Episodi

  • Living with Lipoedema: A Warrior's Journey
    Oct 14 2026

    Jill on recognising lipedema, getting diagnosed, and finding a routine that works

    Shelley speaks with Jill about her lipedema journey, from noticing unusual leg size at 12 or 13 to finally getting diagnosed in October 2024. They focus on the practical side of living with lipedema, including pain, swelling, food choices, movement, and the mindset shift that comes with understanding your body better. Jill also shares the tools and routines that help her most, including structured meals, carb cycling, pool work, and simple lymphatic support strategies. The episode is especially useful for anyone looking for realistic, non-extreme ways to manage symptoms day to day.

    • Jill first noticed differences around puberty, especially bigger thighs and legs compared with her friends

    • She says pain has never been her biggest issue, aside from occasional discomfort when she overdoes it

    • Swelling and fluid retention are more noticeable, especially after busy workweeks and lots of steps

    • Jill describes the relief of finally being diagnosed after seeing the documentary Fat Ass and then finding a practitioner nearby

    • She shares the mindset shift from “I have lipedema” to “lipedema doesn’t have me”

    • Food became clearer after diagnosis, especially how sugar, insulin, and portion size affect her body

    • She explains how she uses carb cycling in a flexible, non-restrictive way rather than strict dieting

    • Water exercise and warm pool movement are a major part of her symptom management

    • She talks through her daily support tools, including legs-up-the-wall, moisturising, dry brushing, massage, and the Chelsea Jean gloves

    • Jill and Shelley both emphasise self-compassion, experimentation, and not blaming yourself when one approach doesn’t work

    00:00 - Introducing Jill and the lipedema conversation

    01:29 - First signs something was different at 12 or 13

    01:37 - Jill’s experience with pain and why it has been mild for her

    02:08 - Swelling, fluid retention, and busy-workday management

    03:00 - Getting diagnosed in October 2024 and the relief it brought

    04:41 - Moving from self-blame to better understanding

    05:09 - Food, vegetarian experiments, and why the right approach is individual

    06:34 - Learning from podcasts, books, and expert advice

    07:24 - Why Jill prefers conservative management over surgery

    08:29 - Why water exercise works so well for her body

    09:31 - The story of the sudden belly change around age 30

    10:16 - A parallel story about overdoing it and misunderstanding energy crashes

    12:23 - How Jill currently supports her lipedema day to day

    13:51 - Why insulin is central to her nutrition choices

    14:16 - Resetting sugar addiction with a 90-day no-sugar approach

    15:05 - Eating carbs with protein and avoiding “naked carbs”

    16:14 - What low-carb, medium-carb, and high-carb days look like in practice

    18:38 - Why carb cycling feels less restrictive than it sounds

    19:21 - Jason Fung, insulin resistance, and fasting

    20:18 - Why keto is not Jill’s preferred long-term approach

    21:11 - Tools, supports, and what she uses instead of heavy compression

    22:29 - Building a positive mindset and making daily care feel purposeful

    23:45 - What Jill wishes she knew before diagnosis

    24:28 - Watching the next generation and helping daughters get earlier answers

    Stay connected: Subscribe to The Lipoedema Podcast for education, lived experiences and conversations with health professionals.

    Shelley ⁠https://www.instagram.com/shell_peers

    Tiana

    ⁠https://www.instagram.com/me_and_my_lipoedema⁠

    The Lipoedema Podcast

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    ⁠https://www.instagram.com/the_lipoedema_podcast/⁠

    Facebook

    ⁠https://www.facebook.com/thelipoedemapodcast⁠

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    ⁠https://www.youtube.com/@thelipoedemapodcast⁠

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    22 min
  • Ep. 144 ~ Compression Pumps for Lipoedema
    Oct 7 2026

    Dr Jen Sanderson joins Shelley and Tiana to explain what compression pumps are, how they work, and who can benefit. The conversation focuses on using pumps for lipoedema, lymphedema, post-operative recovery, and sports recovery, with practical guidance on pressure settings, safety, and when to seek professional support. In this episode, Jen also shares why hydration, breathing, and the right sleeve coverage matter just as much as the pump itself. This discussion is especially useful for anyone deciding whether a pump is worth it, how often to use it, and how to make sure it fits their symptoms and treatment plan.

    00:00 - Introduction to the episode and guest

    01:18 - What a compression pump is

    02:06 - Why people use compression pumps

    04:08 - Graduated compression and how pump cycles work

    05:37 - Why therapist guidance matters

    08:31 - Medical pumps versus sports recovery devices

    10:08 - How lipedema and sports recovery differ in pump use

    12:13 - Body areas that can be treated

    12:59 - Why half the body is usually enough at once

    15:26 - Why fluid can shift to the upper body

    16:57 - Deep breathing to help clear the thoracic duct

    19:04 - Daily use versus a few times per week

    23:31 - How to tell if the settings need adjusting

    25:14 - Why pressure must be individualised

    28:28 - Compression pumps before and after surgery

    32:44 - Pregnancy precautions and pressure changes

    34:46 - Conditions and situations where pumps may not be safe

    37:08 - Long-term use and reducing recurrent cellulitis

    39:39 - Where to try a pump

    40:47 - How the rent-to-buy scheme works

    43:38 - How to contact Medirent for questions

    45:17 - Closing thoughts on individualised care

    Learn more about Medi-Rent via their website https://medirent.com.au/

    Hosts on Instagram

    Shelley ⁠https://www.instagram.com/chai_latte_2go

    Tiana

    ⁠https://www.instagram.com/me_and_my_lipoedema⁠

    The Lipoedema Podcast

    Instagram

    ⁠https://www.instagram.com/the_lipoedema_podcast/⁠

    Facebook

    ⁠https://www.facebook.com/thelipoedemapodcast⁠

    YouTube

    ⁠https://www.youtube.com/@thelipoedemapodcast⁠

    Spotify

    ⁠https://open.spotify.com/show/⁠thelipoedemapodcast

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    40 min
  • 143 Rubenesque Lipoedema Clinic
    Sep 30 2026

    In this episode, Charlotte Wolfenden shares her personal journey with lipoedema, her insights on navigating the healthcare system, and the importance of self-advocacy and tailored treatment options for women with lipedema.

    Chapters

    • 00:00 — Introduction to Charlotte Wolfenden and her journey with lipedema

    • 11:04 — Charlotte’s experience with lipedema symptoms and diagnosis

    • 27:44 — The importance of touch-and-feel services for compression garments

    • 59:58 — Charlotte’s surgical experiences and recovery process

    • 77:44 — Seeking help within the medical system and early challenges

    • 72:11 — The significance of self-advocacy and patient empowerment

    • 72:11 — Impact of personal experiences on professional life and clinic creation

    • 55:32 — The influence of social media and misinformation in lipedema awareness

    • 49:58 — Building a specialised clinic for women with lipedema

    • 05:32 — What to expect during a first consultation at the clinic

    • 33:19 — Range of garments and treatment options available

    • 33:19 — Future hopes for lipedema recognition and support

    • 22:13 — Charlotte’s advice for women navigating lipedema

    • 33:19 — Where to find Charlotte and closing remarks

    Hosts on Instagram

    Shelley ⁠https://www.instagram.com/chai_latte_2go

    Tiana

    ⁠https://www.instagram.com/me_and_my_lipoedema⁠

    The Lipoedema Podcast

    Instagram

    ⁠https://www.instagram.com/the_lipoedema_podcast/⁠

    Facebook

    ⁠https://www.facebook.com/thelipoedemapodcast⁠

    YouTube

    ⁠https://www.youtube.com/@thelipoedemapodcast⁠

    Spotify

    ⁠https://open.spotify.com/show/⁠thelipoedemapodcast

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    29 min
  • 142 - Connective Tissue & Lipoedema
    Sep 23 2026

    In this episode, Shell and Tiana explore the complex relationship between lipoedema, connective tissue disorders, and overall health. They discuss the latest research, personal experiences, and practical tips for managing these conditions holistically.

    Chapters

    • 00.00 — Introduction to Connective Tissue and Lipedema

    • 11.04 — Understanding the Impact of Connective Tissue Disorders

    • 44.24 — Research Insights on Fat Cells and Lipedema

    • 58.23 — The Structure of Connective Tissue: Lasagna vs. Spaghetti Analogy

    • 45.26 — Exercise, Inflammation, and Managing Symptoms

    • 18.54 — Personal Experiences with Flare-Ups and Management

    • 45.53 — Hypermobility, EDS, and Connective Tissue Integrity

    • 26.09 — Holistic Health Strategies and Foundation of Wellness

    • 59.38 — Navigating Diagnosis and the Healthcare System

    • 53.11 — Practical Movement Solutions and Lifestyle Adjustments

    • 53.11 — The Power of Gentle Movement and Digestion Benefits

    Hosts on Instagram

    Shelley https://www.instagram.com/chai_latte_2go

    Tiana

    https://www.instagram.com/me_and_my_lipoedema

    The Lipoedema Podcast

    Instagram

    https://www.instagram.com/the_lipoedema_podcast/

    Facebook

    https://www.facebook.com/profile.php?id=61550287043665&mibextid=ZbWKwL

    YouTube

    ⁠https://www.youtube.com/@thelipoedemapodcast⁠

    Spotify

    ⁠https://open.spotify.com/show/⁠thelipoedemapodcast


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    36 min
  • BONUS - 2027 Lipoedema Conference
    Sep 16 2026

    This episode covers the upcoming Lipoedema Australia Conference in 2027, its significance on the global stage, and insights into the Lipoedema World Congress and international collaborations. Hosts Shelley and Tiana share their excitement and details about the event, highlighting its importance for professionals and patients alike.

    00:00 Introduction to the 2027 Lipedema Australia Conference

    01:14 Growth of Lipedema Australia Conferences

    02:00 Global Attention and Recognition

    03:33 Conference Location and Details in Melbourne

    04:11 Potential Venue and Co-location Details

    05:02 International Speakers and Attendees

    06:00 Lipedema World Alliance and Key Figures

    07:29 Research and Medical Discussions at the Congress

    09:20 The Delphi Consensus and International Standards

    12:27 Conference Dates and Final Remarks

    www.lipoedemaaustralia.org.au

    Hosts on Instagram

    Shelley https://www.instagram.com/shell_peers

    Tiana

    https://www.instagram.com/me_and_my_lipoedema

    The Lipoedema Podcast

    Instagram

    https://www.instagram.com/the_lipoedema_podcast/

    Facebook

    https://www.facebook.com/profile.php?id=61550287043665&mibextid=ZbWKwL

    YouTube

    ⁠https://www.youtube.com/@thelipoedemapodcast⁠

    Spotify

    ⁠https://open.spotify.com/show/⁠thelipoedemapodcast

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    14 min
  • Ep 141 ~ The Lipoedema Store
    Sep 9 2026

    Melanie shares her personal journey with lipoedema, her diagnosis, treatment options, and how her experiences led her to create the Lipoedema Store to support others. This episode offers insights into managing lipoedema and the importance of community and accessible resources.

    00:00 — Introducing Mel Metheringham and the Lipoedema Store

    00:45 — Mel’s long road to diagnosis and years of self-blame

    02:11 — Finding the right clinic and finally getting answers

    03:31 — Lipoedema throughout the body, not just the legs

    04:23 — Pain, inflammation, migraines, and alcohol as a trigger

    05:47 — Why non-scale victories matter more than the number

    06:03 — Questioning whether lipoedema is real and dealing with judgment

    08:07 — Regret, alcohol, and wondering what could have been different

    09:28 — Water, scuba diving, and movement as part of mobility

    10:54 — The overwhelm of diagnosis, compression, and expensive tools

    13:21 — Grieving the body you thought you would have

    14:40 — Letting go of waiting for a smaller future

    15:22 — Why Mel created the Lipoedema Store

    17:31 — Making support feel realistic, accessible, and pressure-free

    18:49 — Choosing products she has actually used and trusted

    19:58 — Facebook groups, surgeon recommendations, and compression that fits

    20:36 — Arm liposuction in Cyprus and the emotional reality of surgery

    21:05 — Life-changing results in everyday tasks like laundry

    21:54 — Future surgery plans, finances, and taking things slowly

    23:12 — Reducing overwhelm for people living with lipoedema

    24:49 — How missed MLD massages affected Mel’s symptoms

    25:45 — Mindset, flare-ups, and not punishing yourself

    26:39 — Remembering what helps when symptoms return

    27:41 — Missing a lymphopress only after it was gone

    29:14 — Future plans for professional programs and more products

    30:38 — Where to find the Lipoedema Store

    Find out more about The Lipoedema Store here: https://thelipoedemastore.com/

    Hosts on Instagram

    Shelley ⁠https://www.instagram.com/chai_latte_2go

    Tiana

    ⁠https://www.instagram.com/me_and_my_lipoedema⁠

    The Lipoedema Podcast

    Instagram

    ⁠https://www.instagram.com/the_lipoedema_podcast/⁠

    Facebook

    ⁠https://www.facebook.com/thelipoedemapodcast⁠

    YouTube

    ⁠https://www.youtube.com/@thelipoedemapodcast⁠

    Spotify

    ⁠https://open.spotify.com/show/⁠thelipoedemapodcast


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    30 min
  • Ep. 140 ~ Compression with Haddenham Australia
    Sep 2 2026

    In this episode, we explore the latest in compression therapy with Haddenham Healthcare, focusing on their innovative products designed for lipoedema and other conditions. Learn about their clinically led approach, product customisation, and upcoming innovations like their new pump.

    Chapters

    • 0:00 — Introduction to Haddenham Healthcare and their focus on compression

    • 3:13 — How clinical feedback shapes product innovation

    • 5:26 — Global reach and manufacturing details of Haddenham products

    • 8:13 — Choosing the right garment for lipoedema: key considerations

    • 9:44 — Differences in compression needs for lipoedema versus lymphedema

    • 12:05 — Features and benefits of the Comfy Wave garment

    • 14:07 — Importance of skin-friendly fabrics and garment care tips

    • 16:44 — Introduction to the upcoming portable pump for lipoedema

    • 20:27 — Adapting garments for other conditions like POTS and venous insufficiency

    • 25:05 — The overlap of conditions and the need for versatile garments

    • 29:44 — Future innovations and the evolution of compression therapy

    • 30:63 — Details about the new pump and its features

    • 37:30 — Supporting skin health and garment maintenance tips

    • 38:66 — Accessing products and the importance of trained therapists

    https://hadhealth.com.au/

    https://lymphshop.com.au/

    Hosts on Instagram

    Shelley ⁠https://www.instagram.com/chai_latte_2go

    Tiana

    ⁠https://www.instagram.com/me_and_my_lipoedema⁠

    The Lipoedema Podcast

    Instagram

    ⁠https://www.instagram.com/the_lipoedema_podcast/⁠

    Facebook

    ⁠https://www.facebook.com/thelipoedemapodcast⁠

    YouTube

    ⁠https://www.youtube.com/@thelipoedemapodcast⁠

    Spotify

    ⁠https://open.spotify.com/show/⁠thelipoedemapodcast

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    30 min
  • Ep 139 ~ Supporting recovery post-op with Laura Hamilton
    Aug 26 2026

    In this episode, Laura Hamilton shares her personal journey with lipoedema, recent surgeries, and innovative post-surgical recovery modalities. She emphasises the importance of self-advocacy, choosing the right medical team, and practical recovery strategies for lipoedema patients.

    Chapters

    00:00 Introduction and guest background

    49:57:34 Laura's recent surgery and recovery update

    197:11:01 Laura's journey with lipedema and weight loss

    3638:51:08 Insights on lipedema surgery and timing

    6333:17:57 The importance of surgical planning and sequencing

    7055:31:19 Post-surgical scars and healing

    9277:44:44 Pre-surgical preparation and managing lipedema fat

    11055:31:31 Advice on choosing the right surgeon

    13972:11:40 Recognising and advocating for complications

    16444:25:05 Self-advocacy in post-surgical care

    22611:05:19 Modalities used in recovery: taping, laser, and more

    29972:12:26 Success stories and patient outcomes

    373055:32:48 The role of support systems and self-care

    422499:59:41 Laura's clinic and online platform

    489722:13:18 Practical tips for compression garment selection

    Find Laura’s services here: www.elegancecare.com.au

    Hosts on Instagram

    Shelley ⁠https://www.instagram.com/chai_latte_2go

    Tiana

    ⁠https://www.instagram.com/me_and_my_lipoedema⁠

    The Lipoedema Podcast

    Instagram

    ⁠https://www.instagram.com/the_lipoedema_podcast/⁠

    Facebook

    ⁠https://www.facebook.com/thelipoedemapodcast⁠

    YouTube

    ⁠https://www.youtube.com/@thelipoedemapodcast⁠

    Spotify

    ⁠https://open.spotify.com/show/⁠thelipoedemapodcast


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    31 min