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London Portrait and Editorial Artist
Chronically ill published female photographer and retoucher
Let’s talk about Disability and Mental Health
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Displaced. Betrayed. Drowning.

The words written across my body in a shoot with @rega_photography aren’t just for effect. They reflect what it feels like to be disabled in Britain today. With the government’s proposed PIP changes, another lifeline is slipping away. For many, PIP isn’t just financial support, it’s the difference between surviving and living.

The system has always been brutal, forcing us to justify our existence, prove our disabilities, and be scrutinized by assessors with no real medical knowledge. Now, it’s becoming even more inaccessible.

Imagine being told you don’t qualify for help because you can walk a few steps-never mind that doing so might leave you in agony for days. Imagine having POTS, an invisible illness, where standing up could make you faint, but because you can physically move, the system sees no issue. Imagine dealing with seizures, chronic pain, fatigue so debilitating that brushing your hair feels impossible, and still being told you’re “not disabled enough.”

Many of us push through pain and exhaustion to work, desperately trying to meet societal expectations. But it comes at a cost: worsened symptoms, hospital visits, and sometimes complete burnout.

We are exhausted-not just from our conditions, but from fighting to be heard. To be seen. To be valued.

These decisions aren’t just about policy-they’re about people. And right now, the disabled community needs allies more than ever. If you’re able-bodied, check in on your disabled friends. Listen to us. Stand with us. Because this fight is about the kind of society we all want to live in.

#pipcuts #disabilityrights #disabilityawareness #disabled #chronicillness #heds #pots #seizures #invisibledisability #disabledcreative #disabledcommunity #disabilityjustice
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Cupid is here! Are you waiting to be hit by a little bit of love this valentines?
Definitely my favourite self portraits so far even if my body was aching the next day from all the balancing 😂 

Self portraits by me @rega_photography 
Headpiece by @mostoryfairy 
Bow and arrow prop by @sanfelicecaio 
Backdrop is Middle Ages Golden by @clickbackdrops (not including clouds)

[Image Descriptions: A variety of images of Becky (a white woman with long brown hair) in a green and gold corset outfit posing with a bow and arrow up in the clouds.]
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#ShotByRega #RegaRetouch #CupidPhotoShoot #Cupid #Valentines #SelfPortraits #SelfPortraitPhotography #PortraitPhotographer #BowAndArrow #UpInTheClouds #CloudBackdrop #FantasyPhotography Becky (a white woman with long brown hair) in a green and gold corset outfit posing with a bow and arrow up in the clouds. She is posed like she is floating, looking down whilst aiming her bow and arrow.
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Let’s talk seizures… yup, we’re going there! 

Coming up to three years ago, I started having unexplained seizures alongside other symptoms. I was regularly being taken to the hospital, having seized or fainted at university, on the train and sometimes in the middle of roads. I was constantly in danger and terrified to leave the house. I was even asked to leave university, lost a job I loved, and felt like my body was constantly betraying me because it was. My home, my body, was doing anything it could to endanger me - I would dislocate joints when collapsing, wet myself in public and be constantly humiliated by the scene that would no doubt ensue the second I fell.

 I started having to go on the search for answers, finding it very hard to be taken seriously… ‘Everybody faints’, ‘Drink more water’, ‘It’s because you’re underweight’, ‘You’re overweight’, ‘You’re being dramatic’ - these are amongst a few of the nicer things people would say to me. I couldn’t get anybody to listen. My seizures remain the most complex part of my condition and are undiagnosed. 

I have multiple daily convulsive seizures and faint-like seizures, and whilst, with time, I have gotten better at managing them and finding methods to protect myself better, I still am at risk every day. Still, I hope that with time, there will be answers and a solution. 

You may be asking why I am finally sharing this part of my life, and the answer is simple: I so often feel alone in my disability, and the truth is I’m not alone; none of us are alone. There are so many people (including models) who look well but might be suffering from health issues that you can’t see.

I wanted to thank everybody for the overwhelming support - I have had so many people reach out with questions and kindness, and I will continue to do my best to share honestly. 

#model #modellife #modeling #londonmodels #disabledmodel #disabilityawareness #disabilty #hiddendisability #chronicallyill #chronicillnessawareness #chronicillnesses #seizures #seizureawareness
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Hiya, Emily here! 👋🏻

I thought it was time to share a bit more about myself…
I was born and raised in Singapore to a Kiwi mother and an Irish/English father. At 17, I left home and moved to Italy, where I learnt to speak some Italian and fell in love with cooking! Now, I live in London and work as a model. 🇬🇧

I have many hobbies, but honestly I love anything creative or outdoors! 
The go-tos include:
- Yoga
- Dance
- Cooking
- Art

I am disabled! I suffer from Chronic Seizures, Postural Tachycardia Syndrome, Chronic Migraines, and Hypermobile Ehlers Danlos. I will start sharing more about my journey, and all questions are welcome! ❤️‍🩹

I have two beautiful and incredibly talented adopted sisters: @lizzie.massey and @bella_massey 💕 Lizzie and I used to live on a boat together with our three cats! 

On this page, I share my modelling journey and some parts of my chaotic life, and I am going to start sharing my battles with disabilities. 

I would love it if you all stuck around for this crazy journey with me and considered giving me a follow! 

I wish y’all the very best!
Emily 😘

#model #modellife #meetme #londonmodel #disabledmodel #disability #disabilityawareness #modelling #chronicillness #londonmodels #ukmodel
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