Lymphoma Net - Home

Sostegnando la gente con linfoma non-Hodgkin

 
Mail a friend Print this page
 Home page >> Testimonianze dei pazienti - Cheryl
  Home page
  Cos’è il linfoma non Hodgkin ?
  L’assistenza clinica ai pazienti
  Come trattare il linfoma non Hodgkin
  Convivere con il linfoma non Hodgkin
 
Cambiamenti dello stile di vita
Vivere in modo sano con il LNH
Testimonianze dei pazienti
Dove e come trovare supporto
Per i caregiver

  Notizie in inglese



  Glossario
  Webmasters
  Comitato redazionale
  Aiuto
  Contatto
  Mappa del sito
  Abbonarsi al bollettino in inglese
  Altre lingue

 
 Testimonianze dei pazienti - Cheryl
Back to patient stories | Comparte tu historia

 

Cheryl, a hard-working manager and mum, is slowly coming to terms with the emotional journey that can follow an NHL diagnosis

'After a great weekend of pottering in the garden, I woke up on Monday morning with a stiff arm. By Thursday I felt a lump in my armpit, so I headed off to the doctors, convinced that I must have pulled a muscle. After all, I had heard that cancerous lumps don't hurt. My doctor suggested an ultrasound and also informed me that it was possible that a sample of the lump might need to be taken, a biopsy.

'On Friday I was at the hairdressers at 8.30 am for a quick trim before heading off to work. The phone call came from my doctor: lymphoma had been diagnosed. After seeing the oncologist, stage 2, large, diffuse cell NHL was confirmed, chemotherapy was mentioned and, somewhere in his discussions, was something about radiotherapy. I don't remember much about that day or the Succesivo 6 months.

'Chemo and radiotherapy have successfully treated the disease, but it is the emotional journey that no-one prepared me for. Waiting for the Succesivo 3-monthly check up, hoping that the disease has not returned, has been really difficult, and not just for me. No-one is game enough to mention the events from last year.

'But here I am a year later, trying to get my life back in some sort of order. I am back at work, although I have to reduce my hours. The journey has left me really tired: I now find that most days I need a "nanna nap" just to Aiuto me get through the normal evenings and activities of family life.

'So how do I cope? I try to avoid being alone. I get up every morning and prepare my "happy face" (make up). One day soon I hope to feel like one of the lucky ones.'

Share your story with others on lymphoma-net.org