🇬🇧 ENGLISH
Hi, I'm Chris – officially Christoph Muth, from Duisburg, Germany.
I'm fighting a progressive, extremely rare neurological multi-system disease.
If it's not treated urgently, it could be fatal.
Update
🚨Official trustee account for donations now available
📌 Please help us by signing the petition:
👉Change.org
💰 Or support our donation campaign:
👉GoFundMe
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🇩🇪 DEUTSCH
Hallo, ich bin Chris – offiziell Christoph Muth aus Duisburg.
Ich kämpfe gegen eine extrem seltene, fortschreitende neurologische Multisystemerkrankung.
Ohne gezielte Hilfe kann sie tödlich verlaufen.
Offizielles Treuhandkonto für Spenden ab sofort verfügbar
✍️ Bitte unterstützt uns mit eurer Unterschrift:
👉Change.org
💰 Oder durch eine Spende:
👉GoFundme
My story
How it all began ✍️
After Accident cold switched from Lexapro 7mg to Cymbalta (DEC. 2022)
Lexapro was taken for far too long. Several attempts were made to phase it out, without success, slow reduction possible, down to 7 mg.
(huge discontinuation symptoms, but no neurological problems with just one drop of
reduction, was well on the way to getting rid of the medication).
Tremor developed directly after switching for the first time, paresthesia immediately, never
under Lexapro/Cipralex .
Stayed on 20 mg Cymbalta until June 2023.
Had tingling, numbness after each dose, areas that tingled repeatedly for a long time
became numb like a layer of ice and it kept moving..
to be continued..
Reports in media about my disease
German TV
https://www.sat1nrw.de/aktuell/mann-leidet-unter-seltener-nervenkrankheit-257029
Online newspaper
https://www.derwesten.de/staedte/duisburg/duisburg-news-krankheit-spende-familie-id301527423.html
Radio Duisburg (German radio station)
Podcast Interview: Jonas Muth on the Dangers of Antidepressants
In this powerful conversation, my son Jonas shares our family’s story: how antidepressants severely damaged my health and led to a rare, complex neurological disease. He explains why urgent international medical help and support are needed.
Apple Podcasts:
Frequently asked questions
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About us
Chris.backtolife
Everyday life with a rare, progressive disease