Brianjeansonne Mp3 Free Sound Fffects Download

After 46-year-old Brian Jeansonne was diagnosed with ALS in 2020, his voice slowly began to disappear. So, he and his family turned to artificial intelligence for a chance to sound more like himself — and express his love and needs. #news #health #ALS #AI
Living with ALS has taken away my control, but not my feelings. My physical therapy sessions mean so much more than physical relief. When my therapist gently guides my limbs, it feels like I'm reclaiming a part of myself. These stretches ease tightness and discomfort, but the real value is in the human connection. It's about shared understanding, genuine care, and knowing I'm not alone. #ALSAwareness #PhysicalTherapy #NotAlone #OnwardForward #brianjeansonne #Blove414 #thejeansonne7 #theJ7 #LivingWithALS #ALSsupport #MotorNeuronDisease #LouGehrigsDisease #ALS
ALS patient Brian Jeansonne has difficulty speaking as a result of the debilitating disease. Now, new technology is helping him find his voice. Dr. Jon LaPook explores the full story tonight on CBS Evening News. #news #ALS #AI
Q&A with Brian and Kristy Q: What do you miss most from before ALS? love. - - - - - - - - 📆Release Date: 9-23-24: Onward.Forward. By B. Jeansonne #BrianJeansonne #thejeansonne7 #ALSawareness #ALS #lougehrigsdisease
Living with ALS means I can't go places alone, but thanks to my amazing family, I still enjoy the things I love. Our visits to my favorite coffee shop, CCs and walks (or wheeling) in City Park fill me with gratitude. #FamilyLove #LifeWithALS #OnwardForward #brianjeansonne #Blove414 #thejeansonne7 #theJ7 #ALSawareness #LivingWithALS #ALSsupport #MotorNeuronDisease #LouGehrigsDisease #ALS
I can’t believe how fast I progressed. This is ALS, brutal. love. #OnwardForward #brianjeansonne #Blove414 #thejeansonne7 #theJ7 #ALSawareness #LivingWithALS #ALSsupport #MotorNeuronDisease #LouGehrigsDisease #ALS
Q: Why did you write this book? Brian shares a candid and introspective account of his journey with ALS, exploring profound themes such as soul, suffering, love, and more. With insight and humor, Brian dives into life's toughest questions, offering a raw perspective on existence. This heartfelt memoir, featuring a foreword by Alanis Morissette, urges readers to embrace life in all its complexities. love. - - - - - - - - 📆Release Date: 9-23-24: Onward.Forward. By B. Jeansonne #BrianJeansonne #thejeansonne7 #ALSawareness #ALS #lougehrigsdisease #onwardforward #findingbeautyandlove #myalsjourney
Brian and I had the incredible opportunity to share our story with CBS about how artificial intelligence is helping ALS patients preserve their voices. We’re excited to give you a behind-the-scenes look at this special moment. It’s a bit long, but it's packed with valuable information and memories we’ll cherish forever. We’re beyond grateful that CBS Evening News discovered us right here on TikTok and reached out to our family. @Norah O’Donnell #BrianJeansonne #thejeansonne7 #ALSawareness #ALS #lougehrigsdisease #ArtificialIntelligence #VoicePreservation #CBSNews #BehindTheScenes
Our journey with ALS has been filled with incredible community support and resilience. From countless meals to a fully funded van, generosity has surrounded us. Despite challenges, the love and kindness of those around us have kept our spirits strong. The outdoors became my sanctuary, whether at my favorite coffee shop, under the oaks, or on my neighbor's porch. The first year of ALS was a whirlwind for us in every way—physically, spiritually, emotionally, mentally, vocationally, and socially. love. - - - - - - - - 📖 Onward. Forward., Chapter 1 Coming Sept 2024: Onward. Forward. #Blove414 #BrianJeansonne #ALSawareness #LouGehrigsDisease  #MotorNeuronDisease #LivingWithALS #ALSsupport #ALSCommunity #ALSJourney #ALSFamily #ALS
Q&A with Brian and Kristy Q: What advice would you give someone recently diagnosed with ALS? love. - - - - - - - - 📖 Onward. Forward., Chapter 5 📆Coming Sept. 2024: Onward.Forward. By B. Jeansonne #Blove414 #BrianJeansonne #thejeansonne7 #ALSawareness #LouGehrigsDisease  #MotorNeuronDisease #LivingWithALS #ALSsupport #ALSCommunity #ALSJourney #ALSFamily #als