Podcasts about Lupus

Thanks for reading this! Please like and share this episode, and also subscribe to the channel. I would greatly appreciate it! Care warning: Breast cancer is discussed in this episode. Jodie Lin is a National Board-Certified Health and Wellness Coach. She is certified in hormone health, holistic cancer health, and she's working on her Holistic Autoimmune Certification. She is also a two-time breast cancer survivor living with Lupus. Most importantly, she is a married mom to five beautifully diverse children. She loves working with others, sharing her knowledge, and encouraging them to find their own individual path to health. Jodie's contact information: www.jklwellhealthcoaching.com www.instagram.com/jklwell_health_coaching www.facebook.com/jklwell My contact information: www.chrisdtgordon.com @chrisdtgordon Chris DT Gordon's TAG and POP Shop: https://chris-dt-gordons-tag-and-pop-store.myshopify.com/ Knowledge sharers: @nateberan

In today's episode Jeffrey invites author and researcher, Stephanie Seneff Ph.D and author and pediatrician, Michelle Perro, M.D. to a discussion on the link between glyphosate and Roundup and autoimmune diseases such as Type 1 Diabetes, JRA, Hashimoto's, Lupus, Rheumatoid Arthritis, MS and Celiac's Disease.  The Institute for Responsible Technology is working to protect you & the World from GMOs (and while we're at it, Roundup®...)  To find out exactly how we do this and to subscribe to our newsletter visit https://www.responsibletechnology.org/ Join us at Protect Nature Now to Safeguarding Biological Evolution from GMOs 2.0. The place to get critical up to date information, watch our short film and most importantly, learn easy ways for you to take action against this existential threat. Visit: https://protectnaturenow.com/ Watch "Don't Let the Gene Out of the Bottle" Get the book: "Seeds of Deception" IG @irtnogmos Facebook @responsibletechnology YouTube @TheInstituteforResponsibleTechinology Twitter @TheInstituteforResponsibleTechnology

Ellen from the US share her experience of LDN Lupus, Sjogren's, Hashimoto's, Pain and interstitial cystitis on the LDN Radio Show 2022

This episode addresses the chiropractic evaluation and adjustments for Dr. Brads' dog, as well as stories from the rest of the crew.

Jessica Serra est éthologue (étude du comportement des animaux). Elle est l'auteure de La bête en nous en 2021. Dans cet épisode, Jessica évoque la période où se cotoyaient sur terre plusieurs espèces d'Homos. Au final, Homo Sapiens, cet espèce modeste qui s'est autosurnommé "sage" a prévalu sur toutes les autres, dont le célèbre homme de Neandertal; Il ne reste d'eux que quelques % d'ADN dans notre génome. Homo sapiens fut un loup pour les autres Homos, ans parler des animaux... Vers -12000 ans, des chasseurs ont commencé à domestiquer un allié précieux, qui n'est pas étranger à son succès évolutif: le loup ... _______  

Well Said has invited Dr. Richard Furie, Chief of the Division of Rheumatology at Northwell Health and a Professor at the Zucker SOM to explain the ins and outs of Lupus, a disease that affects 1.5 million Americans and the progress physicians are making in determining its causes and triggers.

Q & A call-in discussion with a survivor-professional, using an OPEN MIKE forum. We'll feature a survivor-professional co-host who'll field topics brought to the episode by you, the listener. ~~ Tonight's special guest will be Monica Boglin from Puyallup, Washington, a survivor of sexual, physical, and emotional child abuse. Her predictors were all family members, and her parents were intent on passing on to Monica the behavior that their parents had done to them. She also has lived with Lupus since she was 29, a painful autoimmune disease that has long been linked to adverse childhood experiences (ACEs). Monica became a life coach and a therapist and notes, “I've finally found a way to forgive the unforgivable and to firmly keep anyone and everything harmful out of my life been linked to." She's earned her Masters degree in metaphysical science and counseling and is well on her way to earning a PhD in the same field. "I hope to further use my story as a way to become of service and to help those along the path to their own healing, because I now know that hope and help is available.” ~~ On these episodes we welcome various co-hosts, survivor-professionals who'll assist in fielding questions and lead a variety of topics suggested by our call-in participants. Their trauma-informed perspectives as survivor-professionals will help them guide discussions on the issues of child abuse, trauma and healthy human sexuality that spring from questions and topics brought to us by our listeners. ~~ Everyone's invited to engage on tonight's show. ~~ Please visit the NAASCA.org web site.

This week on your favorite house MD rewatch podcast Grimes and Box review Season 3 episode 1- Meaning. House is healed physically but he still struggles while finding meaning... see what I did there.

When Christine De La Rosa was diagnosed with lupus in 2010, her team of nearly a dozen doctors put her on 11 pills a day — five of which were opioids. Christine's health suffered so deeply on this medley of prescription drugs that even basic tasks like eating became too difficult for her to endure. After five years of debilitating symptoms, Christine found medical cannabis, and for the first time since her diagnosis, she began to feel better. In today's inspiring episode, Christine shares how swapping prescription drugs for cannabis saved her life, and she encourages others to advocate for themselves on their journey to holistic healing. Hosted by Ellen Lee Scanlon Sign up for our newsletter at dothepot.com Follow us: IG: @dothepot FB: @dothepot Pinterest: @dothepot LinkedIn: How to Do the Pot Twitter: @dothepot --- Send in a voice message: https://anchor.fm/htdtp/message

Imagine, after years of living on your own, building a 15-year career an award-winning career as a Creative Consultant and Wardrobe Stylist, and essentially checking all the success boxes, a chronic illness drops into your body, leading you back to your hometown to move in with your parents as you work to rehabilitate and heal, and try to not just reclaim, but reimagine your life.Today's guest, Tiffani Moore, knows exactly what it's like to be in this scenario—forced to listen to her body's need for recovery and support after she found out she had Lupus. Tiffani is the Founder and Owner of Moore WellBeings, in addition to being an Intuitive Healer & Coach, Reiki Master, yoga instructor, BreathWork, and MNDFL certified Meditation Facilitator. Before making her mark in the world of wellness, she spent 15+ years building a career as a successful, sought-after stylist and Creative Consultant. But her lupus diagnosis, and the physical and psychological devastation that led up to it, changed everything. Seeking less conventional solutions, she followed her intuition and began to study the power of alternative therapies, including meditation, yoga, herbal medicine, and many of the healing practices she utilizes with clients now. Recovering her wellbeing has been a years-long, painstaking process, fueled by intensive learning, and eventually, a drive to train in and share the many modalities she'd discovered, while also creating a safe, nonjudgmental and well-informed space for marginalized communities to explore holistic wellness. In this conversation with Tiffani today, you'll hear us explore the harsh realities of living with a chronic illness, like feeling like a burden to loved ones or the struggle to balance rest and recovery with the need to work to survive. We talk about intuition and its role in healing, wellness, and self-expression and how it could benefit us to rethink wellness not as a luxury but instead as a birthright or something we all deserve and can access.You can find Tiffani at: Website | InstagramIf you LOVED this episode you'll also love the conversations we had with James Gordon about the power of the mind to heal and work through illness and trauma.Check out our offerings & partners: My New Book SparkedMy New Podcast SPARKEDVisit Our Sponsor Page For a Complete List of Vanity URLs & Discount Codes.ClickUp: 15% off ClickUp's massive Unlimited Plan for a year. Code GOODLIFE.Zocdoc See acast.com/privacy for privacy and opt-out information.

Andy, Bee and Agent C realize the ramifications of the distribution of the L.I.F. Pharmaceutical Drug and will need to do whatever they can to stop it.  

Clinical trials make new and better treatments for lupus possible. In this episode of The Expert Series, we sit down and talk with Stephanie Slan, Director of IMPACT+ (Improving Minority Participation and Awareness in Clinical Trials) at the Lupus Foundation of America about clinical trial participation. Stephanie also debunks some myths about clinical trials might keep people from wanting to participate. It's important for people with lupus to consider participating in these trials to further the advancement of lupus medicines and treatment. This episode breaks down eligibility criteria, what happens during a clinical trial, and what happens with your information after a trial. Listen to learn more To learn more about clinical trials, read more about participating in clinical trials here or about frequently asked questions here If you are interested in participating in research, visit: Lupus.org/RAY SUBSCRIBE to receive an email update when new episodes of The Expert Series are released.

This week we welcome Dr. Alfred Kim to our show as we discuss B-Cell depleting therapies and how patients on these drugs may be more susceptible to COVID-19. During which, Dr. Kim takes us back to the beginning of the pandemic and how he and his patients initially managed the rituximab infusions, how and why people on this drug may be at increased risk of severe disease, the importance of vaccinations, and why they may not work for this patient population. Finally, we finish with Dr. Kim sharing with us important information on how to mitigate the risk of COVID-19 among people taking b-cell depleting therapies, now that there are new therapies for COVID-19 pre-exposure prophylaxis.  

This week on your favorite House MD rewatch podcast the guys recap Season 2! From their favorite moments to listener mail.

Langston and David answer a listener's email about Nick Cannon having a lot of kids only for future bone marrow transplants and other "spare parts". See omnystudio.com/listener for privacy information.

Discussion with a Lupus Nephritis patient (and Pharm.D. student) about manifestations and treatments of SLE and Lupus Nephritis.

In the third episode in our podcast series about Lupus, Mel Brooke, Patient and Public Engagement Programme Director (BIRD) talks with expert guest Dr Jess Ellis, Rheumatology Clinical Research Fellow at the RNHRD, Bath about the annual Lupus clinic and exciting news about a collaborative initiative with BIRD to set up a Patient Advisory Group (PAG) within the hospital. If you can please rate our podcasts on your listening platform. Did you know you can also access all our information podcasts direct from BIRDs website? Simply visit www.birdbath.org.uk/podcasts and scroll down the page to find the one you are looking for. Links mentioned in the show: Lupus UK (charity) RUH/RNHRD Bath Please note: All content for BIRD's PPE podcasts are created for information purposes only and not intended to be a substitute for individual medical advice, diagnosis, or treatment. Always seek the advice of your physician or health provider with any questions you may have about your medical condition. Reliance on any information provided by BIRD or any of the expert podcast guests is solely at your own risk. The Patient and Public Engagement Programme is supported by hands-off sponsorships from Eli Lilly and Company Limited, UCB and Amgen - all of whom have provided grant funding but who have had no involvement in the development, content or editorial control of this podcast, nor the subsequent review and approval of these materials or general running of the patient and public engagement programme. We would also like to thank The Arnold Clark Community Fund, The Cumber Family Charitable Trust, Medlock Charitable Trust, The Ray Harris Charitable Trust. Thank you to all our sponsors for helping us to bring you information that supports you and helps to increase your knowledge of rheumatic diseases. To find out more about BIRD and the PPE Programme visit: The Bath Institute for Rheumatic Diseases Please sign up to our mailing list if you would like to stay in touch and be notified about future podcasts via admin@birdbath.org.uk

In the second episode of our podcast series about Lupus you can listen as Mel Brooke, Patient and Public Engagement Programme Director (BIRD) talks with expert guest Dr Sarah Skeoch, Consultant Rheumatologist at the RNHRD (Bath) to learn about the kinds of medications and treatments that are available to support people with this complex condition. If you can please rate our podcasts on your listening platform. Did you know you can also access all our information podcasts direct from BIRDs website? Simply visit www.birdbath.org.uk/podcasts and scroll down the page to find the one you are looking for. Links mentioned in the show: Lupus UK (charity) RUH/RNHRD Bath Please note: All content for BIRD's PPE podcasts are created for information purposes only and not intended to be a substitute for individual medical advice, diagnosis, or treatment. Always seek the advice of your physician or health provider with any questions you may have about your medical condition. Reliance on any information provided by BIRD or any of the expert podcast guests is solely at your own risk. The Patient and Public Engagement Programme is supported by hands-off sponsorships from Eli Lilly and Company Limited, UCB and Amgen - all of whom have provided grant funding but who have had no involvement in the development, content or editorial control of this podcast, nor the subsequent review and approval of these materials or general running of the patient and public engagement programme. We would also like to thank The Arnold Clark Community Fund, The Cumber Family Charitable Trust, Medlock Charitable Trust, The Ray Harris Charitable Trust. Thank you to all our sponsors for helping us to bring you information that supports you and helps to increase your knowledge of rheumatic diseases. To find out more about BIRD and the PPE Programme visit: The Bath Institute for Rheumatic Diseases Please sign up to our mailing list if you would like to stay in touch and be notified about future podcasts via admin@birdbath.org.uk

Join us for this first episode in our podcast series about Lupus. Listen as Mel Brooke, Patient and Public Engagement Programme Director (BIRD) talks with expert guest Dr Ellie Korendowych, Consultant Rheumatologist at the RNHRD (Bath) who explains about the symptoms that people with this condition can experience and the types of diagnostic techniques used. If you can please rate our podcasts on your listening platform. Did you know you can also access all our information podcasts direct from BIRDs website? Simply visit www.birdbath.org.uk/podcasts and scroll down the page to find the one you are looking for. Links mentioned in the show: Lupus UK (charity) RUH/RNHRD Bath Please note: All content for BIRD's PPE podcasts are created for information purposes only and not intended to be a substitute for individual medical advice, diagnosis, or treatment. Always seek the advice of your physician or health provider with any questions you may have about your medical condition. Reliance on any information provided by BIRD or any of the expert podcast guests is solely at your own risk. The Patient and Public Engagement Programme is supported by hands-off sponsorships from Eli Lilly and Company Limited, UCB and Amgen - all of whom have provided grant funding but who have had no involvement in the development, content or editorial control of this podcast, nor the subsequent review and approval of these materials or general running of the patient and public engagement programme. We would also like to thank The Arnold Clark Community Fund, The Cumber Family Charitable Trust, Medlock Charitable Trust, The Ray Harris Charitable Trust. Thank you to all our sponsors for helping us to bring you information that supports you and helps to increase your knowledge of rheumatic diseases. To find out more about BIRD and the PPE Programme visit: The Bath Institute for Rheumatic Diseases Please sign up to our mailing list if you would like to stay in touch and be notified about future podcasts via admin@birdbath.org.uk

This episode was originally released on January 19, 2021. Microbiome, microbes, microorganisms – these terms may be confusing, but the types of bacteria living in and on our bodies can impact arthritis. Learn what helps or harms the microbiome and the health of your gut and discover dietary changes that can make a difference. Visit the Live Yes! With Arthritis Podcast site to read the blog and get show notes and a full transcript: https://arthritis.org/liveyes/podcast We want to hear from you. Tell us what you think about the Live Yes! With Arthritis Podcast. Get started by emailing podcast@arthritis.org. Special Guests: Arthur Kavanaugh, MD and Monica Guma, MD.

Today's amazing guest, Daniella Djan, is the epitome of all things resilience! Being diagnosed with Lupus at just 18 years old, Daniella's was left feeling helpless, scared and alone. But since then she's gone on to live a big and meaningful life that's given her a whole new way to contribute to the world. If you are someone who's living with a chronic illness or has been dealt a sucker punch by life, be sure to tune in as Daniella shares with us her F.I.T strategy so you can do the same! Want to feel more confident and less stressed every day? Learn more about my personalised teen coacing programs here: www.kategladdin.com/coaching For daily inspiration and tips, follow me on instagram: @kategladdin

Dr. Jun Lu, MD interviewed by Flavia Fedeles, MD, FAAD

Dear friend Melissa back in the hunt as she takes Tom's spot on the show. Today, we talk about Lupus and what it means to be one.We go from camping to hunting, Goosebumps to Jon Tron, Buffy The Vampire Slayer to The Little Mermaid, and Brendan Fraser to Pauly Shore..............? WTF?!Listen in on the fun and find out why.The music is:  Silent Partner - No CultureWant to show us some love?  Support us on Ko-FiWant to Talk to usWebsite:  Rage Across the InternetJoin the Forums to get the Code for our discord and come chat with us!Email: rageacrosspodcast@gmail.comTwitter: @rageacrossFacebook: Rage Across the InternetWe've got a YouTube too, check it Right Here←Previous Episode

An affirmation for this summer.

Imagine being 30 and needing to plan your funeral while also planning your will. This is the exact experience Amanda Ishii had to go through a few years ago. On this week's episode, Amanda discusses her journey living with Lupus, Crohn's disease, Colon cancer and Multi Organ Dysfunction. Amanda explains her initial symptoms and jumps into the importance of social and mental support when it comes to dealing with a chronic illness. Moreover, Amanda brings up therapy, a resource that not only helped her by providing her someone to talk to but also is used by many people in all communities as a tool for support. As the episode progresses, Amanda discusses what life was like throughout college to present day with an ileostomy bag in social settings, while playing basketball and when travelling. Since a young age, basketball was a passion of hers. Even with a medical device, Amanda continues to pursue basketball professionally while knowing her limits; she is unstoppable. Finally, Natasha and Amanda end off the podcast episode by talking about a new initiative Amanda is starting up to supply 3rd world countries with medical and school supplies for free, The Mango House. Check out Amanda's socials: Instagram: @haparae @themangohouse_cebu Sign up for the July Joint Chat Rheum Session: https://us02web.zoom.us/meeting/register/tZ0ofuCspjsoGdduKrpgemnDZa1As6TvwYhL Check out our socials: Website: https://www.takeapaincheck.ca/Instagram: https://www.instagram.com/takeapainch... Twitter: https://twitter.com/takeapaincheck​​​Tiktok: https://www.tiktok.com/@takeapaincheck

Episode Notes In episode 301, I sit down with Disability Rights Lawyer Ashley B. Jacobson as we wheel into the courtroom and talk about how disability impacts our entire legal system.  We explore ableism in law school, policing, etc.  Ashley shares with us her personal experiences of Lupus and Interstitial Cystitis and why self-cathing can be a pain + so much more! Enjoy!  You can follow Ashley and her work here: https://linktr.ee/Ashleybjacobson  Episode Sponsors  Support Bump'n and donate so everyone can access self-pleasure by going to  www.getbumpn.com  Sign up to be a part of the free, virtual Parks Accessibility Conference taking place August 23-25th, 2022 by going to www.parksaccessibilityconference.ca   Clone-A-Willy or Clone-A-Pussy all your own and get 20% off sitewide by using coupon code DARKPOD at Checkout. www.cloneawillycom.  Get 15% off your next purchase of sex toys, books and DVDs by using Coupon code AFTERDARK at checkout when you shop at trans owned and operated sex shop Come As You Are www.comeasyouare.com  Support Disability After Dark on Patreon at www.patreon.com/disabilityafterdark 

Star Wars Rebels Season 4 Episode 9: DUME Reeling from a devastating loss, the Ghost crew rallies together to find new purpose and resolve. Submit corrections to us here: Bit.ly/BothanReport Episode Recap begins at 0:32:08 First aired on February 19, 2018, written by Dave Filoni & Christopher Yost, and directed by Sergio Paez Music by Zen_Man Cover Art by Cherriielle

To have your question featured in a future video, please email: questions@drmdcas.com

Ready for lively living with lupus this summer?? Tune in, and bring a friend. This summer = 2 episodes a week!! There will be information, inspiration, and MORE. Listen to this episode to get started with your lively living with lupus summer. There are a few journal prompts in here to help ✨

While joint pain and inflammation are the hallmark symptoms of arthritis, the physical toll it takes on your body can vary. Depending on what type of arthritis you have, and whether it's an autoimmune inflammatory condition, the physical symptoms can affect many parts of your body — beyond your joints — including your skin and eyes or your heart and kidneys. Learn more in this episode of the Newly Diagnosed With Arthritis series of the Live Yes! With Arthritis Podcast. Visit the Live Yes! With Arthritis Podcast site to get show notes and a full transcript: https://arthritis.org/liveyes/podcast We want to hear from you. Tell us what you think about the Live Yes! With Arthritis Podcast. Get started by emailing podcast@arthritis.org. Special Guest: Dr. Liana Fraenkel.

Grief, anger, anxiety and stress often come with an arthritis diagnosis, and they may continue to come and go. Listen to a rheumatologist/researcher discuss the link between chronic pain and emotions, how they influence each other and strategies to deal with it. Visit the Live Yes! With Arthritis Podcast site to get show notes and a full transcript: https://arthritis.org/liveyes/podcast We want to hear from you. Tell us what you think about the Live Yes! With Arthritis Podcast. Get started by emailing podcast@arthritis.org. Special Guest: Dr. Francis Keefe.

Get the Heart of Freedom III Replay here: https://hof3replay.thefuturegen.com/hof3recording Join the Future Generations Community here: https://community.thefuturegen.com   Remember to Rate, Review and Subscribe on iTunes and Follow us on Spotify Follow us on Instagram: @futuregenpodcast   It's only natural that anyone who cares about health freedom cares about birth as well. Kylee Zeck dives deep into this topic in this episode. Her words serve to remind parents everywhere that they are not alone, regardless of their birthing experiences. Enjoy this episode and the healing that comes from it! Kylee's journey began at age 15, after receiving a diagnosis of mononucleosis (Epstein Barr Virus). She experienced years of unexplained suffering and multiple diagnoses: Lupus, Rheumatoid Arthritis, Fibromyalgia, and Undifferentiated Connective tissue disease. After countless doctors contradicting each other with various autoimmune diagnoses and multiple trials and errors of medication, she realized she needed to become her own advocate and take her health back into her own hands. It has been four years since that turning point, and since then she has experienced relief and healing from lifestyle changes, learning natural and alternative remedies, and soon to be a certification in holistic health.   Stay Connected with Kylee:  Instagram: https://www.instagram.com/kylee.zeck/ Website: https://www.creatingthecure.coach/  Linktree: https://linktr.ee/Kzeck4   ______________________________   Stay Connected with the Future Generations Podcast:  Instagram: @futuregenpodcast, @thefuturegensd  and @drstantonhom5.0 Facebook: Future Generations Podcast and Future Generations | Clinic of Chiropractic  Website: Future Generations | Clinic of Chiropractic  Remember to Rate, Review and Subscribe on iTunes and Follow us on Spotify!

https://www.youtube.com/watch?v=XoJIcGZT58A&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=64&t=4s Featuring Drs. Jack Cush, Kathryn Dao and Yuz Yusof reporting on lupus-related studies and sessions from EULAR 2022.

https://www.youtube.com/watch?v=XoJIcGZT58A&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=64&t=4s Featuring Drs. Jack Cush, Kathryn Dao and Yuz Yusof reporting on lupus-related studies and sessions from EULAR 2022.

- Kathryn Dao: What Patients Want and Are Willing to Risk with SLE https://www.youtube.com/watch?v=lytObQy_UdQ&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=13 - Yuz Yusof: What Symptoms or Targets Mattered Most to People with Lupus? https://www.youtube.com/watch?v=EJKPsegnpS0&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=8&t=6s - Kathryn Dao: AURORA-2 Two-year Results Voclosporin For Lupus Nephritis https://www.youtube.com/watch?v=HZOFQi559S4&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=14 - Kathryn Dao: Severe Hematologic Relapse Risk in SLE https://www.youtube.com/watch?v=j3S-BOhNhDE&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=15 - Eric Dein: Let's Talk about Sex and Autoimmune Disease https://www.youtube.com/watch?v=hi_DqRiLPUw&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=21 - Kathryn Dao: DMARDS, Prednisone, Pregnancy, OH MY! https://www.youtube.com/watch?v=kwzKrzFjIWM&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=25 - Kathryn Dao: Belimumab Use in Pregnancy https://www.youtube.com/watch?v=14MUTorltoU&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=26 - Peter Nash: Deucravacitinib at EULAR 2022 https://www.youtube.com/playlist?list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP - Yuz Yusof: Interview with Dr. Lucy Carter on RNA-Seq analysis to determine who's at risk for SLE https://www.youtube.com/watch?v=PhQvt6IVPfY&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=50

- Kathryn Dao: What Patients Want and Are Willing to Risk with SLE  https://www.youtube.com/watch?v=lytObQy_UdQ&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=13 - Yuz Yusof: What Symptoms or Targets Mattered Most to People with Lupus?  https://www.youtube.com/watch?v=EJKPsegnpS0&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=8&t=6s - Kathryn Dao: AURORA-2 Two-year Results Voclosporin For Lupus Nephritis   https://www.youtube.com/watch?v=HZOFQi559S4&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=14 - Kathryn Dao: Severe Hematologic Relapse Risk in SLE  https://www.youtube.com/watch?v=j3S-BOhNhDE&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=15 - Eric Dein: Let's Talk about Sex and Autoimmune Disease  https://www.youtube.com/watch?v=hi_DqRiLPUw&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=21 - Kathryn Dao: DMARDS, Prednisone, Pregnancy, OH MY!  https://www.youtube.com/watch?v=kwzKrzFjIWM&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=25 - Kathryn Dao: Belimumab Use in Pregnancy   https://www.youtube.com/watch?v=14MUTorltoU&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=26 - Peter Nash: Deucravacitinib at EULAR 2022  https://www.youtube.com/playlist?list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP - Yuz Yusof: Interview with Dr. Lucy Carter on RNA-Seq analysis to determine who's at risk for SLE https://www.youtube.com/watch?v=PhQvt6IVPfY&list=PLbd4uixNDSBSKgUojFF3dfPfHlN8QN2EP&index=50

In this Episode of The Human Upgrade™...​… Dave talks with Lisa B. about the frustration she's experiencing with her health conditions. She says she lives a healthy lifestyle and does the “right things” and still struggles with chronic low energy. Her kids often say, “you never feel well, mom.” She agrees but finds it difficult to explain why. Now in her early 50s, she's had panic attacks and anxiety since childhood and has taken many types of anti-depressants throughout her life. She also struggles with OCD.She's experienced long-time hormonal imbalances, including painful periods, acne, fertility problems, and ongoing PMS “flu” that she says takes over her life during her cycles. She suffers from aggressive seasonal allergies and has a shellfish allergy. She's been on Accutane, was diagnosed with Lupus in college and also diagnosed with exercise-induced urticaria and Mast Cell Activation Syndrome. She got COVID in 2021.In this “Interventions With Dave” episode, Dave examines what's going on with Lisa's varied symptom. They discuss what's working and what's not, and what can help her gain more energy and control of her health. The conversation gets into a bunch of topics, like:PMS “flu” (with sore throat, hot tongue, achy, brain fog, no energy, feverish feeling with no fever present, painful periods) Hormones, the Wiley Protocol and testosterone“Mold cough” and other symptoms of moldOCD and anxietyMTHFR gene mutation Histamine, Mast Cells and Mast Cell Activation SyndromeAllergiesAnd much more…Find biohacking tips, tools and resources particular to this episode on the episode web page: https://daveasprey.com/interventions-with-dave-lisa-b-949/Note: The "Interventions With Dave” recommendations are designed to help you upgrade yourself and your biology so you can perform better at everything you do. They are not, however, a substitute for advice or treatment by a trained medical professional that may be needed for specific health conditions, illness or injury.See Privacy Policy at https://art19.com/privacy and California Privacy Notice at https://art19.com/privacy#do-not-sell-my-info.

Do you want to achieve whole-body healing? Join Amorahki in this new episode of Superpowers of the Soul as she chats with Sandie Gascon. Sandie is an Integrative Healing Practitioner who is on a lifelong quest to help people get to the root of their health issues and achieve their health goals. Not too long ago, Sandie suffered deeply with constant pain and fatigue. She feared she would never be able to have children because she could barely take care of herself due to Lupus, Migraines, Interstitial Cystitis, and a whole host of other symptoms. But Sandie became her first client and discovered the power of Whole Body Healing to completely heal herself and make all her dreams come true, including the birth of her beautiful son. Tune in to know how to attain whole-body healing.

Q & A call-in discussion with a survivor-professional, using an OPEN MIKE forum. We'll feature a survivor-professional co-host who'll field topics brought to the episode by you, the listener. ~~ Tonight's special guest will be Monica Boglin from Puyallup, Washington, a survivor of sexual, physical, and emotional child abuse. Her predictors were all family members, and her parents were intent on passing on to Monica the behavior that their parents had done to them. She also has lived with Lupus since she was 29, a painful autoimmune disease that has long been linked to adverse childhood experiences (ACEs). Monica became a life coach and a therapist and notes, “I've finally found a way to forgive the unforgivable and to firmly keep anyone and everything harmful out of my life been linked to." She's earned her Masters degree in metaphysical science and counseling and is well on her way to earning a PhD in the same field. "I hope to further use my story as a way to become of service and to help those along the path to their own healing, because I now know that hope and help is available.” ~~ On these episodes we welcome various co-hosts, survivor-professionals who'll assist in fielding questions and lead a variety of topics suggested by our call-in participants. Their trauma-informed perspectives as survivor-professionals will help them guide discussions on the issues of child abuse, trauma and healthy human sexuality that spring from questions and topics brought to us by our listeners. ~~ Everyone's invited to engage on tonight's show. ~~ Please visit the NAASCA.org web site.

The Expert Series is happy to have Dr. Bonnie Bermas on our episode about fertility and reproductive health. Dr. Bermas is an internal medicine professor at UT Southwestern Medical Center focusing on rheumatology disorders. She was the Clinical Director of the Lupus Center and co-director of the Program in pregnancy and rheumatic diseases at Brigham and Women's and Harvard Medical School. Her research interests include pregnancy and rheumatic diseases, systemic lupus erythematosus (SLE) and antiphospholipid syndrome (APS), and rheumatic immune checkpoint inhibitor adverse events. Below are resources from the National Resource Center on Lupus related to this episode Read about Lupus and women's reproductive health Read how six men are living with lupus Learn more to understand the role of how sex and gender play in lupus For more information on medication, read about Medications used to treat lupus. SUBSCRIBE to receive an email update when new episodes of The Expert Series are released.

Join us in the next episode of the Our Daily Magic Podcast (LIVE from the Facebook Group and Youtube) as "I am Magickai" aka Kaí and Dell Henderson aka "The True Essence Connector" will be interviewing Sandie Gascon Sandie Gascon is a Health Coach who has helped guide hundreds of people from over twenty-five countries on their healing journey. After suffering severe side effects from medications during her twenty-year battle with chronic migraines, when she was diagnosed with Lupus she committed herself to heal naturally. Through her experiences, she developed a whole body, mind, and spirit approach that addresses the person in a truly holistic manner. She takes the guesswork out of the equation by running functional lab work to see what the body needs. She healed herself of migraines, depression, lupus, interstitial cystitis, and cystic acne. Her purpose is to help educate others on the importance of shifting focus to rebuilding and rebalancing the body and removing internal and external stress so the body can heal itself. The episode started with Dell asking Sandie on how she started her journey that lead her to become a health coach where she iterated, "it doesn't have to be what she went through" (8:45). She then went through her medical history and shared how listening to a certain podcast changed everything (10;39). Dell was curious what podcast was it (13:52).  Kai asks what are some of the little known spiritual aspect that people can integrate into a healthy lifestyle (15:46) where Sandie shares that focusing on our passion is a major aspect. Dell asks about the root stuff she had to battle within her to attain balance for her healing (17:23). She shares her journey with supplements and mentions that supplements are not magic and the magic is the work we do on ourselves (21:33). Dell probes more on the balance and acceptance (25:13) where Sandie says that it's where faith do its magic. Dell then mentions Abraham Hicks and the Law of Attraction (27:21) where Sandie shares she has a section in her book about it called The Stages of Consciousness. She further explained these stages.  Dell opens up a conversation about fibromyalgia (33:25) where Sandie proposed another way to deal with the illness from her book. Kai further explores the topic on epigenetics (39:44) and quantum healing (41:21). They then discuss Sandie's holistic healing practices. They then move on to talk about Sandie's Integrative Healing Academy and what she teaches there (56:01).  The episode ends with Sandie sharing her parting words for the listeners and her contact information (1:06:13).  Join us in this enlightening episode about shifting balance, acceptance and faith. If you're interested to learn more about holistic healing, or interested to  learn to practice it, this episode is definitely for you. Please check it out!  Stay Magical!  ***** Discover your soul's truth so you can get exactly what you want out of life. Book a FREE Soul Chat with Kaí + Dell: https://ourdailymagic.as.me/soulchat

Dr. Prather opens the show with a COVID-19 update about the future of vaccine mandates. Then, we share three patient success stories from Dr. Prather's office that will inspire you on your own health journey. In this episode, you'll find out:—How 14 states, including Indiana, require that businesses allow their employees religious and medical exemptions from vaccine mandates.—The necessity of public pushback to defeat vaccine mandates and demand health freedom from the government. —Why Dr. Prather says "the science and the data don't support the vaccine".—The reason the government has had a tunnel-vision approach to vaccines being the solution to the pandemic and ignored all other treatments.—The new vaccine that is a potential alternative to the new Pfizer and Moderna vaccines that is more along the lines of traditional vaccines. —The shocking COVID results being seen in Australia after they strictly followed a strategy of lockdowns and vaccine mandates.—What policy the airlines are trying to change concerning international travel. —Why Pam decided to come see Dr. Prather after suffering from extreme stress and discovered for the first time that she has Scoliosis. And why she says, "I didn't know I could feel this good" until she experienced the treatments at Holistic Integration. —How Katy went to almost 20 different specialists for help after a random neck fracture, including The Cleveland Clinic and The Mayo Clinic, and found no answers until she came to Dr. Prather's office. And how she's so excited to be WALKING again after being close to needing a wheelchair. —And in a special treat for long-time patients of Dr. Prather, we will be joined by Pat, a beloved employee in Dr. Prather's office who retired after 17-years. Hear how she first came to Dr. Prather as a patient after being diagnosed with Lupus and why her general practitioner said she wouldn't be alive today if it weren't for Dr. Prather.www.TheVoiceOfHealthRadio.com

This episode was originally released on April 28, 2020. Staying active is important for managing arthritis, but it can be difficult for some people to do, especially when they're in a lot of pain. Walking is a good way to ease into adding physical activity to your routine. Dr. Leigh Callahan talks about the many benefits of walking, from managing the pain of arthritis to improving your physical and mental health. She shares strategies for taking the first step by using the Walk With Ease program. Visit the Live Yes! With Arthritis Podcast site to read the blog, get show notes and a full transcript: https://arthritis.org/liveyes/podcast We want to hear from you. Tell us what you think about the Live Yes! With Arthritis Podcast. Get started by emailing podcast@arthritis.org. Special Guest: Leigh F. Callahan, PhD.

Join Yvonne Brandenburg, RVT, VTS SAIM and Jordan Porter RVT, LVT, VTS SAIM as we talk about: When the immune system attacks DNA. That is right, I said DNA. But it doesn't go around attacking ALL DNA. We discuss DLE and when the body attacks skin cells.    Question of the Week Who is going to ACVIM 2022?  Leave a comment at https://imfpp.org/episode129  Resources We Mentioned in the Show  VCA: Discoid Cutaneous Lupus Erythematosus:  https://vcahospitals.com/know-your-pet/discoid-cutaneous-lupus-erythematosus   VIN: https://veterinarypartner.vin.com/default.aspx?pid=19239&catId=102899&id=4952581   Thanks so much for tuning in. Join us again next week for another episode!  Want to earn some RACE approved CE credits for listening to the podcast? You can earn between 0.5-1.0  hour of RACE approved CE credit for each podcast episode you listen to.    Join the Internal Medicine For Vet Techs Membership to earn and keep track of your continuing education hours as you get your learn on!   Join now! http://internalmedicineforvettechsmembership.com/   Get Access to the Membership Site for your RACE approved CE certificates Sign up at https://internalmedicineforvettechsmembership.com  Get Access to the Technician Treasure Trove  Sign up at https://imfpp.org/treasuretrove    Thanks for listening!  – Yvonne and Jordan   

In this episode, listen as Karen H. Costenbader, MD, MPH, and Brad H. Rovin, MD, answer key questions about identifying patients at high risk for lupus nephritis, whether an elevated serum creatinine always signals lupus nephritis, the safety of newer therapies for lupus in women who are pregnant or breastfeeding, and the possibility of using SGLT2 inhibitors in patients with lupus nephritis.Presenters: Karen H. Costenbader, MD, MPHProfessor of MedicineDepartment of MedicineHarvard Medical SchoolDirector, Lupus ProgramDivision of Rheumatology, Inflammation and ImmunityBrigham and Women's HospitalBoston, MassachusettsBrad H. Rovin, MDProfessor and Director, Division of NephrologyThe Lee A. Hebert Professor of NephrologyMedical Director, The Ohio State Center for Clinical Research ManagementThe Ohio State University Wexner Medical CenterColumbus, OhioReview the downloadable slidesets at: https://bit.ly/3mlHOlaLink to full program:https://bit.ly/3aC2NNL

Good people,Today I'm joined by Ardenia Brown, also known as Chef Butta. Ardenia is part of my family, one of my cousins; she is the personal chef for Ahmir Thompson, Questlove, specializing in Farm-To-Fork Cuisine and Holistic Juicing using local organic wild ingredients. Chef Butta's truth is about self-acceptance. Throughout her childhood, she felt ignored, not heard, and forced to be what she was supposed to be. She built a successful career in the music industry in Los Angeles, and one day, Ardenia had to abandon everything and come back to take care of her sick mother. Far from home, Ardenia explored and found out who she was, she found her true self, and that is how she showed up many years later in her hometown to her mother and her family. We had a fantastic conversation about health, food, and the food industry, the "heartset" used by Ardenia to switch from the entertainment industry into a celebrity chef, how she managed to differentiate herself and cut through the noise in the food industry, and the vital relevance of family and connections. In This Episode, You Will Learn:Ardenia shares her truth (5:26)About the pressure families put on us rewarding what and how we are supposed to be (11:39)How it was for Ardenia to abandon her lifestyle in LA and come back home to take care of her mother (15:06)What turns food into good food (19:18)About how Ardenia differentiated herself from other chefs (22:45)First Impressions:LA (33:49)Western Medicine (33:49)Eastern Medicine (34:01)Marketing (34:13)Garlic (34:24)Lupus (34:30)Juicing (34:39)Soul Food (34:46)Destiny (34:53)Chef Butta (35:01)Resources:Chef Butta websiteConnect with Chef Butta:Instagram See acast.com/privacy for privacy and opt-out information.

This is a Step 5 Episode*   In this episode, Tiffany, CEO of AiArthritis, is joined by Catherine Ames, from the Young Patients' Autoimmune Research & Empowerment Alliance, both persons living with AiArthritis diseases and both who attended the 16th Annual Personalized Medicine Conference in May 2022. Precision Medicine (PM) may currently be in the cancer space, but it's quickly moving into the autoimmune/autoinflammatory space and there are some things they want you to know. What is it? Why is it important to understand and what can you do to make sure you can benefit most from it as it enters our space?    They talk about its impact on prevention (yes, we said it), early detection, diagnosis, and even matching treatments based on genetic profiles and biomarkers (blood, tissues, for example). Also, PM may be a solution to capping the high cost of healthcare, which means it's as much of a research issue as a public policy issue.  *All main episodes that air on the 1st Sunday of each month are either Step 2 in our 6 step problem solving process (first time the topic is on the table) OR a Step 5, which is a revisit to the table. In a Step 5, we are ready to take action to solve a problem (create a resource, ask to join a project, etc.) Show Notes: Episode 74 – “EveryONE's Voice Precisely Matters”   00:52 – Tiffany welcomes listeners. 01:12 - Tiffany is a patient living with non-radiographic axial spondyloarthritis. 01:32 - Tiffany is joined by Catherine Ames, a college student living with Lupus. 04:10 - Catherine is here today to represent the Young Patients' Autoimmune Research & Empowerment Alliance which works to include patients age 16-23 in medical research. 08:00 - Catherine and Tiffany met at a conference on Personalized (Precision) Medicine. 08:28 - AiArthritis distinguishes between Personalized Medicine and Precision Medicine because Personalized Medicine is more about patient preference and Precision Medicine is based on biomarkers. 10:01 - The conference they attended was largely dedicated to treatment of cancer more so than treatment of autoimmune disease because cancer treatment really spawned the field of Precision Medicine based on genetic sequencing of excised tumors. 13:07 - AiArthritis and AREA are at the forefront of Precision Medicine research in the autoimmune arena because most experts don't anticipate serious breakthroughs in the immunology sphere with regard to Precision Medicine until 2025 or later. 15:05 - The keynote speaker of the conference talked about the importance of teaching the FDA and other regulatory agencies about innovative research. 17:08 - Early intervention with Precision Medicine could reduce the risk of comorbidities and increase the odds of achieving remission. 18:30 - Precision Medicine is intended to be expanded beyond cancer to other spheres within medical care, but there are access issues within the current healthcare system, especially in the United States. 19:23 - Precision Medicine has the potential to decrease healthcare costs in any system by intervening early to avoid patients developing complicated and expensive conditions. 23:20 - One example of Precision Medicine applications in AiArthritis is the use of biomarkers within RA to predict more aggressive forms of the disease. 24:10 - The reality is that AiArthritis diseases require expensive treatments that impose a significant cost burden on all healthcare systems, but only a minority of patients will respond to any specific treatment. 26:20 - The current practice of trial and error of drugs that have never even been tested in a clinical setting on a specific subgroup of autoimmune patients is wasteful and inefficient. 30:47 - AiArthritis encourages patients to get involved in clinical research by participating in the FORWARD National Databank or via other means. 31:27 - Visit AiArthritis.org/research for more information on how you can get involved in any of our research efforts. 33:33 - The concept of Precision Medicine sounds wonderful, but many patients are facing seemingly insurmountable barriers to access to care that may make them reluctant to participate in data collection efforts that might help move the field along. 38:16 - High costs of healthcare are driving access issues within all healthcare systems, so Precision Medicine should eventually - by way of reducing costs - increase access for all people. 45:18 - If patients could find treatments that better matched their specific conditions, they could improve their quality of life even if their disease is too advanced for remission to be possible. 46:00 - Tiffany and Catherine discuss pharmacogenetics. 49:43 - Pharmacogenetics has the potential to help match patients with the right pharmaceutical therapy based on their genome. 51:12 - Pharmacogenetics also has potential to anticipate drug-related toxicity before a patient develops an adverse reaction. 54:08 - Visit AiArthritis.org/research or aiarthritis.org/advocacy to get involved in promoting Precision Medicine. 55:01 - You can find Catherine @ChronicallyCatherine on social media or email her at chronicallycatherine@gmail.com.  55:35 - Find Young Patients' Area @yp_area on instagram or email them at youngpatientsarea@gmail.com. 56:29 - Tiffany thanks Catherine for her contributions to today's episode. 57:03 - Tiffany invites listeners to participate in any of the ensuing 360its following this episode. 58:12 - If you have something to say about today's episode, email us at podcast@aiarthritis.org or submit an anonymous comment at aiarthritis.org/rant. 58:56 - We are @IFAiArthritis on all social media platforms. 59:10 - Stay tuned for our brand new talk show website that will be premiering soon.   __________________________________________________________________ Patient Voices and All Other Stakeholders - Join our AiArthritis Voices Program and Connect to Opportunities to Have Your Voice Counted If you are a patient, a parent of a juvenile patient, or any other stakeholder (doctor, nurse, researcher, industry representative, or other health services person) - are you ready to join the conversation? It's your turn to pull up a seat. Join our new AiArthritis Voices program, where people living with AiArthritis diseases and other stakeholders who we need 'at the table' to solve problems that impact education, advocacy, and research sign up to have a voice in our initiatives. By signing up, you'll get notified of opportunities to be more involved with this show - including submitting post-episode comments and gaining insider information on future show topics. Patients and all other stakeholders are encouraged to join so we can match you with opportunities to pull up a seat and TOGETHER - as equals - solve the problems of today and tomorrow. JOIN TODAY! AiArthritis Voices 360 is produced by the International Foundation for Autoimmune and Autoinflammatory Arthritis. Visit us on the web at www.aiarthritis.org/talkshow. Find us on Twitter, Instagram, TikTok, or Facebook (@IFAiArthritis) or email us (podcast@aiarthritis.org).  Be sure to check out our top-rated show on Feedspot! 

We are back this week with another autoimmune disorder and this episode is all about different autoimmune connective tissue disorders such as Lupus, scleroderma, and Osler Rendu as just to name a few. Listen to Dr. Nicole as she dives into why some of these disorders manifest in the first place and where do they originate from. She dissects why most of the people suffering from these disorders might not have been able to find a proper solution that is outside of just living on immunosuppressants. Tune in to learn more! Interested in working with IWG? Book a complimentary consult call to learn more using this link: https://bit.ly/IWRcall2022  Noteworthy Time Stamps: 01:34 Why you might resonate with this topic? 05:16 Foundational principle to understanding connective tissue disorders 10:42 Why would the immune system attack the connective tissue? 14:51 A case study 24:47 What is ‘PANDAS' disorder? 29:01 You won't know until you do better testing 30:15 A patient with a 10-year history of Lupus 35:50 You can't always rely on the bloodwork markers 41:37 It's about therapy and acknowledgment 46:05 The biggest myth of autoimmunity

Kayla Stevens is a 27-year-old woman from Atlanta, Georgia. She has a Bachelor of Science in Kinesiology and Health Sciences from the University of Maine, a Master of Health Administration (MHA) from Georgia State University, and she's currently finishing up her Integrative Health Practitioner (IHP) certification. Prior to contracting Lyme disease, Ms. Stevens worked for a local hospital, was known as the “party girl,” and traveled frequently. At the age of 25, Ms. Stevens quickly fell ill from Lyme disease the day after a tick bite with flu-like symptoms and a bullseye rash. Within a week her symptoms rapidly progressed and included severe psychiatric symptoms she'd never before experienced, such as suicidal thoughts, panic attacks, severe depression, a constant feeling as if she were dying, seeing shadows, and feeling schizophrenic. Ms. Stevens went to the Emergency Room (ER) 3 times, saw an infectious disease specialist, rheumatologist, and Lyme literate doctor before she was diagnosed with Lyme disease through IGeneX and muscle testing a few months after getting sick. Her infectious disease doctor said she “couldn't possibly have Lyme disease” while all the ER doctors suggested it was a mental health disorder or Lupus. Ms. Stevens first treated using antibiotics for 16 months in combination with a mix of herbs. She then went on to treat at LymeStop in Idaho for 4 months. If you would like to learn how Lyme disease inspired a western trained medical professional to study and utilize integrative medicine, then tune in now! PS Kelsey Watkins special guest co-hosted this interview with Matt from Tick Boot Camp!

“There are huge tropes around people of color to not look for holistic medicine. And you have to first work through the tropes, the propaganda tropes around people of color and the use of cannabis.” - Christine De La RosaWelcome back to the To Be Blunt podcast! In this episode, Shayda Torabi welcomes Christine De La Rosa, CEO and Co-Founder of The People's Ecosystem. Christine is a well-respected business leader, advocate, and activist. Everything changed after she was diagnosed with lupus, and she shares she was able to take her life back with the help of cannabis. Now, she's committed to opening access to medical cannabis for the chronically ill and providing opportunities for minorities in the industry.[00:01 – 05:40] What the Hell Is Going On With Texas Hemp and Cannabis?[05:41 – 21:08] Using Medicinal Cannabis for Life-Altering Conditions[21:09 – 32:48] Creating Social Equity for Women and People of Color[26:49- 45:42] Challenges in Operating and the Importance of Brand SOPs[45:43 - 55:25] Executing SOPs and Understanding Licensing[55:26 – 1:11:14] Democratizing Access to Funding Through Web 3.0Christine De La Rosa is passionate about the industry that saved her life. At the top of her tech career, she almost died from complications of undiagnosed Lupus. In 2015, she found cannabis as an alternative medicine to treat her lupus. No longer bound to 11 pills a day or monthly infusions, she was inspired by her experience to open The People's Dispensary in 2016, along with her co-founders to help those who most need access to cannabis. Together, they continue to grow their multi-state supply chain footprint and build a fiercely sought-after national social equity model and enterprise now known as The People's Ecosystem and its subsidiaries. She is currently the CEO and National Co-Founder of The People's Ecosystem, Founder & Fund Manager of The People's Group and Founder of CBxShield.Connect with Christine De La Rosa!Visit The People's Ecosystem website and follow them on Instagram, LinkedIn, Facebook, and Twitter.Shayda Torabi has been called one of the most influential Women in WordPress and now she's one of the women leading the cannabis reformation conversation building one of Texas' premier CBD brands. She's currently the CEO and Co-Founder of RESTART CBD, a female-run education first CBD wellness brand. And has formerly held marketing positions at WP Engine and WebDevStudios. Shayda is the host of a podcast for cannabis marketers called To Be Blunt, where she interviews top cannabis brands on their most successful marketing initiatives. When Shayda's not building her cannabiz in Texas, you can find her on the road exploring the best hikes and spots for vegan ice cream. Follow Shayda at @theshaydatorabiKey Quote:“You're constantly in a battle for safe banking, you're constantly in a battle to keep your business open. Know that it's difficult and also wildly rewarding.”  - Christine De La RosaSPONSORSHIP is brought to you by Restart CBD. Check them out for your CBD needsLEAVE A REVIEW + help someone who wants to join me for episodes featuring some serious cannabis industry by sharing this episode or click here to listen to past epRESTART CBD RESTART CBD is an education first CBD wellness brand shipping nationwide. restartcbd.com