Funeral of Judith Schossböck
Anyone who would like to come to the funeral is welcome!
Please register by email at:
info@blackferkstudio.com
or using the contact form on the website:
https://blackferkstudio.com/en/contact/
Other ways to get involved:
For those who cannot come, there is the opportunity to participate in the funeral and/or on a memorial page by leaving a message or a small farewell gift. We will make these messages visible at the funeral and/or later on the memorial page on this website.
Please send gifts and letters to this address (the mailbox will be open from Tuesday, December 17th, 2024):
Postfach 0004
1050 Wien (Vienna)
Austria
It is also possible to send emails to
info@blackferkstudio.com
which we will print and stick in the condolence book.
Please send an email here with the subject “Condolences for Judith”.
Judith Schossböck, Ph.D. – 1981–2024
Content warning: The following text is about serious illness and death.
Dear friends and acquaintances of Judith,
with great sadness but also gratitude, I would like to inform you that my partner Judith Schossböck passed away on December 10th, 2024, in the presence of her loved ones. She leaves behind an abundance of love and connections that we will carry into the world and live in her memory.
Judith’s illness was progressive (very severe ME/CFS, cerebrospinal fluid leak, very severe MCAS, pancreatic disease, hormonal disorders, POTS…) and unfortunately could not be stopped even by the best medical team. Her illness has been steadily worsening since 2021, until in the end there was not much room left. Even the ingestion of water led to massive physical reactions in the last phase, and her limit was already exceeded by drinking or washing or speaking. People in the room were also difficult to bear.
Judith was in a permanent crash at the end, even though her illness was very dynamic at times and she was able to write a lot and kept finding new, beautiful things. Hospital stays were no longer possible, however, and she reacted with severe symptoms and long reactions even to simple electrolyte infusions, temperature changes and harmless odour. She could no longer try medication, which always led to a permanent deterioration of her condition, most recently triggered by liquid and food.
Judith lived an active and full life with a great love for people, science, art and activism, and achieved incredible things even with her serious illness. She completed her dissertation on health activism, founded the Black Ferk Studio with me, and realized various art projects, e.g. the first international exhibition on ME/CFS in the Künstlerhaus Vienna. She used art and activism to help others and contribute to their visibility, and, as an artist, created an impressive number of paintings and drawings, some of which received awards.
She did all of this from her bed. She loved life and people with all her heart and was loved and appreciated by her family and friends. Despite everything, she felt very connected to the world and was committed to achieving something good.
Unfortunately, the unlucky combination of illnesses ultimately left her with no choice. There were simply too many problems that even a creative, intelligent and cheerful person like Judith could not overcome. Until the end, she was fearless and brave and tried not to let her symptoms determine her.
The online communities and the possibility of including people with disabilities were very important to Judith. With this in mind, we will soon provide further information on ways to participate in farewell rituals and celebrations. Everyone is welcome.
The Black Ferk Studio will also live on and continue to realise some of her ideas.
Judith’s words to you:
Until the end, I had the unconditional love of my family and partner as well as my best friends and a community by my side who always found creative ways to include me. We would certainly have thought of many more things if this beast had not been so outrageously progressive. I loved everything so much — about the little world in my bed and the big one out there, about our connections. For example, how I decorated everything here and kept finding creative little things. I am proud of every single one of my pictures and our activities and I carry you all in my heart. Unfortunately, this atypical progression left me no other way, but I also saw this intensive process as an act of love with a lot of understanding and as a gift.
You will find me everywhere in our memories, and in every happy piglet you meet 😉
My life has made a lot of sense to me, from my adventures in faraway countries, to science, to art, and finally activism from bed — I have always been connected to these areas. I feel like I have lived and loved for five or more, thanks in part to you. My life is not a tragic one, because it was full of wonderful things right up to the end, and I hope to have left something good behind and created something beautiful.
Please do not take my story as a reason for less hope: this illness gives most people more opportunities and stability than it did for me. And I had a particularly insidious combination of different illnesses. Above all, a drug sensitivity that is unparalleled.
Celebrate life, enjoy the small and big things: I hope my story can be seen as that of a person who made the best of the cards she was dealt. Thank you so much to my family, my love, my network, everyone I’ve ever been in love with, all my friends. Love as much as you can.
Archive
Body, Illness, Art
A discussion evening organized by @ourbodies.at and @feministische.medizin
5 November 2024, 07:00 to 08:30 pm
Depot, Breite Gasse 3
1070 Vienna
depot.or.at
Video recording of the evening:
https://www.youtube.com/live/882GOkm7Iqk?si=SjJUTgK3kYUp5dvA
There are still too few spaces for us to talk about health and our bodies — especially for people who are affected by various forms of discrimination. Artistic initiatives are finding new, creative ways to take a critical look at the health system: They are educating people about symptoms and illnesses that doctors do not take seriously. In this way, artists are also making a contribution to health communication — to raising awareness about mental illnesses, ME/CFS or endometriosis. Our Bodies presents artists and projects: Why do we need a new feminist health movement?
The Other Life
Performance by Matthias Mollner
31 October, 1 and 2 November 2024, 07:30 pm
ARTIST AT RESORT | TERM 24
Tanz*Hotel | Resort 1020 Studios at Zirkusgasse 35, 1020 Vienna
In his performance, Matthias Mollner deals with the reality of life of chronically seriously ill people who are often invisible or made invisible in society. Based on personal experiences — his partner suffers from a severe form of the multisystem disease ME/CFS — Mollner develops a work that delves into the existential dimension of the topic. The dark sides of life such as suffering, isolation and dying are revealed, as are the strength, dreams and hopes of those affected and their relatives.
Conference “Health without barriers”
17 October 2024
ÖGB Catamaran
Johann-Böhm-Platz 1
1020 Vienna
Conference of the Austrian Disability Council on the topic of “Health without barriers”.
With an exhibition stand from Black Ferk Studio.
Parallel Vienna 2024
Art fair
11 to 15 September 2024
Otto-Wagner-Areal
Pavillon 16
Baumgartner Höhe 1
1140 Vienna
As part of the Parallel art fair we show the work of five artists who deal with the dark side of human existence and address taboo topics such as illness and death. Two of these artists are themselves affected by multisystem diseases such as ME/CFS and work with sometimes severe physical limitations, e.g. bedriddenness or severe neurological symptoms.
Further information about our contributions can be found on the Parallel website. There you can also purchase the exhibited works of art directly online.
30% of proceeds will be donated to ME/CFS research organisations or NGOs.
Artists:
Hazel Hughes
Ernst Miesgang
Matthias Mollner
Judith Schoßböck
Nikolina Žunec
Pictures from left to right:
Judith Schoßböck — Goth Moth, Nikolina Žunec — Wound II, Matthias Mollner — Portrait with cage and fresh air, Ernst Miesgang — Rotting Christ, Hazel Hughes — Switch
Art Lovers for ME/CFS
Charity auction on the occasion of severe ME Day on 8 August
4 to 9 August 2024
All auctions can be found on:
https://www.instagram.com/judyintheskynet/
Pain Portraits
18 February — 29 March 2024
Lutherische Stadtkirche (Lutheran City Church)
Dorotheergasse 18
1010 Vienna
Exhibition: 18 February to 29 March 2024, open daily from 9 a.m. to 6 p.m
Matinee: 18 February 2024, 11:30 a.m. following the service
Workshop and reading: 9 March 2024, 1 p.m. to 5:30 p.m and 6 p.m., Lutheran City Church, Raum der Begegnung (community room)
During the Passion season, the “Pain Portraits” series by the artist Matthias Mollner will be exhibited in the Lutheran City Church in Vienna.
In this picture cycle, Mollner deals with the severe multisystem illness of his partner Judith Schossböck. The program includes a workshop and a reading in which passion and suffering can be reflected in a special way and are allowed to coexist.
Many people with ME/CFS, but also other painful illnesses, report not only the medical but also a humanitarian and spiritual crisis or challenge of their situation, for which our society often lacks the language. The lack of recognition, being overwhelmed by the suffering of others and the often difficult to understand condition of those affected often lead to the suffering being euphemised, blended out or rationalized. The exhibition project understands itself as a counter-idea to these tendencies and invites to take a closer look and create understanding.
Matthias Mollner: Resistive milling
The source material for the “Pain Portraits” are photos that I took of my bedridden partner in several stages in 2021/22. It was important to me to document the situation and, in particular, to show this ambivalent perception that often occurs when looking at people affected by ME/CFS. Who is not connected to any technical devices, has no bandages, prostheses or other medical material on their body, and is not lying in a white hospital or nursing bed cannot be that seriously ill, can they? I wanted to examine this false perception of illness and process it in images.
In 2022, the series of 9 “Pain Portraits” was created, in which I expanded the documentary nature of my photographs into a mental and physical space. The images are photos, paintings and objects; they are flat and three-dimensional at the same time. The “wormholes” milled and cut from chipboard break through a smooth surface. They twist back and forth and stand in contrast to the images as a physical-spatial dissonance. I also cut holes in some of the images that swallowed up parts of the motifs.
Milling is a dusty and slow process that requires sharp tools and a precise hand. In this activity I fight against the resistance of the material and work my way into the depths layer by layer. At the end, these furrows almost come to life and emerge from the picture.
Judith Schossböck: Passionflower thoughts
The three upright stigmas of the passion flower are also interpreted as the nails with which Jesus was nailed to the cross. I take extracts of this flower as medicine, among other things. They help me (unfortunately only very minimally) with neurological states of emergency.
Some experiences associated with ME/CFS are occasionally described by my friends as a kind of spiritual experience. In particular, the extreme condition in which in the severe stage or “crash” one may be too weak to express the suffering itself, and the experience of proximity to death, sometimes require a philosophical or religious orientation.
Looking at my own medical history, I have had several such near-death experiences, and some of them occur regularly. In my brain it feels as if an area that is responsible for pain is inflamed or activated and sometimes as if my mind is leaving my body. In this extreme vulnerability, an out-of-body experience, normal sensations and connections suddenly seem part of the impossible, and our language fails. The pain is then omnipresent, and occasionally universal.
I can only speak from my perspective, but there should actually be tens of thousands of portraits of various people affected hanging in this church. It would not seem strange to me that we would then kneel in awe before these people, but rather appropriate: a corrective mechanism to the usual “treatment” of society or authorities, in which the personal quickly becomes political. Because people with ME/CFS, no matter how peaceful or sleeping they may look in some pictures (warning: appearances are deceiving), are, given their great suffering, among the strongest but most invisible of the world.
Lead by: Matthias Mollner
Date: 9 March 2024, 1 p.m. to 5:30 p.m., Lutheran City Church Vienna, Raum der Begegnung (community room), next to the church
Registration via contact form or E‑mail: info@blackferkstudio.com
Limited number of participants. If required, you can start at a later time.
In this performative workshop, participants will work with the artist to create images on the topic, using images created by both humans and AI.
The results of the workshop are collected and further developed into collage images by Mollner in an artistic process. The perception of those affected, relatives or allies as well as the perspective of outsiders come together in this joint work.
Notes:
- No experience with art, the disease ME/CFS or AI programs is necessary, but you are welcome to bring your own work.
- Drawing and painting utensils and paper are available on site. You can also use your own material.
- Air cleaners are installed in the room.
- FFP2 masks: As some of our participants have a severe neuroimmunological illness or belong to vulnerable groups, masks will be available for free in the room.
Dear Silja. My sister, an unexplored illness, and a death that honors life.
Date and location: 9 March 2024, 6 p.m., Lutheran City Church Vienna, Raum der Begegnung (community room), next to the church
In her book and other texts, Birte Viermann portrays her sister, seriously ill with ME/CFS, from the perspective of a close relative. With a lot of love and openness, but also radical honesty and gentleness, the text deals with the decision of assisted suicide, the experiences and feelings as a carer and relative, but also the “network of love” that Silja left behind after her death.
A portrait of very special people that is not just about ME/CFS, but also openly addresses many things that are worth tracing and thinking about.
Notes:
- Air cleaners are installed in the room.
- FFP2 masks: As some of our visitors have a severe neuroimmunological illness or belong to vulnerable groups, masks will be available for free in the room.
The WE&ME Foundation was founded in 2020 by the Ströck family and is based in Vienna, where the family is known for its “Ströck” bakeries, which have delighted generations with their baked goods.
The Ströck family’s journey has been profoundly influenced by ME/CFS and has shaped the nature and purpose of the WE&ME Foundation with unshakable determination. Two brothers in the family, Christoph and Philipp Ströck, both suffer from ME/CFS.
Over the years, the Ströck family became increasingly aware of the serious deficiencies in social security and support for millions of ME/CFS sufferers. Most patients are on their own when it comes to diagnosis and the necessary support, a situation that often leads to an irreversible deterioration in the patient’s health. In many cases they are unable to return to work or even participate in social life, resulting in a lack of social support. The additional burden on patients and their families due to this cruel disease is unacceptable.
The WE&ME Foundation is committed to funding groundbreaking research that uncovers the complexities of ME/CFS and enables effective treatments and cures.
Link: WE&ME Foundation
When you purchase an image from the Pain Portrait series, 30% of the proceeds will be donated to the WE&ME Foundation’s ME/CFS research projects.
Please send your request via our contact form or E‑mail: info@blackferkstudio.com
Of course, you also have the option of donating directly to the WE&ME Foundation:
www.weandmecfs.org/
Idea: Sabine Hermisson
Concept: Black Ferk Studio (Matthias Mollner and Judith Schossböck)
Organisation:
Marie-Therese Burka, WE&ME Foundation
Sabine Hermisson
Johannes Modeß, Lutheran City Church Vienna
Black Ferk Studio (Matthias Mollner, Judith Schossböck)
Support and Funding:
WE&ME Foundation
Symposium CRASH! on Youtube
The symposium about ME/CFS took place on August 18th as part of our exhibition at Künstlerhaus Factory. You can now find it online on the new Black Ferk Studio Youtube channel.
The event with expert talks, a reading and a performance ist available as full video (divided into chapters), or as single slideshows (for people who can’t watch moving images so well or prefer to read or less visual input).
Subtitles are available in German and English. Please select your language and turn them on or off as needed.
Full Playlist:
https://www.youtube.com/playlist…
Symposium CRASH!
18 August 2023, 7 p.m.
Künstlerhaus Vienna, Factory
Bösendorferstraße 10,
1010 Wien
Moderators:
Univ.-Prof. Dr. Joachim Hermisson and Matthias Mollner
6:30 pm
Admission to the Factory
7:00 – 7:15 pm
Welcoming
Presentation of the project partners:
Austrian Society for ME/CFS,
WE&ME Foundation (previously TEMPI-Foundation)
7:15 – 7:30 pm
Reading Barbara Kaufmann:
Die Verdächtigen (The Suspects)
7:30 – 7:50 pm
Talk Dr. Martin Komenda-Lett:
Beyond Known Structures: ME/CFS as a challenge for medical practice
afterwards Q&A and discussion
8:00 – 8:20 pm
Talk Dr. Jennifer Blauensteiner:
MicroRNAs of Blood Vessels in ME/CFS
afterwards Q&A and discussion
8:30 – 8:45 pm
Break
8:45 – 9:05 pm
Talk Andrea Strohriegl:
Community and Activism: What difference can one make together?
afterwards Q&A and discussion
9:15 – 9:35 pm
Talk DDr. Markus Gole:
Fatigue and Mental Illness: Differential diagnostic ways to ME/CFS
afterwards Q&A and discussion
9:45 – 10:00 pm
Performance Matthias Mollner:
Stop and Go
Further information:
- Free admission to the symposium
- No registration required
- Barrier-free access
- Entrance via the Bösendorferstraße 10 (the backside of the Künstlerhaus/House of Artists)
- Face masks: As many of our participants and visitors have a severe neuroimmunological illness or belong to vulnerable groups, masks will be available for free in the exhibition place.
CRASH!
Exhibition
Künstlerhaus Vienna, Factory
11 to 27 August 2023
Opening: 10 August, 7 p.m.
Curated by BLACK FERK STUDIO
Works by
Christina Baltais, Broken Battery, Ruth Braham, Martine Brandt, Whitney Dafoe, Sibylle Dahrendorf, Faraz Fallahi, Franziska Hannig, Mila and Sabine Hermisson, Hazel Hughes, Sunniva Innstrand, Noli Kat, Matthias Mollner, Renate Mowlam, Martin Keogh aka The Missing Neighbor, Kristine Cornelia Paulsen, Anna Parker, Judith Schossböck, Ilse Sjouke, James Strazza, Olivia, Anil van der Zee
ME/CFS (myalgic encephalomyelitis/chronic fatigue syndrome) is a monster: one that many affected people and their loved ones in Austria and around the world are fighting. A severe and not uncommon multi-system illness, there is no treatment for the root causes nor generally accessible therapy to date. Due to the COVID-19 pandemic and the millions of individuals affected by Post or Long COVID, this often unrecognised and trivialised illness has shifted more into the public awareness.
“Even trying to put on an exhibition with this terror is complete madness,” was one of the thoughts that went through the minds of Judith Schoßböck and Matthias Mollner in autumn 2021, when they came to the decision to translate their experience into art. Expressing their personal stroke of fate as art is a way of processing their experiences and intimate insights into a silent and invisible world lived each day by millions of people who are missing from society (#MillionsMissing), who mobilise their meagre energy reserves for daily survival and recognition. This is an illness that stands in diametric opposition to the commonly accepted ideals of motivation and performance, as simple activities and exertion are punished with a worsening of symptoms.
In this exhibition Mollner, Schoßböck (a.k.a. Black Ferk Studio), and other artists and creatives reflect on the reality of living with ME/CFS. To create art in this context becomes a special activity that is tied to risk, as sufferers of the disease experience physical consequences. The hypersensitivities the illness often causes are further challenges to artistic endeavour and community participation.
The exhibition shows various artistic perspectives together with information on the illness in different contexts: From the personal views of those affected to the standpoint of society, from helplessness to activism, from the isolation of the individual to the collective view, from the emotional experience of perpetual crisis to scientific fact. The exhibition tells stories from the “nightside of life” (as Susan Sontag called illness), provides insight into coping strategies, and seeks to utilise openness and dark-yet-colourful humour to counteract suffering and neglect.
Symposium: 18 August, 7 p.m.
Speakers:
Dr. Jennifer Blauensteiner. ME/CFS Research, FH Joanneum, Graz. DDr. Markus Gole. Psychologist and philosopher, Linz. Barbara Kaufmann. Filmmaker and author, Vienna. Dr. Martin Komenda-Lett. Neurologist and ME/CFS expert, Vienna. Andrea Strohriegl. Community and activism, Vienna
Live performance by Matthias Mollner
Project partners and support:
Österreichische Gesellschaft für ME/CFS
WE&ME Foundation (formerly TEMPI-Stiftung)
Can anybody hear me?
Group Show in the ip.forum
U4 Center, Stiege B, 2. Upper floor
Schönbrunner Straße 218–220
1120 Vienna
Austria
Opening: Thursday, 13 Oktober 2022
Exhibition duration: 13 October to 15 December 2022
Curators: PJ Maguire und Gabriele Baumgartner
In recent years, we’ve all had to abandon or adapt our social habits and interactions, creating a domino effect in our present and future interaction habits.
Artists have also had to adapt in order to be heard or seen and to be able to communicate to the viewers. Art is usually a mouthpiece to communicate issues that move a person in some way. In this exhibition, we ask about the ways artists have created to be „heard“ and how others have taken the path of communication in their artistic work to date.
Congress of the Knowing
9 to 10 September 2022
Public space under the Lentos Art Museum
Doktor-Ernst-Koref-Promenade 1
4020 Linz
Austria
“A burning stone. Why you need to know about ME/CFS”
The Black Ferk Studio is pleased to be present with two installations and a lecture performance at the “Congress of the Knowing” in Linz. All interested people can take part in the congress. Admission is free, registration is requested: https://kdw.institute
On September 9th and 10th, the “Congress of the Knowing” will take place in Linz under the Lentos Art Museum. Knowledgeable people from all over Europe will come together at this magical place to exchange and share secret, special and unique knowledge. Events, debates and performances are open to the public and will take place on both days. The open space under the Lentos hence becomes a form of “democratic knowledge zone” in a public space. People will meet there to exchange knowledge with expertise and experience valuable to others: scientists, artists, performers, researchers and experts in other, special areas: such as people affected by poverty, people with experience of discrimination, socially disadvantaged people, or people whose special knowledge has little public reach. The lectures and audience discussions address current discourses. There is also the opportunity to gain access to complex content in a playful way through workshops and interactive formats.