Black and white photo of a happy family, two adults and a young girl with Down syndrome, sharing a moment of affection outdoors. There is a transparent purple and white logo overlay with an illustrated girl and DNA strand design, and text reading "Saving Sasha from SLC6A1."
Epilepsy Foundation logo with purple and white stylized 'e' symbol and text.
Australian flag flying in the wind with the Union Jack in the upper left corner and constellation of the Southern Cross.

Australian Donors: Make a Tax-Deductible Donation Today.

Help raise the $1.6 million AUD needed for Sasha's toxicology testing and pave the way for life-changing genetic therapy for millions.

Without your support, Sasha will never develop —

she will be an infant trapped in a woman's body,

severely disabled and needing 24/7 care for the rest of her life.

100% of the proceeds go to Saving Sasha

This is our only chance to help our daughter. 

We must fight for her, and we must move fast. Her future depends on it. We are facing the pain of seeing the person we care for most in the entire world deteriorating. Anything you can do to help will change countless lives.

David and I ask for your help today. We will be forever grateful.

Sasha Lipworth can't even use a toy she used to play with when she was 2yrs old due to SLC6A1.
Sasha in her mothers arms on a hospital bed due to SLC6A1.
Sasha who has SLC6A1 in her wheelchair pram waiting to have a general anaesthetic for an MRI to check brain function.
Sasha lying in a hospital bed recovering from her muscle biopsy to help diagnose her rare disease SLC6A1
Sasha's mother, Nadine had no idea that her baby girl had a rare disease that is akin to childhood dementia.
After having seizures, Sasha being comforted by her father David in hospital.
On the day that Sasha was born being held by her loving father David.
Saving Sasha from SLC6A1 and the journey to diagnosis took 6 years.