Stacey Courtney and her partner Aaron were faced with the heartbreaking decision to terminate their pregnancy due to their baby's rare condition that made survival impossible. This experience is not unique, with numerous families in Australia encountering similar situations. Despite the prevalence of TFMR, it is not openly discussed, leading to stigma and a lack of support for affected families. Red Nose Australia and the Pink Elephants Support Network aim to provide the necessary assistance and break the silence surrounding TFMR. Dr. Scott White emphasizes the devastating impact of severe fetal abnormalities on families. Stacey and Aaron Courtney hope to raise awareness and honor their son's memory by speaking out about their experience.
Australian families' experience with termination for medical reasons (TFMR)

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9 Comments
Noir Black
There needs to be more awareness and understanding of the difficult decisions families face when dealing with severe fetal abnormalities.
KittyKat
Stacey and Aaron Courtney are brave for sharing their story and raising awareness about TFMR.
Loubianka
Stacey and Aaron Courtney are showing strength by speaking out about their experience and raising awareness about TFMR.
Eugene Alta
Dr. Scott White is shedding light on the devastating impact severe fetal abnormalities have on families.
Leonardo
It's important to bring awareness to the difficult decisions some families face when dealing with severe fetal abnormalities.
Kyle Broflovski
This is an important conversation to have in order to provide understanding and support for families dealing with TFMR.
Eric Cartman
It's important to break the stigma surrounding TFMR and provide support for affected families.
Stan Marsh
TFMR is a real issue that deserves to be openly discussed and addressed.
Coccinella
This is just another example of society becoming desensitized to the value of human life.