26/05/2026
๐๐ง๐ฏ๐ข๐ญ๐๐ญ๐ข๐จ๐ง ๐ญ๐จ ๐๐๐ซ๐ญ๐ข๐๐ข๐ฉ๐๐ญ๐ ๐ข๐ง ๐๐ ๐๐ฆ๐ฉ๐๐๐ญ ๐๐ญ๐ฎ๐๐ฒ
Weโre sharing an important opportunity for AK Warriors, family members, close friends, and caregivers to take part in a new research project that aims to better understand what living with Acanthamoeba Keratitis is really like.
This study is being conducted by Dereje Hayilu Anbesse from UNSW Sydney, under the supervision of A/Prof. Nicole White Carnt. It focuses on ๐ญ๐ก๐ ๐ซ๐๐๐ฅโ๐ฅ๐ข๐๐ ๐ข๐ฆ๐ฉ๐๐๐ญ ๐จ๐ ๐๐โ not just the medical side, but the emotional, financial, and dayโtoโday challenges that so many of you know firsthand.
Your experience may help improve future care and support for people with AK, and this research is designed to make sure those experiences are finally heard and recognised.
๐๐ก๐จ ๐๐๐ง ๐ญ๐๐ค๐ ๐ฉ๐๐ซ๐ญ?
Anyone diagnosed with AK (2015โ2027)
Family members, partners, close friends, or caregivers who supported someone through AK
Eyeโcare professionals involved in AK care
๐๐ก๐๐ญโ๐ฌ ๐ข๐ง๐ฏ๐จ๐ฅ๐ฏ๐๐?
A short screening
A 45โminute online interview (Zoom or Teams)
Everything you share is confidential and handled only by the UNSW research team
๐๐ง๐ญ๐๐ซ๐ฏ๐ข๐๐ฐ ๐ฅ๐ข๐ง๐ค:
๐ https://redcap.link/AKIDI
If youโd like more information, you can contact Dereje Hayilu Anbesse directly at:
๐ง [email protected]
The Acanthamoeba Keratitis Eye Foundation is helping share this study so that the voices of our community โ your voices โ can help shape better care and better understanding for future AK patients.
Thank you to everyone who chooses to take part or share this with others. Your experiences truly matter.