Niko Suvisto
@nikosuvisto
Life on hold by severe #MECFS, currently 99% bedbound 🛌 Documenting my life like it is now, advocacy through photography 📷 📍Finland
It’s Severe ME Awareness Week and sleep problems are one of the more significant symptoms of the illness, which in my experience are heightened in the severe stage. Insomnia always reminds me of those darkest moments. 12/12
Insomnia, one of the miserable symptoms of myalgic encephalomyelitis. It causes the time to stand still while every minute feels like an hour. A moment when you think about the what-ifs. Or when you reminisce about the past as there is not much of a future ahead. 1/12 TW: Death #SevereMEAwareness
On Sunday, I shared my most recent blog post that told the story of how I was transferred while having very severe ME. Today, I’d like to share my online exhibition, ‘In the Absence of Light’, which tells my whole story of surviving very severe ME. 1/3 #SevereMEAwarenessWeek
It’s August now and the official Severe ME Awareness Day is the 8th of August. In past years our community has talked about how a single day for severe ME is not enough. 1/5 #SevereME #MECFS #pwME #Photography nikosuvisto.com/this-is-how-...
Part of my morning routine is to drink a glass of water with supplements. Yesterday, I noticed how the light glimmered in the water and reflected off the spoon. The title of this new panoramic project is ‘The Light Only Passes By’, and I chose it for several reasons. 1/3 #MECFS #Photography
Yesterday was my mom’s name day, and a few relatives visited us. I stayed isolated, and my door was kept shut because too much noise makes my symptoms worse. But I did overhear a conversation about my situation. 1/10 #MECFS #pwME #Photography
They have denied all my disability pension and sickness benefit applications. The appeals are denied as well. I’m deemed fully fit for work and made to collect unemployment "benefits". 1/2 nikosuvisto.com/denied-denie... #MECFS #pwME #Photography #Kela #SocialSecurity
This photograph, titled ‘Suffocated’, was my submission to the A Quiet Storm’s online group exhibition ‘Myalgic Encephalomyelitis Kills’, which launched today on the International ME/CFS Awareness Day. 1/10 www.aquietstorm.me/myalgic-ence... #MECFS #Photography #OnlineExhibition
Today is Mother’s Day, and my plan was to write a longer text in honour of my mom, who is my sole caregiver, but I don’t have the energy for that right now. I feel more ill than I usually would. This photograph was taken last week when she came to my room to celebrate Vappu. #Photography #MECFS
Last week my godmother brought me flowers. Image is part of my ongoing self-documentary series ‘Enduring: Life with Severe ME/CFS’.
I basically never post any photos the same day I take them. Mostly because my illness, ME, won’t allow me to do that. But this image is from today. 1/3
All sorts of supplements are often more readily available. The pile of them grows and grows, but their effect to tackle the symptoms is at best hard to judge. 2/4
We try to find hope wherever we can, which often means we try out all sorts of "treatments". There are some (off-label) medications to try, but nothing is guaranteed to work and the risks can be high – if you even have access to them. 1/4 #MECFS #pwME #Photography
I like writing captions for my photographs, but lately my mind has been way too clogged for it. I have managed to take a few images I’d like to share, but I also want to write texts for them as they feel like important topics. 1/5 #MECFS #pwME #Photography
My Easter meal in 2025. I ate alone in my room while others gathered in the dining room, which is right at the other end of our house. 6/6
My mother in our living room during that same Easter photography "trip" in 2024. When my illness was at its most severe I couldn’t even hold a camera. Back then I daydreamt of documenting my mother’s life. 4/6
I think it’s always worth to document whatever's in front of you. However mundane or boring it might feel in that moment there might be a time when those captures become important. 1/6 #MECFS #pwME #Photography
To make matters more complex, I have to travel fully supine, which means only an ambulance or a stretcher taxi can take me anywhere. Or let’s be real—my only destination would be a hospital in an emergency or if a doctor blackmails me to go. 3/7
It’s been exactly two years today since the last time I was outside of my house. Since June 2022, I’ve been outside only a handful of times, and all have been hospital visits. Such was the case two years ago as well. 1/7 #MECFS #pwME #Photography
The only clues of the passage of time are the changing view from your window, how the light plays differently in the corners of your dark room from season to season, or when your loved ones get older.’ The full essay, including all images and captions, can be viewed on my website. 6/6
For two years, I have documented the passage of time through my window. The project has turned into a photo essay, and is now live on my website! A short excerpt from it below: 1/6 nikosuvisto.com/the-time-sta... #MECFS #pwME #PhotoEssay #Photography
If there are flowers in our house, I try to use the opportunity to photograph them. The light in my room is a big problem, and I can’t stay upright for long without my symptoms worsening. So, any close-up or macro work is usually out of the question. #MECFS #Photography #Flowers
Every morning, my mother comes to my room and opens my curtains. I can’t do it myself as I’m 99% bedbound due to severe myalgic encephalomyelitis (ME/CFS). During the winter months, the rays of the morning sun reach my room from the other side of the house. #MECFS #pwME #Photography
Our gallery currently features 8 artists and 9 different exhibitions, with new artist introductions, exhibitions, and blog posts in progress. 5/7
We have finally finished updating our online art gallery into a dark theme! A Quiet Storm showcases art made by people who have experienced severe ME/CFS. Our full statement is below. www.aquietstorm.me #MECFS #pwME #Art #OnlineArtGallery
For some reason, I haven’t photographed the door of my room. Maybe it is because I’m always faced the other way around. 1/5 #Photography #MECFS #pwME
The lifts in the video are from 2015 to 2018. To you, it might look like an average exercise montage. Maybe you think to yourself, ‘He moves well.’ 5/11