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Transitions Daily Alcoholics Anonymous Recovery Readings Podcast
The daily distribution consists of different recovery quotes daily from various resources, including; Twenty-Four Hours a Day, A.A. Thought for the Day, Daily Reflections, Big Book Quote, Just for Today, As Bill Sees It, plus more! This podcast is a short daily audio provided by the online recovery group Transitions Daily. Transitions Daily also distributes this same content in a daily email with a secret Facebook group for discussion. Go to www.DailyAAEmails.com for more information. Do you want to stop drinking? Have you ever listened to sobriety podcasts? Does alcoholism or addiction run in your family? Have you tried Alcoholics Anonymous or the 12 Steps of A.A.? Are you considering how to get sober? Are you seriously thinking about sobriety for the first time? Is alcohol controlling your life as never before? If so, you will definitely want to check out this recovery podcast.
ADHD is NOT well understood by most doctors. I know, shocking, right? We often expect our doctors to be the "know all, be all, end all" of medical information, and as much as they want to help us... they just don't get the in-depth training necessary on every single area... And ADHD is one of them. This Q&A session covers my top recommendations when it comes to prepping for an ADHD Diagnosis appointment. Don't get me wrong, I truly believe most doctors want to help us and their hearts are in the right place. I also believe it's important to be our own advocates by making sure we understand our diagnosis and we're prepared to ask the right questions. The question, "How should I prepare for my ADHD Diagnosis appointment?" comes up a lot so I thought it was time I shared my two cents on the subject. Don't worry, Successful Mama. The info in this episode will help you feel confident talking with your doctor about your options and what the right path FOR you will be on your ADHD journey. What other tips would you give someone who's about to talk to their doctor about getting an ADHD diagnosis? Drop your thoughts in the comments. P.s. Real quick - I wanted to mention the totally free Motherhood in ADHD Facebook community. If you're looking for other moms who "get it"...I invite you to join us. Always accepting new members. :-) Click here for transcription.
Bulletproof Hygiene Podcast Episode 44 Hosts: Charissa Wood, RDH & Brittany Simon, CRDH, BASDH Key Takeaways:Introduction Sympathy Vs. Empathy 10 Reasons Why Empathy Is Important Walk Through It As A Practitioner What Empathy Looks Like What Empathy Is Not References: Summit 2022 Mighty Networks: Bulletproof Hygiene Bulletproof Hygiene: The Guide For Finding Fulfillment Through Purposeful, Profitable Hygiene Tweetables:Difficult emotions are not problems to be fixed, they are experiences to be validated. Charissa Wood We cannot ask someone to process the diagnosis faster than they do. Brittany Simon Focus on active listening. Charissa Wood We are all empaths on some level. Charissa Wood Shame is disempowering. Brittany Simon Just because silence is awkward, doesn't mean it's bad. Charissa Wood When you prioritize problems over people, you make people feel like problems. Charissa Wood When people are struggling they want connection, not information. Charissa Wood
Join Todd C. Villines, MD, MSCCT as he takes a deep dive into the newly released 2021 AHA/ACC/ASE/CHEST/SAEM/SCCT/SCMR Guideline for the Evaluation and Diagnosis of Chest Pain: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. Our special guests are Ron Blankstein, MD, MSCCT; Michelle Williams, MBChB, PhD, FSCCT; Stephan Achenbach, MD, MSCCT and Pamela Douglas, MD .This episode will explore:2021 AHA/ACC/ASE/CHEST/SAEM/SCCT/SCMR Guideline for the Evaluation and Diagnosis of Chest Pain: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice GuidelinesSupport the show (https://scct.org/donations/donate.asp?id=18823)
This week the Our MBC Life podcast hosts a panel to discuss what it's really like to be diagnosed stage 4 from the beginning of de novo MBC. Those of us diagnosed de novo don't get an introduction to breast cancer at earlier stages and that presents some unique issues. OMBCL Podcast team member, Miranda Gonzales, moderates our panel of Shonte Drakeford, Deltra James, Lisa Laudico, and Anne Woodward. Miranda brings her passion for bridging the gap between individuals who have had an early-stage breast cancer diagnosis and those of us who are living with MBC. Join us for a wide-ranging discussion on the challenges we face and how we have navigated those challenges with our family and friends. More info is available on our website www.ourmbclife.org Be sure to rate, review us, and sign up for our newsblast. Got something to share? Feedback? Email:Ourmbclife@sharecxancersupport.org Send us a voice recording via email or through speakpipe on our website. Follow on Facebook, Instagram, and Twitter @ourmbclife
What's good about...CANCER? Crystal Carson is going to tell us what - and how - she found her good. She's a wife, a mother, a daughter, a sister - she's also an actor and an acting coach - and she's living with stage 3 breast cancer. She's lived the dark part, now she's ready to share the light, the good she's discovered within others, and most importantly, within herself. Nine out of ten people will deal directly with cancer in their lifetime and that makes finding the positives all the more important.
When a life science worker has a life science problem, where do they turn? Mix Talent's KC McAllister talks with Jessica Krauser. Jessica is a Marketing Advisor for Two Labs, a pharmaceutical services company in Columbus, OH who faced a difficult diagnosis of Early Onset Parkinson's, and chose to make a difference regardless. Hear her inspiring story in this week's episode! For more details on the causes and organizations mentioned in today's episode, check out these websites: The 5K For JK Michael J. Fox Foundation pDNextSteps T&J No Limit Fitness
When the television presenter Melanie Sykes and the model Christine McGuinness revealed they had been diagnosed with autism as adults, it brought new attention to the challenges for others like them whose symptoms have been missed. This is the story of one autistic woman - and how diagnosis in her thirties changed her life. Help support our independent journalism at theguardian.com/infocus
This is #JustATouchof_J and I got somethin else to say. Ep.5
Commentary by Dr. Valentin Fuster
Commentary by Dr. Valentin Fuster
Alan Lightman is an American writer, physicist and social entrepreneur. He served on the faculties of Harvard and MIT, and was the first person at MIT to receive dual faculty appointments in science and in the humanities. Currently, he serves as professor for the practice of the humanities at MIT. In his scientific research, he has made fundamental contributions to the astrophysics of black holes and cosmic radiative processes. He is the author of numerous books, both fiction and nonfiction, including Einstein's dreams, an international bestseller, The Diagnosis, a finalist for the National Book Award in Fiction, and his latest book, Probable Impossibilities: Musings on Beginnings and Endings, where he discusses questions of nothingness and infinity, the mind, and the specialness of life. Alan's essays and articles have appeared in the Atlantic, Granta, Harper's, Nautilus, The New Yorker, The New York Review of Books, Salon, and many other publications. EPISODE SUMMARY In this conversation we talk about: Growing up in Memphis, Tennessee, and living between physics and the humanities What it was like to study physics at Princeton and Caltech Working with Richard Feynman Writing Einstein's Dreams The connection between physics and spirituality The topics of entropy and life The rarity of life On nothingness and infinity On the value of wasting time, and many other topics. This conversation with Alan Lightman is one of a dozen or more upcoming conversations with bestselling authors, thinkers, designers, scientists, and makers who are reimagining our world and experience. So please follow us on your favorite podcasting app, if you haven't already, so that you can make sure you don't miss them. And now, let's jump right in with Alan Lightman. TIMESTAMP CHAPTERS [3:12] Life During Covid [6:40] Early Influences [12:42] On Writing and the Origin of Einstein's Dreams [17:53] A Convergence Between Physics and Spirituality [19:42] The Origin of the Universe [24:40] The Rarity of Life [29:06] A Distinction Between Life and Death [33:26] Nothingness and Infinity [36:39] Finding Meaning in a Multiverse [39:34] The Benefit of Wasting Time [42:33] A Sermon on Disconnection EPISODE LINKS Alan's Links
How am I going to teach my kid to be good at stuff that even I'm not good at? Today's episode is an ADHD Q&A session focused on helping you find ways to teach your child the important life skills they need to be responsible adults. Okay, so maybe you aren't great at being on time or keeping up with laundry or remembering someone's name...but there are lots of things that you ARE GOOD at. Let's focus on the good stuff, shall we? Listen and learn how you can use what you ARE good at to create a path that helps your kiddo learn those life skills and reminds you that you ARE a Successful Mama. One quick tip - keep things simple and positive. I hope this episode helps you realize teaching responsibility to your child doesn't have to feel overwhelming or scary. You got this! Oh, and since you're here I want to remind you I have some free resources to help you, parent, as a mom with ADHD. There are LOTS of goodies for you so head over to the resource page on my website and grab them up. patriciasung.com/resources Click here for transcription.
How would react if you were given a diagnosis you weren't expecting? What if it was for your unborn child? Today Jen O'Hara shares her experience with her son Will receiving a neurodivergent diagnosis of Down Syndrome. Later in the episode Dean and I share how we aim to create an environmnet where our children don't fear others, and lead with acceptance.. Stick around for my 3 favourite things for the week! Thank you for being here! Explore my shop: http://www.hellofriendo.com Thank you Jen for your contribution to Friendo. Follow along on social: Instagram @hellofriendoshop Instagram @amandamuse Twitter @museamanda Facebook /museamanda YouTube AmandaMuse Advertising Inquiries: https://curiouscast.ca/advertise-with-us/ See omnystudio.com/listener for privacy information.
Let's take a closer look at 18 papers published in September 2021 that rely on positron emission tomography (or PET) to detect amyloid and tau pathology in the brain, within the context of Alzheimer's disease! If you're interested in learning about tau and amyloid based detection, alternative PET tracers in AD research, or combining PET with different imaging modalities, make sure to tune into this episode. Sections in this episode: Amyloid-based detection (2.35) Tau-based detection (9.35) Amyloid & Tau (21.30) Other targets (24.25) -------------------------------------------------------------- You can find the numbered bibliography for this episode by clicking here, or the link below:https://drive.google.com/file/d/19bbDKI8EJifGuwe-bVPkInWCuSEFc2-Y/view?usp=sharingTo access the folder with all the bibliographies for 2021 so far, follow this link (it will be updated as we publish episodes and process bibliographies), or click the following link below:https://drive.google.com/drive/folders/1N1zx_itPkCDNYE1yFGZzQxDDR-NiRx3p?usp=sharingYou can also join our mailing list to receive a newsletter by filling this form. Or tweet at us: @AMiNDR_podcast --------------------------------------------------------------Follow-up on social media for more updates!Facebook: AMiNDR Twitter: @AMiNDR_podcastInstagram: @AMiNDR.podcastYoutube: AMiNDR PodcastLinkedIn: AMiNDR PodcastEmail: amindrpodcast@gmail.com -------------------------------------------------------------- Please help us by spreading the word about AMiNDR to your friends, colleagues, and networks! Another way you can help us reach more listeners who would benefit from the show is by leaving us a review on Apple Podcasts or wherever you listen to podcasts. It helps us a lot and we thank you in advance for leaving a review! Our team of volunteers works tirelessly each month to bring you every episode of AMiNDR. This episode was scripted, hosted, and edited by Alexandra Pavel, and reviewed by Naila Kuhlmann and Anusha Kamesh. The bibliography was made by Anjana Rajendran and the wordcloud by Sarah Louadi (www.wordart.com). Big thanks to the sorting team for taking on the enormous task of sorting all of the Alzheimer's Disease papers into episodes each month. For September 2021, the sorters were Jacques Ferreira, Ellen Koch, Christy Yu, Sarah Louadi, Kate Van Pelt, Nicole Corso, Eden Dubchak, Kira Tosefsky, Dana Clausen, and Elyn Rowe.Also, props to our management team, which includes Sarah Louadi, Ellen Koch, Naila Kuhlmann, Elyn Rowe, Anusha Kamesh, Jacques Ferreira, and Shruti Kocchar for keeping everything running smoothly.Our music is from "Journey of a Neurotransmitter" by musician and fellow neuroscientist Anusha Kamesh; you can find the original piece and her other music on soundcloud under Anusha Kamesh or on her YouTube channel, AKMusic. https://www.youtube.com/channel/UCMH7chrAdtCUZuGia16FR4w -------------------------------------------------------------- If you are interested in joining the team, send us your CV by email. We are specifically looking for help with sorting abstracts by topic, abstract summaries and hosting, audio editing, creating bibliographies, and outreach/marketing. However, if you are interested in helping in other ways, don't hesitate to apply anyways. --------------------------------------------------------------*About AMiNDR: * Learn more about this project and the team behind it by listening to our first episode: "Welcome to AMiNDR!"
There are few cancers more challenging than glioblastomas. While there is currently no cure for these brain tumors, patients and their caregivers can take steps to maximize their quality of life once they learn their diagnosis. Dr. Akanksha Sharma and TV meteorologist and author Maria Quiban Whitesell both know a lot about doing just that. Dr. Sharma is a neuro-oncologist at PNI, where she treats patients with brain cancer. She says that what makes glioblastomas so difficult is that they spread throughout glial cells in the brain like flakes of pepper in a pile of salt. Glial cells support and protect neurons in the brain, and surgery can only remove so many of the malignant ones. As a palliative medicine specialist, her aim is to open and hold space for patients to have meaningful conversations and honest dialog with their nearest and dearest, for them to savor and create new cherished memories, and to make the most of their time. Maria lost her husband to glioblastoma and wrote a book about her loss called You Can't Do It Alone: A Widow's Journey Through Loss, Grief and Life After. This conversation shows how caregivers can muster the strength to do some of the hardest work there is and keep going—for their patients and their families—in the face of one of life's most difficult challenges. For more information please visit https://www.pacificneuroscienceinstitute.org/people/sharma/
Lauren shares her stories of birth and loss. Today's episode is sponsored by Motif Medical. See how you can get Motif's Luna breast pump covered through insurance at motifmedical.com/birthhour. Know Your Options Online Childbirth Course: https://courses.thebirthhour.com/limited-time Beyond the Latch Course: https://courses.thebirthhour.com/enroll-b2w/ Support The Birth Hour via Patreon!: https://patreon.com/birthhour
We conclude our discussion of Jay Galbraith's portfolio of books and articles focusing on organizational design with a look at contemporary challenges facing managers. We raise common misconceptions about design, including those also found in Galbraith's own work. In the process of revisiting the meaning of design, we consider how managers can leverage it to make their organizations better.
This week we are joined by Natalie Bates, an amazing woman who was diagnosed with Turner's Syndrome at birth. The ladies talk about how Turner's, a rare chromosomal disorder has impacted Natalie's childhood and relationships. She shares how bottling in her story led to depression and isolation and how drastically her life has changed since opening up about her diagnosis. You can expect to hear: - Why diagnosis for Turner's Syndrome during the developmental years is imperative for proper treatment - How Natalie is navigating life without medical insurance - Physical indicators that your child might have Turner's Syndrome - Natalie's milestones: getting married this month & graduating from college Connect with us: @officalboxowner @fullcourtpumps officialboxowner.com Connect with our guest: @NEB198807 =========== Official Box Owner: We are so honored to not only partner with other brands but also support your needs by offering our own OBO products. Visit us at www.officalboxowner.com to buy, Balanced Box Boric Acid suppositories, Yummy box apple cider vinegar gummies, & our custom OBO pouch to carry your feminine products with style!
Neuro Pathways: A Cleveland Clinic Podcast for Medical Professionals
Aaron Abrams, MD discusses the efforts that have led to, and continue to evolve, the understanding that earlier, higher efficacy treatments improve outcomes for patients with pediatric-onset demyelinating diseases.
11/15/2021 | CT of Splenic Anomalies from Splenosis to Polysplenia: Potential Pitfalls in Diagnosis - Part 2
Curiosity led a biostatistician down an unusual path. Intrigued by the concept that the SARS-COV-2 virus has not been isolated ever, our guest began inquiring of health departments around the world: Do you have evidence of an isolated virus? To date, over 100 institutions from all over the globe have responded...and there has been no evidence in sight of SARS-COV-2. Christine Massey, a former biostatistician for cancer researchers, today discusses her research on the concept of viruses (and this “virus” in particular) and what she's learned through hundreds of FOIA requests (freedom of information act) from health departments all over the world. She goes over how the cultures or samples used to "isolate the virus" are actually interfering with the process. She exposes the flaws in this methodology and the problem with PCR testing. She also explains why talk of “variants” is essentially nonsense. Visit Christine's website: fluoridefreepeel.ca Check out our website: westonaprice.org Thank you to sponsors: Primal Pastures, Paleo Valley, BetterHelp
Shoulder popping left right and center? Hearing or feeling weird noises from your shoulder? Let's combat your assumptions about what is happening in the shoulder in this episode! DocJen & Dr. Dom explain the medical diagnosis - shoulder crepitus- for noises in the shoulder. Explaining the anatomy of the shoulder, they break down the types of noises that could be associated with pathologies around the shoulder. Furthermore, Docjen & Dr. Dom dive into how rounded shoulders could be related to different noises occurring in the shoulder, and the importance of getting it checked out and assessed by a physical therapist in person. Then, they describe their best tips to improving shoulder function, speaking into mobility and strength, and what to consider if there is no pain associated with the noises from your shoulder. Tune in! Manscape Performance Package 4.0. Look forward to shaving again with the new signature lawnmower, an electrical trimmer with skin-safe technology. Prevent nicks and cuts, look, feel, and smell fresh throughout the day. Another gift checked off as the holiday season approaches. Use code 'OPTIMAL' to get your Manscape Performance Package! What You Will Learn In This PT Pearl: 2:30 - What is Shoulder Crepitus? 4:30 - Anatomy around the shoulder 5:57 - Noises with pathologies 7:20 - Are the crack sand pops bad? 8:51 - Get it checked out early! 10:09 - Diagnosis associated with shoulder noises 13:20 - Could rounded shoulders be related? 16:54 - Get it checked out with a physical therapy 18:44- How to improve shoulder function 24:09- What happens if you improve mobility around the shoulder? 25:21- What to do if you are having pain with your noises To Watch the PT Pearl on YouTube, click here: https://youtube.com/watch/ For research and full show notes, visit the full website at: https://www.docjenfit.com/podcast/episode154/ Thank you so much for checking out this episode of The Optimal Body Podcast. If you haven't done so already, please take a minute to subscribe and leave a quick rating and review of the show! --- Send in a voice message: https://anchor.fm/tobpodcast/message
Dr Fred Moss is a thought leader and transformative psychiatrist who has served the mental health industry for four decades. While his initial interest in psychiatry was to expand on communication and human connections as primary healing tools, a shift in the medical paradigm in the 1980's led to physicians diagnosing patients with imbalances and prescribing medications as a primary way of dealing with life's distress. That led him to take a new approach with his patients, assisting them to reclaim their lives without psychiatric diagnoses and medication. As an advisor, speaker and educator, he is committed to humanity and to globally transforming our mental health conversations. He is also the host of the 'Welcome To Humanity' podcast, which explores what it means to be human and how to live an extraordinary life.
Toyota and Tesla chiefs downplay the speed of EV acceptance. Bill applies proper diagnostic techniques to vehicle with mystery issues. Popular, common vehicles prevent headaches on road trips. We love to hear from you! CarsThePodcast@gmail.com
In this episode, climate change as a medial diagnosis. South African Doctor explains how an Engineered Vector (virus) and Engineered Substance (vaccine) were created to tackle this global problem.
On this episode of Cock & Bull, Cyrus is joined by Amit and Silverie to talk about bucket baths, Silverie's boarding school days, dogs on men's dating profile pics, a Canadian woman becoming the first woman to be diagnosed with 'climate change' as she is suffering from breathing problems and asthma, and more.Subscribe to our new YouTube channel: https://www.youtube.com/channel/UCmY4iMGgEa49b7-NH94p1BQAlso, subscribe to Cyrus' YouTube channel: https://youtube.com/channel/UCHAb9jLYk0TwkWsCxom4q8AYou can follow Amit on Instagram & Twitter @DoshiAmit: https://twitter.com/doshiamit and https://instagram.com/doshiamitYou can follow Antariksh on Instagram @antariksht: https://instagram.com/antarikshtDo send in AMA questions for Cyrus by tweeting them to @cyrussaysin or e-mailing them at whatcyrussays@gmail.comDon't forget to follow Cyrus Broacha on Instagram @BoredBroacha (https://www.instagram.com/boredbroacha)In case you're late to the party and want to catch up on previous episodes of Cyrus Says you can do so at: www.ivmpodcasts.com/cyrussaysYou can listen to this show and other awesome shows on the new and improved IVM Podcasts App on Android: https://ivm.today/android or iOS: https://ivm.today/ios
On this episode of the “Cancer Horizons” podcast, a young mother living with lung cancer shares the story of her cancer diagnosis and describes the once-in-a-lifetime coincidence of learning her neighbor has the same cancer type and mutation.
ONCE UPON A GENE - EPISODE 108 Finding Hope: From Diagnosis to Action - LMNA Related Congenital Muscular Dystrophy - Hannah Lowe Hannah Lowe is the President and Co-Founder of the L-CMD Research Foundation. Her son Austin has a rare form of muscular dystrophy (L-CMD) caused by a genetic mutation and she's urgently working to find a cure for her son and other kids like him. EPISODE HIGHLIGHTS Can you tell us about your children? I have two sons— Ean who is four and Austin who is two. Last year, Austin was diagnosed with a rare disease resulting from a randomly occurring genetic mutation. He was about 6 months old when he was diagnosed. Austin wasn't gaining weight, so after 6 months he was admitted to the hospital to get a feeding tube to aid in nutrition. He was in the hospital for three weeks while they ran a series of tests to find the underlying cause of his low weight. Every test came back clear until the genetic tests came back. That's when it was discovered that Austin has a single point mutation on the LMNA gene which results in L-CMD, which is a rare form of muscular dystrophy. What did you do after you got Austin's diagnosis? After getting a new routine worked out, we turned our attention to figuring out what we can do. We started making connections, talking to everyone and gathering information. L-CMD has a fair amount of research happening for the gene itself because genetic mutations of the gene cause about 12 other diseases. Through networking, we connected with a group of other rare disease families working on treatments and cures for their own rare diseases. With some helpful connections, we took baby steps to start a nonprofit. What roadblocks have you hit and what would you do differently? The biggest roadblock is expectation versus reality. When we first started, researchers told us the pace of research is slower than the progression of the disease. We didn't accept that, but it has been a big mindset shift to know this is in fact the case. CONNECT WITH THE L-CMD RESEARCH FOUNDATION L-CMD Research Foundation Website https://www.lcmdresearch.org/ L-CMD Research Foundation on Instagram https://www.instagram.com/lcmd.foundation/ L-CMD Research Foundation on Facebook https://www.facebook.com/LCMD.foundation L-CMD Research Foundation on Twitter https://twitter.com/foundationlcmd RESOURCES AND LINKS MENTIONED Discord Chat https://discord.com/invite/7UFUPAFs8K ONCE UPON A GENE - Episode 104 - A Rare Collection- Stories of Courage with Felix Townsin, Erica Jolene Stearns, Mahrynn McLaughlin and Brianna Colquitt https://effieparks.com/podcast/episode-104-rare-collection-courage Givebutter https://givebutter.com/ 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/
Alzheimer's Disease International's World Alzheimer's Report 2021 recently found that 75% of people with dementia are undiagnosed, equating to 41 million people across the globe. The report, subtitled “Journey through the diagnosis of dementia,” also found clinician stigma is still a major barrier to diagnosis, and one in three believe nothing can be done about dementia. Dr. Serge Gauthier, co-author of the report, joins the podcast to discuss these findings, recommendations for improving dementia diagnoses, and more from the report. Episode Topics 2:00 - How did you get into this field, and why did you choose to study dementia? 3:04 - What was the methodology behind this research? What was that process like to collect this data? 5:47 - What are some of the key findings that you took away from the report? 7:59 - What did you discover about stigma while conducting this report? Why is that important to this discussion about diagnosis and subsequent care? 9:47 - How can people encourage their healthcare systems to have better diagnoses practices in place? 12:04 - What role do PET scans and blood-based biomarkers play in this effort for more diagnoses? Should everyone get these tests done? 13:56 - How do you think new therapies like Aducanumab are going to change how we view diagnosis? 16:33 - What are some of the key recommendations for government agencies from the report? 18:33 - Most agencies in the United States do not recommend screening for cognitive impairment without symptoms. Is that a mistake, and if so, how do we change those policies? 19:31 - What role do specialists, memory centers, and community agencies play in improving diagnosis? Should we have a primary care focus or should we train more specialists and organizations to help with diagnosis? 21:59 - Do you think there needs to be a change in how we use terms like dementia and major neurocognitive disorder? Should we adopt a universal terminology surrounding cognitive impairment, and do you think dementia should be retired due to the stigma it carries? 22:57 - What are some of the easiest things we can do to help our system diagnose people with dementia? 24:42 - What gives you hope that things will get better in the diagnosis and care of people with dementia? Show Notes The World Alzheimer Report 2021 includes over 50 essays from leading experts from around the world and is supported by findings from 3 key global surveys, which received responses from 1,111 clinicians, 2,325 people with dementia and carers, and over 100 national Alzheimer and dementia associations. Find more information about the 2021 World Alzheimer's Report from Alzheimer's Disease International on their website. A PDF of the report, “Journey through the diagnosis of dementia,” is also available on their website to read. To learn more about Dr. Serge Gauthier, read his bio on the McGill University website.
Showing our kids success with ADHD is 100% obtainable for them is NOT impossible. Today is Part 2 of a conversation I was lucky enough to have with my friend Katelyn Mabry. (If you missed us last week go check out Episode 117 and hurry back!) Katelyn's a special education teacher and author who grew up having an ADHD diagnosis and that led her to want to help others like her through teaching. During this episode, Katelyn gets deeper into her professional opinions about: - How to explain to your child that they have ADHD - What to do to teach them new responsibilities and skills - How to help our ADHD children move forward when they are feeling stuck - And what we can do to connect with our kids on a deeper level to form solid safe foundations. If you're feeling a little overwhelmed by a potential ADHD diagnosis for your kiddo or if you're already there and still working out how to talk with your child about their ADHD THIS is the episode for you, Successful Mama! Check out Katlyn's book, “Hi, It's Me! I have ADHD!” and her podcast for kids titled “Journey With Me Through ADHD." Special thanks to Katelyn for hanging out with me and sharing her empathy-inducing knowledge with us! Learn more about Katelyn on her website here and check out her book “Hi, It's Me! I Have ADHD” on Amazon. You can listen to her podcast, Journey With Me Through ADHD: A Podcast for Kids and follow her on Facebook and Instagram. REMINDER: There's a place where you can get your calendar and to-do list organized one step at a time, so you enjoy more time with your kids while feeling confident + capable in your day... even when your ADHD hijacks your plan. Sign-ups for Daily Planning for ADHD Moms are open! Click here to sign up --> bit.ly/adhdplan Listen to full episodes at www.motherhoodwithadhd.com or find us on your favorite podcast listening app. Click here for transcription.
Hi friends! I hope you're having a lovely week so far! I'm excited to share a new podcast episode up with you with Renea Jones-Hudson. I LOVED talking with her and getting to learn more about her — I hope you'll take a listen to this one! Here's what we talk about: - How she became involved with fitness and opened her own gym - Her experience with Ulcerative Colitis and how it lead to her plant-based lifestyle - Her go-to plant-based meals - Her tip for staying Healthy in Real Life and so much more. A little bit more about Renea: I was born and raised in Kingston, Jamaica. Migrated here at the age of 14, four years later I joined the military, and retired as a Captain after 21.5 years. I am married to my husband of 24 years, he is also a retired Army veteran (22 years) and we have two amazing children. When I decided to retire, it was an absolute spur of the moment decision. I had no plans. I did not have a next step but I was ready for a change. I spent my whole life in the military and I just wanted to do more with myself. With no plan, I decided to do what I was always good at: FITNESS. I opened IslandJam Fitness in October 2016 in my garage, moved to my own studio after 9 months, and now I am completely online. As a wife and mother, and after moving around so much in the military, time freedom and stability was and still is a priority. As an entrepreneur, I am able to have the flexibility I desire to be available for my family. You can connect with Renea on Instagram or on her website. Birthday promo starts now!! Get all of the details here. I'm so excited to share these fitness programs with you at a 50% discount :) Get 15% off Organifi with the code FITNESSISTA. I drink the green juice and red juice daily, and also love adding the gold powder at night for relaxation and sleep. I love love love the meals from Sakara Life. Use this link and the code XOGINAH for 20% off their meal delivery and clean boutique items. The goji rose donut is my very fave! Thank you so much for listening and for all of your support with the podcast! Please leave a rating or review if you enjoyed this episode. If you leave a rating, head to this page and you'll get a little “thank you” gift from me to you.
On this episode of The Power of Love Show we welcome author, podcast host, SurvivorTHRIVER, S.O.A.R. Strategist & life coach: Tiffany R. Easley! Learn More: Website: www.TiffanyREasley.com Instagram: @TiffanyREasley Twitter: @TiffanyREasley YouTube: Tiffany R. Easley Facebook: Tiffany R. Easley Enterprises Podcast: ‘SOARING After A Diagnosis With Tiffany' S.O.A.R.: See it, Own it, Attain it, Regift it! WIN: Work hard, Inspire others, Never give up! Subscribe to our YouTube channel: https://www.youtube.com/watch?v=2-Nd1HTnbaI Like Our Facebook Page: https://www.facebook.com/884355188308946/ Have you subscribed to our Podcast? Apple Podcasts: https://podcasts.apple.com/fr/podcast/the-power-of-love-show/id1282931846 Spotify Podcasts : https://open.spotify.com/show/6X6zGAPmdReRrlLO0NW4n6?si=bhNl9GjJRxKXUvTdwZme6Q Google Podcasts: https://podcasts.google.com/feed/aHR0cHM6Ly9wb3dlcm9mbG92ZS5saWJzeW4uY29tL3Jzcw Other podcasts: https://anchor.fm/thepowerofloveshow Did you know you can support DDJF through any of your Amazon purchases? Simply click link below and select Dee Dee Jackson Foundation as your charity of choice: https://smile.amazon.com/gp/chpf/dashboard/ref=smi_nav_surl_mi_x_mkt Once done… bookmark and use your smile link to support DDJF! The Power of Love Show is a weekly show sponsored by The Dee Dee Jackson Foundation where we shine a light on loss and grief and how it impacts our lives. Our aim is to build a community where we share inspiring stories, interview experts, learn, grow and empower one another to find proper and healthy healing. Visit the DDJF official website: http://www.ddjf.org/ Donate to DDJF (501c3): https://app.mobilecause.com/form/xDJ0Cg?vid=74qmm Check Out DDJF Merch: https://teespring.com/.../collection/All%20Products... Join the Dee Dee Jackson Facebook Group https://www.facebook.com/groups/1500933326745571 Follow us on Instagram: @DeeDeeJacksonFoundation • https://instagram.com/deedeejacksonfoundation?utm_medium=copy_link --- Support this podcast: https://anchor.fm/thepowerofloveshow/support
Should I get an official diagnosis for Dyslexia? In this episode I am not going to talk about where to get one, what type to get and how it works. I am going to dig into the deeper question of should I just self diagnose dyslexia or should I get an actual test done. This question is asked by so many people and I wanted to weigh in. Want to be on the pod and share your story? >> https://www.videoask.com/fzg9j7p5j Get On The Waiting List For Our Next Course >> https://tcd.truthaboutdyslexia.com/The-Confident-Dyslexic Join our Private Facebook Community Here >> https://www.facebook.com/groups/adultdyslexia Support the Pod on Patreon and get some cool videos along the way! >> https://www.patreon.com/adultdyslexia Subscribe to watch 'My Dyslexic Life' on Youtube here >> https://www.youtube.com/channel/UC6eO96kabO3y66aUeaEKbIg
In the first interview of our ADD series, Madeline Spolin aka Spo tells us how she realized she had ADD, why it took until her late 20's for someone to figure this out and what gender has to do with it. Find us at: Patreon.com/bipolarbicoastal Facebook.com/groups/bipolarbicoastalsecret On Facebook and Instagram by searching "Bipolar Bicoastal"
In this episode I talk to a person who has multiple diagnosis and is part of the LGBT community
Over the past year and a half, the NKF and ASN have been leading the effort to develop race-free eGFR test results while maintaining the accuracy of the test. The NKF-ASN Task Force on Reassessing the Inclusion of Race in Diagnosing Kidney Diseases has recently released its final report that recommends a new, race-free approach to estimate eGFR. In this collaborative episode with the ASN, the Task Force discusses how they approached the work and what efforts are being made to ensure the new equation is implemented as quickly as possible. Our guests, Dr. Cynthia Delgado, Dr. Lesley Inker, Dr. Joe Vassalotti and Tod Ibrahim discuss the goals of the Task Force and how the healthcare team came together to come up with a solution that better served kidney patients. They discuss the implications for patients, how clinicians and researchers can adopt these new guidelines, and what resources are available for both patients and the medical community to learn more. Developed in accordance with the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) and recommended by the National Kidney Foundation and American Society of Nephrology Task Force Reassessing the Inclusion of Race in Diagnosing Kidney Diseases, the new app is available for free by visiting the NKF website. If you enjoyed this episode, please follow us on Apple Podcasts, Spotify, Podbean or wherever you listen to your podcasts. Have ideas for future episodes? Email us at nkfpodcast@kidney.org or tweet us @NKF_Nephpros. Thank you for tuning in!
Cast:Dr. Tara Egan, hostJustina Hinterberger, LCMHC - guest expertToday's episode is for the moms out there. Tara welcomes her guest, Justina Hinterberger. Justina is a Board Certified (NCC) counselor that specializes in women and trauma located in Cornelius, NC . She offers treatment for complex issues such as depression, anxiety, bipolar disorders, perinatal mental health, grief and loss, infertility and personality disorders. Our topic is " What is Postpartum Depression? Diagnosis, Symptoms, and Treatment."I'd like to highlight something that I found to be particularly relatable on her website. She writes, “as women, we often take on many roles; professional, friends, sisters, daughters, mothers, grandmothers. We so often are forced by others in our lives and by society to lose ourselves in our roles, especially after becoming mothers. Justina seeks to walk alongside women as they rediscover who they are without the pressure or stigmas of who they "should" be. Not every women has to have children, not every woman has to get married, not every woman has to live a life pleasing someone else. Women are unique individual human beings with different experiences, needs, thoughts, desires and goals.”Tune in to learn:- Many mom's do not report that they are feeling post partum depression.- What is post partum depression? What are the symptoms?- How is it diagnosed?- Why do we call it PPD when it often looks like anxiety? - Can we predict who is more likely to demonstrate symptoms? (Family history, environmental factors, past history of mental illness)- How does it impact romantic relationships, connecting with the baby, self-esteem, confidence as a mother? -How can husbands/partners support a mother with PPD? Can dads get PPD?- What is the first step you should take if you think you may be experiencing PPD? What can you do if you feel like a friend or family member is experiencing it?To find out more and connect with Justina Hinterberger visit, https://www.carolinascenter.com/justina-hinterberger.Website - To learn more about Dr. Tara Egan's books, webinars, public speaking opportunities, and coaching/consultation services, Go HERE.Facebook - learn more HERE.YouTube - learn more HERE.Instagram - learn more HERE.Website - To learn more about Dr. Tara Egan's child & adolescent therapy services, visit HERE.E-Course -To learn more about Dr. Egan's online mini-course called "Managing Your Family's Technology and Social Media", created to help parents eliminate power struggles, keep your family safe from internet misuse, and reconnect with your family, go HERE.Podcast edited by Christian Fox
Drs Heather Bell and Kurt DeVine return to a discussion on things that don't play well with opioids. What are the big diagnoses that patients have that can predispose them to increased morbidity/mortality when prescribed opioids? To learn more about the doctors as well as keep up with current happenings follow us on twitter: @echocsct and Facebook: @theaddictionconnectionhk
In this episode, we discuss the diagnosis and treatment of multigestation pregnancies with Dr. Beth Kline-Fath, Chief of Fetal and Neonatal Imaging at Cincinnati Children's Hospital. To see all the images watch the video: https://youtu.be/AXHwmSAcKzc Host: Todd Ponsky
We discuss several works by Jay Galbraith on the theory and practice of organizational design, which is about creating organizations to provide better outcomes and serve the organization's purpose and strategy. This episode begins with a focus on one of Jay Galbraith's earlier publications, an article titled, “Organizational Design: An Information Processing View” for designing organizations to make better decisions in times of high uncertainty, and then brings in his more recent works promoting his five-point “Star Model,” a design tool for use by managers.
Nevertheless, She Persisted: Surviving Teen Depression and Anxiety
Find extended show notes, timestamps, transcriptions, and the episode's YouTube video https://www.shepersistedpodcast.com/podcast-episodes/ep74 (here)! Today I am joined by Dr. Kojo Sarfo a social media content creator, mental health nurse practitioner, and psychotherapist to discuss all things ADHD. Connect with Dr. Sarfo: https://beacons.page/drkojosarfo (https://beacons.page/drkojosarfo) This week's DBT skill is the PLEASE skill. Learn more https://www.mindsoother.com/blog/using-please-mastery-skills-to-maintain-emotional-control (here). Dr. Sarfo and I dive into the following topics…+ What is ADHD? How does it present and how do these presentations change depending on age and gender? + What is the diagnosis and treatment process for ADHD? + ADHD vs. ADD + Are ADHD medications addictive and Dr. Sarfo's perspective on prescribing them + Is ADHD more often a primary and secondary diagnosis and how delayed diagnosis impacts this + the importance of a balanced diet, good routine, and healthy habits on for ADHD + Dr. Sarfo's favorite ADHD resources + how to support a peer that has ADHD and supporting your child if they have ADHD + so much more! Mentioned In The Episode…+ https://www.shepersistedpodcast.com/podcast-episodes/ep75 (Ep. 75 Adolescent Substance Use feat. Dr. Jay Faber) + https://pod.link/1463051730/episode/169f8c8ef4d798b5a3a8bea9f78bb2eb (Ep. 39 Your Foolproof Guide to a Good Night's Sleep) + https://www.additudemag.com/ (https://www.additudemag.com/) + https://www.tiktok.com/@dr.kojosarfo?lang=en (https://www.tiktok.com/@dr.kojosarfo) + https://www.youtube.com/c/HowtoADHD (https://www.youtube.com/c/HowtoADHD) SHOP GUEST RECOMMENDATIONS: https://amzn.to/3A69GOC (https://amzn.to/3A69GOC) EPISODE SPONSORS
Jayne Vinson's grandson Jayden was diagnosed with colon cancer when he was 11 years old, a from of cancer that normally strikes adults in their middle age years or even later. Jayden went through an excruciating 17 hour surgical procedure which cost him his colon, spleen, gallbladder, and part of his liver and pancreas in the process. Jayden passed away of July 17th of this year. As rare as this cancer is when it comes to children, it unfortunately may not be as rare in the years to come.
11/08/2021 | CT of Splenic Anomalies from Splenosis to Polysplenia: Potential Pitfalls in Diagnosis - Part 1
Cheryl is an author, a speaker and a recovered chronic pain patient. She was told she would never be able to do the things she loved ever again at a young age. Now Cheryl is not merely surviving, but she is thriving.In this episode, we talk about the struggles Cheryl lived with and it wasn't until she took her own health into her hands that her life began to change. This isn't about not listening to your doctors, and please note that this is in no way medical advice - speak with your own practitioner about what's right for you. Cheryl listened to what felt right for her, and made changes through her own investigation and research. Often once we get into the medical system, we never get better, and we continue down a path of slow demise. After 2 years of not getting better, and even feeling worse, Cheryl's life took a turn when she took matters into her own hands - and she hasn't looked back since.We talk about Feldenkrais, about her book Forever Fit and Flexible, her podcast The FemiNinja Podcast and her coaching program. To find out more, check her out at https://www.cherylilov.com/about/.If you enjoyed this episode, please share. It means the world to us podcasters when you do this! Also, follow me! I'm on Twitter, YouTube, TikTok, Instagram, Facebook, Pinterest - Sandy K Nutrition everywhere.My contest is still running. I will be giving away a biological age DNA kit to a lucky winner, valued at $300 US in a draw. To enter, subscribe, rate, and review my podcast with a few kind words. In order to be considered, proof must be provided via email to sandy@sandyknutrition.ca. North American entries only. To review with a few kind words, you can go here: https://lovethepodcast.com/sandyknutrition.
What do I do if I think something is "wrong" with my kid? How do I know if my kid is developing okay? I hear these questions a lot. Today I'm talking about how to choose a professional and how to know what the best step is to find the support your child needs. The post Diagnosis appeared first on Simple Families.
The Joyful Mourning - A Podcast for Women Who Have Experienced Pregnancy or Infant Loss
Listen in as I spend time with Carolyn Keller as she shares with me about her daughter Bethany who had trisomy 13. This episode is full of so much wisdom -- Caroyn shares about her pregnancy journey with Bethany as well as her life in the NICU. She talks about what it was like to receive a life-limiting diagnosis and how she navigated that news with her husband and her 3 living children. And then we talk about what it was like to say goodbye and navigate life after loss. Again, we talk about marriage and parenting and what her faith looked like during that time. Carolyn gives so much wisdom in this episode as well as a ton of practical advice including her favorite resources and books for navigating a life-limiting diagnosis and life after loss and how to walk living children through both of those. Carolyn said something towards the end of our time together, something that only another grieving mom would be able to hear and understand, she said: “I look forward to the sadness because through the sadness, I can have joy remembering my daughter.” Such a beautiful and honest and accurate sentiment. Make sure to listen all the way to the end when Carolyn shares a few more words that I promise will offer you freedom and hope today in your grief journey. I am so thankful to Carolyn and her willingness to share her story and wisdom with us -- I pray it is a blessing to you. FREE RESOURCE FOR LIFE AFTER BABY LOSS Over the past 5 years we have helped thousands of women navigate life after the loss of a baby and we pulled our best and most helpful resources all into one easy to access resource. There is a separate bundle for miscarriage, infant loss and life-limiting diagnosis so the resources are very specific, tailored to you and your grief journey. To get your free resource bundle head to themorning.com/resourcebundle CHRISTMAS BIBLE STUDY GUIDEwww.themorning.com/christmas RESOURCE FOR HOW TO LOVE A GRIEVING MOM www.themorning.com/friendsandfamily SHOW NOTESwww.themorning.com/blog/episode137 FREE ONLINE COMMUNITY www.themorning.com/community
"The diagnosis is well-established. A cure is within our reach, and the wisest among our practitioners of the healing arts are offering valuable counsel. When the U.S. government and science, in its most principled form, work together, insulated from a culture of insidious and invidious profiteering, they can put a man on the moon, and launch a helicopter on Mars. They can also deliver better health care in a much more equitable and cost-effective way. It is time for the patient to listen to her best doctors. They are giving it to her straight." Jeffrey Fraser is a neurologist. He shares his story and discusses his KevinMD article, "Diagnosis: malformation of a health care system." (https://www.kevinmd.com/blog/2021/07/diagnosis-malformation-of-a-health-care-system.html)
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