Cancer Blogs

Blogging can be a great way to journal your experiences and share with others. Why not create your own cancer journey blog, or have a read of other blogs created by our members?

Unsure how to get started? Take a look at our help pages on blogs. 

  • My journey

    My journey through Stage 2 Hodgkin's Lymphoma
  • Infrared Saunas ???

    Looking for experience and recommendations of infrared Saunas?
  • One Voice

    A place for me to put down my thoughts about my mum and her battle with GBM4.
  • Husband told he has prostate cancer, does not want anyone to know

    Thanks for those who replied to my earlier post. My husband does not want anyone to treat him any different and to keep asking him how he is.At the moment nobody would know as he is still working, feeling and looking fit.
  • Help

    One employee’s husband is diagnosed with stomach cancer. My dear friends, would you like provide us with useful information? On behalf of the patient and his family,
  • Radiotherapy advice, please?

    Has anyone had radiotherapy, during the past year? I was wondering how it was? How did it effect your skin? Did it make you feel tired & sick? Any advice most welcome? Looking forward to chatting on here. Blessings to all.
  • Healthy living

    Healthy living blog guides you to survive from deadliest diseases and help you to take precaution about cancer and other diseases.
  • The road to nowhere

    Hi there, my name is Mick I am 51 and about a month ago I was diagnosed with inoperable Liver Cancer, to top it off I also have Hep C and Cirrhosis. All the best to you all both carers and sufferers alike. Mick
  • Still waiting for radiotherapy dates? Worrying!

    I had my op on 22 October, and have my first radiotherapy session, 27 Dec. I hope it continues, from there? Does anyone know? A friend thinks it may be a few more weeks! Or it will virtually be 3 months.. Any advice appreciated. Blessings, xxxxxx
  • Lynch in London - looking for a GP / medical team / office which actually knows about it

    My dear friend is 32 and has HNPCC PS2. She has had years of doctors misdiagnosing her and even now, when she's been diagnosed with Lynch and has had 19 tumors removed, her GP clinic still don't know anything about the syndrome. Can you help?