Post-Mortem of a Broken Heart

So todayI finally took the leap and publish the short story I have been working on for the few last week.

In a play like form, it is the story of unrequited love, obsession and finding closure on our own; when you still have so much left to say; so many questions unanswered.

You can read for free on: Wattpad

I look forward to reading your comments and writing more story.

Until next time my lovely,


Story cover


How to deal with others emotional labour?

Lately, I have seen a general exhaustion in the different communities; either Fat, Queer, Disabled, Mental Health; in regards to the amount of emotional labour required from writers and activists.

As a social worker, I am trained and have the tools to deal with other people emotional labour on a daily basis, and may be more inclined to do so with my fellow tweeps, let’s call it occupational hazard. However, even to me it can become too much and I have to put the limits I have learned to establish over the years.

This guide is for the well-meaning people who get a lot of request or are dumped emotional labour on them and are unsure how to manage it.

1. You are responsible for the means, not the results.

This is something I tell myself every day, whether I am working with a client or doing emotional labour with a friend or fellow tweep. While we genuinely want to help others with their problems, they are not your problems. You can made recommendations, give advices, refer them to organisations, but whether or not this people use them or not is outside your control. You can’t be held accountable for the results. Which leads be to my second point.

2. People are responsible for their own action; of their own life

You can’t carry the burden for them. Sure, they may be going through a rough patch, difficulties in their professional or personal lives, but the actions they take, or don’t take, is not your responsability. Once this person unloaded on you and you gave them an active listening, advices and supported them, the outcome of the situation is not on your shoulder.

3. Establish clear limits and boundaries

It is very important to establish boundaries and limits upfront when a person unload their labour on you. Tell them what you can and can’t do. Reflect that you are not a professional and might not be equiped to help them adequately. It is okay to refuse to do emotional labour with someone. It requires a lot of energy and knowing your own limits is an healthy behavior. Saying no does not make you a bad person. Don’t let people manipulate you into thinking you failed to help them or you were responsable for something you were not unless previously agreed. By putting clear boundaries, failed expectations and misunderstanding can be avoided. It also decreases the stress on the helper.

4. You cannot save them

And this is a very important point. Professionals of the helping relation field have to remind themselves constantly. We wish we could uplift pain, solve all the problems, stop wars. We are only human with our own set of problems. We are limited by our own knowledge and understanding of the world. While you can empathize with them, the best thing you can do is provide them the tools to find a solution to their problems. IF YOU CAN. It’s okay not to know what to do. The healthiest thing to do would be to be honest with that person and encourage them to seek proper care. People are much more resilient than we think. Sometimes, they just need to be reminded of the obvious.

Now you’re going to ask me; but what if the person is suicidal? What if they kill themselves because I “turned them down”?

5. You do not hold that much power over someone’s life

If you truly believe someone is at an immediate risk of danger to themselves or others, please call the emergency services if you have access to these informations or try to reach someone in their close network. While most people say they are lonely, which is a valid emotion, they still might have some sort of network around them. If you feel someone is using suicidal ideations as a way to get your attention, it may be better to refer them to mental health services and, once again reflect your limitations. You are not responsable if someone decide to take their own life. Unless you encourage them too, but this is another story.

6. Do not carry the burden of others on your shoulders

You have enough as it is. You cannot hold the weight of the world on your shoulder. That person might feel relieve for a moment after dumping their emotional labour on you, but at the end of the day, it is their mind chaos and it belongs to them. Try to distance yourself. Don’t absorb the other person feelings. You may as easily fell down the rabbit hole with them.

7. You can’t pour from an empty cup

While it may be rewarding to do emotional labour with others, it can be extremely psychologically depleting if you are not careful and taking proper care of yourself. It can lead to caregiver’s burnout; with similar symptoms as stress and depression. If after talking with the person you feel depressed, sad, stressed, unwell, guilty. If you notice changes in your eating and sleeping patterns after talking with the person; it may be time to end the relationship and seek proper care for yourself. You have to prioritize your mental health first. You can’t help others if your cup is empty.

Sometimes people are unsatisfied with the solution I propose and may respond: “So there is nothing I can do?”
My answer is always “not quite”. There is always something that can be done, but it may not be something you wanted or expected. Sometimes it’s taking baby steps and some things takes time. We rarely can do grandiose thing to help people, but the smallest change is already an improvement and should be reinforced positively.

Now I know some of these advices may sound cold and harsh. I want to remind everyone that while I believe everyone is genuinely doing their best, being untrained and unequiped to deal with intense emotional labour can lead to change in one own’s mental health and physical state. There are trained professional in your communities eager to help. I will say it again, you cannot save other people. They are responsable for their own actions and decisions and while it may be tempting to want to take over their pain, this will only double the suffering. Empowering people by giving them tools and resources to overcome their problems is the best thing you can do for them and for yourself.

I remain available if people want more detailed tools and approaches to deal with difficult situations. Sensitives people or HSP may be more susceptible to get into those delicate circles. However, I think it can be equally damaging for the other person to receive emotional labour from someone who is not equiped to do so. I am not pointing fingers, I believe most people act from the best of their knowledge, but sometimes, it is not enough.

Encourage them to build a network in their community, it could be community based organisation, health services, local volunteer groups, whatever is best for them. The bigger the safety net the better. Think of yourself as a link in the long chain of this person’s life and problems.

Remember, you are not alone. I am always available.

Until then,

Take care my lovelies

Visibly Invisible Illness

Some say it’s an invisible illness

But I see it everyday as I look in the miror

The rolls, the stretchmarks, the cellulites

All these bites eaten to soothe the pain

To hide this endless void of suffering

Forgetting what hunger fills like, fearing the emptiness.

All this weight I am still wearing as an armor

To shield myself against the harm of the world

I wear the shame and the disgust as another layer of clothing

As I was thought as a little girl, it only flared up since

It may be invisible to others, but it’s the only thing my reflection shows to me

Not the heartwarming smile, the gentle eyes, the compassion to others.

Not the love of those surrounding me, only what is absent, my own.

Focussing on the lack when the rest abounds.

Coming to terms with a body that is scarred, marked by mental illnesses and eating disorder

A body I fail to see its beauty doesn’t make it any less beautiful, desirable, worthy.

A body some would deemed lazy, stupid or ugly.

A body I inflicting more violence than it deserved

By a mind that is invisibly ill to others.

20 years of suffering in silence, invisible to most.

To you, a smiling young woman, with all her life in front of her.

To me, a self-reflection filled with disgust, self-hatred, failing to see what you do.

You tried with all your might. You can’t save me.

But I haven’t given up yet.

Just watch me.

I survived a car crash

Wednesday morning, 7:05 Am. The kind of day where you wished you stayed in bed. On my way to work. I was far from knowing how the next few minutes would change my life forever. This January had been hell, the last day would finish it with a bang.

As I crossed the first street corner away from my house, once the light turned green, I see a car moving forward my way. Anyone that ever lived in a big city knows how cars engaged in the way in a passive-agressive manner as you strut to the other side of the street. I thought it was one of them. I thought the car would stop. Boy was I wrong. This car didn’t stop.


Everything is in slow motion. My mind tumbles as I fall back. I remind myself to stay soft. I try to make sense of what is happening. Why didn’t it stopped? My knees are the first to collide into the car bumper. Then my head hit the hood, breaking my glasses along the way. I fall in a crouched position. For a few seconds, a searing pain through my right knee renders me immobile. I fear a concussion. I can’t move. All this time, I think to myself this is what dying feels like.

Seconds passes, driver exits the car. Ask me if I’m okay. If I can move. With all my might, I stand up and move to the opposite street corner. There is definitely something wrong with my leg. I still fear a concussion. I am in shocked. The driver move their car to the side and join me. They insist on taking me inside their car to avoid the freezing weather, it is -25c, typical winter weather. I refuse. They offer me to take me to the hospital. HELL NO. I won’t sit in your car from hell, I think to myself.

The driver seems as distress as I am. Tears stream down their cheeks. They say they are sorry. That they never saw me. Because my coat is the same color as the road. Grey.

Setting: Beautiful wednesday morning, cold but sunny, no precipitation. A tall 5’7’’ fat woman cross the street. She also wears a green bag, a yellow hat and a checkered grey white and red scarf.

They never saw me. In broad daylight. A fat tall woman in a grey coat. Because of what I wore. Sounds like victim-blaming doesn’t it. Sounds way too familiar. And it worked. I did feel guilty.

After a few minutes, I am the most cold-headed of the two. Adrenaline must have kicked him. I take my phone out. Call the husband. We live one minute away from the accident site. He is coming. He tells me to call the police. I feel like I needed someone validation to do so. All this time, I tell myself I should have taken her license number but I can’t walk to the back of the car, or even move. Thinking straight is hard. Standing is the most I can do at this point.

911. “Yes, I’d like to report an car accident.” The operator ask me if I am okay. I tell her I think so, they will send an ambulance anyway. Thank you. I called the ambulance for my own accident. Irony.

Ambulance arrives. Relief floods over. I painfully walk toward the truck with all my will. They asked me questions. My brain functions at a lowered capacity. I finally start crying, nerves braking out. I apologized profusely. Maybe I overreacted. Reassurances abound. I did the right thing. They take my vital signs, assess the trauma. He talks to me in a soothing voice.

Police arrives. They take my short statement. He looks at my coat and laugh. “It’s daylight” he says. I feel validated. This lone statement makes all the difference. Everything feel surreals. My first ambulance ride. I don’t see much without my glasses, but I feel safe inside, my husband next to me. It’s over, but this day was far from over.

Waiting in the emergency room is my own definition of purgatory. You know when you came in, you never know when, and if, you will exit. At some point, desperation and anxiety take over, they must have forgotten you.

Parked in the waiting room in a wheelchair, I was replaying the last hour in my head. Poor driver. It will be a bad day for them too. What if I had wore a different coat that morning? What if I didn’t assume they would see me crossing the street? I was feeling guilty, blaming myself, looking for ways this could be avoided. I was tired and in pain. I was blind from lack of glasses. I was hyper aware for any signs of concussion. All I wanted was to lay in bed and sleep forever.

But this day, like any day reached to an end and I was discharged. Diagnosis; broken fibula. Leg needs to be straight and kept this way by a zimmer. I was given crutches I have yet to understand how they work.

Since then, other symptoms have emerged but no concussions or other life threatening consequences. I have to sleep on my back and it is incredibly uncomfortable. My knee hurts most of the time. I need assistance for most thing. Going to the bathroom is an incredibly tough chore and I tip my hat to everyone dealing with reduced mobility and bathroom on a daily basis. I am covered with scary bruises.

This accident could have been much worst. I could have died that morning, on that last day of this cold January. I am ever grateful for all the support and love I have received.

This is a life changing moment for me. There will always have a before and an after the accident. I feel different. I see it as an opportunity to grow, to learn and to be grateful of this life I was given.

For the driver, I doubt I will ever know the rest of their story but I wish them luck. I truly believe it was an accident and this person will also live with some consequences for the rest of their life. I do not resent them. I hope they will also grow and learn from this.

In the meantime, I am taking time to heal my physical and psychological wounds, cursing everyday I don’t have new glasses and drinking my usual quantities of coffee.

I blame all of this on the super full blue blood moon. I am a survivor.

Writing this has been for me a cathartic way to clear my head of the events. I do not seek validation or any other type of attention from this. I do not want people to demonize the driver. It helps me make a bit of sense of what happened in those few chaotic minutes that felt like an eternity. I am ever grateful to be alive and well surrounded. I want to give special thanks to everyone that supported me throughout this ordeal, especially my husband, my parents, my family, my friends and all my beloved twitter community.

I am a fraud

Lately, I’ve felt extremely tired. Physically. Mentally. Emotionally. And yesterday I finally put words on something that had been unconsciously bothering me, imposter syndrome. I feel like a fraud, even though I am part of many communities, many labels. I still feel like an outsider trying too hard.

In the writing community, where I have met wonderful people, even some I would call friends, I feel like a fraud. I can’t write anything more than a few tweets and lines here and there. I have a hard time sitting down to write, I fear the white pages, I fear myself. What right do I have to call myself a writer? I have yet to produce anything. Only trails of abandoned novels; ideas and a few short story contests. My words fail me, they sound stupid, they lack depth, personality. I am just one amongst the many. I lost sight of writing for the sole pleasure of doing it and it paralyzes me.

In the disability community, I have a really hard time owning this label. Not because I am ashamed of it, but mostly because most of my struggles are invisible. I am functional enough. I don’t struggle with chronic pain or physically limiting illness. I keep thinking that some have “worst conditions” and I hate myself for thinking this. I also don’t think it’s how the community works, but I have this fear of being called out; for not being enough. The chronic pain is in my mind. I have yet to sleep restfully. I have a degenerative eye disease that was caught early and that in all likeliness, will remain like this. I have other health problems that while bothersome, makes me hard to tailor my place in the disabled community. I feel like a fraud.

In the LGBTQAP+ community, I struggle to own my queer label. I am a cis white woman married to a cis white man. While my sexual preference definitely puts me in the spectrum, it doesn’t change the fact that I am a boring married woman, in a traditional relationship. My marriage is not open. Polyamory is definitely not for me. I am comfortable with my assigned at birth gender. I am in no way marginal and I have a hard time relating to the queer community where everyone looks so cool and beautiful. Perhaps my vision of the community is warped, but I have yet to relate. I feel like a fraud.

In my beloved fat community, while fat and very vocal about our issues, I feel like a fraud. I don’t have a plus size fashion instagram account. I don’t look as pretty or cute or marginal as public figures. I am not as cool as Roxane Gay. I can’t relate to anyone in the community other than by ideas. I am not fearless, I won’t wear a crop top because a) they are fugly and b) I still hate my body. While I preach fat and body acceptance, I failed to internalize these ideas to myself. I wake up every day hating myself, disgusted by my body. I am a fraud.

In the mental health community, I feel alone. It would be presomptuous to say that I am the only one living with said conditions or loneliness, but I fail to find role models or individuals with whom I share a true connexion, that makes me feel understood. While I am a fearless advocate, I still put some of the stigmas on myself. It’s okay for others but not for me. I would dare to say that at some point, everyone in the community feel alone and misunderstood and I dare not pretend I am unique in this regard.

I am tired. I feel the pressure to perform, to please, to impress endlessly. To feel accepted. To have a sense of belonging. Seeking validation. But it’s all ephemeral. I think about changing my self, but it’s only in superficial terms. I doubt having half shaved pink hair and a septum piercing will make me feel magically belonging somewhere.

I seek an ethereal coolness that doesn’t exist.

Where do I belong? I try to take these labels, the communities where I share interests, beliefs and ideas, but at the end of the day, I feel alone and exhausted. I put so much pressure on myself to be someone I am not, someone I wish I could be. Unrealistic expectations weigh me down, but I can’t shut these voices in my head.

I am not looking for solutions or fishing for compliments. I just realize that even though I have nearly reached my 30s, I am still this little girl longing for acceptance and love. Thinking she has to compromise herself to belong somewhere. I may be trying too hard. I may be looking at the wrong places. My vision is probably skewed. But to shut down this mind chaos, with all these voices that reminds me constantly that I am not enough, that I am a fraud, requires a strength I have yet to gain. Today, I can’t fight them, it’ll have to do for now.

Coming out

I wondered for a few weeks now how to present this.

I have known for about two months now, but the diagnosis was confirmed yesterday. It felt like a meat clever on a butcher block.


My name is Catherine, I am 28 years old and I have glaucoma.


A simple yet, fear loaded word.

For those who don’t know, glaucoma is a degenerative eye disease that affects the optical nerve and can lead to a loss of vision including blindness.

As a writer and avid reader, this diagnosis is hard to digest. The idea that at some point in my life, I can lose my sight is frightening. I can lose my windows to the world, what I use to do the things I love the most.

I’m sure most of us have thought at a time or another about what we would do if we were to lose our vision, a fearful idea, but we brush it off. Most of us are born with this privilege. The thought of losing it, like any other privilege, is dreadful.

I can’t brush this off. While unlikely, it is a possible future.

In my case, it is very early onset. I have no loss of vision, since my other eye is compensating. I was lucky enough to have a cautious optometrist who took the extra step to refer me to a specialist, ‘’just in case’’.

This ‘’just in case’’ revealed a case. One that can be treated early on and prevent further damage and loss. I was told not to worry. Easier said than done.

Having a disease that commonly affects the elderly and diabetics made me reflect on my own aging and vulnerability. I feared fatmisia from the doctors, knowing they often put together larger body size with diabetes and high blood pressure. I have none of those, but it’s irrelevant.  I always had a shitty vision, but I never anticipated it would get to this point.

Yesterday, I put anti-glaucoma drops in my right eye for the first time. It is supposed to lessen the pressure in my eye. The thing is, I have normal eye pressure. I had no indicator that it could be glaucoma. Just a bad visual field on the left side of my right eye. I don’t know what this treatment will do.

Regardless, I am grateful my condition was caught early. I am hopeful a treatment might exist to cure this disease before I die. We often assign some diseases and illnesses to elderly. The more I talk to people, the more I realized there is no set age to develop it. I am lucky to live in a country where healthcare is universal.

Still, I am only talking from my own perspective, projecting my own fears, from an abled standpoint. Individuals dealing with partial or total loss of vision can and have full and rich life. People are resilient and if I am ever faced with this reality, I sure will roll with the punches.

I think it is time we open this conversation to end ageism toward diseases and disability. I am a young adult and I have glaucoma. It doesn’t change who I am. And if I ever get to the point where I lose my sight, then I’ll just do erotic audiobook.

The silver lining is that the drops will apparently make my lashes longer. Only on one eye at this time. Oh well.

No matter what your health situation is, your age and the diseases/disabilities you carry, they do not define you. You are a warrior that slay every day. Even when you stay in bed. Stay strong. Take care. Reach out.

Brain fog on head city

My body is betraying me and I feel helpless. I am exhausted. My body hurts. I am physically uncomfortable. My brain feels to big for my head; like it will ooze out from my ears. I don’t usually feel like that and it worries me.

My mental health status has never been a secret. I struggle from chronic depression and anxiety on a moderate to severe level. I don’t think I will ever “heal” from it and testimonies from celebrities who “overcame” their mental illnesses deeply aggravates me. It invalidates my reality. It erases my experience. One that doesn’t have a happy ending. At best, a good enough for now; and I am okay with it. I have an chronic illness that requires treatments and management. It is also invisible. Some days are harder than others, but I know I am not alone with these illnesses.

Until recently, my mental illness stayed in my head, with typical physical symptoms of tiredness and medications side effects.

Lately, my body feels uncomfortable. No amount of sleep will find me rested. I keep waking up from nightmares, a bit lessen by a lot of nighttime medication. I spend most of my spare time sleeping. My body hurts, most likely from oversleeping. I feel hot; cold; groggy. I feel my body has left me down.

Canadian winters are extremely hard on mind and body. Harsher on sensitive people. I also have to remind myself that the past two months have been extremely challenging and stressful; between upcoming emergency relocating from water damages, relationships problems and obsessive thinking.

Perhaps I just need to give myself some time. But I don’t feel I have time to spare anymore. For the first time; I realize how physically challenging mental illnesses can be, having been mostly spare this far. I have never felt this uncomfortable, restless while lethargic at the same time.

I want to write, and see a lot of prolific writers around me, struggling with mental illnesses and I feel like I failed. Why can they do it and not me? Perhaps I am not trying hard enough. Perhaps I let my fears overwhelm me.

But this thick brain fog is leaving me walking in the dark. Struggling to find the words, the ideas, the outlines. Between working and daily life; I am an empty cup. I have nothing else to spill on the hungry paper.

I am lucky to be surrounded with kind, understanding people, who tell me to take care of myself, that it is okay, to take some time. But I feel I stuck at the same place for so long, it makes me sad. I feel so lonely.

I wish I could finish on a positive note but I’m not sure I will ever be a writer. I am uncertain this brain fog and fatigue will ever leave. As a social worker, it is easier to give those advices to others than to ourselves. But today, I don’t want people trying to find solutions, I just want to be heard.

Aces and Aros: More than a card game

Until recently, I have to shamefully admit that I did not know asexuality and aromantic inclination were a possibility. I have to humbly say, it blew my mind. That some individual have little to no inclination to sexuality or romantic relationship was a totally foreign concept to me. Having dedicated most of my life to ponder on the great matters of love and sexuality, it seemed surreal. Why? How? To love and be loved; To desire and be desired were my life purpose. Obviously, I knew about the spectrum but had yet to be confronted with this reality before. I was simply not aware.

On my part, I consider myself on the opposite side of the spectrum. I want it all. Sometimes, it causes problems. I wish I thought less about it. I envy the free space it would liberate in my mind to focus on something else than my emotions, my desire, my feelings. Not to say that those on the other end of the spectrum don’t experience feelings or emotions, but I have a hard time envisioning what it feels like. I can’t help but feeling envious. In my mind, it seems so freeing. I am probably wrong and understand everything badly and please correct me if I do, but liberating one’s mind of such trivial subjects may lead to greater discoveries. Again, some of the greatest writers dedicated their life to write about trivial matters, but in this day in age, it seems we have much more to do than spend days writing poetry to a blond virginal beauty.

I am the type of person that can’t compartiment. I feel intensely most of the time. Sadness, excitement, exaltation, desire, love, hate. I wish I could feel nothing, but I don’t seem to have been programmed this way. The few times I can empty my mind is a time of great distress to me. It feel uncomfortable, suffocating. It seems there is always a million things running at the background of my head at the same time. Focusing is a hard thing to do. I wish I could empty my head just be able to focus on what really matters. Instead, I feel it takes so much place, it creates problems, unnecessary pain and troubles, disassociation, anxiety and depression.

This year, I want to pursue the work to distance myself from my emotions. I know it won’t be easy. I know most of my emotions are valid. But perhaps if I give them time to bloom, they might be something much more positive. Just the thought of taming my intensity makes me anxious, but this intensity also hurts me the most.

I definitely want to educate myself more on asexuality and aromanticism, it might teach me a thing or two about myself, about being a better person to others and how to relate to this big great world.

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