#SelfDocumentary
It has been one year since I started sharing more openly about my life with severe ME/CFS. I chose to do it through my photography, resulting in my ongoing series ‘Enduring: Life with Severe ME/CFS’. 1/10

#MECFS #pwME #Photography #SelfDocumentary
October 21, 2025 at 7:22 AM
In need of some rest.

Last Saturday, I drank an alcohol-free beer, listened to music, and sat upright (in my hospital bed) for about 30 minutes. And now, because of that, I have PEM (post-exertional malaise, a hallmark symptom of ME/CFS). 1/8

#pwME #MECFS #SelfDocumentary #Photography
April 7, 2025 at 3:11 PM
POV: You are bedbound and need a wash.

I haven’t had a shower yet this year, which feels a bit surreal, if I’m being honest. I could do it, but it just isn’t worth suffering so much, as it would trigger a huge PEM (post-exertional malaise). 1/2

#MECFS #Photography #SelfDocumentary
August 13, 2025 at 2:07 PM
Today, in the morning, a few bright rays of sunshine managed to reach my darkened room. It’s almost as if the sun is reluctant to show itself in this part of the ”world”. 1/5

#MECFS #pwME #selfdocumentary #photography
January 4, 2025 at 3:49 PM
I’ve not posted here for a while now. I’ve not felt good this summer, and I still don’t. Opportunities for self-portraits or meaningful photos have been mostly absent.

Although I did took this one earlier, and wrote some words.

#MECFS #pwME #Photography #SelfDocumentary #Enduring
July 28, 2025 at 3:53 PM
Last summer I lost some of my baseline. It was because LDA started to become less effective. It’s my primary medication and the one that keeps my head above the water. A small increase in its dosage helped me to gain some of that baseline back. 1/3

#MECFS #pwME #photography #selfdocumentary
February 3, 2025 at 3:52 PM
I’ve not been doing that great this summer. In all honesty, these past years have been extremely hard, and my body has given up on me. In the end, I’m just grateful I’m still here to experience life. 1/8

#MECFS #pwME #Photography #SelfDocumentary
August 18, 2025 at 6:40 AM
Good Night

Every night this routine of ours is the same: when everything is done for the day, my mother closes my room’s door, so I can go to sleep. I can’t close the door myself, I can’t just leavy my bed like that. 1/3

#pwME #MEcfs #selfdocumentary #photography
November 28, 2024 at 6:57 PM
Lately, I’ve started using hearing protection again while resting—it helps me reach a deeper state of rest. 1/9

#MECFS #pwME #Photography #SelfDocumentary
April 24, 2025 at 4:21 PM
I’m fortuned that I’ve help from my mother. We’ve come up with other solutions to keep me clean. Once every two weeks we do a more thorough cleaning in bed. We wash my body and my hair. 3/5

#photography #selfdocumentary
December 15, 2024 at 8:28 AM
New year, huh? I don’t know what to think about that. These ”milestones” are nowadays just strange, as you are chronically ill. The passage of time is cruel, as you rot in bed and you feel like your life is wasted away. 1/10

#MECFS #pwME #selfdocumentary #photography
December 31, 2024 at 4:04 PM
I haven’t seen most of the rooms in our house for years now, although I live inside one 24/7. They might as well be on the other side of the world.

I’m imprisoned by my own body.

Part of my series ‘Enduring: Life with Severe ME/CFS’. 2/2

#MECFS #pwME #Photography #SelfDocumentary
June 1, 2025 at 7:36 AM
I feel numb all the time. You have to detach yourself from the reality because it’s too painful to live like this. ME/CFS does this to you—it makes you feel empty. 1/9

#MECFS #pwME #photography #selfdocumentary
January 14, 2025 at 1:00 PM
A rare photograph outside of my room.

Part of my series ‘Enduring: Life with Severe ME/CFS’.

#Photography #SelfDocumentary #MECFS
May 25, 2025 at 7:15 AM
It’s ME/CFS Awareness Month, and I wonder — what is life?
According to Wikipedia, life consists of these seven traits ⬇️

1/10
@openmedf.bsky.social @lowenergylounge.bsky.social
#Photography
#SelfDocumentary
#MECFS
#MECFSis
#pwME
May 2, 2025 at 6:55 PM
Yet Another Thing I’ve Lost

Usually once a month we cut my hair. I used to have a long hair for a couple of years. I started to grow it when I still had a mild #MECFS and I tried to maintain a somewhat normal life. 1/7

#pwME #selfdocumentary #photography
December 1, 2024 at 4:37 PM
I hope that one day there will be more light than dark, for all of us.

All photographs part of my series ‘Enduring: Life with Severe ME/CFS’. 2/2

#Photography #MECFS #pwME #SelfDocumentary
August 31, 2025 at 7:31 AM
This week it was time for a refreshing cleanup. I made a short video about it.

As I’m a severe #pwME I can’t shower much. So the cleaning has to be done in a different way.

I can trim my beard, but for the rest of it I need some help from my mom - she’s my caregiver.

#selfdocumentary #MECFS
January 26, 2025 at 8:15 AM