Acanthamoeba Keratitis

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If you are going through AK know you are not alone!

My name is Juliette and I have had AK in 2017, since then i've become an AK patient advocate, set up a website, created a support group so anyone who is going through AK, supporting someone with AK or wants to learn more about AK can join.

The more we raise awareness, educate, and support the more we can avoid misdiagnoses .. and isolations.

acanthamoebakeratitis.info

#AcanthamoebaKeratitis #akpatientadovate

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Acanthamoeba keratitis again

My 18 year old daughter is fighting AK for a second in two years. This is a horrible nightmare.

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