{"id":11704,"date":"2025-03-16T17:17:53","date_gmt":"2025-03-16T17:17:53","guid":{"rendered":"https:\/\/mecfs-research.org\/?page_id=11704"},"modified":"2026-04-25T18:29:50","modified_gmt":"2026-04-25T18:29:50","slug":"pm-lemonchallenge-werderbremen-2025-03","status":"publish","type":"page","link":"https:\/\/mecfs-research.org\/en\/press\/press-releases\/pm-lemonchallenge-werderbremen-2025-03\/","title":{"rendered":"2025-03 Pressemeldung Werder Bremen Nachbericht"},"content":{"rendered":"
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Premier League club Werder Bremen supports the #LemonChallengeMECFS<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Bremen, Hamburg, 17 March 2025<\/p>

On the day of the match at Werder Bremen, players and numerous fans bit into lemons on Saturday.<\/strong> With the #LemonChallengeMECFS, they called for more attention to be paid to the serious and often invisible disease ME\/CFS, which also affects many football fans.<\/strong> <\/span><\/p>

On Saturday, Werder Bremen and its fans supported the #LemonChallengeMECFS<\/span><\/a>\u00a0on match day against Borussia M\u00f6nchengladbach, calling for more attention and research for ME\/CFS patients. The players Leonardo Bittencourt, Larissa M\u00fchlhaus, Oliver H\u00fcsing, stadium announcer Arndt Zeigler, as well as numerous fans in front of and inside the sold-out Weser Stadium were there. The match day event was the first ME\/CFS awareness event with the official participation of a Bundesliga club.<\/p>

Stadium visitors were motivated and informed with information stands, posters, flyers and a video in the stadium. Stadium announcer Arndt Zeigler interviewed Joerg Heydecke (founder of the foundation) live in the stadium before the game. Several hundred fans did the #LemonChallengeMECFS on their way to the stadium. The campaign was initiated and supported by the \u2018Empty Stands\u2019 (Instagram profile)<\/a>, an initiative of football fans from many clubs who are patients with ME\/CFS, and the ME\/CFS Research Foundation.<\/p>

The sour faces can be seen on all social media channels and are growing every day. With the #LemonChallengeMECFS, the ME\/CFS Research Foundation has been generating public attention, raising awareness and collecting donations for ME\/CFS research since the end of last year. Since its launch in December, the #LemonChallengeMECFS has generated over 70,000 euros in donations. Many celebrities from the worlds of culture, sport and politics have shown their support with a short video. Among them are Robert Habeck, Heidi Reichinnek, Ricarda Lang, Julia Kl\u00f6ckner and Johannes Rauch (Austrian Minister of Health). The #LemonChallengeMECFS has been going viral on Instagram, Facebook, X, Threads, LinkedIn, YouTube Shorts and TikTok since the end of last year.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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In the sold-out Weser Stadium, Werder Bremen fans demand more ME\/CFS research and draw attention to a patient fan. Use for editorial purposes is free of charge. All rights: ME\/CFS Research Foundation and Empty Stands.<\/figcaption>\n\t\t\t\t\t\t\t\t\t\t<\/figure>\n\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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#LemonChallengeMECFS in front of and inside the Weserstadion. Werder Bremen and many football fans are raising awareness of the severe illness ME\/CFS. Use for editorial purposes free of charge. All rights: ME\/CFS Research Foundation and Empty Stands.<\/figcaption>\n\t\t\t\t\t\t\t\t\t\t<\/figure>\n\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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Football fans with ME\/CFS launch the \u2018Empty Stands\u2019 initiative<\/strong><\/p>

With the claim \u2018Missing in the stands - lost to ME\/CFS\u2019, fans suffering from ME\/CFS founded the \u2018Empty Stands\u2019 initiative. They want to go back to the stadium and cheer on their teams. Football clubs and fans are called upon to support the initiative with actions and donations for education and research on ME\/CFS. In addition to Werder Bremen, other clubs have pledged their support.<\/p>

Fabian Fritz is one of the co-founders of Empty Stands. This is what he says about his life with ME\/CFS: \u00a0\u2018I just check the score on the app. That's all I can physically manage. Unfortunately, activities lasting more than 30 minutes are already too much. When I'm having a good day, I listen to the radio of our active fan scene. But I've only managed that once in the last six months. After that, I had to lie in the dark for two days.\u2019<\/em><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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Research funding for ME\/CFS<\/strong><\/p>

More than 40 million patients worldwide suffer from this severe, often invisible disease. In Germany, it is assumed that over 620,000 people are affected. The bite into the lemon is symbolic of the sensory overload that patients experience \u2013 one of the many symptoms of this severe multisystem illness. So far, little research has been done on ME\/CFS and there is no causal therapy. The donations from the #LemonChallengeMECFS will go entirely towards research funding.<\/p>

Joerg Heydecke, founder and CEO of the ME\/CFS Research Foundation, comments: \u2018We are thrilled and encouraged by the great success of the #LemonChallengeMECFS. We are getting a lot of positive feedback from patients and their families, but also increasingly from celebrities and the general public. With this challenge, we want to draw attention to the medical and social catastrophe of this common but so far under-researched disease. Thanks to everyone who supports the #LemonChallengeMECFS and our work with their actions and donations!\u2019<\/em><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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How to do the #LemonChallengeMECFS<\/strong><\/p>

Nominees are asked to (symbolically) bite into a lemon and to document their reaction to the extreme irritation of the sense of taste on video. Three more people will be nominated for #LemonChallengeMECFS. The campaign is accompanied by an appeal for donations in favour of ME\/CFS research.<\/p>

The ME\/CFS Research Foundation is documenting the campaign on its website, providing instructions and showing selected \u2018best of\u2019 videos:
https:\/\/mecfs-research.org\/lemonchallengemecfs-fussball\/<\/a><\/span><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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Verwendung des Bildmaterials (Teil 1 und Teil 2) f\u00fcr redaktionelle Zwecke honorarfrei. Alle Rechte: ME\/CFS Research Foundation und Empty Stands.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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Press contact<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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Thank you for your interest. Please feel free to contact us, sign up to our press mailing list and subscribe to our newsletter.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\"Petra\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t
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Petra Dohrendorf
e-Mail: presse@mecfs-research.org<\/a><\/span>
phone: +49-179-1419112<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t

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Further information on ME\/CFS, the foundation and current media coverage can be found in the press section of our website: https:\/\/mecfs-research.org\/press\/\u00a0<\/p>

Donation info<\/strong>: https:\/\/mecfs-research.org\/spenden\/<\/a><\/span><\/p>

Donation account<\/strong>: DE35 2004 0000 0628 5316 00 (Commerzbank)<\/p>

ME\/CFS Research Foundation is a non-profit limited liability company and fulfils the statutory requirements according to \u00a7\u00a7 51, 59, 60 and 61 AO (German tax laws). It may issue donation receipts within the meaning of Section 10b of the German Income Tax Act.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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About ME\/CFS Research Foundation<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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The non-profit ME\/CFS Research Foundation, based in Hamburg, funds and supports biomedical research into ME\/CFS (myalgic encephalomyelitis\/chronic fatigue syndrome) and Long COVID. The aim is to develop diagnostic and therapeutic approaches to improve the current inadequate standard of care. The foundation works closely with researchers and ME\/CFS patient organisations.<\/p>

Due to a lack of research to date, there is still no effective treatment for these common and serious multisystemic diseases. The foundation funds research projects, connects researchers, ensures transparency regarding research progress, and provides facts and resources to raise awareness.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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About ME\/CFS (myalgic encephalomyelitis\/chronic fatigue syndrome) and long COVID:<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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ME\/CFS (Myalgic Encephalomyelitis \/ Chronic Fatigue Syndrome) is a chronic, severe multisystemic condition characterised by a wide range of disorders, primarily affecting the nervous and immune systems. ME\/CFS is predominantly post-infectious in origin, including as a consequence of COVID-19. It is the most severe form of Long COVID. People with ME\/CFS experience pronounced physical and cognitive symptoms, a very low quality of life and often a high degree of disability. Between 60 and 75 per cent of all sufferers are unable to work, and many are confined to their homes or beds. The key symptom is severe exercise intolerance with a worsening of symptoms following everyday activities (post-exertional malaise, or PEM for short). Due to the current lack of biomarkers, diagnosing ME\/CFS is only possible through a detailed medical history and multidisciplinary diagnostic process to rule out other conditions. Many doctors lack the necessary expertise. It often takes years for those affected to receive a diagnosis. To date, there is no effective treatment. Adults with ME\/CFS currently have little prospect of recovery and reintegration into working life. The prognosis is better for children and young people, yet long-term absences from school are the norm. For most sufferers, participation in normal life\u2014including work, education, friends, sport, hobbies, etc.\u2014is not possible.<\/p>

In Deutschland lag die Zahl der Menschen, die mit ME\/CFS leben, im Jahr 2025 bei mehr als 657.000. Ein Teil der durch COVID-19 an Long COVID bzw. Post-COVID-Syndrom erkrankten Personen erf\u00fcllt die Diagnosekriterien f\u00fcr ME\/CFS. Bereits vor der COVID-19-Pandemie lebten etwa 400.000 Menschen in Deutschland mit ME\/CFS. Weltweit liegt die Zahl der Betroffenen bei weit \u00fcber 40 Millionen. Die medizinische Versorgungslage der Erkrankten ist ungen\u00fcgend. Oft kommt es zu Fehldiagnosen und daraus resultierenden Folgesch\u00e4den.<\/p>

Die hohe Zahl der Betroffenen ist f\u00fcr alle Bereiche der Versorgung sowie auch \u00f6konomisch, durch den krankheitsbedingten Ausfall von Ausbildungszeit und Arbeitskraft, ein zunehmend kritischer Faktor.<\/p>

All the figures and sources mentioned can be found on our website: https:\/\/mecfs-research.org\/was-ist-me-cfs<\/a><\/span><\/p>

\u00a0<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t<\/div>","protected":false},"excerpt":{"rendered":"

PressEmitteilung Werder Bremen unterst\u00fctzt die #LemonChallengeMECFS Bremen, Hamburg, 17. M\u00e4rz 2025 Zur Spieltagsaktion bei Werder Bremen bissen Spieler und zahlreiche Fans am Samstag in Zitronen. Mit der #LemonChallengeMECFS forderten sie mehr Aufmerksamkeit f\u00fcr die schwere und oft unsichtbare Krankheit ME\/CFS, die auch viele Fussballfans betrifft. Werder Bremen und seine Fans unterst\u00fctzen am Samstag beim Spieltag […]<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":8866,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"_seopress_robots_primary_cat":"","_seopress_titles_title":"","_seopress_titles_desc":"","_seopress_robots_index":"","site-sidebar-layout":"no-sidebar","site-content-layout":"page-builder","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"disabled","ast-breadcrumbs-content":"","ast-featured-img":"disabled","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"class_list":["post-11704","page","type-page","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/mecfs-research.org\/en\/wp-json\/wp\/v2\/pages\/11704","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/mecfs-research.org\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/mecfs-research.org\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/mecfs-research.org\/en\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/mecfs-research.org\/en\/wp-json\/wp\/v2\/comments?post=11704"}],"version-history":[{"count":36,"href":"https:\/\/mecfs-research.org\/en\/wp-json\/wp\/v2\/pages\/11704\/revisions"}],"predecessor-version":[{"id":16860,"href":"https:\/\/mecfs-research.org\/en\/wp-json\/wp\/v2\/pages\/11704\/revisions\/16860"}],"up":[{"embeddable":true,"href":"https:\/\/mecfs-research.org\/en\/wp-json\/wp\/v2\/pages\/8866"}],"wp:attachment":[{"href":"https:\/\/mecfs-research.org\/en\/wp-json\/wp\/v2\/media?parent=11704"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}