Daily Life Holly Warland Slowly Dying With Euthanasia

My partner and I have been documenting daily life with a disability through Instagram without the filters and mushy inspo-porn. I’m brutally honest and open with my photos, revealing aspects of disabled life that you don’t often hear about. I’m Holly Warland, a 27-year-old woman from Australia and I have a rare condition called Limb...


Daily Life Holly Warland Slowly Dying With Euthanasia

My partner and I have been documenting daily life with a disability through Instagram without the filters and mushy inspo-porn. I’m brutally honest and open with my photos, revealing aspects of disabled life that you don’t often hear about.

I’m Holly Warland, a 27-year-old woman from Australia and I have a rare condition called Limb Girdle Muscular Dystrophy. My LGMD involves the gradual deterioration of all my muscles from the chin down leaving me predominantly bed bound and reliant on care.

I was diagnosed at 11 but led a mostly typical life with great support from family and friends. I worked hard getting my Bachelors and Honours in Psychology and had planned my life around my doctorate; I wanted to be Dr. Warland by 25. I was halfway through my Ph.D. in neuroscience when I noticed my physical strength diminishing.

In 2016 I had to pull out of my Ph.D. studies as well as give up my beloved teaching job at my university. Every day I began waking up to waves of nausea, a racing pulse, sore muscles, hyperventilation, and uncontrollable shaking. My life was thrown into chaos. As my condition worsened, I found a real lack of true representation of severe disability. It seemed like every social media personality with a disability fell into the category of ‘inspirational’. Worse still, the fitness blogs posting inspo-porn memes of amputees with captions like ‘GET AFTER IT!’ and ‘WHAT’S YOUR EXCUSE?’ Gross.

I couldn’t relate to that, so my partner Luke (who is also my full-time carer and a part-time photo/videographer) and I decided to take some photos of my naked body and post them online so people could see the toll a disability has on the human body. The response I got was encouraging (and relatively non-creepy) and spurred me to share some more of the intimate parts of disabled life.

Most of the photos come with a backstory or a musing on an issue from my crippled point of view. Luke catches me at my best and worst; from fancy dinners to vomiting in the shower, nothing is sugar-coated. I’ve reached thousands of people around the world and have been given the opportunity to advocate for issues close to my heart.

What started as a way for a bored, bed bound cripple to vent her frustrations and clear the air on a few topics has turned into a window for those who may never encounter a fatal disability in the wild.

More info: Instagram

I wanted to show more of this darker and more honest side to disability, so my partner and I have been documenting my daily life

I have a rare condition called Limb Girdle Muscular Dystrophy. It involves the gradual deterioration of all my muscles from the chin down leaving me predominantly bed bound and reliant on care.

I figure if people are going to stare at me, make them laugh. I’ve always tackled things with humor and a sprinkling of pessimism. I know that doesn’t sound healthy, but it’s impossible to feel positive and ‘inspirational’ when you have a degenerative condition with no cure in sight. Things are literally only going to get worse. I wanted to show more of this darker and more honest side to disability.

Luke: a partner, a carer, a cat-wrangler. I’m convinced some philanthropist is paying him millions to make my final years the happiest they can be


This is Luke; my photographer, partner, carer, kitty dad, and all-round incredible human.

He’s the one behind the scenes of every one of these pictures. He never leaves my side, regardless of my mental or physical condition.

I’m convinced some philanthropist is paying him millions to make my final years the happiest they can be. There is no other explanation because look at him. He’s gorgeous, loves cats, and gives great massages.

I love him with all my brain.

I used to be unstoppable. I was halfway through my neuroscience Ph.D. specializing in ASD children’s ability to read facial expressions when my MD exacerbated


Giving a speech at a conference, pre-bodily breakdown.

I’m not humble about my achievements because I feel proud of the obstacles I overcame to achieve what I did


Presenting my Honors thesis (also pre-BB).

I’d present at conferences about my research, be on science panels, teach at my university, and write academic articles.

Now it’s gone. But I’ve realized I stressed my whole life over a piece of paper. I went straight from high school onto 7 years of university. I worked my crippled arse off and now I have no future to use my skills.

It’s hard to let go of your entire life plan but also oddly satisfying.

This photo was taken a few months before everything went downhill


I felt happy and healthy and had the strength to do fun things like go out to dinner or concerts.

As well as dealing with physical problems, I also had to come to terms with my loss of autonomy. I can’t be spontaneous anymore, everything has to be planned. People have to work around me and how my body has decided to feel on any given day.

I used to be well enough for a weekly walk

Now, it’s been long 4 years of hospital visits

My condition is so rare that when I tell the doctors what’s wrong with me, I’m often left with blank stares. It’s not the doctor’s fault, I just feel like every time I am there for treatment I’m also a mini sideshow for the medical students.

This is one of many hospital visits. But due to the freezing temperatures they keep hospitals in I’m better off at home self-medicating. I can’t make my own body heat so you can cover me in blankets but I won’t warm up without an external heat source.

Life in bed is not a dream come true

As aforementioned, I’m basically bed bound. I can get up periodically to go to the toilet or have a shower but it takes a lot of energy and I’m often left gasping for breath. I know living in bed might sound like a dream to some but think about how bored you get after a week at home with the flu and just pretend that’s forever.

When I’m not trying to manage my pain or other physical maladies I’m watching TV, snoozing, or reading. Because of all the medication I’m on, it’s very difficult for me to concentrate so I can’t even keep myself busy with writing or working online. I feel my once alert and task orientated brain is turning to mush.

Even showers can be tiring, but at least no one can see your tears

A shower for me is simultaneously heart racing and relaxing. I sit in a specialized chair and with my right hand can direct the water. It makes my heart race because I’m sitting up using strength to hold my back and neck up. Luckily the glass acts as a head and shoulder rest. But the hot water also relaxes my muscles so it’s not an entirely negative experience.

This has nothing to do with nudity by the way. Luke caught me having a shower rest and figured it’d show another glimpse into the experience that is being Holly with the MD.

At the doctor’s; my second home

I had to have a difficult conversation with my doctor about how I’m petrified of becoming addicted to painkillers but need to increase my dosage due to my dip in strength and mobility now. I shed a few tears and he calmly explained that because of my condition, I was only going to get worse and there’s no possible treatment so I am kind of allowed to become addicted because there’s essentially nothing to lose. Of course he said it in a more professional way, he wasn’t advocating pill addiction!

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