News from Germany


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“It’s as if she were lying in a coffin”: Daughter Nele (22) has ME/CFS​

Nele (22) has been bedridden since May due to her ME/CFS. Her mother, Doreen Schmidt, cares for her around the clock, pushing herself to the point of exhaustion. She is now planning a specialized shared living arrangement for people affected by the disease.​




Doreen Schmidt works as a physiotherapist at Schön Klinik Bad Bramstedt and is familiar with a wide range of medical conditions. But caring for her own daughter around the clock is pushing her to her limits. “I myself have started having panic attacks and anxiety. This is about my daughter.” Caring for someone with ME/CFS is particularly challenging, she says. Even the slightest stimulus—a scent or a sound—can be too much for Nele.

She has already contacted residential care facilities, but they turned Nele down. She is either considered too young, or the facilities are not sufficiently familiar with ME/CFS. “There simply isn’t a proper medical care concept yet,” she says. Many people do not know how to deal with the illness.

And yet Doreen Schmidt cannot help but ask herself: What will happen if she can no longer care for her daughter? In order not to be broken by this seemingly hopeless situation, she has come up with a plan. Her vision is to establish a specialized assisted shared living arrangement in the Bad Bramstedt or Neumünster area for people with ME/CFS.

She envisions an apartment with three or four rooms. Instead of constantly changing home-care providers, dedicated assistants would provide round-the-clock care. Each resident would have their own room, protected from the others’ presence and stimuli, while still not being alone. “This is meant to be my appeal. Is there anyone else caring for a relative and looking for a compassionate solution?”

Families affected by ME/CFS experience every day how helpless the healthcare system is in responding to the disease, Doreen Schmidt says. “It’s a catastrophe. There is no one to guide us through this.” Some doctors are quick to dismiss the physical illness as psychological or simply brush patients off. “Parents are crying out for help because they can’t even find a family doctor anymore who is willing to care for their sick child.”
 




Demand for Legal Advice from the VdK Social Association on the Rise
Sascha Peter has multiple sclerosis and suffers from severe sleep disorders as a result. However, his application for rehabilitation was summarily rejected on the grounds that it was not medically necessary.​
Nearly One-Quarter Increase in Legal Consultations
His case is one of nearly 5,000 cases in which the social law advisory service of the VdK Social Association provided support in 2025. According to the VdK, more than half of these proceedings were successful, as in Sascha Peter’s case. Last year, the social association says it secured more than five million euros in back payments and pension entitlements.​
The demand for legal advice has increased by almost a quarter since 2020. “We are noticing that the waiting times for consultation appointments with us are getting longer and longer,” says Peter Springborn, Managing Director of the VdK’s state office.​
Additional Advice Center Planned
The organization now intends to take measures to counter this trend. Around the turn of the year, it is hoped that an additional office can be opened.​
“At the moment, we have six social advisory centers distributed across the entire Saarland. A seventh, virtual center will be added,” Springborn says.​
The virtual advice center is scheduled to offer additional telephone consultations with specialists starting in January. Video consultations are also expected to be introduced in the foreseeable future.​


 

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Everyone in the Family Has ME/CFS: When an Entire Family Disappears from Everyday Life

The ME/CFS Kids Mobile visits patients who are barely able to leave their homes. The *Abendblatt* was able to accompany the team on one of its visits.​




This is the life of a father who worked for Airbus for 23 years. The life of a mother who loved her job as a childcare worker. And the life of a daughter who liked horses and loved playing outdoors. Today, there are three beds in the middle of the family’s living room: one for the mother, Enrike; one for her husband, Marco; and one for their eight-year-old daughter, Nele. All three are seriously ill. All three have ME/CFS.

On this Friday afternoon in August, the father, mother, and daughter have managed to make it from their beds to the dining table. They have carefully rationed their energy to do so. The visitors they have been waiting for have arrived: the ME/CFS Kids Mobile.

Since February, multidisciplinary teams have been travelling from their headquarters in Hamburg-Eppendorf to the homes of children who are so seriously ill that even making the journey to a doctor’s office can be too much for them. So far, the project has been financed entirely through donations. The team is now caring for more than 60 families in Hamburg and the surrounding area. The S. family is one of the particularly severe cases, because here it is not “just” the child who is ill—the parents are affected as well.

Today, the S. family does not have to go anywhere to receive help. There is no difficult journey to the car, no waiting room, and no conversation in which they have to explain everything all over again. Instead, paediatrician Sönke Siefert and Kirsten Mainzer, co-founder of the Kids Mobile, are sitting with them in the place that was once the central setting of the family’s life: the dining table.

Is there a medical explanation for why three members of the S. family have become so seriously ill? Siefert shrugs. “No, there isn’t,” he says.

Then he adds something that says a great deal about the idea behind the Kids Mobile: “That isn’t decisive for our work, either. Most people affected already have more than enough to deal with in terms of doubt and pressure. We are here first of all to listen, and then to organise help wherever it is most urgently needed.”

The team therefore focuses on what is possible—on the practical adjustments that can be made in everyday life. Sometimes a family needs help applying for an assistive device. Sometimes it needs nutritional counselling because a child no longer has the strength to eat. Sometimes someone has to speak with a school, daycare centre, or youth welfare office. That is why the team includes not only doctors and nursing professionals, but also psychosocial support staff, nutritional counsellors, a social services team, and music therapists.

And sometimes helping also means warning families about something. Precisely because there is no curative treatment, families are particularly vulnerable to promises, Siefert says. Part of his job is therefore to advise against procedures whose potential harm is greater than their possible benefit. Above all, however, the team tries not to focus exclusively on the sick child.


The ME/CFS Kids Mobile Needs Support

The idea for the ME/CFS Kids Mobile arose from the Hamburg Outpatient Paediatric Care Network (KVN). Since February 2026, the project has been supporting seriously ill children and adolescents, as well as their families, through medical, nursing, and psychosocial assistance in the home. Its aim is to provide early training, advice, and support for affected young people and their family members who provide care, thereby sustainably improving the care situation at home.

So far, the Kids Mobile has been financed entirely through donations. After initial hopes of finding a quick solution, the health insurance funds announced at the beginning of 2026 that they would not cover the project’s costs for the time being. As things currently stand, there is still no solution in sight.

The care provided to date has been made possible thanks to the Holistic Health Institute, *Ein Herz für Kinder*, *Hamburg macht Kinder gesund*, and the Blunk Foundation. The ME/CFS Kids Mobile depends on donations. Anyone wishing to support the project can do so using the following bank details:

IBAN: DE66 2019 0003 0009 2495 08
BIC: GENODEF1HH2,
Betreff: KinderVersorgungsNetz Hamburg
 

From Bettina Grande‘s Psychotherapie-Netzwerk ME/CFS.

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For a differentiated, respectful, and factually appropriate approach to people with ME/CFS​

Regarding the Joint Statement from Healthcare and Academia​
Endorsed by more than 30 signatories from the fields of medicine, psychotherapy, and academia.​
Published on 15 September 2026.​




Joint Statement from Healthcare and Academia

In Support of a Differentiated, Respectful, and Factually Appropriate Approach to People with ME/CFS​

In our medical, psychotherapeutic, and/or scientific work, we regularly encounter people with ME/CFS who are living in an exceptionally challenging situation. Most are severely restricted by their illness in their independence, social participation, and ability to pursue their professional and private lives. At the same time, only limited therapeutic options are currently available. Adequate healthcare structures are still largely lacking, and all too often people affected by the disease are, in practical terms, left to cope with their severe illness largely on their own by our healthcare system.

Against this background in particular, in our clinical and/or scientific work we frequently experience a high degree of gratitude and appreciation from people with ME/CFS for reliable support, careful diagnostic assessment, and an approach that fully recognizes and takes into account their individual limits of exertion as well as the often devastating extent of the limitations caused by their illness. Many people affected also have a strong interest in professional and scientific matters. They closely follow developments in research, engage thoughtfully with new findings, and often themselves devote what little energy they have left to improving healthcare, public awareness, and research.

Our shared experience is that the vast majority of people affected approach medical, therapeutic, and scientific questions in a constructive, reflective, and solution-oriented manner. Many contribute their own experiences in ways that provide important additional insights for healthcare and research. As medical and psychotherapeutic practitioners or scientists, we can benefit from this wealth of experience. Particularly in view of an illness that remains insufficiently understood and the existing deficiencies in healthcare provision, the perspective of those affected can be of considerable value.

As in any other patient population, there may of course occasionally be difficult or conflictual encounters involving people with ME/CFS. In our experience, however, such situations are neither characteristic of this patient population nor more frequent than in other medical contexts. Individual negative experiences must therefore never be generalized or used as the basis for attributing particular characteristics to an entire group.

Against this background, we are particularly concerned by portrayals that characterize people with ME/CFS as having a “combative and accusatory tone,” emphasize “aggressiveness” among affected individuals as a characteristic problem, or otherwise frame this patient population as generally “difficult.” Such sweeping statements turn individual negative experiences into a purported distinctive feature of this patient population, even though our experience in clinical practice and research provides no basis for such a characterization. Such portrayals can foster unwarranted mistrust of people with the disease, encourage the premature psychologization of physical symptoms, and contribute to medical concerns not being assessed without prejudice. In this way, they further impede the already inadequate healthcare available to people with ME/CFS.

We therefore strongly advocate for differentiated, respectful, and factually appropriate language, as well as a corresponding attitude toward this patient population. Both are essential prerequisites for trusting and effective healthcare and for constructive scientific collaboration.


The undersigned listed below support this statement in their personal capacity. Information regarding their professional roles and institutional affiliations is provided solely for professional context; it does not imply endorsement of the statement by the institutions named.

Dr. med. Christoph Bammer
Specialist in Internal Medicine and Nephrology; PAIS Clinic, BKH Kufstein.

Dr. med. Michaela Bauer
Specialist in Psychiatry and Psychotherapy (FMH); private practice, Bern.

Dr. med. Judith Bellmann-Strobl
Specialist in Neurology; Head of PAIS/Post-COVID Clinic; Senior Physician, Neuroimmunology Outpatient Clinic, Experimental and Clinical Research Center (ECRC), Charité – Universitätsmedizin Berlin and Max Delbrück Center for Molecular Medicine (MDC).

Dr. med. Anna Brock
Specialist in Internal Medicine; PAIS Practice Brock, Erbach; Charité Fatigue Center, Charité – Universitätsmedizin Berlin.

Ronja Büchner, M.Sc.
Psychologist and Research Associate; Faculty of Medicine, Leipzig University.

Dr. med. Monika Dräger
Physician, lecturer, and author specializing in ME/CFS, Long COVID, and PAIS; Dr. Lindner Medical Practice, Berlin.

PD Dr. rer. nat. Laura Froehlich
Acting Professor of Social Psychology; Faculty of Psychology, FernUniversität in Hagen.

Prof. Dr. med. Patrick Gerner
Specialist in Pediatrics and Adolescent Medicine; Chief Physician, Department of Pediatrics and Adolescent Medicine; Ortenau Klinikum Offenburg.

Dr. med. Christian Gogoll
Specialist in Internal Medicine and Pulmonology; Head of the Long COVID Network of the Association of Statutory Health Insurance Physicians (KV) Berlin; Lungen-MVZ Weißensee, Johannesstift Diakonie, Berlin.

Dipl.-Psych. Bettina Grande
Psychological Psychotherapist; Charité – Universitätsmedizin Berlin; Board Member, Psychotherapie-Netzwerk ME/CFS e.V.

Dr. Dipl.-Psych. Tilman Grande
Psychological Psychotherapist; Charité – Universitätsmedizin Berlin; Board Member, Psychotherapie-Netzwerk ME/CFS e.V.

Dr. med. Isabelle Greber
Physician in private practice, Dr. Isabelle Greber Medical Practice, Boppard-Buchholz.

Dr. med. Lotte Habermann-Horstmeier, MPH, MSc
Director, Villingen Institute of Public Health, Villingen-Schwenningen.

Univ.-Prof. Dr. med. Kathryn Hoffmann, MPH
Head of the Department of Primary Care Medicine, Center for Public Health; Medical University of Vienna.

Prof. Dr. med. Dr. phil. Martina King
Full Professor of Medical Humanities; Faculty of Science and Medicine, University of Fribourg/Switzerland.

Prof. Dr. rer. soc. Eva-Maria Klinkisch
Catholic University of Applied Sciences Freiburg.

Prof. Dr. Vivienne Matthies-Boon
Head of the Department of Ethics and Political Philosophy; Radboud University, Nijmegen.

Dr. med. Julia Möbius
Specialist in Internal Medicine; Diamedikum, Potsdam.

Prof. Dr. Bhupesh K. Prusty
Associate Professor, Institute of Microbiology and Virology, Rīga Stradiņš University, Riga.

Dr. med. Herbert Renz-Polster
Specialist in Pediatrics and Adolescent Medicine, Vogt.

Dr. med. Wolfgang Ries
Specialist in Internal Medicine, Nephrology, Angiology, and Internal Intensive Care Medicine; Dr. Wolfgang Ries Medical Practice, Handewitt.

Dr. med. Claudia Schilling
Specialist in Psychiatry and Psychotherapy; Specialist in Neurology; Sleep Medicine; Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, Mannheim.

Prof. Dr. med. Georg Schomerus
Specialist in Psychiatry and Psychotherapy; Director, Department and Outpatient Department of Psychiatry and Psychotherapy, Leipzig University Hospital.

Ann-Kristin Specht, M.A.
Sociologist; Weber-Bartz-Papendieck Group Practice, Long-/Post-COVID Anchor Center Rhineland-Palatinate, Koblenz.

Univ.-Prof. Dr. med. Dr. h.c. Jürgen Michael Steinacker
Specialist in Internal Medicine, Cardiology, Sports Medicine, and Rehabilitation Medicine; Institute for Rehabilitation Medicine Research, Ulm University.

Dr. med. Michael Stingl
Specialist in Neurology, CerePrax – Practice for Neurology & Psychology, Vienna.

Dr. med. Maja Strasser
Specialist in Neurology, Neurology Practice, Solothurn.

Jesko Streeck
Diploma-qualified Physiotherapist, lecturer, and professional textbook author; Osteofit Practice, Alzey.

Dipl.-Sozialpäd. Philipp Theis
Child and Adolescent Psychotherapist; Munich Chronic Fatigue Center for Young People (MCFC), TUM University Hospital Rechts der Isar, Munich.

Dr. med. Astrid Weber
Specialist in Internal Medicine and Psychotherapy; Weber-Bartz-PapendieckGroup Practice, Long/Post-COVID AnchorCenter Rhineland-Palatinate, Koblenz.

Dr. med. Andreas Weiß
Specialist in Anesthesiology and Emergency Medicine, Oberreute.

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