with Shandra Trantham, a Ph.D. candidate at the University of Florida.  Shandra was destined for a life in science. As a young child, science and math were her favorite subjects. She and I share the childhood dream of becoming an astronaut. I never followed my dream, but Shandra didn’t even have the choice. When she was 9 years old, she began to lose her balance and things got progressively worse. When she was 12, she was diagnosed with Friedreich’s Ataxia. Our regular listeners may be familiar with Friedreich’s Ataxia because we have talked to other’s about the rare disorder (https://salemoaks.com/captivate-podcast/kyle-bryant-remember-why-we-are-doing-all-this/ (Kyle Bryant in episode 2) way back in 2019, and https://salemoaks.com/captivate-podcast/emerging-researcher-layne-rodden/ (Layne Rodden in episode 013)). For Shandra, her diagnosis gave her a focus on science, a reason to study, and a purpose.  Her story is informative and inspiring.  You can contact Shandra at shandra.trantham@gmail.com Plese support us a https://patreon.com/salemoaks Support this podcast

Lucky to have Kyle Bryant, host of YouTube channel Daily Skate Undertake, join me this week to talk skating, his journey and what it's like having his son on his YouTube channel. #podcast #skateboarding #youtubecollab #dailyskateundertake #progressdaily #skateboardingisfun #brailleskateboarding #oklahoma #bayarea --- Support this podcast: https://podcasters.spotify.com/pod/show/dreadful-talk-podcast/support

Key Topics: What is Sean and Kyle's mission that led up to the launch of the Podcast (01:26) With a diagnosis like FA, how did you react and respond to the news (2:53) Living with FA, what does life look like for Sean and Kyle (5:17) How is the charity Determinence supporting the community (6:19) What made podcasting the right medium to add to the brand (9:38) Starting a podcast with a big mission in mind (12:26) How has creating a community help support the Podcast (14:40) Starting a podcast isn't always easy, what challenges did they find along the way (16:40) Does having a non-profit connected to your podcast help (18:50) Biggest advice Sean and Kyle have for others looking to start a Cause focused podcast (20:17) Looking back, what are some of the best memories (21:45) Can podcasting be a self-less exercise of our time (24:33) The best piece of advice for others who are focused on moving a cause forward (25:40) Website link: https://twodisableddudes.com/ (https://twodisableddudes.com/) Charity: https://determinence.com/ (Determinence) https://determinence.givingfuel.com/general-donation-page) (Donation) Social Links Twitter: https://twitter.com/2ddpodcast (2DDPodcast) Facebook: http://facebook.com/TwoDisabledDudes (Two Disabled Dudes) Facebook: https://www.facebook.com/Determinence/ (Determinence) Instagram: http://instagram.com/2ddpodcast (2DDPodcast) Instagram: https://www.instagram.com/determinence/ (Determinence) Thanks for Listening! Be sure to subscribe onhttps://itunes.apple.com/us/podcast/causecasts/id1398644299?mt=2 ( Apple),https://www.google.com/podcasts?feed=aHR0cDovL2ZlZWRzLnBvZGlhbnQuY28vY2F1c2VjYXN0cy9yc3MueG1s ( Google),https://open.spotify.com/show/3hmQQrfFDPznEqEAEeRVm8 ( Spotify), https://music.amazon.com/podcasts/67ea3876-ad03-4d6f-814c-c5395544f5c6/Causepods?ref=dm_wcp_podcast_link_th (Amazon), or wherever you get your podcasts. And feel free to drop us a line at mathew@causepods.org. Follow Mathew on Social Media to stay up to date on Causepods – https://www.facebook.com/MathewPassy (Facebook) |https://twitter.com/MathewPassy ( Twitter) |https://www.instagram.com/mathewpassy/ ( Instagram) |https://www.linkedin.com/in/mathewpassy/ ( LinkedIn) For help, resources, and community support, please join thehttps://www.facebook.com/groups/causepods ( Causepods Facebook Group) if you are already producing podcasts for a cause or are thinking about launching one. And if you would like to be a guest on Causepods, please fill out this form and schedulehttps://bookme.name/thepodcastconsultant/lite/causecast-podcast-booking ( your chat here).

ONCE UPON A GENE - EPISODE 045 Two Disabled Dudes - Kyle Bryant and Sean Baumstark When I became a part of the rare disease community after Ford was born, I didn't feel like I had any community at all. After Ford was born, I felt less connected to my friends and I sought out a new community through podcasts because hearing stories made me feel connected. Sean Baumstark and Kyle Bryant, the hosts of Two Disabled Dudes podcast, both have Friedreich’s ataxia (FA). They have been an impactful resource in my journey and I'm so excited they're joining me. EPISODE HIGHLIGHTS Can you tell us how you became friends and connected as podcasters? We met through cycling, raising awareness and did a couple bike rides together, including The World’s Toughest Bike Race - Race Across America (RAAM). It starts in San Diego, California and ends in Annapolis, Maryland. A documentary crew followed us and that experience really brought us together.  What is FA? Friedreich’s ataxia (FA) is a rare neuromuscular disease that affects muscle coordination from the toes to the fingertips. It also has symptoms of scoliosis, diabetes, vision loss, hearing loss and life-shortening heart complications. It's a rare disease that affects about 1 in 50,000 people. The condition is dual recessive so both parents can carry the damaged gene, but there's no warning indicators that it will affect the children. The average diagnosis age is 5-15 years old.  Can you share the background of The Ataxian? The film is our race against time in the Race Across America. It's relay style and we had 4 cyclists. The team has 9 days to get from the west to the east coast with no time to stop. We used this race as an opportunity to call attention to FA and raise awareness about life in the rare disease world. Everyone on the team had one mission- to finish before the clock stopped.  Sean, tell us about your organization, Determinence. After being diagnosed, I started doing day hikes with friends to think, talk and wrestle with the new outcomes we thought life was going to bring. It was on one of these hikes that we realized a lot of other people in my community at that time were inspired because they knew I didn;t walk well and struggled with hiking and climbing. People were inspired to get out, which turned into a 5K, then a 10K and eventually a half marathon. This idea of helping people accomplish something physically challenging for them was the driving inspiration behind Determinence. Determinence is a non profit I founded with a mission to help people in the world of disability to climb mountains and cross finish lines. Supporters can donate to the cause or get involved with a team.  Kyle, tell us about your book, Shifting Into High Gear. All of my cycling adventures are documented through blog posts, articles and the documentary. My first ride from San Diego, California to Memphis, Tennessee wasn't documented anywhere so I worked with a writer to publish the book, Shifting Into High Gear. It was an amazing process, thinking about my experience, what it meant to me and what it may mean to someone else who reads my story. LINKS AND RESOURCES MENTIONED The World’s Toughest Bike Race - Race Across America (RAAM) https://www.raceacrossamerica.org/ Two Disabled Dudes podcast https://twodisableddudes.com/ The Ataxian http://theataxianmovie.com/ Determinence https://determinence.com/ Shifting Into High Gear https://kyleabryant.com/ TUNE INTO THE ONCE UPON A GENE PODCAST Spotify Apple Podcasts Stitcher Overcast CONNECT WITH EFFIE PARKS Website https://effieparks.com/ Twitter https://twitter.com/OnceUponAGene Instagram https://www.instagram.com/onceuponagene.podcast/?hl=en Built Ford Tough Facebook Group https://www.facebook.com/groups/1877643259173346/

Friedreich's ataxia (FA) is a rare disease and is often misunderstood by those who are not affected by it. This episode explores the ways to talk about FA with those who may not be familiar with the condition. Guest hosted by Kyle Bryant and Sean Baumstark of the Two Disabled Dudes podcast.

People living with Friedreich's ataxia (FA) sometimes have difficulty with daily activities. This episode dives into the many life hacks that people living with FA and their caregivers have instituted into their daily lives. Guest hosted by Kyle Bryant and Sean Baumstark of the Two Disabled Dudes podcast.

This introductory episode of FA Talks welcomes some individuals living with FA and their caregivers as they talk about their experiences with Friedreich's ataxia. Guest hosted by Kyle Bryant and Sean Baumstark.

https://www.jamesmillerlifeology.com/feed/ Kyle Bryant @kyleabryant reviews his book Shifting Into High Gear that highlights his remarkable tenacity of how he turned his ataxia diagnosis into a mission to help you create your identity. KyleABryant.com #kyleabryant #ataxia #bicycling #motivation #inspiration #disability The post Create your Identity – Kyle Bryant appeared first on James Miller | Lifeology®.

Kyle Bryant reviews his book Shifting Into High Gear that highlights his remarkable tenacity of how he turned his ataxia diagnosis into a mission to help you create your identity. KyleABryant

Kyle Bryant reviews his book Shifting Into High Gear that highlights his remarkable tenacity of how he turned his ataxia diagnosis into a mission to help you create your identity. KyleABryant

We welcome Kyle Bryant of the Friedreich’s Ataxia Research Alliance (FARA) to discuss his journey as a patient with Friedreich’s Ataxia (FA), as an active patient leader, and in his job as a liaison between the FA community and researchers. After being diagnosed with FA when only 17 years old, Kyle has dedicated his life to helping other people with FA and exemplifying the adage “Life is how we react to it!” He has reacted by becoming a long-distance bike rider, podcast host, author, and full-time patient advocate.  Kyle opens up about his drive to help others deal with the challenges of life with FA and other disorders. It started when he wrote a daily blog during his first big bike ride from San Diego to Memphis. The comments and responses to this blog made him realize “Oh my gosh, we can make a real impact” by giving people hope and community. It was life-changing for him. Kyle has a very healthy perspective on participation in clinical trials. He talks about his understanding that he may be just one small “mouse” in a study, but he can be the most powerful mouse that ever lived, an essential ingredient to make a drug a reality.   Kyle Bryant is the author of The Ataxian (https://smile.amazon.com/Ataxian-Sean-Baumstark/dp/B079YMBNGQ/ref=sr_1_1?keywords=The+Ataxian&qid=1570029801&sr=8-1) .  

Growing up in northern California, Kyle Bryant (https://kyleabryant.com/) loved being outside and being active. But, his late teens would change everything. He began experiencing a loss in balance, coordination and strength. A battery of doctors and tests eventually led to a diagnosis of Friedreich’s Ataxia (FA), a rare, progressive neuromuscular disease that currently has no treatment or cure. While grappling with this diagnosis and all it meant, Kyle discovered cycling, and, along with it, a new lease on freedom. He's now completed numerous ultra-distance rides including "The World's Toughest Bike Race", Race Across America in 2010, as part of 4-man Team FARA which is the subject of the documentary The Ataxian. He is the co-host of the Two Disabled Dudes Podcast and the author of a moving new memoir, Shifting Into High Gear (https://amzn.to/31R1QaR). Bryant is also the founder and director of the bicycle ride fundraiser, rideATAXIA for the Friedreich’s Ataxia Research Alliance (FARA). rideATAXIA is currently held annually in 6 locations and has raised over $7 million for Friedreich's ataxia (FA) research since 2007.Check out our offerings & partners: Peloton: Try the Peloton Bike in your home for 30 days. Free pick-up and a full return if you still aren’t certain the Peloton Bike is for you! Learn more about Peloton’s 30-Day Home Trial at onepeloton.com and use promo code GOODLIFE to get $100 off accessories with the purchase of a Peloton.ThirdLove: Go to ThirdLove.com/GOODLIFE now to find your perfect-fitting bra... and get 15% off your first purchase!Legacybox: There’s never been a better time to digitally preserve your memories. Go to Legacybox.com/GOODLIFE to get 40% off your first order.

https://www.jamesmillerlifeology.com/feed/ Kyle Bryant @kyleabryant reviews his book Shifting Into High Gear that charts the course of his transformation as he journeys on a recumbent tricycle across the United States in the throes of Friedreich's ataxia, a life-shortening and disabling disease. KyleABryant.com The post Shifting into High Gear: Guest – Kyle Bryant appeared first on James Miller | Lifeology®.

Today on the show, learn how you must never allow your limitations define who you are. How to gradually shift your career into something more meaningful to you and your community. This is Alberto's conversation with Kyle Bryant, a man whose diagnosis drove him to ride his bike for thousands of miles and inspire us all with his story. You can find Kyle on all social media platforms by searching for @kyleabryant. To purchase Kyle's book titled "Shifting into High Gear: One Man's Grave Diagnosis and the Epic Bike Ride That Taught Him What Matters" click here: https://amzn.to/2ThLbdn Kyle Bryant graduated from the University of California at Davis with a degree in Civil Engineering. After working five years as an engineer, he found his calling through cycling and helping others. He is the founder/director of rideATAXIA for the Friedrich's Ataxia Research Alliance (FARA), and together with his team they produce family-friendly bike rides across the country to empower those with FA and raise funds for research. Looking to turn your passion into profit and your full-time activity? Alberto Sardiñas is one of the world’s leading experts on how to successfully turn a passion project into a lucrative career. As someone who has started multiple side passion projects that have all turned into full-time day jobs, Alberto knows how to properly plan and execute a vision into a reality. On the Passion Accomplished podcast, he shares his own tools, as well as those of his guests. With a social media following of close to 2.8 million fans, people all over the world look to Alberto for advice and inspiration on how they can achieve their dreams. Alberto’s greatest passion is helping people accomplish their goals and live out their dreams. As a show host and a mentor, Alberto can help anyone feeling frustrated with where they are in life to fulfill their greater calling, while still working their day job.

Kyle Bryant is the founder and director of Ride Ataxia, a fundraising program of the Friedreich's Ataxia Research Alliance (FARA). This man's story of riding 2,500 miles in a recumbent trike is amazing! What is behind this personal story? Tune in and find out. It will not only touch your heart but make you realize that dreams can be fulfilled in the most unique and amazing ways.

My guest today is Kyle Bryant

Hi #kNOwATAXIA Nation! Happy #thoughtfultuesday. Today, I’m sharing a podcast I did with my good friend Kyle Bryant. I was able to get a few minutes with him in Las Vegas at the Annual Ataxia Conference. Listen in as we talk about Kyle’s new book, Shifting Into High Gear and learn about his motivation for writing it. I think you’ll really enjoy hearing Kyle’s story. We discuss the rollercoaster of emotions experienced with the diagnosis of a rare disease, the impact this diagnosis has on the family, the importance of becoming an expert in that disease, the road to acceptance (not always a straight line) and the realization that your involvement can make an impact. Please enjoy and let me know your thoughts in the comments below. iTunes https://itunes.apple.com/us/podcast/k... SoundCloud https://soundcloud.com/user-536040137... Facebook https://www.facebook.com/ataxiadidyou... Website http://www.rideforjohn.org/ Instagram https://www.instagram.com/ataxian_/ Twitter https://twitter.com/AtaxiaFacts

Kyle Bryant joins host Frankie Picasso on Mission Unstoppable Radio. Kyle Bryant was diagnosed with Friedreich's Ataxia, at 17, a life shortening illness that threatened to put this athlete in a wheel chair in his 20’s. Needing some control over his life, Kyle decided he would ride 2500 miles on his bike to raise money and awareness for his disease. Little did he know, he would really find himself.As the miles passed on by, Kyle Bryant made a huge self discovery, one that not only changed his own life, but impacts the lives of anyone who reads his brilliant memoir, Shifting into High Gear. You see, whether one is able bodied, have a rare disease like Kyle or face a hang nail, each of us has a choice about three things. 1. How we choose to define ourselves, 2. What limits we place on ourselves, and 3. How much of ourselves we are going to give back for the greater good!However, as time moved on, Kyle began to see that he was not in this disease by himself. That there were opportunities for him to build community and be an example for others despite the obstacles that lay before him, the FA community and their families Kyle chose to break free from self imposed limits and limited thinking. He allowed the definition of himself to expand even as his disease took away. some of his others see defeat. abilities. It is a courageous person who shows up to really Live live where

Kyle Bryant reviews his book Shifting Into High Gear that charts the course of his transformation as he journeys on a recumbent tricycle across the United States in the throes of Friedreich's ataxia, a life-shortening and disabling disease. KyleBryant.com

Episode 6: Kyle Bryant by Prep Insider

San Fernando senior running back Kyle Bryant talks about his commitment to Eastern Washington and his history as a Tiger at SanFer.

“The Ataxian” follows Kyle Bryant, a charismatic Californian with Friedreich’s ataxia, whose ability to walk and speak is impaired, as he tirelessly works to raise awareness and funds for research for the neuromuscular disorder he was diagnosed with at age 17, Friedreich’s ataxia, a little-known, progressive, fatal disease, that has no cure. Its onset usually occurs in adolescence and lifespan is roughly the age of 30. Kyle says he wants “to do something crazy!” and pulls together a team of four bicyclists — himself (on a recumbent bike) and Sean Baumstark, a friend who also has the disease, along with two friends who happen to be stellar athletes — to take part in Race Across America, an annual competition that covers 3,000 miles in nine days traveling from Oceanside, CA to Annapolis, MD. “The Ataxian” takes its viewers on a journey of inspiration, beauty, even euphoria. But its lasting contribution is in making the world a little more familiar with this disease, and a little less lonely for the families struggling against it.

1st ever Facebook LIVE interview with Kyle Bryant. Check out the video on the Remix: The Dad page. We discuss music, fitness,books and changing the world. --- This episode is sponsored by · Anchor: The easiest way to make a podcast. https://anchor.fm/app Support this podcast: https://anchor.fm/remix5280/support

Dana Mauro Up close and personal with @KyleaBryant. Learn about what Kyle's been up to, the inspiration behind his newly released movie the Ataxian, his mission to raise awareness and his personal ataxia journey. @ataxiadidyouknow About the Movie https://itunes.apple.com/us/movie/the-ataxian/id1336806410 The Ataxian examines the life of Kyle Bryant, a man diagnosed with the fatal progressive neuro-muscular disorder, Friedreich’s ataxia. Despite being unable to walk, Kyle, along with a team of friends, attempt the most grueling bicycle race in the world—The Race Across America. Kyle’s determination and unbreakable spirit carry them through sweeping landscapes and a life-changing cross-country trip. iTunes https://itunes.apple.com/us/podcast/know-ataxia-ataxia/id1312495222?mt SoundCloud https://soundcloud.com/user-536040137-843024175 Facebook https://www.facebook.com/ataxiadidyouknow/ Website http://www.rideforjohn.org/ Instagram https://www.instagram.com/ataxian_/ Twitter https://twitter.com/johnnyjots

Kyle Bryant is one of the most positive, upbeat people you’ll meet. He also has Friedreich’s ataxia, a degenative neuro-muscular disease. We talk about FARA, CrossFit, and having a positive outlook.

This week we're joined by Kyle Bryant, host of the Two Disabled Dudes Podcast and founder of RideATAXIA. We discuss Friedreich's ataxia, a rare neuro-muscular disorder, what it was like to be diagnosed with it at 17, and how a chance encounter with a recumbent trike altered the course of his life. Show Notes Jamie: Moving On From NV Access Ryan and Rob briefly discuss the news that James Teh, one of the lead developers at NV Access (makers of the open source screen reader, NVDA) is leaving to work at Mozilla. https://www.nvaccess.org/post/jamie-moving-on-from-nv-access/ rideATAXIA http://www.rideataxia.org Two Disabled Dudes Podcast http://twodisableddudes.com Friedreich's Ataxia Research Alliance http://www.curefa.org The Ataxian Trailer https://vimeo.com/127990377 Visit us online at www.atbanter.com or you can drop us an email (we LOVE email) at atbanterpodcast@gmail.com!

Leading up to the 8th Annual Ride Ataxia NorCal (2017), Kyle Bryant was interviewed on KHTK Sports 1140 to promote the bike ride, The Ataxian and spread awareness of Friedreichs Ataxia!

To learn more about Butterflies of Wisdom visit http://butterfliesofwisdom.weebly.com/ Be sure to FOLLOW this program https://itunes.apple.com/us/podcast/wins-women-of-wisdom/id1060801905. To find out how Win walk and about Ekso go to http://www.bridgingbionics.org/, or email Amanda Boxtel atamanda@bridgingbionics.org.   On Butterflies of Wisdom today, Best-Selling Author, Win Kelly Charles welcomes Kyle Bryant. Kyle was diagnosed with Friedreich’s ataxia (FA) at age seventeen and found that as the disease progressed he had to give up the sports so interwoven in his life growing up in Northern California; sports such as golf, baseball, basketball and football.  When Kyle's FA had progressed to a point where it became unsafe for him to continue riding his bike, he put a stop to the loss of the activity he cherished.  He took back control, purchased a recumbent trike, and resumed his riding with passion. Kyle started small with an initial ride of 7 miles.  However, fueled with a passion for pushing the limits and do more with his life Kyle built up to a century ride (100 mi in a day) within four months of his first ride.  Upon completion of his first time, he decided that the sky was the limit. In 2007 Kyle founded Ride Ataxia with a 2,500-mile 59-day ride from San Diego, CA to Memphis TN. The goal of the ride was to raise awareness and much-needed research funds for FA, a disease that has no treatment, no cure, no hope…until now. Kyle and Ride Ataxia did not stop in Memphis.  Kyle’s cycling feats include Sacramento to Las Vegas, NV, Portland, OR to Seattle, WA, and completion of Race Across America in which his four-man team finished the 3,000-mile race in 8 days, 8 hours, and 14 minutes. With his trike as the vehicle of change, Kyle took his hopeless situation of no treatment, no cure, no hope and turned it into an opportunity to do something great for himself and many others. In 2009 Kyle became the Spokesperson for the Friedreich’s Ataxia Research Alliance (FARA) in their mission to cure FA.  With Kyle as the program director, Ride Ataxia has become FARA’s Marquee fundraising event with challenging yet family friendly bike rides all over the USA – welcoming 2500 participants and raising $800,000 per year. To learn more about Kyle visithttp://kyleabryant.com/. To find out more about Win Kelly Charles visithttps://wincharles.wix.com/win-charles. Please send feedback to Win by email her at winwwow@gmail.com, or go to http://survey.libsyn.com/winwisdom andhttp://survey.libsyn.com/thebutterfly. To be on the show, please fill out the intake at http://bit.ly/1MLJSLG. To look at our sponsorships go tohttp://www.educents.com/daily-deals#wwow. To learn about the magic of Siri go to https://www.udemy.com/writing-a-book-using-siri/?utm_campaign=email&utm_source=sendgrid.com&utm_medium=email.    

In this special bonus episode of Ryan Watches a Movie, we talk about the The Ataxian, a new documentary from directors Zack Bennett andKevin Schlanser about Kyle Bryant and his bike ride across America despite having Friedreich's Ataxia, the same neurological disease as Ryan. We speak about the film, as well as what FA is, and we have a conversation with the directors and Kyle Bryant. This is the most important episode we've ever done, so be sure to give it a listen. Fara website: https://www.curefa.org/FA Patient Registry: https://www.curefa.org/registry.htmlRyan's rideAtaxia donation page: Click Here web: filmpulse.nettwitter: twitter.com/filmpulsenetfacebook: facebook.com/filmpulsepatreon: patreon.com/filmpulse

En este episodio, Hablamos del blog de bicicletas recumbentes, la culminacion de el Ataxia Ride por Kyle Bryant y de nuestra noticia especial: La Primera vuelta por la Ruta Panoramica en Puerto Rico. Esta actividad, auspiciada por Los Patriotas Cycling, tiene un enfoque diferente y mas afin al concepto de cicloturismo. Se discuten los diferentes aspectos que envuelven la actividad. Visiten la pagina de los Patriotas Cycling para mas información: http://www.lospatriotas.com Ademas queremos invitarlos a visitar la pagina de nuestro amigo Ramón Rodriguez quien a traves de su pagina ciclismopr.com siempre nos patrocina. Visiten su pagina para informacion del ciclismo en general y muy buenos enlaces a la industria: http://www.ciclismopr.com Visiten la pagina de Kyle Bryant para informacion acerca de la condicion de Ataxia y para que lean su interesante blog acerca de sus aventuras: http://www.rideataxia.org El nuevo telefono del podcast es 1-206-350-3691: Dejen sus mensajes de voz y los transmitiremos en el proximo programa. Tambien comentamos acerca de un interesante blog acerca de bicicletas recumbentes, manejado por nuestro amigo Allan Barnard. Pueden verlo en: http://www.recumbentblog.com En la Foto, de izquierda a derecha: El honorable alcalde de la ciudad de Caguas William Miranda Marin, Juan Gonzalez de los Patriotas Cycling, Fernando Arevalo de Ciclismo Tropical y Ramon Rodriguez de CiclismoPR.com

En este episodio, se habla de las diferentes clases de bicicleta, desde el punto de vista cicloturista. Para ejemplos de bicicletas de las que se habla en el programa, sigan los siguientes enlaces: Bicicletas de Calle: http://www2.trekbikes.com/bikes/bike.php?bikeid=1467000&f=1 Bicicleta hibrida http://www2.trekbikes.com/bikes/bike.php?bikeid=1494020&f=8 Bicicleta Turista http://www2.trekbikes.com/bikes/bike.php?bikeid=1432000&f=6 http://www.cannondale.com/bikes/06/cusa/cats/spec_touring.html Bicicleta Reclinable (Recumbente) http://www.ransbikes.com http://www.barcroftcycles.com/ http://www.actionbent.com Para buscar informacion acerca de la aventura de Kyle Bryant titulada "The Ride Ataxia interview" vayan a la pagina en ingles: http://biketourist.podomatic.com En la foto Se muestra la bicicleta de Anna Bromley, la Barcroft Dakota justo antes de salir en su aventura de 4000 millas con su padre. Para leer acerca de su aventura, busque el diario titulado "Pedal to the Sea" en el siguiente enlace: http://www.crazyguyonabike.com

In this episode, we interview Mr. Kyle Bryant, who will embark into a 2800 mile bike tour to raise awareness of this rare disease, which is almost unknown. Being a patient himself of this debilitating disease, Kyle wants to make a statement for the people who can no longer be active and on behalf of future patients. Having a goal to raise $30,000 to be destined for research and treatement, he wants to make sure that at the end of his adventure, everyone knows about the disease. Check Kyle's website: http://www.rideataxia.org/ Kyle would love that you accompany him, at least a part of the adventure. Go to his website and learn about the route and contact him for details!