Genre: young adult contemporary
Release date: January 1, 2020
Synopsis: It’s My Life follows Jenna, as she struggles with growing up, figuring out who she is, and how her disability plays into that. She navigates family, friendship, and finding her voice, both at school and as the director of her own care. The author writes that this book is primarily not about her disability, but about a girl who “believes something about herself that is not true”. However, Jenna’s negative feelings around her disability drive the bulk of the plot points and are central to the story.
Disabilities represented: cerebral palsy, depression
Disclosure: I received digital access to the ARC in exchange for my review, which was shared on Edelweiss.
Review contains spoilers.
I found It’s My Life choppy and disorganized. First person perspective can be challenging for authors. In this case Jenna’s thoughts come through as pressured, fast-paced, and highly disorganized. The plot contained significant jump points with weak transitions. I often found myself wondering, “How did we get here?” or “Would this really happen?” I mean, would someone’s uncle really randomly help them complete lal the paperwork for medical emancipation out of nowhere? The text message conversations between Jenna and her crush are especially choppy, as was the whole “cat-fishing” scheme. Jenna spends so much of the novel as her alter-ego that I honestly forgot her name several times.
I wanted to love this book. I did. I think there is a real dearth of coming of age novels for teens with disabilities. They face the same struggles as any teen, but with the added stress of a society that doesn’t often accommodate them. I think that following Jenna’s struggle for medical autonomy, the constant decision-making, the risk/benefit analysis of “is this treatment worth it? are these side effects worth it? for what purpose?” would have yielded a whole depth of emotions and plot to explore. I would have loved for that to be at the forefront. Instead, I struggled to understand whether this book was about Jenna’s understanding of her disability (which was very, very negative), about her struggle to have a “normal” life, about her depression, about her friendships… I just don’t even know.
I will say that I very much thing that Ramey wanted to portray to the world that Jenna is capable and brilliant and perfect, as she is. I do not think that Ramey herself has a negative view of cerebral palsy. She especially portrayed Jenna’s family beautifully. There’s a moment between Jenna and Jenna’s dad, towards the end of the book. Jenna asks if he ever had to grieve the diagnosis of cerebral palsy. He talks about how, from the beginning, he saw what a fighter she was and how beautiful and perfect she was, as herself, completely. It was a heart cracking moment — and an unconditional love that I wish more people had the privilege to experience.
So, no, I don’t think that Ramey is intentionally ableist. I don’t think she believes the world would be better without Jenna, or that Jenna would be better without her disability. The ableism in this novel is the subtle stuff, the “I don’t like the word disability” stuff. Late in the novel, when Jenna meets another person with a disability, the other person says she runs a club at her college for students with disabilities. The other person, though, talks about how she prefers the term “differently abled” or something (and I rolled my eyes). Similarly, of course the happy ending for this novel is that Jenna gets a baclofen pump, the baclofen pump works beautifully, and Jenna’s whole life is changed! She is less physically impacted! Hurray! (Sense the sarcasm.)
I do think this is a risk when well-meaning professionals write from the perspective of a disability. We have to really spend a lot of time analyzing what we are writing to see if we are unintentionally reflecting the ableist culture we live in, or if we are using our writing to subvert that oppression. I think that It’s My Life could have done with a lot more subversion.