Resources for glioblastoma care partners
Receiving a GBM diagnosis can be very lonely and frightening. But you are not alone.
Receiving a GBM diagnosis can be very lonely and frightening. But you are not alone.
My Brother Died of Brain Cancer. 20 Years Later, I Had It, Too.
I was told it didn’t run in families. Was it just chance?
We Are Living With Brain Cancer. Here’s How Biden Could Help Us.
Like Beau Biden, we have glioblastoma. It doesn’t get the attention it should.
Margaret writes about her and her husband Glenn’s glioblastoma experience, including becoming activists for better treatment.
The National Brain Tumor Society has good tips on what to expect when having brain surgery, including ideas for care partners. People who receive a glioblastoma diagnosis are usually completely shocked and not prepared, this information may help.
Prof. Richard Scolyer is an Australian pathologist who’s bravely sharing his GBM journey
Our survey showed serious disparities in GBM care across the USA. Let’s tell the country and make change!
We have been collaborating in the UK with a group of brain tumour charities and a non-profit organisation to ensure that patients have timely access to innovative treatments.
Nicola Nuttall writes movingly about her daughter Laura who lived an incredible vivid life even after being diagnosed with glioblastoma.
Glioblastoma Awareness Day: Help us spread the word about GBM.
