Embodying Hope

Embodying Hope Embodiment is political. Recovery is messy. Hope is radical. Embodying Hope is a recovery space rooted in narrative therapy, lived experience & body liberation.

26/11/2025

It’s abt how you respond to the feelings that matters. If hating your body leads you to starving, compulsively exercising, binge eating, purging, missing events with friends, avoiding outings, not wearing what you want to wear, and other things that basically keep you out of life, then that’s a problem. But the problem isn’t the body hatred itself, it’s the actions in response to it. You can hate your body AND still decide to go to class. Hate your body and wear the dress you thought was cute. Hate your body and go to the beach.

Believe me, I know this isn’t easy. That voice is SO loud. But I really thought I had to wait for that voice to get quieter before I could start to do things I wanted and start to feel better. And that’s not how it works. Slowly (and I do mean S-L-O-W-L-Y) by doing life while hating my body, that voice started to get a little quieter and show up a little less.

It’s still there and makes appearances. And yes, I am recovered. And yes, I still can hate my body. Maybe not all the time. But I also have a lot of practice at living my life in a body that I may not love, but is allowing me to live in a life I do.

If you like what you read and would like to work with me or chat more, or perhaps something I said resonated and you are struggling with body hatred and can’t imagine how to live life more fully in the face of that body hatred, reach out! I have space for a few new clients as we move into the holiday season.

bodyimageissues

If you know a teen who’s struggling with food or body image, this group gives them a supportive space to talk about the ...
26/11/2025

If you know a teen who’s struggling with food or body image, this group gives them a supportive space to talk about the real-life pressures they face — school stress, friendships, identity, family dynamics, social media, and the constant “be this / look like that” messaging everywhere they turn.

Over 8 weeks, teens will learn grounding tools, build confidence, and feel less alone through meaningful peer connection — all within a HAES-aligned, inclusive, neuroaffirming approach. 💛

Tuesdays | Dec 2 – Feb 3
5:00–6:00 PM PST | Ages 13–18
Signup link: https://bit.ly/teenedgrp
(Link in bio)

If you’re supporting a teen who’s struggling with food or body image, they don’t have to navigate it alone.This 8-week T...
25/11/2025

If you’re supporting a teen who’s struggling with food or body image, they don’t have to navigate it alone.

This 8-week Teen Food & Body Image Group creates a supportive space to talk about school stress, friendships, family dynamics, identity, and the pressure of social media + diet culture — all within a HAES-aligned, neuroaffirming approach.

Teens will learn grounding tools, build confidence, and connect with peers who understand their experiences.

📅 Starts Dec 2 (break Dec 23 + 30)
📍 Virtual
👥 Ages 13–18 (high school)

Details + signup: https://bit.ly/teenedgrp

23/10/2025

Did you know, one of the hardest things about having an invisible disability…is that it doesn’t look like anything’s wrong.

People see me out here walking my dog or smiling and assume I’m fine.

But what they don’t see are the flare-ups, the fatigue, or the mental gymnastics it takes just to get through the day.

So if you’re out here doing life with an invisible illness — I see you.

You’re not faking being sick. You’re fighting to live fully. 💛

It’s Invisible Disabilities Week — let’s make the unseen visible.

15/10/2025

Did you know they call Glossopharyngeal Neuralgia “the su***de disease”. This is because the pain is so severe and, for some (like myself) it’s constant and unrelenting.

Glossopharyngeal Neuralgia (GPN) is caused by a compression of the 9th cranial nerve. I was lucky enough to actually have 4 cranial nerves compressed, but since my pain started with the Glossopharyngeal nerve pain, and was the hardest to get help and a diagnosis for, I speak abt it the most.

This is a very rare disease. Most doctors and medical professionals have not even heard of it.

Living with a rare disease is challenging. I adjust a lot of my life to try and mitigate the symptoms. One of the big ones post-surgery that has remained is come wind.

Cold wind, barometric temperature changes, spicy food, sugary foods, are just some of the things that can trigger or exhaserbate the pain.

After 5 years in windy San Francisco I made the move to SE Queensland (the Sunshine Coast). It’s hard to put to words how much this has improved my quality of life.

Stay tuned for more info on living with this rare disease, my path to a diagnosis, and what it means to be a recovered eating disorder professional navigating this journey

Do these statements feel all too familiar? 👉 A new diagnosis or chronic illness has increased anxiety about food & eatin...
30/09/2025

Do these statements feel all too familiar?
👉 A new diagnosis or chronic illness has increased anxiety about food & eating
👉 You’ve been recommended to eliminate certain foods to help reduce symptoms, and you worry this will lead to a relapse in your recovery
👉 You’re stuck between doing what is best for your body and honoring your mental health
👉 You find it difficult to make peace with your body when you feel betrayed by yours
👉 You’re tired of being accused of not “really being sick”
👉 Your life has become an endless rotation of doctors appointments, tests, and hospitals, and with that, there comes an increased focus on “health” and exposure to numbers that is becoming triggering?

If so, then this group is for YOU 🙌

Join us in an 8 week online therapy group, SupportED Spoonies, for those navigating eating disorder recovery while living with a chronic health condition/disability.

🗓️ Mondays, Oct 7th- Nov 25
🕛 5pm - 6pm PST
📍 Online via Zoom
🤝 Adults 18+

Meet others who may validate, encourage, and understand your experiences. In this compassionate and inclusive space, we hold the belief that all bodies are good bodies, while also acknowledging and addressing the personal and structural challenges of illness and disability.

This group will provide discussions around:
💛 Disability justice, Accessibility, & Medical Advocacy
💙 Coping Mechanisms, Self-Care Strategies, & Medical Management
💚 Accommodations and Adaptations for lifestyle and ED treatment
❤️ Relationships and Social Support
🧡 and much more…

Rooted in , principles, , and affirmative of folks across the gender and sexuality spectra. We are committed to justice and strive to create an environment where everyone feels seen, valued, and supported.

It is EXHAUSTING living with chronic illness and then navigating eating disorder recovery on top of that. Join a space with others who get it and you never need to justify your experience.

Sign ups open!
For more information or to register please complete the registration form bit.ly/SSgrp

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Sunshine Coast, QLD

Opening Hours

Tuesday 9am - 7pm
Wednesday 9am - 7pm
Thursday 9am - 7pm
Friday 9am - 7pm

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