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Mantelcellymfoom

Leven met mantelcellymfoom


De inhoud van deze pagina is opgedragen aan patiënten met de diagnose mantelcellymfoom en hun omgeving.

Dit materiaal kwam tot stand door een samenwerking tussen de Belgische vereniging voor Hematologie (Belgian Hematology Society, BHS), de patientenorganisaties Lymfklierkanker Vereniging Vlaanderen vzw (LVV), Hodgkin en non-Hodgkin vzw, Lotuz vzw, vzw SuperNils, Wildgroei vzw, Action Lymphome Wallonie-Bruxelles asbl (ALWB) en Johnson&Johnson.

Wat deze patiëntengids uniek maakt is dat deze vertrekt van de persoonlijke ervaringen en verhalen van lotgenoten en hun omgeving. Hierdoor komen ook onderwerpen zoals nazorg en praktische tips aan bod, en hopen we een antwoord te geven op concrete vragen die de aandoening met zich meebrengt.

Wij hopen van harte dat we met deze gids ons steentje kunnen bijdragen aan begrijpbare informatie over mantelcellymfoom.

Wat vind je in onderstaande gids?

  • Wat is mantelcellymfoom?
  • Diagnose
  • Behandeling
  • Empowerment
  • Mantelzorger
  • Leven met mantelcellymfoom
  • Nuttige links

Benieuwd? Lees de digitale gids hieronder of vraag een gedrukt exemplaar aan bij jouw hematoloog of behandelteam.


Let wel: deze gids is niet bedoeld ter vervanging van deskundig medisch advies, waarvoor je steeds bij je arts en je behandelteam terecht kunt.

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