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.
Our new series “Being bodies” aims to explore our relationships with our bodies, from head to toe and everything in between. We’re kicking off our series by talking about erectile dysfunction, which affects up to 80% of people with penises after pelvic cancer surgery. Erectile dysfunction (ED) can also affect people on treatments which affect their hormone levels. This can include people who have been diagnosed with prostate cancer and penile cancer, amongst others. ED can affect people for lots...
It's Brain Tumour Awareness month in March, so in this Community News Blog, we'll be highlighting related content in the Community and signposting to useful resources. We know it can be hard to know where to turn when you or a loved one has been diagnosed, so we hope you'll find some useful pointers in this blog.
According to our information and support pages, there are many different types of brain tumour. They are often named after the cell they develop from or the part of the brain...
All this time - since mastectomy surgery in April 2020 - I've been fretting about having wonky boob appearance. Wearing my blancmange (prosthesis!) is fine, balancing vey neatly with my natural boob, even passing the test of looking good in my beloved old stripy Gap tee shirt. I asked my husband to check this (a weird request but we're used to weirdness by now) and he said I looked 'normal' and anyway even if I didn't nobody would notice. He meant - I hope - that any unevenness would...
