“i was like 14, but i’ve lived my life knowing that things are going to be tough,” she says. “you’ve got to trudge along and do the thing that’s hard because sometimes you don’t know what that’s going to result in. like i didn’t know that she was going to apologize.”
another time, one of her friends wanted to invite her to hang out at her house, and she told ashley that her parents said they would need to give her plastic plates, cups and utensils (for fear of hiv transmission). her friend stood up and told her parents that that wasn’t right or ok. “it was really inspiring to see that my friend had taken that upon herself to try and educate her parents a little bit. we were 15.”
there’s so much uncertainty about living with hiv and how people will react, even though ashley was born with hiv, contracted from her birth mother. it was beyond her control and all she ever knew. she was adopted by a family who helped manage her normal—all the doctor’s appointments, support groups, summer camps for kids with hiv, and daily medications that are lifesaving, making the virus undetectable and untransmissible.
her family has also seen her through sickness, bone loss and hair loss, which are some of the medication side effects. still, early on, when treatment wasn’t as advanced as today, there was no telling if she would live to go to university or get married, if those were things she wanted. ashley went on to study theatre at york university in toronto. she works on the york campus for the non-profit hillel international to support jewish students, and she’s engaged, planning her wedding for july 2027.