Nutrição e Canetas Emagrecedoras: comer pouco, porém bem | Evolution 15
from Lipedema Hosted by Letícia Miyamoto, Danilo Dib | Amato Podcast
Neste episódio do Lipedema Talks, gravado no congresso Lipedema Evolution 2026, Letícia Miyamoto conversa com o nutricionista Danilo Dib sobre como se alimentar durante o uso das novas medicações para emagrecimento, os análogos de GLP-1 como Ozempic, Saxenda e Monjaro. Danilo explica que a medicação é uma ferramenta poderosa, mas que o resultado a longo…
Embed this episode
No transcript yet.
Similar podcasts
Lipedema Mamas Podcast
Ashley Fisher & Shawn Bigby
This is a space where we talk all things Lipedema. A place for education, resources, and inspiring personal stories. You are not alone on this journey, and we are thrilled to have you join us!
ليبيديما بالعربي | Lipedema in Arabic
Dina Braiwish
مبادرة ليبيديما بالعربي هي مبادرة توعوية باللغة العربية للتثقيف الصحي عن مرض الوذمة الشحمية أو ما يُعرف بمرض الليبيديما، صاحبة هذه المبادرة دينا ابريوش مصابة بذات المرض، حيث أنشأت صفحات توعوية ومجموعات دعم لمصابات هذا المرض منذ بداية عام 2022، وتقوم بجولات سنوية في فلسطين والأردن والإمارات لعقد لقاءات توعوية وجاهية وتوثيقها، وتجمع السيدات المصابات مع الأطباء والمختصين في تشخيص وعلاج مرض الليبيديما، وتقدم مساحة للمصابات للتعبيرعن أنفسهم ونشر تجاربهم الشخصية والعلاجية مع مرض الليبيديما، وتسعى جاهدةً لتوسعة دائرة التوعية في المجتمعات العربية والتعاون مع المراكز الصحية والأطباء لتقديم المساعدات الطبية والنفسية لمصابات الوذمة الشحمية تستضيف دينا في بودكاست ليبيديما بالعربي عدة أطراف مهمة للحديث عن مرض الليبيديما، حيث تناولت الجانب النفسي، والعلاج الجراحي والعلاج التحفظي لمرض الوذمة الشحمية، والجانب الرياضي وكذلك تجارب شخصية لمصابات الليبيديما (Lipedema in Arabic) initiative has been created by its owner (Dina Braiwish) - who also suffers from Lipedema - for raising awa
Lipedema Link
Don-Ellen Ray
"Lipedema Link" is your essential podcast connecting individuals navigating the challenges of Lipedema. Join host Don-Ellen Ray, a passionate advocate and Lipedema survivor, as she explores this misunderstood condition. Through expert insights, personal stories, and empowering discussions, we provide support, information, and inspiration. Join our community, gain knowledge, and embrace resilience on your Lipedema journey. Tune in for valuable resources, practical tips, and a sense of unity. You are not alone—discover the power of the "Lipedema Link" today!
Living Well with Lipedema Surgery Simplified
Lipedema Simplified
Lipedema, the disease they call fat, is a chronic fat disorder that affects 17 million women in the USA and as many as 350 million women worldwide. It is often mistaken for simple obesity. Generally under-recognized and misdiagnosed, symptoms include pain, swelling, and weight gain disproportionately distributed in the thighs, buttocks, legs, and hips with a smaller upper body. Lipedema fat is resistant to diet and exercise and without intervention, progresses and worsens over time. This flash briefing offers tips, news, and updates with the founder and CEO of Lipedema Simplified, Catherine A. Seo, Ph.D., and guest experts. Please note DISCLAIMER: The information in Living Well with Lipedema - Surgery Simplified is provided for informational and educational purposes only.
Frequently asked questions
How long is this episode of Lipedema?
This episode is 32 minutes long.
When was this Lipedema episode published?
This episode was published on September 16, 2026.
Can I download this Lipedema episode?
Yes. Use the download control on the episode player to save the publisher-provided media file.