Krebs [be]trifft seltene Erkrankungen episode artwork

EPISODE · Apr 24, 2026 · 32 MIN

Krebs [be]trifft seltene Erkrankungen

from Krebs [be]trifft · host Merck GmbH, Wien

Wie sieht der Diagnoseweg bei der seltenen Erkrankung Neurofibromatose Typ 1 (NF1) aus? Welche Unterstützungsmöglichkeiten helfen Betroffenen und ihren Angehörigen, Herausforderungen besser zu bewältigen? Claas Röhl, Obmann des Vereins NF Kinder, gibt in unserem Podcast persönliche Einblicke in den Alltag mit NF1. Er betont, wie wichtig der gegenseitige Austausch zwischen Betroffenen, Angehörigen und medizinischen Fachpersonal ist. Außerdem erzählt er, warum er NF-Kinder gegründet hat, welche Hürden es auf dem Diagnoseweg gibt und warum Selbsthilfe und Begleitung so wichtig sind. Der Titel ‚Krebs [be]trifft‘ ist eine Hommage an eine Gruppe Menschen, die man nicht einschränken kann, denn Krebs trifft, betrifft und macht betroffen. Alle Interessierten sind deshalb herzlich eingeladen, in die Folgen reinzuhören und teilzunehmen an der Konversation zum Thema Krebs. Für Fragen, Anregungen und Kritik zu unserem Podcast könnt ihr uns jederzeit über die österreichische Webseite der Firma Merck, oder über die e-Mail Adresse [email protected] kontaktieren! www.diagnose-krebs.at , www.merck.at

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Krebs [be]trifft seltene Erkrankungen

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This episode is 32 minutes long.

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This episode was published on April 24, 2026.

What is this episode about?

Wie sieht der Diagnoseweg bei der seltenen Erkrankung Neurofibromatose Typ 1 (NF1) aus? Welche Unterstützungsmöglichkeiten helfen Betroffenen und ihren Angehörigen, Herausforderungen besser zu bewältigen? Claas Röhl, Obmann des Vereins NF Kinder,...

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