Real stories from families affected by Atypical Teratoid/Rhabdoid Tumour, also known as AT/RT or ATRT.
Here you can read personal experiences of diagnosis, treatment and family life following an AT/RT brain tumour diagnosis.
AT/RT is a rare, fast-growing cancer of the brain and central nervous system that most commonly affects young children, although it can occasionally occur in older children and adults. Treatment may include surgery, chemotherapy and radiotherapy, depending on the individual diagnosis and circumstances.
Every family’s experience is different, and these stories are shared to help others feel less alone and better understand the realities of living through an AT/RT diagnosis.
Browse the stories below and hear directly from families affected by AT/RT.
