Group of genetic disorders that mainly affect the bones
POPULARITY
5 episodes with Osteogenesis imperfecta
2 episodes with Osteogenesis imperfecta
2 episodes with Osteogenesis imperfecta
2 episodes with Osteogenesis imperfecta
2 episodes with Osteogenesis imperfecta
2 episodes with Osteogenesis imperfecta
2 episodes with Osteogenesis imperfecta
2 episodes with Osteogenesis imperfecta
2 episodes with Osteogenesis imperfecta
2 episodes with Osteogenesis imperfecta
2 episodes with Osteogenesis imperfecta
6 episodes with Osteogenesis imperfecta
2 episodes with Osteogenesis imperfecta
2 episodes with Osteogenesis imperfecta
12 episodes with Osteogenesis imperfecta
2 episodes with Osteogenesis imperfecta
2 episodes with Osteogenesis imperfecta
3 episodes with Osteogenesis imperfecta
Have you ever ignored shoulder pain, thinking it was just muscle soreness? In this eye-opening episode of Health Happy Life Podcast, I share the critical story of a 46-year-old woman whose "simple shoulder pain" turned out to be a heart attack - a wake-up call we all need to hear.This podcast is intended to be informational only. It is not a medical consultation, nor is it personalized medical advice. For medical advice, please consult your physician.As a board-certified kidney specialist and internal medicine physician, I break down several headline-making health stories that could affect you or your loved ones. We examine Tracy Morgan's unexpected health scare at the Knicks game, giving you practical tips to tell food poisoning from stomach viruses.The episode also tackles RFK Jr.'s concerns about toxic metals in baby formula through "Operation Stork Speed" - I'll teach you exactly what to look for on formula labels to protect your little ones. Plus, we celebrate Will Smith's inspiring $50,000 health challenge with Big Boy and explore Christina Applegate's powerful MS journey, including insights from her 30+ hospital visits.Whether you're worried about heart attack symptoms, dealing with chronic illness, or trying to make safer choices for your family, this replay offers clear, practical medical knowledge without the confusing doctor-speak. Your health matters to me - let's learn together.#HealthHappyLife #DrFrita #MedicalMondays #HeartHealth #ChronicIllnessHere are a few helpful resources to help on your journey to wellness:▶️ Subscribe so you will never miss a video.
Meet Sparsh Shah, a 21-year-old musical prodigy, inspirational speaker, and Guinness World Records holder. Known to many as Purhythm, Sparsh is a singer, rapper, songwriter, music producer, and philanthropist. Despite being born with Osteogenesis Imperfecta, a rare and incurable disorder that makes his bones extremely fragile, Sparsh has turned his challenges into a platform for inspiring others.Leveraging Social Media for Good - Learn how Sparsh uses platforms like YouTube, Instagram, and TikTok to share his music and story with the world. He'll share practical strategies for creating authentic content that resonates with audiences.Dealing with Haters and Staying Positive - Sparsh shares his approach to handling negativity on the internet. There is power in focusing on the good and letting your message shine louder than the criticism.Inspiring the Next Generation - Learn about Sparsh's impactful work as an inspirational speaker for schools and youth organizations. He connects with students to empower them to overcome obstacles and embrace their unique potential. Interested in having Sparsh visit your school? We'll share how you can make it happen!SPECIAL GUESTSparsh ShahSinger, Songwriter, Rapper, Inspirational Speaker, Philanthropist, Guinness World Records HolderSparsh-Shah-Purhythm, New JerseyEmail: hirenonweb@gmail.com Twitter: @sparshpurhythmWebsite: http://www.SparshShah.com Facebook: https://www.facebook.com/purhythm Instagram: @shahsparshYoutube: http://www.youtube.com/SparshPurhythmTikTok: @sparshpurhythmSnapchat: @ShahSparshUSEFUL INFORMATIONViral video - Eminem - "Not Afraid" Clean Cover by Sparsh Shah (PURHYTHM)Video referenced in K12prtip at the start of the episode - Click hereOrder your copy of my book Social Media for Schools: Proven Storytelling Strategies & Ideas to Celebrate Your Students & Staff - While Keeping Your Sanity now!Interested in our membership program? Learn more here: https://socialschool4edu.com/MORE RESOURCESFree Video Training: Learn the simple secrets behind social media for K12 schools!Sign up for our free e-newsletter - click herewww.SocialSchool4EDU.com
Pastor Jonathan Stokes takes us through a journey of deepening faith and trust in God through the extreme challenges of having a child with O1.Started in the ministry in 2007 as a youth pastor at First Baptist Church in Wellsburg. Studied at Bobby Wood School of Christian Studies. I've been in the ministry for 18 years. I am the Interim Pastor at First Baptist Church of Weirton, a medical assistant at WMC.#osteogenesisimperfecta #faith #community
Osteoporose tritt meistens bei Frauen nach den Wechseljahren oder bei Männern ab dem Alter von 50 auf. Es gibt aber auch Fälle, in denen die Osteoporose oder Knochenbrüche schon in jüngerem Alter auftreten. Bei der sog. „Early-onset Osteoporosis“ sind häufig andere Erkrankungen oder Medikamente die Ursache. In den Fällen, in denen keine Ursache gefunden wird, muss dann auch an eine genetische Ursache ausgeschlossen werden. In unserer heutigen Folge ist Dr. Erik Kelter, niedergelassener Orthopäde und Unfallchirurg aus Köln, zu Gast. Mit ihm sprechen wir über einen spannenden Patientenfall und das Vorgehen bei „Early-onset Osteoporosis“.
Send us a textC4 Leaders – the ONLY nonprofit to utilize the pizza making process to create space for our companions to be seen, heard, and loved. We also write children's books, host this podcast, and use the most amazing handmade, hand-tossed, sourdough pizza to bring out the best in each other. Please check out PIZZADAYS.ORG to support our important work. Season 4 Episode #17 Katherine Klimitas is coming from Metairie, LA (inform, inspire, & transform)You can find via her website https://kakartnola.comAbout our guest: Artist, Story Teller, Public Speaker, Entrepreneur, Dog Lover, Hard Worker, Jeweler, and someone still yet defined. When Katherine was five, her mother gave her, her first watercolor set and Katherine's love for art was born. Fast forward a few years and Katherine was graduating from Loyola University New Orleans with a BA in graphic design and shortly thereafter began her art and design business. Katherine has published two books and has her work exhibited in many public entities, including the West Baton Rouge Museum of Art. Katherine was born with Osteogenesis Imperfecta, better known as Brittle Bone Disease. Katherine is 2 feet, 7 inches tall and by age 10, she had broken 500+ bones. Growing up with brittle bone disease, Katherine's life was always a little different from her able-bodied friends. Katherine was blessed to be born into a family of veterinarians and there was no way her parents were going to let her disease dictate her happiness. Her parents made her want to make something of herself, and she was going to be happy doing it—end of story.Currently, Katherine puts most of her energy into expanding her reach and capabilities as a watercolor artist and motivating others to contribute to their communities. Katherine, thanks for sharing your many gifts with people all over the world, for continuing to push yourself to be your best, and for being our guest on Life's Essential Ingredients. Welcome to the show!TOTD – “Some believe in destiny and some believe in fate, but I believe that happiness is something we create.” Sugarland song – Something MoreBuild a habit - to create intention - to live your purpose! In this episode:What was life like growing up?What are your life's essential ingredients?Why is GIVING BACK so important to you?The importance of family…Find Your SomethingLiving in Pain… what are some of your pain management tipsPerspective being 2'7”, lying down to work…I know you love MUSIC… dad inspired you (he passed) and love how it brings people together just like your art…Dogs…you have five…WatercolorsGraphic DesignPet PortraitsJewelryLegacy
In this episode, we review the high-yield topic of Osteogenesis Imperfecta / Brittle Bone Disease from the MSK section. Follow Medbullets on social media: Facebook: www.facebook.com/medbullets Instagram: www.instagram.com/medbulletsofficial Twitter: www.twitter.com/medbullets
Imagine treating complex cases faster and more accurately - without the guesswork. That's exactly what Dr. Jean Marc Retrouvey is doing by merging digital orthodontics with groundbreaking research.In this episode, Dr. Retrouvey shares how he's using AI and digital tools to treat rare bone diseases like osteogenesis imperfecta. His career journey spans teaching across continents and working on research that's changing lives.Dr. Retrouvey believes these tools should be fundamental knowledge, and he's here to share how they are already transforming the way orthodontists plan and treat cases.AI-powered systems are helping predict treatment outcomes and assist in complex case planning. This doesn't just save time—it improves the precision of treatments.But AI isn't without its limitations. While AI can align teeth based on thousands of past cases, it still struggles with personalized elements like facial aesthetics.Beyond the academic world, Dr. Retrouvey opens up about his love for fast cars and motorcycles, sharing stories of racing and adventure that balance his professional life.Don't miss this opportunity to hear from a leader in the field. Tune in now!Key TakeawaysIntroduction (00:00)Dr. Jean Marc Retrouvey's background and career journey (00:49)Researching osteogenesis imperfecta with Baylor College of Medicine (02:39)Invisalign's role in treating complex orthodontic cases (06:34)Digital orthodontics in modern residency programs (10:28)AI in orthodontics and its current applications (19:32)Dr. Retrouvey's passion for fast cars and racing (24:44)Additional ResourcesConnect with Dr. Jean Marc RetrouveyLinkedIn: https://www.linkedin.com/in/retrouvey/Facebook: https://www.facebook.com/jeanmarcretrouvey/—-- Register for the OrthoPreneurs Summit 2025: http://opsummit2025.com/- For more information, visit: https://orthopreneurs.com/- Join our FREE Facebook group here: https://www.facebook.com/groups/OrthoPreneurs
This week @sbship8_dpt discusses a recent case who presented with shoulder pain and history of osteogenesis imperfecta and her PT management throughout her plan of care. Want to make sure you stay on top of all things geriatrics? Go to https://MMOA.online to check out our Free eBooks, Lectures, & the MMOA Digest!
Daniel Lee was born with Osteogenesis Imperfecta commonly known as brittle bones disease. He has not let that define him and is now a para-athlete, motivational speaker, and a social impact leader. He is also the founder of 360 All Ability that works to create an inclusive world for people with disabilities. Join us in this chat with Daniel to learn more about his journey. 00:06 Introduction 01:11 Current Work 03:55 Childhood 07:57 Interests as a child 09:10 Thoughts on career as a young person 15:20 Journey to becoming a leader and mentor 17:45 Journey to becoming a motivational speaker 21:45 Designing a portfolio career 26:16 Intrinsic Drivers 34:20 Introduction to formal para-sports 39: 26 Sporting ecosystem for para-athletes 42:15 What is next? 43:41 Proudest Achievement 46:15 Sharing wisdom on finding your purpose 47:30 Closing Remarks Guest: Daniel Lee| LinkedIn Profile
Don't be deceived by the Gary Patti's easy smile. He knows more than a little about knockdowns and rebounds. These days as a keynote speaker, life coach, business consultant, and bestselling author, his unique comeback story is teaching others how to stay in the game and win. Gary was a two-week-old infant when a fractured femur (thigh bone) led to a diagnosis of Osteogenesis Imperfecta—brittle-bone disease. Before he was 12, he would have 80 fractures; as an adult he'd land in a body cast for months at a time. Instead of a sheltered existence, however, Gary's remarkable life and career came together while mending through 100 broken bones and a dozen-plus surgeries. Learn more about Gary and order the book at: unbreakablehope.com
I serien Foreldrestemmer møter vi foreldre til barn med sjeldne diagnoser. Felles er at de har behov for tilrettelegging på skolen. Her får vi vite litt om hvordan dette har gått og om disse foreldrene har noen råd til andre i samme situasjon. I denne episoden snakker vi med Jan-Helge som er far til en sønn med Osteogenesis Imperfecta. Tekstversjon: https://www.sunnaas.no/fag-og-forskning/kompetansesentre-og-tjenester/trs-kompetansesenter-for-sjeldne-diagnoser/foreldrestemmer---podkast-transkribert/
We are joined on this episode by Courtney and Thomas Hawthorne III, or T3! You may have seen him on social media when a video of him hitting a home run went MEGA viral! We saw the clip and knew we had to get them on to share their story! Thomas is your everyday 9-year-old kid, but also has a condition called Osteogenesis Imperfecta, or brittle bone disease, which is a genetic bone disease that causes fragile bones that easily break. Though T3 has this diagnosis, he still loves sports, playing with friends, playing video games and exploring the world! His mom, Courtney, created his platform to share his story and show the world that even when diagnoses can cause limitations, life should still be lived to the fullest! In the episode, we hear the story of his diagnosis from his mom's perspective. She talks about how she never expected to be on this turbulent journey and how the family has fully embraced it. We also discuss the impact that sharing milestones in life can have on people's perceptions. T3 then tells us a bit about his joys, dreams, and aspirations in life! This heart-filled episode shows us that, regardless of what life throws at us, we can all hit it out of the park! See the video version of this episode here
Loretta Smith, celebrated as the bestselling author of A Spanner in the Works, the gripping biography of Alice Anderson, the 'garage girl,' now invites us into her extraordinary life in Corpus in Extremis. A life shaped by pain, resilience, and the relentless pursuit of creativity despite the constraints of Osteogenesis Imperfecta—a condition known colloquially as brittle bone disease. #disability https://tinyurl.com/mt94d7mtSupport the Show.Check out more content on www.lotl.com
Katherine Klimitas was born with Osteogenesis Imperfecta, better known as Brittle Bone Disease. Despite this, she has created a design and art business that has been extremely successful. Learn more about how she uses physical limitations to still create the work and life she loves.Find Katherine's work at https://kakartnola.com/.Episode 447 How Brittle Bone Disease Made Katherine Klimitas A Better Designer_________ Love to create, design and craft? Have you always wanted to know how to turn your passions into profit? Carina's new book – Design Profit & Prosper will lead you down the path of making your dreams a reality. Get your copy today! https://www.designsuitecourses.com/designprofitprosper__________About Carina Gardner:Carina Gardner is a fabric designer, paper designer, and design educator who is passionate about helping other designers fulfill their creative dreams by teaching them her strategies for making money as a designer. She has a Ph.D. in Design and taught design at the University of Minnesota before starting Carina Gardner, Inc.Carina Gardner, Inc design brand has been featured in dishware, holiday decor, sewing patterns, and more. Her exclusive Design Suite Program helps creatives make money designing as they learn to design. Her programs include Illustrator and Photoshop training, surface pattern design, paper design, Silhouette & Cricut file design, and running a design business. She started the Make and Design Podcast so that she could share inspiration, stories, and experiences about design and life with crafters and designers.Find out more at https://www.carinagardner.comWatch this episode as a video at https://www.makeanddesign.com/
Is "safe" always best? This episode of Baby Banter challenges the idea. Host Nicole Pates, a paediatric physiotherapist, chats with Belinda, a mum who knows all about navigating risk. Her son Will has osteogenesis imperfecta (OI), also known as brittle bone disease. Belinda doesn't let OI hold Will back! She's found ways to create a world of exploration, even with the added challenge of keeping Will safe. Listen in to discover how Belinda empowers Will to assess risks and embrace outdoor play. In this episode you'll learn: How to approach risky play with a child with OI Strategies for building confidence and independence The importance of calculated risks in development Links: More on Osteogenesis Imperfecta Follow Nicole Pates on Instagram Baby Play Academy Toddler Play Academy The Ultimate Guide to Tummy Time Head Preference & Head Flattening Webinar Positioning and Play ideas for babies with hip dysplasia in braces
In this episode, we review the high-yield topic of Osteogenesis Imperfecta from the Pediatrics section. Follow Orthobullets on Social Media: Facebook Instagram Twitter LinkedIn YouTube --- Send in a voice message: https://podcasters.spotify.com/pod/show/orthobullets/message
Often, the more we learn about a disease, the more we learn about ourselves and the world around us. The story of the genetic disorder osteogenesis imperfecta (OI), colloquially known as brittle bone disease, illustrates this perfectly. As researchers continue to uncover the mechanisms responsible for OI development and progression, the better we understand the varied and crucial roles collagen plays in all parts of our biology. As historians attempt to trace how that knowledge has accumulated over time, the more we can clearly see how science rarely progresses consistently but rather erratically and is prone to interruption. And as we assess where we are with OI treatment and research today, the more apparent the gap is between knowledge and application, and just how critical lived experiences are in understanding a disease. In this episode, we explore these aspects of osteogenesis imperfecta, and we are thrilled to be joined by Natalie Lloyd, who shares her experience with OI as our firsthand account. Natalie is a New York Times bestselling author of novels for young readers, whose recently published award-winning book Hummingbird tells the story of a young girl with OI. Heartwarming, magical, and brilliant, this wonderful book is a must-read. Tune in today!See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.
Join Sheila and Sara this week as they cover Osteogenesis Imperfecta and Neuromuscular Diseases (with a primary focus on DMD). We also touch on Becker MD, congenital MD, facioscapulohumeral muscular dystrophy, Myotonic dystrophy, Emery-Dreifuss MD and SMA. Please note, the content for SMA is from Campbell, but we recognize the quickly evolving presentation of that disease with the introduction of Spinraza and other medications. Please be mindful of this during the episode. Enjoy. Affiliate Codes: ------------------------------------------ Medbridge Affiliate website: https://www.medbridgeeducation.com/pushing-pediatrics Medbridge Affiliate Code: PUSHINGPEDS ----------------------------------------- Resources: Palisano, R. J., Orlin, M. N., & Schreiber, R. (2023). Campbell's physical therapy for children. Elsevier.
In this week's episode I sat down with Emily Voorde. Emily is the Founder and CEO of INTO Strategies, a disability-led inclusion consultancy committed to bringing people with disabilities into campaigns, moments, and movements. Prior to starting INTO Strategies Emily was an Associate Director with NEWCO Strategies, a majority-women, majority-LGBTQ progressive consulting firm, served in the White House as the Associate Director in the White House Office of Public Engagement under President Biden, and worked on Mayor Pete's 2020 Presidential campaign. We discuss our shared experiences with the Osteogenesis Imperfecta (OI) Foundation and Little People of America respectively, who these organizations are actually for and serve, the role advocacy does and should play within these types of organizations and much, much more. Follow Emily: Instagram: @shortyvoorde LinkedIn: Emily Voorde Follow INTO Strategies: @intostrategies LinkedIn: INTO Strategies Website: https://www.intostrategies.com Email: emily@intostrategies.com Follow Me: Instagram: @jill_ilana , @alwayslookingup.podcast Website: https://www.jillianilana.com Email: alwayslookingup227@gmail.com This episode was edited and produced by Ben Curwin.
Jamie and Doug took an online course to help tackle the challenges with putting their 6yr old and 3yr old to bed. For the last 6 + months, they have struggled with catering to their kids during bedtime. Doug had a routine with Hendrix that would take 45 minutes, and include rubbing his back, and staying in his room until he was nearly asleep. Jamie would lay in bed with Henley and read, and then try to fall asleep to sleep stories. Doug is very anti-letting the kids sleep in their bed. Both Jamie and Doug were waking up multiple times a night, whether it was their daughter crying and climbing in bed with them, or their 3yr old son crying that he was scared. The nail in the coffin for them was when their son was able to climb out of his crib and run into their bedroom multiple times a night. Jamie and Doug discuss the parenting course they took, and the advice that some of their Frans messaged them. They have had some success so far, and have a few tricks and tips that have helped them tackle this sleep issue….and it has been working for the last few days!!! Plus, Jamie and Doug had a friend Trisha Taylor on the show (Episode 109), who they hung out with on their RV road-trip. Trisha was a mom, blogger, and truly an inspiration. Trisha had Osteogenesis Imperfecta which is a brittle bone disorder, and at that time, she had suffered over 600 broken bones and seven surgeries! She was 2ft. 10in tall and only weighed 60lbs and 6 years ago she defied the odds and became pregnant! Unfortunately Trisha recently had and accident and passed away. Jamie and Doug share a little about their interactions, and the relationship that Jamie and Trisha had built. Rest in Peace Trisha, and thoughts and continued prayers to her son Maven! Learn more about your ad choices. Visit megaphone.fm/adchoices
Jeff Black, owner of Iron House Strength & Conditioning and Relentless Forever, bodybuilder, podcaster and published author joins us today to chat about (a bit !) of his story and how he has developed into the man he is today. He shares what it was like growing up with and living with Osteogenesis Imperfecta, his experiences with psychedelic-assisted therapy, the process of writing his book and what drives him forward in all his endeavors. We think you will be inspired by this episode!Give Jeff a Follow on Intagram @jeffunbreakableblackWebsite and Podcast Links Unnamed & Untamed Meredith @merepaci_scoobyprephttps://linktr.ee/MerepaciSarah @sarahfordbishophttps://linktr.ee/sarahfordSonia @soniaspilhttps://linktr.ee/soniaspil
Jeannette welcomes Alycia Hirani, the founder of Emiah Couture, a unique clothing and design business. Despite her osteogenesis Imperfecta, otherwise known as brittle bones, which is a lifelong condition that requires her to use the assistance of crutches and a wheelchair, she now creates bespoke garments for a wide range of clientele across the country and the abroad. Alycia shares her journey of turning her creative passion into a viable business, starting with her love for drawing and painting and transitioning into fashion and wearable art. Alycia also discusses the challenges of balancing her creative side with the demands of running a business and the importance of having a supportive network, stressing the value of diversity, equity, and inclusion in her work and shares her aspirations for the future, including expanding her offerings and exploring opportunities in public speaking and TV work KEY TAKEAWAYS Having the right people in your life, whether they are friends, mentors, or fellow entrepreneurs, can provide valuable support and guidance on your journey. Valuing different perspectives and experiences can enrich your work and help create a more inclusive environment. Consider the needs and preferences of diverse individuals in your business and strive to make your products or services accessible to all. Clear communication is essential, especially when working on bespoke projects. Regularly check in with clients, ask detailed questions, and maintain open lines of communication to ensure you understand their needs and expectations. As a business owner, be open to change and willing to explore different avenues. Don't be afraid to try new things, pivot your business model, or expand into new areas. Stay flexible and continuously adapt to meet the needs of your clients and the market BEST MOMENTS "Having good friends and having that kind of really supportive network is really helpful." "I think it's really important to surround yourself with people that will lift you up at a moment's notice." "Having that kind of support kind of like net of like-minded people really helps just to kind of make the process easier and it just makes it more positive for you as well." "I think it's always nice to relate to someone else and that you can have that kind of bond, especially when you work on your own or having other things." This is the perfect time to get focused on what YOU want to really achieve in your business, career, and life. It's never too late to be BRAVE and BOLD and unlock your inner BRILLIANCE. If you'd like to jump on a free mentoring session just DM Jeannette at info@jeannettelinfootassociates.com or sign up via Jeannette's linktree https://linktr.ee/JLinfoot VALUABLE RESOURCES Brave, Bold, Brilliant podcast series - https://podcasts.apple.com/gb/podcast/brave-bold-brilliant-podcast/id1524278970 ABOUT THE GUEST Alycia is a bespoke designer specialising in bridal, corsetry and couture. Alongside her condition, Osteogenesis Imperfecta; otherwise known as brittle bones, she creates one of a kind garments featuring exquisite embellishments for a wide range of clientele who are looking for heirloom pieces and a decadent experience. Social media links that they want us to tag www.emiah.co.uk www.instagram.com/alycia.emiah / @alycia.emiah www.instagram.com/emiahcouture / @emiahcouture www.facebook.com/emiahcouture / @emiahcouture ABOUT THE PRINCE'S TRUST NatWest has a long and proud history of supporting communities across the country and creating opportunities today to help others thrive tomorrow. We are proud to work side-by-side with The Prince's Trust on its Enterprise programme. Over the past 20 years this partnership has supported tens of thousands of young people to turn their ideas into sustainable businesses. NatWest colleagues also take part in volunteering and fundraising; since 2019 The Prince's Trust has welcomed more than 882 NatWest Group volunteers across 437 different sessions, supporting 3,372 young people. We are committed to supporting entrepreneurs to start, scale and grow and offer a range of fully-funded support for businesses at every stage, including online learning with Business Builder, a six-month Accelerator programme for businesses with ambitions to expand, and Local Enterprise Managers who offer regular events and 1:1 support. THE CHALLENGE WE FACE IN WALES Wales continues to experience a variety of entrenched social and economic challenges. Workless households, significant health inequalities and high youth unemployment in some areas are the main issues that continue to prevail. It's widely recognised that growing up in poverty can have an unjust and detrimental impact on young people, placing barriers on future opportunities. According to The Prince's Trust annual Youth Index report (2022) 24% of young people in Wales agree they will never recover from the emotional impact of the pandemic More than half (56%) of young people in Wales agree that the pandemic has left them feeling “burnt out” and 44% reveal that the pandemic has caused a long-term negative impact on their stress levels While over half (55%) of Wales' young people report experiencing a mental health problem 46% say the pandemic has made their mental health worse, and 28% of young people in Wales surveyed feel like they will fail in life Today, The Prince's Trust is one of the UK's leading youth charities, founded by King Charles in 1976. Our programmes have been developed in response to society's changing needs, give young people the support they need to overcome hardship and lead full and successful lives. Our plans in Wales will directly help to alleviate the issues this generation are experiencing. The rising cost-of-living is having a significant impact on unemployed young people supported by The Prince's Trust. The Prince's Trust deliver a number of programmes for young people aged 11-30. The focus on Education, Employment and Enterprise. All of our programmes embed confidence and resilience building; to enable young people to enjoy long term positive outcomes. Our gentle plea for support We really need your help! If you would consider being a business mentor for young people at The Prince's Trust, or want to support via your business or as an individual; we would be delighted to hear from you. You will be helping us to change the lives of young people for the better, and supporting young people into meaningful education and employment; with the confidence to know they can succeed. Let's create brighter futures for young people in Wales, and inspire future generations to come. hello@princes-trust.org.uk, or 020 7543 1384 ABOUT THE HOST Jeannette Linfoot is a highly regarded senior executive, property investor, board advisor, and business mentor with over 25 years of global professional business experience across the travel, leisure, hospitality, and property sectors. Having bought, ran, and sold businesses all over the world, Jeannette now has a portfolio of her own businesses and also advises and mentors other business leaders to drive forward their strategies as well as their own personal development. Jeannette is a down-to-earth leader, a passionate champion for diversity & inclusion, and a huge advocate of nurturing talent so every person can unleash their full potential and live their dreams. CONTACT THE HOST Jeannette's linktree - https://linktr.ee/JLinfoot https://www.jeannettelinfootassociates.com/ YOUTUBE - https://www.youtube.com/channel/UCtsU57ZGoPhm55_X0qF16_Q LinkedIn - https://uk.linkedin.com/in/jeannettelinfoot Facebook - https://uk.linkedin.com/in/jeannettelinfoot Instagram - https://www.instagram.com/jeannette.linfoot/ Email - info@jeannettelinfootassociates.com Podcast Description Jeannette Linfoot talks to incredible people about their experiences of being Brave, Bold & Brilliant, which have allowed them to unleash their full potential in business, their careers, and life in general. From the boardroom tables of ‘big' international businesses to the dining room tables of entrepreneurial start-ups, how to overcome challenges, embrace opportunities and take risks, whilst staying ‘true' to yourself is the order of the day.Travel, Bold, Brilliant, business, growth, scale, marketing, investment, investing, entrepreneurship, coach, consultant, mindset, six figures, seven figures, travel, industry, ROI, B2B, inspirational: https://linktr.ee/JLinfootThis show was brought to you by Progressive Media
Welcome back to our weekend Cabral HouseCall shows! This is where we answer our community's wellness, weight loss, and anti-aging questions to help people get back on track! Check out today's questions: Cindy: I love Fatlossity PM for the best sleep, but I often get jittery with caffeine so I have only used the AM short term. I don't get the same effect with your Sleep Support supplement (melatonin tends to awaken me after only a few hours). I do benefit from the amino acid L-trypophine, on occasion. Since Fatlossity PM cannot be purchased separately, do you have any suggestions for improving sleep or which supplement is likely to help me? My sleep has improved over the last 6 years from learning from you, but I often still wake up after 5 or 6 hours of sleep to go to the bathroom. I am post-menopasusal, but I do take estrogen replacement- which has helped. But, Once my brain starts thinking, sadly sleep is usually over! Anonymous: Hello Dr. Cabral. 39 year old male here. My issue is related to “Incomplete Bowel Movement” and I have been experiencing this issue for at least 10 years and I'm unsure what I should do about it. Basically, I have a normal bowel movement but it sometimes feels like not everything came out. So then I use an anal douche and every single time there is more poop coming out with the water. This happens with every single bowel movement. I'm a “fitness guy” with a healthy diet and lots of fiber. Thank you! Joy: Thanks for all you do Dr Cabral! (Q #1 of higher importance) I'm a 30y/o F & would consider myself to be decently healthy & aware of my body. I however experience awful joint pain & weakness. It tends to hold me back from enjoying an active lifestyle. It's literally every joint from my neck to my ankles. My brother was born with a disease -Osteogenesis Imperfecta but has the more mild type 1. It affects the production of collagen. I don't think I have OI also. Curious what would you recommend me take/do to help my joint pain. Q#2 I recently read of the “earthing” concept, which is supposed to have a range of health benefits. It involves the natural electricity of the earth, here is a link for more info. I'm skeptical, but would like to know what u think! https://groundingofficial.com/ Jade: Hey there. I've been invested in my health for some time now and have been doing my best to encourage people around me to be healthier versions of themselves. However, I have one aunt in her late 50s whose diet isn't necessarily the best. She drinks Diet Coke mostly every day, eats out regularly and doesn't exercise. She also has an extremely stressful job which doesn't help. It‘s always been difficult to encourage her to change her eating habits, but she was just diagnosed with carpal tunnel. I told her I would do my best to get information on small changes she can make to better her condition and overall life. Is there anything she can do or take that may not be drastic? I would recommend your detox and less processed foods and drinks of course, but that's too extreme for her. Erica: Hi Dr. Cabral! I wanted to ask you your thoughts on what could be the root of my symptoms. I've had dizziness for about 3-4 years now and it's very consistent almost every day. However, it hasn't gotten worse it's stayed very consistent over this time. It seems to be worse around the time of my period and also when under stress. In addition, I have a lot of popping in both of my ears and sometimes my ears feel itchy and almost like my eustachian tubes have to release pressure. I went to the ENT who said I might have Eustachian tube dysfunction but ruled out any fluid in my ears or other issues. I also tried the maneuver for crystals in my ears which didn't seem to have an effect either. Any thoughts on things I could try? Dizziness got worse when I took antibiotics 3/4 years ago. Thank you Thank you for tuning into today's Cabral HouseCall and be sure to check back tomorrow where we answer more of our community's questions! - - - Show Notes and Resources: StephenCabral.com/2766 - - - Get a FREE Copy of Dr. Cabral's Book: The Rain Barrel Effect - - - Join the Community & Get Your Questions Answered: CabralSupportGroup.com - - - Dr. Cabral's Most Popular At-Home Lab Tests: > Complete Minerals & Metals Test (Test for mineral imbalances & heavy metal toxicity) - - - > Complete Candida, Metabolic & Vitamins Test (Test for 75 biomarkers including yeast & bacterial gut overgrowth, as well as vitamin levels) - - - > Complete Stress, Mood & Metabolism Test (Discover your complete thyroid, adrenal, hormone, vitamin D & insulin levels) - - - > Complete Food Sensitivity Test (Find out your hidden food sensitivities) - - - > Complete Omega-3 & Inflammation Test (Discover your levels of inflammation related to your omega-6 to omega-3 levels) - - - Get Your Question Answered On An Upcoming HouseCall: StephenCabral.com/askcabral - - - Would You Take 30 Seconds To Rate & Review The Cabral Concept? The best way to help me spread our mission of true natural health is to pass on the good word, and I read and appreciate every review!
We all have limitations. We all have challenges. And we all have a choice when we face them head-on: We can either shrink back in isolation, distancing ourselves from God and others; or we can lean into God's strength, depending on Him and the people He's put in our lives. Today's guest, Meagan Anne, was born with a rare condition called Osteogenesis Imperfecta. But despite living with a disability, she lives life to the fullest!! Her story is a beautiful testimony of God's faithfulness and all He can do with our willingness to come to Him — limits and all. To connect with Meagan, head over to @meagannanne on Instagram and subscribe to her YouTube channel here: https://www.youtube.com/@MeaganAnne Get your By Words Story candle here: https://www.juneandblume.com/shop/p/storycandle (Use code BYWRDS10 for 10% off your June + Blume order!) Shop my favorite Bible studies + devotionals: thedailygraceco.com/HANNAHH Get 20% off your BIOHM Health order with code HANNAH: https://www.biohmhealth.com/ Connect: www.thehannahhughes.com Instagram: @thehannahhughes @thebywordsshow Shop my Amazon faves: https://www.amazon.com/shop/thehannahhughes --- Support this podcast: https://podcasters.spotify.com/pod/show/bywords/support
Laura is back and she is joined by the truly exceptional McKenzie Coan, a Paralympic swimmer whose remarkable journey has resulted in thoroughly stellar achievements. McKenzie's story is a testament to the indomitable human spirit, demonstrating that anything is possible when you put your heart and mind to it. In today's powerful conversation, she reveals the mindset skills that have fueled her success, and emphasizes the significance of resilience, determination, staying present, and embracing challenges as opportunities for growth. From being diagnosed with Osteogenesis Imperfecta at just 19 days old, McKenzie's life has exceeded all expectations as she consistently defied limitations set by others. Through aqua therapy and unwavering support from her parents, McKenzie's love for water became a source of rejuvenation that propelled her to ultimately become a three-time U.S. Paralympian, a six-time Paralympic medalist, and a world record holder. In today's episode, she delves into such topics as the emotional turmoil of team selection, the impact of the Paralympic Games, and the importance of mental strength in facing uncertainties leading up to the Tokyo Paralympics. McKenzie also offers her insights on adaptive sports, strength training, and the emotional rollercoaster of pursuing Paralympic excellence. Noting the profound impact of support from family, coaches, and teammates, she also highlights the power of embracing life's challenges to pursue your dreams with belief and determination. Join Laura and McKenzie here today for this remarkable journey of defying limitations and achieving greatness, as they reveal the fact that the pursuit of gold is not just about winning medals; it's about finding freedom in your passion and pushing yourself to new heights. Episode Highlights: The belief McKenzie's parents instilled in her that anything was possible How swimming became McKenzie's refuge Balancing ambitious goals with living in the present moment How McKenzie's discovery of the Paralympic Games inspired her The power of resilience and determination Overcoming adversity and pursuing dreams The emotional turmoil of team selection McKenzie's journey towards Paris 2024 Growth, resilience, and the power of rewiring the mind for success Quotes: "Through every broken bone, every setback, every obstacle, McKenzie has never lost hope, and neither should you." "I think it is really good to have your mind already set in what your next goal might be or achieving the goal that you're just starting to work towards now." "For the first time in my life, I saw athletes who had a disability, who looked like me, with gold medals around their neck and… I realized that this dream is a possibility for me.” "The things that happen to us either become things that happen to us or things that happen for us. That's up to you to decide in the moment." "Everything I've been through in the last few years has led me to this moment. This is my time to go out and show them how strong I am." "Seeing all the athletes from all the other nations, and we're all so different…but we all are coming together to do one thing, and none of that matters for the next week or two." Links: The Pursuit of Gold Website Grab the Top 10 Mental Skills Guide! Laura's Social Media: Laura's Instagram Laura's Facebook Connect with McKenzie: McKenzie Coan's Website McKenzie Coan on Twitter McKenzie Coan on TikTok Breaking Free
This week a six-year-old from French River talks about living with Osteogenesis Imperfecta, the Crosses for Change memorial in Sudbury is vandalized, we look at at the new plan for a library and art gallery in Sudbury, the mayor of Gore Bay has an update on local issues, domestic rabbits are running wild in Sudbury, and we meet an insect collector at Sudbury city hall.
Tony Jacobsen is an author, speaker, motivator, and coachHe has Osteogenesis Imperfecta, a rare disorder that makes his bones brittle. Tony has suffered 75 fractures, and have had 12 surgical procedures. Each of the long bones in his legs is equipped with steel rods. Tony used a wheelchair when he was a kid, started using crutches in high school, and took his first unassisted steps when he was 24 years old.At 42, Tony thought he'd had a heart attack and was prompted to make some big changes. It was quite a journey as Tony navigated the delicate relationship between exercise and his brittle bones. But once he did, it was magic! He's the healthiest he's ever been, and he realize how much he can help others get past their barriers!This passion has led to Tony writing his book, speaking at various events, and creating resources that will spread the Be #UNBREAKABLE message!www.tonyJacobsen.comTry Nom Nom today, go to https://trynom.com/curveball and get 50% off your first order plus free shipping.
As the daughter of veterinarians, Katherine expresses her family's life-long love of animals through her meticulous life-like paintings. She earned a B.A. from Loyola University in 2011, and today at age 33, runs her multifaceted business KAK ART & Designs from home. When clients learn that Katherine has Osteogenesis Imperfecta, also known as brittle bone disease, they are captivated by her unique perspective. She and her parents stopped counting her broken bones at 500 at age 10. She's 2 feet 7 inches tall, gets around in an electric wheelchair, and creates all of her art, jewelry and commercial graphic design while lying on her side. To learn more about Katherine, pick up a copy of her book: Looking Up, subscribe to her blog, or connect with her on social media.https://kakartnola.com/__________________________________________________Please LIKE
Born with the rare genetic disorder, Osteogenesis Imperfecta (aka ‘brittle bone disease'), and a wheelchair user since the age of six, Athena grew up navigating an ill-fitting narrative about being disabled in our society. On one end of the spectrum is the highly medicalized representation of the disabled body that typically focuses on pain, deformity and lack of function. Frida Kahlo's surrealist self-portraits depicting the painful and distorting aspects of her body and her disability are an example of how this interpretation of disability has shown up in the world of art. On the other end of the spectrum is the objectification of people with disabilities as “super crips” that are held up as inspirational for simply living with their disability. This viewpoint has become even more prevalent with the rise of social media and is articulately critiqued in Stella Young's TED talk, “I'm Not Your Inspiration, Thank You Very Much”. https://www.instagram.com/athenacreative/ My Life Without Limits is a podcast by Cerebral Palsy Alberta Music from Soundstripe: Astro Jetson by Mikey Geiger https://app.soundstripe.com/royalty-free-music Carlos is a Hispanic male with cerebral palsy. He has short dark hair, dark eyes, some facial goatee hair, and uses crutches/canes to help him walk. Leah is a white female with shoulder length red hair, freckles, green eyes, wears glasses and is able bodied. Follow us on Instagram @mylifewithoutlimitspodcast Support our podcast by buying us a coffee here: https://www.buymeacoffee.com/mlwlpodcast lison@cpalberta.com for any questions! We acknowledge that what we call Alberta is the traditional and ancestral territory of many peoples, presently subject to Treaties 6, 7, and 8. Namely: the Blackfoot Confederacy – Kainai, Piikani, and Siksika – the Cree, Dene, Saulteaux, Nakota Sioux, Stoney Nakoda, and the Tsuu T'ina Nation and the Métis People of Alberta. This includes the Métis Settlements and the Six Regions of the Métis Nation of Alberta within the historical Northwest Metis Homeland. We acknowledge the many First Nations, Métis and Inuit who have lived in and cared for these lands for generations. We are grateful for the traditional Knowledge Keepers and Elders who are still with us today and those who have gone before us. We make this acknowledgement as an act of reconciliation and gratitude to those whose territory we reside on or are visiting.
In this episode of Championship Leadership, we are honored to interview Jeffrey Black, Founder of Iron House Strength Conditioning-a health and fitness facility where everyone can empower themselves and can be their own hero. He will share how he battled through a very rare genetic disorder Osteogenesis Imperfecta and his successful journey into health and fitness thus creating Iron House Strength Conditioning. Today, Jeff is guiding people to understand the power of having a healthy physical and mental lifestyle to live a fulfilling life. These and more!! Tune in to this episode!!
For this episode, I speak with Ryan Wilson, the director of Team Trust Productions. Ryan created Team Trust to help mission-driven organizations reach and serve their communications. He wants to help connect people with the entities, organizations and resources they deserve to grow and flourish. Ryan's heart is advocating for persons with disabilities, because he is one. Ryan has befriended persons with the same disability as his (Osteogenesis Imperfecta), and established life-long relationships with persons with visual impairments, hearing impairments, cognitive disabilities and mental illnesses. Each one of these relationships changed his life. Thanks for listening, and if you haven't already, please give us a ⭐⭐⭐⭐⭐ review on Apple Podcasts or Spotify.Otter.ai Transcript: https://otter.ai/u/Upr-Nwv5MGzuBu_HNMWlmkaRMGoPDF Transcript: https://3bd6e695-b492-4878-afa9-f79d8b09e0c4.usrfiles.com/ugd/3bd6e6_1f3eabbdc10a41ef91270b7847d98415.pdfShow Notes: https://bit.ly/TI-Ryan-WilsonCover Art Image Description: black background; think inclusive logo in the top left; rainbow-colored waves overlayed with the headshot of Ryan Wilson; text reads: Ryan Wilson, Team Trust; MCIE logo in the bottom rightCreditsThink Inclusive is written, edited, and sound designed by Tim Villegas and is produced by MCIE.Original music by Miles Kredich.Support Think Inclusive by becoming a patron!Thank you to our sponsor, TogetherLetters. Hosted on Acast. See acast.com/privacy for more information.
In this episode I speak with Professor Kara Ayers, who is a Writer, Speaker, Wife and Mom of three children. Professor Ayers accomplished all of this while also having Osteogenesis Imperfecta. She is currently The Director for The Center For Disability, Equity & Intersectionality.
In this episode, we review the high-yield topic of Osteogenesis Imperfecta from the Pediatrics section. Follow Orthobullets on Social Media: Facebook: www.facebook.com/orthobullets Instagram: www.instagram.com/orthobulletsofficial Twitter: www.twitter.com/orthobullets LinkedIn: www.linkedin.com/company/27125689 YouTube: www.youtube.com/channel/UCMZSlD9OhkFG2t25oM14FvQ --- Send in a voice message: https://anchor.fm/orthobullets/message
Jen interviews her neighbor, Deborah Lapkin, in this week's episode. Deborah gave birth to Haley almost 40 years ago. They did not know at the time of her delivery that Haley has Osteogenesis Imperfecta or Brittle Bone Disease.In this episode, Deborah discusses their journey as a family within a small community and how they both helped to transform much of how our school operates today. She gives us tips on what helped her get out from under the solitude and loneliness of parenting a child with special needs.Jen gets honest about how she doesn't ask for help because sometimes she doesn't even know what she needs. Can you relate? She has some ideas for how those that support us on this journey can offer their own solutions to take help.We celebrate love this week on our Valentine's episode. We hope you enjoy. And, let us know what you think! We love to hear from you. Send emails to ForOurSpecialKids@gmail.com if you have questions, topics, or an amazing person we should highlight. And, please tell a friend or caregiver about us! Follow Us on Instagram & FaceBook, @ForOurSpecialKids or go to https://www.ForOurSpecialKids.comhttps://uppbeat.io/t/lane-king/journeyLicense code: E3DYP1B4L21HSX8E
Jack Flynn and Alex Gornitzky from CHOP and University of Michigan, respectively, join the show to discuss their recent article on the psychology of scoliosis bracing. The lightning round focuses on recent publications by Dr. Flynn with some controversies mixed in to give the guests a chance to "stir the pot." Your hosts are Carter Clement from Children's Hospital of New Orleans, Josh Holt from University of Iowa, and Craig Louer from Vanderbilt. The episode is sponsored by nView Medical. Music by A. A. Alto. “Main Event” article: Why Don't Adolescents Wear Their Brace? A Prospective Study Investigating Psychosocial Characteristics That Predict Scoliosis Brace Wear. Gornitzky et al. JPO Jan 2023. https://pubmed.ncbi.nlm.nih.gov/36194756/ Lightning (a.k.a. “Jumpin Jack Flash”) Round articles: Lengthening Behavior of Magnetically Controlled Growing Rods in Early-Onset Scoliosis: A Multicenter Study. Heyer et al. JBJS Oct 2022. https://pubmed.ncbi.nlm.nih.gov/36367763/ Best Practice Guidelines for Surgical Site Infection in High-risk Pediatric Spine Surgery: Definition, Prevention, Diagnosis, and Treatment. Badin et al. JPO Nov-Dec 2022. https://pubmed.ncbi.nlm.nih.gov/36037438/ A Modern Day Timeline for In-Hospital Monitoring in Perfused, Pulseless Pediatric Supracondylar Humerus Fractures. Heyer et al. JPO Nov-Dec 2022. https://pubmed.ncbi.nlm.nih.gov/35980760/ Preoperative MRI Reliably Predicts Pedicle Dimensions on Intraoperative CT Images in Structural Main Thoracic Curves in Patients With Adolescent Idiopathic Scoliosis. Mitchell et al. Spine (Phila PA 1976) Sept 2022. https://pubmed.ncbi.nlm.nih.gov/35867611/ Early Knee Range of Motion Following Operative Treatment for Tibial Tubercle Avulsion Fractures Is Safe. Huang et al. JPO Oct 2022. https://pubmed.ncbi.nlm.nih.gov/35968996/ Getting the Message: The Declining Trend in Opioid Prescribing for Minor Orthopaedic Injuries in Children and Adolescents. Krakow et al. JBJS Jul 2022. https://pubmed.ncbi.nlm.nih.gov/35793795/ Complications following surgical treatment of adolescent idiopathic scoliosis: a 10-year prospective follow-up study. Hariharan et al. Spine Deformity Sept 2022. https://pubmed.ncbi.nlm.nih.gov/35488969/ Evidence Behind Upper Instrumented Vertebra Selection in Adolescent Idiopathic Scoliosis: A Systematic and Critical Analysis Review. Baghdadi et al. JBJS Reviews Sept 2021. https://pubmed.ncbi.nlm.nih.gov/35417439/ Better Patient Care Through Physician Extenders and Advanced Practice Providers. Milewski et al. JPO May-June 2022. https://pubmed.ncbi.nlm.nih.gov/35405696/ Thoracic Curve Correction Ratio: An Objective Measure to Guide against Overcorrection of a Main Thoracic Curve in the Setting of a Structural Proximal Thoracic Curve. Landrum et al. Journal of Clinical Medicine Mar 2022. https://pubmed.ncbi.nlm.nih.gov/35329871/ Benchmarking surgical indications for adolescent idiopathic scoliosis across time, region, and patient population: a study of 4229 cases. Heyer et al. Spine Deformity July 2022. https://pubmed.ncbi.nlm.nih.gov/35258846/ When Is an Isolated Olecranon Fracture Pathognomonic for Osteogenesis Imperfecta? VanEenenaam et al. JPO May-June 2022. https://pubmed.ncbi.nlm.nih.gov/35200208/ Unplanned Return to the Operating Room (UpROR) After Pediatric Diaphyseal Femoral Fractures. Baghdadi et al. JPO Feb 2022. https://pubmed.ncbi.nlm.nih.gov/34923506/ Awake serial body casting for the management of infantile idiopathic scoliosis: is general anesthesia necessary? LaValva et al. Spine Deformity Oct 2020. https://pubmed.ncbi.nlm.nih.gov/32383143/ Do Year-Out Programs Make Medical Students More Competitive Candidates for Orthopedic Surgery Residencies? Bram et al. Journal of Surgical Education Nov-Dec 2020. https://pubmed.ncbi.nlm.nih.gov/32505668/ Why Irrigate for the Same Contamination Rate: Wound Contamination in Pediatric Spinal Surgery Using Betadine Versus Saline. Cohen et al. JPO Nov-Dec 2020. https://pubmed.ncbi.nlm.nih.gov/33044376/ Mistakes Made and Lessons Learned: A Mid-Career Pediatric Orthopaedic Surgeon's Journey to Sustain Energy and Avoid Burnout. Flynn. JPO July 2020. https://pubmed.ncbi.nlm.nih.gov/32502065/
Welcome to season number 3 of the podcast. We are starting off this season with a two-part special episode with McKenzie Coan. Mckenzie is a 3x Paralympian and a 6x Paralympic medalist for the US in Swimming. McKenzie was diagnosed at 19 days old with a condition called Osteogenesis Imperfecta, otherwise known as brittle bone disease. This condition causes Mckenzie's bone to break easily, doctors said that McKenzie would never walk, never sit upright, never talk, and maybe not even live a very long life. Well, you know this podcast is a two-parter. So McKenzie can talk and her never take no for an answer attitude is truly inspiring. Please enjoy part 2 of the McKenzie Coan journey. McKenzie Coan Instagram: @McKenzie_Coan Facebook: @McKenzieCoan Twitter: @McKenzie_Coan Website: www.mckenziecoan.com Book: Breaking Free: Shattering Expectations and Thriving With Ambition in Pursuit of Gold https://www.amazon.com/Breaking-Free-McKenzie-Coan/dp/1735919322/ref=zg_bsnr_16674_7?_encoding=UTF8&psc=1&refRID=QN5DWMBQBCYHFWGCA0ZT Tim Loves the Olympics Instagram: @tltopodcast Twitter: @tltopodcast Facebook: @tltopodcast
Welcome to season number 3 of the podcast. We are starting off this season with a two-part special episode with McKenzie Coan. Mckenzie is a 3x Paralympian and a 6x Paralympic medalist for the US in Swimming. McKenzie was diagnosed at 19 days old with a condition called Osteogenesis Imperfecta, otherwise known as brittle bone disease. This condition causes Mckenzie's bone to break easily, doctors said that McKenzie would never walk, never sit upright, never talk, and maybe not even live a very long life. This is a journey story you won't soon forget. And as always, thank you for your support. McKenzie Coan Instagram: @McKenzie_Coan Facebook: @McKenzieCoan Twitter: @McKenzie_Coan Website: www.mckenziecoan.com Book: Breaking Free: Shattering Expectations and Thriving With Ambition in Pursuit of Gold https://www.amazon.com/Breaking-Free-McKenzie-Coan/dp/1735919322/ref=zg_bsnr_16674_7?_encoding=UTF8&psc=1&refRID=QN5DWMBQBCYHFWGCA0ZT Tim Loves the Olympics Instagram: @tltopodcast Twitter: @tltopodcast Facebook: @tltopodcast
Andy and Jamie Stewart were expecting their first child when they received the crushing news their baby was not going to survive. How could they trust a God who would let that happen? Full show notes at: https://compelledpodcast.com/episodes/andy-jamie-stewart Learn more about Osteogenesis Imperfecta type 2 here: https://oif.org/ ++++++++++++ Compelled is a seasonal podcast using gripping, immersive storytelling to celebrate the powerful ways God is transforming Christians around the world. These Christian testimonies are raw, true, and powerful. Be encouraged and let your faith be strengthened! Support the podcast on Patreon and listen to episodes 1 week early: https://www.patreon.com/compelledpodcast Help us create more stories by donating on PayPal or Venmo: https://compelledpodcast.com/support-us Show notes, emails, and more at: https://compelledpodcast.com/ Learn more about your ad choices. Visit podcastchoices.com/adchoices
Gary Patti was born with Osteogenesis imperfecta. A life of about 100 fractures with first coming at 2 weeks old. He competed in various wheelchair sports, basketball and track events. Ranked 3rd in the world at the mile event in 1978. 43 years in the fitness industry owning numerous Health and Fitness Clubs. International motivational, inspirational and business speaker.
Katherine Klimitas is a New Orleans-based artist and designer who sold her first watercolor at age 10. As the daughter of veterinarians, Katherine expresses her family's life-long love of animals through her meticulous life-like paintings. She earned a B.A. from Loyola University in 2011, and today at age 33, runs her multifaceted business KAK ART & Designs from home. When clients learn that Katherine has Osteogenesis Imperfecta, also known as brittle bone disease, they are captivated by her unique perspective. She and her parents stopped counting her broken bones at 500 at age 10. She's 2 feet 7 inches tall, gets around in an electric wheelchair, and creates all of her art, jewelry and commercial graphic design while lying on her side. TODAY'S SPONSOR LOVEHelp Us in Supporting Our Sponsor!*Find ALL links and details at the end of the Show Notes. LINKS FOR TODAY'S GUESTKatherine Klimitas WEBSITE: https://kakartnola.com/ (KAKArtNOLA.com) FACEBOOK: https://Facebook.com/kakartnola (@KAKArtNOLA) INSTAGRAM: https://instagram.com/kakartnola (@KAKArtNOLA) LINKS FOR THE PODCASTThe Lowe Down with Kevin Lowe Checkout our https://www.thelowedownwithkevinlowe.com (Website!) Follow us on https://instagram.com/thelowedownwithkevinlowe (Instagram!) Like us on https://facebook.com/thelowedownwithkevinlowe (Facebook!) Experience the POWER of http://kevinlowecoaching.com (Transformative Coaching )in Both Your Life & Business Mentioned in this episode: SPONSORED BY MANSCAPED Get 20% OFF + FREE Shipping with Promo Code LOWE @Manscaped! CLICK to start shopping! https://the-lowe-down-with-kevin-lowe.captivate.fm/manscaped (SHOP @Manscaped.com)
This week, we once again honor one of the most inspiring people we've had the pleasure of interviewing in the podcast, Sean Stephenson. Sean is a therapist, self-help author and motivational speaker. He was born with a rare bone disorder called Osteogenesis Imperfecta that stunted his growth and caused his bones to be extremely fragile. Despite all the medical challenges he has faces over his life, Sean made the decision to lead an extraordinary life and has inspired millions worldwide, including Sir Richard Branson, President Clinton, Tony Robbins and the Dalai Lama. Enjoy listening to this inspiring episode!
Katherine Klimitas is a New Orleans-based artist and designer who sold her first watercolor at age 10. As the daughter of veterinarians, Katherine expresses her family's life-long love of animals through her meticulous life-like paintings. She earned a B.A. from Loyola University in 2011, and today at age 33, runs her multifaceted business KAK ART & Designs from home. When clients learn that Katherine has Osteogenesis Imperfecta, also known as brittle bone disease, they are captivated by her unique perspective. She and her parents stopped counting her broken bones at 500 at age 10. She's 2 feet 7 inches tall, gets around in an electric wheelchair, and creates all of her art, jewelry and commercial graphic design while lying on her side. kakartnola.com facebook.com/kakartnola instagram.com/kakartnola
Atticus Shaffer of The Middle on ABC discusses life with osteogenesis imperfecta and his acting career.
Katherine Klimitas is a New Orleans-based artist and designer who sold her first watercolor at age 10. As the daughter of veterinarians, Katherine expresses her family's life-long love of animals through her meticulous life-like paintings. She earned a B.A. from Loyola University in 2011, and today at age 33, runs her multifaceted business KAK ART & Designs (https://kakartnola.com) from home. When clients learn that Katherine has Osteogenesis Imperfecta, also known as brittle bone disease, they are captivated by her unique perspective. She and her parents stopped counting her broken bones at 500 at age 10. She's 2 feet 7 inches tall, gets around in an electric wheelchair, and creates all of her art, jewelry and commercial graphic design while lying on her side. If you want to learn more about or reach out to Katherine, you can do so directly through her website or on Instagram (https://www.instagram.com/kakartnola) and Facebook (https://www.facebook.com/kakartnola). . . . For all the latest about the podcast, follow us on LinkedIn (https://www.linkedin.com/showcase/as-diverse-as-two-peas-in-a-podcast), Instagram (https://www.instagram.com/asdiverseastwopeasinapod), Facebook (https://www.facebook.com/AsDiverseAsTwoPeasInAPod) or Youtube (https://www.youtube.com/channel/UC-UyuMYX-QAvJKztBTm94NQ) To reach out to Julien Lefort, you can contact him on LinkedIn (https://www.linkedin.com/in/julienl) or directly through his website (https://www.wearefutureminds.com)
Help us to defend our title as the Best Science and Medicine Podcast! Go to podcastawards.com and select “DNA Today” in the Science and Medicine category. Bonus if you tweet/post that you nominated DNA Today (and tag us), then we will share your post and give you a shoutout on the show as a thank you. You have the power to get DNA Today nominated again! On Friday, June 24th, 2022, the US Supreme Court released its decision in Dobbs v. Jackson Women's Health Organizationvoting to overturn Roe v. Wade— the 1973 ruling that guaranteed federal constitutional protections of abortion rights. In this discussion we will be explaining the abortion laws and how this decision specifically affects genetic counseling with Laura Hercher. Laura is a seasoned genetic counselor and the host of The Beagle Has Landed podcast. She is also on the team at Sarah Lawrence College's Genetic Counseling program coordinating student research, directing the ethics course and facilitating the weekly current events discussion. In the week leading up to this episode we asked our listeners to submit their questions on our social media channels, be sure to listen to see if your question was answered!On This Episode We Discuss:Trigger laws and when they go into effectThe effect of this decision on pro-choice states (CT, NY, CA, etc)How this ruling disproportionately affects people who can't afford to travel for abortionsGenetic counseling in a post-Roe world and how this decision affects the fieldThe legal ramifications for genetic counselors discussing patients' options in abortion banned statesHow the overturning of Roe is going to impact pedigrees Receiving care (medication, D&C, D&E) in states that now have abortion bansHow this affects pregnancies that are non-viable and people with conditions where a pregnancy is life-threatening The value of pursuing NIPS if patients cannot access abortionsRecommended resources/organizations for people to donate money or volunteerTo stay up to date on the latest developments in the overturning of Roe v Wade and hear Laura's thoughts on these issues, follow her on Twitter and LinkedIn. You can also follow her podcast, The Beagle has Landed, on Twitter and Facebook.Stay tuned for the next new episode of DNA Today on July 8th, 2022 where we'll be welcoming Atticus Shaffer, who played Brick Heck on the ABC sitcom The Middle, to discuss his experience with Osteogenesis Imperfecta ! New episodes are released on Fridays. In the meantime, you can binge over 190 other episodes on Apple Podcasts, Spotify, streaming on the website, or any other podcast player by searching, “DNA Today”. Episodes since 2021 are also recorded with video which you can watch on our YouTube channel. DNA Today is hosted and produced by Kira Dineen. Our social media lead is Corinne Merlino. Our video lead is Amanda Andreoli. See what else we are up to on Twitter, Instagram, Facebook, YouTube and our website, DNApodcast.com. Questions/inquiries can be sent to info@DNApodcast.com. PerkinElmer Genomics is a global leader in genetic testing focusing on rare diseases, inherited disorders, newborn screening, and hereditary cancer. Testing services support the full continuum of care from preconception and prenatal to neonatal, pediatric, and adult. Testing options include sequencing for targeted genes, multiple genes, the whole exome or genome, and copy number variations. Using a simple saliva or blood sample, PerkinElmer Genomics answers complex genetic questions that can proactively inform patient care and end the diagnostic odyssey for families. Learn more at PerkinElmerGenomics.com. (SPONSORED)HemoShear Therapeutics is a clinical stage company developing new treatments for patients with rare metabolic disorders. By partnering with fellow biopharma companies, HemoShear is accelerating their drug discovery and development programs in metabolic disorders, and also liver diseases and gout. HemoShear is currently conducting a clinical trial for a new therapy for propionic and methylmalonic Acidemia. Learn more about these conditions and the clinical trial in an upcoming episode of DNA Today! You can also visit hemoshear.com. (SPONSORED)In my free time during the summer I am usually with friends at our apartment's pool. My spot is right next to the water reading a book, most recently “A Crack In Creation”, which might come up in a future episode. I like keeping cool by sipping on some ice tea while I read, but I don't like all the sugar. So I've been enjoying Sound drinks instead. Sound makes unsweetened, organic sparkling waters made with tea and botanicals. No natural flavors or sugar. My fav is the blueberry with cinnamon and hibiscus tea. Try it out by ordering at DrinkSound.com using promo code DNATODAY for 20% off! Plus you are supporting the podcast. (SPONSORED)A bunch of my friends at my apartment have dogs and I love being able to offer them a treat when I take them for a walk or when they visit my place. So I got Sundays for Dogs. Now this is dog food, but can also be used as dog treats. My friend Annie's dog, Frank, gets so excited when he sees me, and if I'm being honest, I think it's more the food than me. Sundays For Dogs is real food formulated by a Vet with high quality meat, veggies, fruit and superfoods, then air-dried to perfection. Since you are a DNA Today listener, you can visit SundaysForDogs.com and use code “DNATODAY” for 35% off your first order. Support your pup and the podcast! (SPONSORED)
Want to learn how you can contribute to school inclusion? In this segment, Katherine Klimitas discusses living with a disability and her focus for school inclusion. She talks about growing up and being the only one in her entire school in a wheelchair, adulthood, and now the work she is doing by embracing her creativity and helping others who have a disability. See video here - https://youtu.be/bWy1AK4V8-I WHO IS KATHERINE? Katherine Klimitas is a New Orleans-based artist and designer who sold her first watercolor at age 10. As the daughter of veterinarians, Katherine expresses her family's life-long love of animals through her meticulous life-like paintings. She earned a B.A. from Loyola University in 2011, and today at age 33, runs her multifaceted business KAK ART & Designs from home. When clients learn that Katherine has Osteogenesis Imperfecta, also known as brittle bone disease, they are captivated by her unique perspective. She and her parents stopped counting her broken bones at 500 at age 10. She's 2 feet 7 inches tall, gets around in an electric wheelchair, and creates all of her art, jewelry and commercial graphic design while lying on her side. KATHERINE'S CALL TO ACTION Everyone has something to contribute to society. Find your "something," get out and DO IT! Stop making assumptions when you see someone in a wheelchair. https://kakartnola.com/ Facebook.com/kakartnola instagram.com/kakartnola GENESIS'S INFO https://genesisamariskemp.net/ CALL TO ACTION Subscribe to GEMS with Genesis Amaris Kemp Channel, Hit the notifications bell so you don't miss any content, and share with family/friends. **REMEMBER - You do not have to let limitations or barriers keep you from achieving your success. Mind over Matter...It's time to shift and unleash your greatest potential. If you would like to be a SPONSOR or have any of your merchandise mentioned, please reach out via email at GEMSwithGenesisAmarisKemp@gmail.com --- Send in a voice message: https://anchor.fm/genesis-amaris-kemp/message Support this podcast: https://anchor.fm/genesis-amaris-kemp/support
Katherine Klimitas is an artist, motivational speaker, author, and graphic designer. She is living with Osteogenesis Imperfecta, better known as Brittle Bone Disease. Katherine gets around in an electric wheelchair and she is 2 feet, 7 inches tall. By age 10, my guest had broken over 500 bones because of the disease. However, she and her parents refused to let Osteogenesis Imperfecta disease dictates her happiness and upward mobility. During her senior years at Loyola University, she started KAK Art & Designs. She is now expanding her reach and capabilities as a watercolor artist and motivating others to contribute to their communities. “Some believe in destiny and some believe in fate, but I believe that happiness is something we create.” (Katherine Klimitas quoted this from her favorite hit by Sugarland) Guest's Links: https://www.instagram.com/kakartnola/ https://kakartnola.com/ Now, subscribe to our YouTube channel ( https://youtube.com/channel/UCoc-QGLBLQxIYRa7N-OaRqA). Also, rate, comment, and share this and other episodes with others. #brittlebonedisease #disability #inspiration Please subscribe and share. Also, please donate to this podcast to keep it going. Click the link to donate: https://www.paypal.com/donate?hosted_button_id=KT5DSZEECRSL8 The Canyouth's Exploration social media Links: Facebook page: https://www.facebook.com/CanXplore/ Instagram: https://www.instagram.com/canyouthsexploration/ Twitter: https://twitter.com/CanyouthsN Find and purchase books by Dr. Canute White through this link: https://www.amazon.com/s?k=Canute+white&crid=R4C1V5L88L5O&sprefix=canute+white%2Caps%2C147&ref=nb_sb_noss --- Send in a voice message: https://anchor.fm/radio-white/message
All Home Care Matters was honored to welcome a remarkable guest, Katherine Klimitas. Katherine is an artist, public speaker, author, designer, and an inspiration. Katherine is a New Orleans-based artist and designer who sold her first watercolor at age 10. As the daughter of veterinarians, Katherine expresses her family's life-long love of animals through her meticulous life-like paintings. She earned a B.A. from Loyola University in 2011, and today at age 33, runs her multifaceted business KAK ART & Designs from home. When clients learn that Katherine has Osteogenesis Imperfecta, also known as brittle bone disease, they are captivated by her unique perspective. She and her parents stopped counting her broken bones at 500 at age 10. She's 2 feet 7 inches tall, gets around in an electric wheelchair, and creates all of her art, jewelry and commercial graphic design while lying on her side.
Watch Here: https://youtu.be/wYfZsSB0rZE CAN YOU IMAGINE BREAKING OVER 500 BONES BY THE AGE OF 10? On this episode we are joined by Katherine Klimitas. Katherine has Osteogenesis Imperfecta, better known as Brittle Bone Disease, resulting in her frequently breaking bones (over 500 by the age of ten) and shares her experiences both growing up and being an entrepreneur. On this episode we discuss: Katherine discovering her talent for art at a young age Leveraging your talent to make a living Inclusion in the classroom For places to listen, places to connect on social media, to be a guest, collaborate with or sponsor DTE visit: https://linktr.ee/DisruptTheEveryday Katherine's website: https://kakartnola.com/ About Katherine in her words “Some believe in destiny and some believe in fate, but I believe that happiness is something we create.” If you're a Sugarland fan, too, then you recognize this lyric. It's my favorite from their hit song, Something More. It's completely true. We're presented opportunities for happiness in life and work. But unless we make the effort to pursue those opportunities, we'll never know what it means to be happy. I'm Katherine Klimitas, artist, speaker, author and graphic designer. I have Osteogenesis Imperfecta, better known as Brittle Bone Disease. I get around in an electric wheelchair. I'm 2 feet, 7 inches tall. And by age 10, I had broken 500+ bones. But there was no way my parents and I were going to let my disease dictate my happiness. They made me want to make something of myself, and I was going to be happy doing it—end of story. During my senior year at Loyola University, I started KAK Art & Designs. While my services have changed since 2011, I've stayed focused on 2 key areas: 1) expanding my reach and capabilities as a watercolor artist; and 2) motivating others to contribute to their communities. After owning my business for nearly a decade, what keeps me striving for something more? I want my work to bring people joy. I paint, speak, write, donate my paintings to animal causes and take on music industry creative projects.
Establishing a creative outlet can open the door to infinite possibilities. For Katherine Klimitas she says: we're presented opportunities for happiness in life and work. But unless we make the effort to pursue those opportunities, we'll never know what it means to be happy. She's an artist, speaker, author, and graphic designer. She has Osteogenesis Imperfecta, better known as Brittle Bone Disease. She gets around in an electric wheelchair.” I'm 2 feet, 7 inches tall. And by age 10, I had broken 500+ bones. But there was no way my parents and I were going to let my disease dictate my happiness. They made me want to make something of myself, and I was going to be happy doing it—end of story. During my senior year at Loyola University, I started KAK Art & Designs. While my services have changed since 2011, I've stayed focused on 2 key areas: 1) expanding my reach and capabilities as a watercolor artist; and 2) motivating others to contribute to their communities. After owning my business for nearly a decade, what keeps me striving for something more? I want my work to bring people joy. I paint, speak, write, donate my paintings to animal causes and take on music industry creative projects.” She joined me this week to tell me more. For more information: https://kakartnola.com/ LinkedIn: @KatherineKlimitas Follow: @kakartnola
© 2020-2025 Ivy Podcast Discovery LLC
