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Вміст надано Two Alpha Gals. Весь вміст подкастів, включаючи епізоди, графіку та описи подкастів, завантажується та надається безпосередньо компанією Two Alpha Gals або його партнером по платформі подкастів. Якщо ви вважаєте, що хтось використовує ваш захищений авторським правом твір без вашого дозволу, ви можете виконати процедуру, описану тут https://uk.player.fm/legal.
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Holding Hope: A Conversation on Healing Through Purpose with Ali, Founder of The Tick Chicks
Manage episode 464047437 series 3383882
Вміст надано Two Alpha Gals. Весь вміст подкастів, включаючи епізоди, графіку та описи подкастів, завантажується та надається безпосередньо компанією Two Alpha Gals або його партнером по платформі подкастів. Якщо ви вважаєте, що хтось використовує ваш захищений авторським правом твір без вашого дозволу, ви можете виконати процедуру, описану тут https://uk.player.fm/legal.
Ali knew something was not right, even when she was told repeatedly, “everything is normal.” Although relentless in her pursuit to find answers, it still took more than six years for her lyme diagnosis. Ali walks us through her journey and how it began by shifting her mindset to show up each day. Her “5 Minute Mindset” inspired her work at The Tick Chicks, a platform built to help others see the light at the end of the tunnel. You won't want to miss this empowering conversation, so tune in now!
Ali, lives in LA with her family and is the founder of the Tick Chicks, a platform where she blogs, hosts The Lyme Time podcast, and offers incredible resources for diagnosing, managing, and healing Lyme disease.
To learn more about the work Ali is doing at the Tick Chicks visit: https://thetickchicks.com/
Find Ali on all social media platforms @thetickchicks
Listen to inspiring stories and interviews on the Lyme Time Podcast
…
continue reading
Ali, lives in LA with her family and is the founder of the Tick Chicks, a platform where she blogs, hosts The Lyme Time podcast, and offers incredible resources for diagnosing, managing, and healing Lyme disease.
To learn more about the work Ali is doing at the Tick Chicks visit: https://thetickchicks.com/
Find Ali on all social media platforms @thetickchicks
Listen to inspiring stories and interviews on the Lyme Time Podcast
72 епізодів
Manage episode 464047437 series 3383882
Вміст надано Two Alpha Gals. Весь вміст подкастів, включаючи епізоди, графіку та описи подкастів, завантажується та надається безпосередньо компанією Two Alpha Gals або його партнером по платформі подкастів. Якщо ви вважаєте, що хтось використовує ваш захищений авторським правом твір без вашого дозволу, ви можете виконати процедуру, описану тут https://uk.player.fm/legal.
Ali knew something was not right, even when she was told repeatedly, “everything is normal.” Although relentless in her pursuit to find answers, it still took more than six years for her lyme diagnosis. Ali walks us through her journey and how it began by shifting her mindset to show up each day. Her “5 Minute Mindset” inspired her work at The Tick Chicks, a platform built to help others see the light at the end of the tunnel. You won't want to miss this empowering conversation, so tune in now!
Ali, lives in LA with her family and is the founder of the Tick Chicks, a platform where she blogs, hosts The Lyme Time podcast, and offers incredible resources for diagnosing, managing, and healing Lyme disease.
To learn more about the work Ali is doing at the Tick Chicks visit: https://thetickchicks.com/
Find Ali on all social media platforms @thetickchicks
Listen to inspiring stories and interviews on the Lyme Time Podcast
…
continue reading
Ali, lives in LA with her family and is the founder of the Tick Chicks, a platform where she blogs, hosts The Lyme Time podcast, and offers incredible resources for diagnosing, managing, and healing Lyme disease.
To learn more about the work Ali is doing at the Tick Chicks visit: https://thetickchicks.com/
Find Ali on all social media platforms @thetickchicks
Listen to inspiring stories and interviews on the Lyme Time Podcast
72 епізодів
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In the Tall Grass

1 Could IBS Be AGS? A Conversation with Gastroenterologist, Dr. Sarah McGill, about the GI-Only Onset of Alpha-Gal Syndrome 24:05
Dr. Sarah McGill, gastroenterologist at the University of North Carolina, identified a pattern in her patients testing positive for alpha-gal syndrome when presenting with only GI symptoms, specifically after eating red meat. In this episode, we talk to Dr. McGill about what led her to start testing her GI patients for alpha-gal syndrome, as well as the guidance she co-authored for the American Gastroenterological Association regarding her findings. Listen now to learn more about Dr. McGill's research and how she's helping to raise awareness of the GI-only onset of AGS. For more information about Dr. McGill's practice or to book an appointment visit: https://www.med.unc.edu/medicine/gi/people/sarah-mcgill-md-msc/ Read Dr. McGill's Guidance Here: https://www.cghjournal.org/article/S1542-3565(23)00040-X/fulltext…
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In the Tall Grass

Tick-borne disease often feels like it takes everything from you. Meghan Bradshaw is no exception. As a healthy 20-something, Meghan’s health suddenly declined. Her journey led her from misdiagnosis to multiple joint replacements, fusions, and physiological and emotional devastation. Rather than sitting back and accepting her illness, Meghan instead chose to use her experience to inspire change. Check out her story and listen in to what she’s doing now! To learn more about the work Meghan is doing visit: https://www.meghanbradshaw.com/ Be sure to follow Meghan on social media platforms @mcbradshaw To learn more about Center For Lyme Action and the 2025 Virtual Fly In visit: https://centerforlymeaction.org/events/ The Alpha-gal Allergen Inclusion Act (HR 9382) In August 2024, Congressman Van Drew introduced H.R. 9382, the Alpha-gal Allergen Inclusion Act (AGAIA). This bill will amend the Federal Food, Drug, and Cosmetic Act to add alpha-gal to the definition of “major food allergen.” If enacted, the bill will require labeling of alpha-gal on packaged foods sold in the U.S. in the same way other top allergens such as milk, eggs, and peanuts are currently labeled. To fill out the two-minute form asking your Representative for support visit: https://alphagalaction.org/take-action-on-the-alpha-gal-allergen-inclusion-act/…
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In the Tall Grass

1 Holding Hope: A Conversation on Healing Through Purpose with Ali, Founder of The Tick Chicks 44:56
Ali knew something was not right, even when she was told repeatedly, “everything is normal.” Although relentless in her pursuit to find answers, it still took more than six years for her lyme diagnosis. Ali walks us through her journey and how it began by shifting her mindset to show up each day. Her “5 Minute Mindset” inspired her work at The Tick Chicks, a platform built to help others see the light at the end of the tunnel. You won't want to miss this empowering conversation, so tune in now! Ali, lives in LA with her family and is the founder of the Tick Chicks, a platform where she blogs, hosts The Lyme Time podcast, and offers incredible resources for diagnosing, managing, and healing Lyme disease. To learn more about the work Ali is doing at the Tick Chicks visit: https://thetickchicks.com/ Find Ali on all social media platforms @thetickchicks Listen to inspiring stories and interviews on the Lyme Time Podcast…
Using your auto-injector is NOT like pulling the pin on a grenade! In this episode, we share our experiences with anaphylaxis and how we let fear cloud our understanding of the relief brought by proper treatment, including epinephrine. Anaphylaxis can be scary, but it doesn’t have to be. Preparation is key. We discuss the steps we take and the tools we have in place for when a reaction hits. Join us for an open conversation on preparing for the worst case scenario. To learn more about allergy & anaphylaxis emergency plans visit FAACT: https://www.foodallergyawareness.org/food-allergy-and-anaphylaxis/what-is-anaphylaxis/allergy-and-anaphylaxis-emergency-plans/…
In this episode, we welcome Amanda Orlando back to the podcast to chat about the Free To Be Me Society’s 2025 retreat, happening April 4-6, 2025 in Toronto, Canada. This year’s retreat focuses on repose: a state of rest, sleep, or tranquility. Amanda shares the inspiration behind the event and explains why the emphasis of the retreat this year is on rest and mental wellbeing. Early bird registration ends January 2, so get your tickets today! https://www.freetobeme.ca/ Learn more about Free to Be Me Events and Amanda at: @EverydayAllergenFree My blog: Everyday Allergen-Free Free To Be Me @FreeToBeMeEvents…
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In the Tall Grass

1 Check Yo Self: A Conversation with Olivia and Steve Abrams, the Father-Daughter Duo Behind TiCK MiTT 49:39
Olivia and Steve Abrams have every reason to hate ticks. After navigating their own battles with Lyme disease, the dynamic duo set out to find a solution to reduce tick exposure. But what started as a personal journey became a mission to help others reduce the risk of tick-borne disease transmission through the development of TiCK MiTT. Tune in now to hear more about the passion and innovation behind Olivia and Steve’s simple, effective tool to remove ticks before they attach! Follow TiCK MiTT on social media @tick.mitt To learn more about TiCK MiTT, tick tips, to purchase your TiCK MiTT and Check Yo Self Merch visit: https://tickmitt.com/ Use code TICKFREE for 10% off your entire order!…
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In the Tall Grass

1 Elijah’s Echo: A Conversation with Thomas Silvera, Co-Founder of the Elijah-Alavi Foundation 1:03:40
1:03:40
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Thomas Silvera and his wife Dina lived through a parent’s worst nightmare when they tragically lost their three-year old son to an allergic reaction at his daycare facility. In this conversation, Thomas shares how they have turned their tragedy into a mission to help save the lives of other food-allergic children across the country through awareness, education, and changing the law. You won't want to miss this inspiring conversation, so tune in now! To learn more about the Elijah-Alavi Foundation visit: https://www.elijahalavifoundation.org/ Follow along on social media @elijahsecho…
It’s that time of year again! And because so many of our holiday traditions revolve around food, we thought we would re-release our Thanksgiving episode. We often feel like we miss out on delicious comfort and tradition due to our alpha-gal restrictions. Not this year, because it’s all about safe foods! In this Holiday Mini, The Gals share some of their favorite Thanksgiving recipes & tips for having a joyful experience. Find some of our favorite holiday recipes on our blog at: https://www.twoalphagals.com/blog/feasting-ag-safe https://www.twoalphagals.com/blog/thanksgiving https://www.twoalphagals.com/blog/comfort-joy…
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In the Tall Grass

1 Moving the Needle: A Conversation with Changemaker Ali Moresco on Moving from Illness to Advocacy 52:00
Ali Moresco didn’t always feel well enough to be the advocate she is now. But her long fight with Lyme Disease inspired her to influence and change the world around her. As founder of Moresco Public Relations and Communications where she marries patient needs with client goals, and her service to various Lyme advocacy groups where she continues to lobby and fundraise, Ali is a champion for healthcare causes. Listen now and be inspired! Follow Ali on social media: @alitmoresco To learn more about the work Ali is doing with Moresco PR visit: https://www.amorescopr.com/ To learn more about Project Lyme visit: https://projectlyme.org/…
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In the Tall Grass

1 Rx Champions: A Conversation with Andrew Mize and Corrie Newman of Debbie's Family Pharmacy 1:04:01
1:04:01
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Pharmacist Andrew Mize and Pharmacy Tech Corrie Newman are making their pharmacy alpha-gal safe. But they aren’t stopping there - they’re on a mission to help other pharmacies do the same. In this episode, we discuss the steps they’re taking to help the AGS community and how they plan to expand that across the country. And you won’t want to miss the wealth of tips they offer for getting your medications safely. Andrew Mize is a pharmacist and owner of Debbie’s Family Pharmacy in Rogers, Arkansas. Corrie Newman also works at Debbie’s Family Pharmacy as Compounding Director and Pharmacy Tech. Andrew and Corrie started to notice an increase in the number of alpha-gal patients needing services at their pharmacy, so they decided to address the rising issue. Learn more about Debbie's Pharmacy at: https://www.debbiesfamilypharmacy.com/ Corrie and Andrew wrote a very informative blog post and created an amazing Alpha-gal Patient Resource for navigating your pharmacy needs safely. Check it out on our website!…
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In the Tall Grass

1 Uncovering Heroes: A Conversation with Dr. Bill Rawls on Owning Your Recovery 1:01:08
1:01:08
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Every good story has a hero and a villain. And a solution. Dr. Bill Rawls is on a mission to get people to become the hero of their own story to reach healing. As a practicing physician, Dr. Rawls noticed that people with chronic illnesses weren’t getting well. So he is using what he learned in his own healing journey to help others own their recovery. If you’re still struggling with chronic illness, this episode is for you! Let Dr. Rawls be your guide to becoming the hero of your story. For over 30 years, Dr. Bill Rawls has dedicated his life to medicine. When a health crisis with chronic Lyme disease abruptly changed his quality of life, he came face to face with the limitations of modern medicine and began to explore the vast possibilities of alternative treatments. Restoring his health through holistic and herbal therapies inspired him to share his revelations on the importance of cellular wellness for defending against microbes and other root causes of illness. Today, he works to bring life and vitality to others as he helps them establish their own paths to wellness through modern herbology. Through his bestselling books, Unlocking Lyme and The Cellular Wellness Solution, Dr. Rawls demonstrates why crucial herbal phytochemicals are key to protecting cellular health and strengthening the body's defense against illness. Dr. Rawls is also the founder of Vital Plan, a holistic health company, where he developed the signature Restore Kit™, an advanced herbal protocol that has helped thousands to reclaim vibrant health. Dr. Rawls is a #1 bestselling author and seasoned speaker and interviewee. With a compassionate approach and an incredible depth of knowledge, Dr. Rawls has a distinct ability to make scientific concepts accessible and enriching for everyone. To learn more about Dr. Bill Rawls visit: https://rawlsmd.com/ Follow Dr. Rawls on social media: @rawlsmd To learn more about Vital Plan visit: https://vitalplan.com/ Follow Vital Plan on social media: @vitalplan…
As Founder of Bundle x Joy, a purpose-driven pet brand that focuses on allergy-friendly products, Jess Berger is on a mission to create a space where everyone is welcome. Jess recognized a need and bravely stepped out of her comfort zone to follow her passion after years in corporate America. In this episode, Jess shares her story of living her purpose, and how she’s helping others - two-legged and four-legged - do the same. Named Pet Age's Women of Influence in 2021, Jess Berger is the fearless founder leading this purpose-driven, next generation brand. After 15 years in the pet industry working with some of the largest pet retailers and manufacturers, Jess found herself disillusioned with the lack of representation, inclusivity and alignment in leadership in the pet space. As a first-generation American Latina, Jess asked herself what it would look like to create a pet company where women could come together and lean on each other to create a diverse network of purpose-driven partnerships to serve pet people today. She quickly left her corporate desk behind to pursue JOY and her purpose in entrepreneurship. Now, Jess is building the brand she wished existed, and personally crafting formulas she believes in to simplify pet nutrition and create more time for joy with our pups. To learn more about Bundle x Joy visit: bundlexjoy.com. Use promo code ALPHAGALS for 25% off your first order at https://bundlexjoy.com/discount/ALPHAGALS Be sure to follow Bundle x Joy on social media @bundlexjoy…
We’re sending you back to the beginning! As we get ready to expand on the work we’ve been doing for the last five years, we invite you to revisit how it all got started. Debbie and Candice went a cumulative 30 years with undiagnosed symptoms that included everything from brain fog to joint pain and GI distress. Hear about the symptoms of alpha-gal syndrome and how they finally discovered the impetus of their misery was a tiny tick.…
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In the Tall Grass

1 Like Mother, Like Daughter: A Conversation with Natalie Nichols on Navigating AGS as a Young Adult 22:37
Peyton Owen and Natalie Nichols have several things in common. They’re both young adults. They both love the outdoors. And they’re both living with AGS AND with mothers who also have AGS. In this episode, our teen contributor Peyton chats with Debbie’s daughter Natalie on what it’s like having AGS in the family and how they’re both managing AGS in high school and college. These young gals speak to the challenges and the wins, and they offer great advice for the newly diagnosed. Their conversation is sure to brighten your day!…
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In the Tall Grass

1 I Believe You: A Conversation with Mandy Irby on Trauma-Informed Care & Living with Alpha-Gal. 1:21:11
1:21:11
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In this conversation, Mandy Irby, Founder and CEO of The Birth Nurse, shares how she shifted the focus of her career as a labor and delivery nurse to a patient-centered, trauma-informed approach. Not only is she fostering healthy relationships and birthing experiences for expectant parents and medical professionals, but she is applying her knowledge to her own life as she navigates alpha-gal syndrome. Mandy’s vulnerability inspired a validating conversation you won’t want to miss! You can find Mandy on all social media platforms @thebirthnurse. To learm more about the trauma-responsive work Mandy does with The Birth Nurse visit: https://mandyirby.com/…
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