Podcasts about aicardi goutieres

I was so eager to sit down and chat with my special guest this week, the incredible Lauren Lowery. Lauren is a wife, mama to two (one of whom is diagnosed with the ultra rare disease, Aicardi-Goutieres syndrome), ICF certified and trauma-informed life coach for special needs moms, and podcast host of Overcome the Overwhelm. What I love most about Lauren (besides her soothing and cheerful "disney princess-esque" voice) is her ability to get to the root issues of WHY some of us are stuck living in survival mode. Through her 12 week coaching program, she helps other moms get out of survival mode and into a life that is easier, peaceful, and balanced. I also share some SUPER exciting news that we received last week!Happy listening! Learn more about Lauren's 12 week course here.Follow Lauren on insgram: @lauren_nia_loweryListen to Overcome the Overwhelm for Special Needs Momshttps://www.confessionsofararediseasemama.com/Learn more about my children's fight with ASMD and donate to our cause:https://www.saveromanandstella.com/Follow on instagram: https://www.instagram.com/confessionsofararediseasemama/

On today's episode of the podcast we hear from Lauren about her son's diagnosis of Aicardi-Goutieres Syndrome (AGS.) She shares how her uneventful pregnancy followed by a NICU stay and numerous hospital visits with unanswered questions eventually resulted in a diagnosis. Lauren shares how coaching changed her life and how she is now a life coach for mothers of children with disabilities. [4:32] How ranch living was a dream come true [5:20] After an uneventful pregnancy, Lauren gives birth [7:00] A nurse tells Lauren to get a second opinion [9:15] Lauren and Katie chat about the NICU life [11:00] How staying at the hospital added to the emotional and stressful times [12:25]  Asking about Lauren's pregnancy history [14:00] An MRI reveals some answers [16:50] Living in flight or fight mode [19:50] Leo stopped eating and had a swallow study [21:00] The doctors grasp for answers [26:30] Genetics appointment results [27:30] How diagnosis day holds trauma [29:11] Finding a specialist who has experience working with children who have AGS [31:20] How Lauren found healing through coaching [35:28] Lauren shares Leo's love language [37:24] Self care is what works for your stress management [39:22] What is driving your action and feelings? [42:27] Our definitions of being a good mom Connect: Lauen's Coaching Website Lauren's Instagram Page Whether you are a parent or professional, we want you to join our community. Sign up for our newsletter here. Parents, download our free parent starter kit. When you download our starter kit, you'll learn how to: Give medicine to your child without it becoming a wrestling match Prepare your child (and yourself) for a shot so they can feel less anxious Create and use a coping plan for any medical appointment or procedure The first sign of sniffles, or worse, shouldn't send you into a tailspin. Feel confident in your role as a parent and advocate, no matter what medical situation you're facing. Child life specialists, get affordable PDUs on-demand here. Shop for your CLOC gear here. Catch up with CLOC on Instagram, Facebook and meet Katie for a Q+A every Monday at 10 AM CST.  

"Sometimes you stand up and say this is how can can help. This is what we need. And this looks different for every caregiver."  Lauren and her husband live in Stillwater, Oklahoma with their 5 year old son Leo and 4 year old foster daughter. They run a cattle operation, and she serves as a life coach for special needs moms. Their son Leo has a rare genetic disorder called Aicardi-goutieres syndrome, which affects the brain, spinal cord, and immune system. To learn more about Lauren's coaching, find her at www.lowerylifecoaching.com.  To stay connected with Jess, head to www.jessplusthemess.com.  If you are interested in being a guest please contact me at jess@thelucasproject.org I'd love to hear what you think, so please rate and review! --- Support this podcast: https://anchor.fm/jess-ronne/support

Pesquisadores do programa de células-tronco da Universidade da Califórnia em San Diego usaram uma doença rara, a Síndrome de Aicardi Goutieres (AGS), para investigar os mecanismos fundamentais do cérebro. Usando organóides corticais, ou cérebros, em um disco, eles monitoraram o neurodesenvolvimento enquanto descobriram novas informações sobre a correlação entre retrotransposão e neuroinflamação. Series: "O Canal de Células-Tronco" [Health and Medicine] [Spanish Language] [Show ID: 32916]

Investigadores en el Programa de Células Madre en UC San Diego han utilizado un raro desorden, Aicardi Goutieres (AGS), para explorar mecanismos fundamentales del cerebro. Utilizando organoides corticales, o cerebros en una placa, han seguido el neurodesarrollo a medida que encontraban nueva información sobre la relación entre los retrotransposones y la neuroinflamación. Series: "El Canal de Células Madre" [Health and Medicine] [Spanish Language] [Show ID: 32917]

Pesquisadores do programa de células-tronco da Universidade da Califórnia em San Diego usaram uma doença rara, a Síndrome de Aicardi Goutieres (AGS), para investigar os mecanismos fundamentais do cérebro. Usando organóides corticais, ou cérebros, em um disco, eles monitoraram o neurodesenvolvimento enquanto descobriram novas informações sobre a correlação entre retrotransposão e neuroinflamação. Series: "O Canal de Células-Tronco" [Health and Medicine] [Spanish Language] [Show ID: 32916]

Investigadores en el Programa de Células Madre en UC San Diego han utilizado un raro desorden, Aicardi Goutieres (AGS), para explorar mecanismos fundamentales del cerebro. Utilizando organoides corticales, o cerebros en una placa, han seguido el neurodesarrollo a medida que encontraban nueva información sobre la relación entre los retrotransposones y la neuroinflamación. Series: "El Canal de Células Madre" [Health and Medicine] [Spanish Language] [Show ID: 32917]

Researchers at the UC San Diego Stem Cell Program have used a rare disorder, Aicardi Goutieres (AGS), to explore fundamental brain mechanisms. By utilizing cortical organoids, or brains in a dish, they have tracked neurodevelopment while discovering new information about the relationship between retrotransposons and neuroinflammation. Series: "UCTV Prime" [Health and Medicine] [Show ID: 32743]

Researchers at the UC San Diego Stem Cell Program have used a rare disorder, Aicardi Goutieres (AGS), to explore fundamental brain mechanisms. By utilizing cortical organoids, or brains in a dish, they have tracked neurodevelopment while discovering new information about the relationship between retrotransposons and neuroinflammation. Series: "UCTV Prime" [Health and Medicine] [Show ID: 32743]

Researchers at the UC San Diego Stem Cell Program have used a rare disorder, Aicardi Goutieres (AGS), to explore fundamental brain mechanisms. By utilizing cortical organoids, or brains in a dish, they have tracked neurodevelopment while discovering new information about the relationship between retrotransposons and neuroinflammation. Series: "UCTV Prime" [Health and Medicine] [Show ID: 32743]

Researchers at the UC San Diego Stem Cell Program have used a rare disorder, Aicardi Goutieres (AGS), to explore fundamental brain mechanisms. By utilizing cortical organoids, or brains in a dish, they have tracked neurodevelopment while discovering new information about the relationship between retrotransposons and neuroinflammation. Series: "UCTV Prime" [Health and Medicine] [Show ID: 32743]

1) Pitfalls in electronic health records and 2) Topic of the month: Cerebellar ataxias. This podcast for the Neurology Journal begins and closes with Dr. Robert Gross, Editor-in-Chief, briefly discussing highlighted articles from the print issue of Neurology. In the second segment Dr. Mike Brogan interviews Dr. Jim Bernat about his paper on pitfalls in electronic health records. Dr. Stacey Clardy is reading our e-Pearl of the week about Aicardi-Goutieres syndrome. In the next part of the podcast Dr. Ted Burns interviews Drs. Susan Perlman and Jeremy Schmahmann about the topic of other acquired cerebellar ataxias. The participants had nothing to disclose except Drs Bernat, Clardy, Burns, Perlman and Schmahmann.Dr. Bernat serves as an editorial board member of Neurocritical Care, Neurology Today and Multiple Sclerosis and Related Diseases, receives compensation for serving on the editorial board of The Physician's Index for Ethics and Medicine and receives royalties from the publication of the book Ethical issues in Neurology.Dr. Clardy served on the editorial team for the Neurology® Resident and Fellow Section. Dr. Burns serves as Podcast Editor for Neurology®; and has received research support for consulting activities with CSL Behring and Alexion Pharmaceuticals.Dr. Perlman serves on Medical Research Advisory Board for the National Ataxia Foundation, receives research support from Santhera Pharmaceuticals, Edison Pharmaceuticals, Friedreich Ataxia Research Alliance, and ARRAS funding via the RDN-CRC.Dr. Schmahmann serves as an editorial board member for The Cerebellum; receives royalties from the publication of the books The cerebellum and cognition, MRI atlas of the human cerrellum and Fiber pathways of the brain; holds stock options in Brother and for legal counsel to Johnson & Johnson; receives research support from Birmingham Foundation MINDlink Foundation Sidney R. Baer Jr., Foundations and the NIH and has a patent pending for transcranial magnetic stimulation.