I’ve had the good fortune to see many of my “old” neuroscientist
friends over the past year through book tour and speaking event travels or
through the research I’m doing for my next book. I love listening to them talk passionately about their
research, and I especially love that I can still understand it all, as I now
spend my time writing novels rather than scientific research grants or papers.
Alzheimer’s, anxiety, bipolar, Huntington’s, autism,
schizophrenia, Parkinson’s.
Cytokines, glutamate receptor upregulation, gene expression,
caudate nucleus, amygdala, CAG expansion, GABA.
These brilliant scientists are making exciting and
significant contributions to the body of knowledge that will someday lead to
medical treatments and cures.
While I still love hanging out with scientists and learning about their
latest research results and next set of hypotheses, and I always leave feeling
awed and inspired, I also invariably leave feeling a bit stirred up.
I used to do what they do! I have a Ph.D. in neuroscience from Harvard. I used to do brain research at prestigious
places such as Mass General, McLean Hospital, and the NIH. I still could, but I’ve chosen to
dedicate my career to writing novels instead. At times, this feels like a really strange choice. My former colleagues are making
critical contributions to science.
What am I doing?
I write about people living with neurological diseases or
conditions who are ignored, feared, and misunderstood. I write novels. Not scientific research papers, not
clinical review papers, not even non-fiction. Why on earth do I do this? What is the value in a neuroscientist writing fiction? What is my contribution? Is it to science or literature or
something else entirely?
I’ve spent considerable time pondering these questions. Here’s what I’ve come up with.
Fiction is accessible.
Unless directly affected, most people aren’t going to read a scientific
research article about Alzheimer’s, brain injury, or autism. Most people probably aren’t going to
read a non-fiction book about these topics either. Those texts tend to be too dry, too clinical, too technical,
too impersonal, too intellectual.
They’re often filled with facts and statistics.
Every 68 seconds, someone in the US is diagnosed with
Alzheimer’s.
1 in 88 children in the US is on the autism spectrum.
The science is necessary (and fascinating to neuro-geeks
like me), and the facts and statistics are staggering, but numbers aren’t what
we’re all looking for. Five and
half million Americans have Alzheimer’s Disease. They and all the people who love them are all in desperate
need of learning more about this disease, but they want to understand it in a
way that’s accessible. They want
to understand it with their hearts, not just their heads.
What does it feel like to have Alzheimer’s, a traumatic
brain injury, autism, Huntington's? Most of us
don’t know, and reading the clinical literature is either too daunting or too
scary or both.
Fiction is a powerful way in. Most people aren’t going to read the article about autism in
the April issue of the Journal of
Neuroscience. But they might
read a novel about a family living with autism. Fiction gives us access to what might otherwise be too overwhelming
to consider. Fiction can give us
the humanity behind the science and the statistics.
If you read my novels, you will learn some real science and
clinical information (yes, I sneak it in). But beyond intellectual knowledge, what I think and hope most
readers take away from my books is a compassionate awareness.
Compassionate awareness. This is my contribution. And I believe it’s an important contribution because it is
this kind of awareness that can help break down the stigma and alienation imposed
on families affected by these diseases and conditions. It is compassionate awareness that says
to the world, “I see you. You
exist. You matter. And I care.”
While I’m proud of this contribution, I’d like to do more,
and I’d like to ask for your help.
This month is Autism Awareness Month. My third novel, Love Anthony, is about autism. If you’ve read Love
Anthony, and it’s made you more compassionately aware of autism as you walk
through the world, if you finished it and felt educated, entertained, inspired,
if you feel like you now have more sensitivity and empathy for families living
with autism, then I’m asking you to get involved.
I’m asking you to take that compassionate awareness you now
have and donate something to Autism Speaks or an autism organization of your
choice. It doesn’t have to be much
to make a big impact. I think it’s
fair to guesstimate that at least two million Americans have read Still Alice. Imagine if each reader had donated $1 to the Alzheimer’s
Association. That would’ve made a
powerful and amazing contribution to Alzheimer’s care and research. Let’s do that for autism. Let’s see how powerful and amazing this
readership can be.
Please consider making a contribution to Autism Speaks
though this link:
And if you do, please comment here or shout it out on
Facebook or Twitter. Let others
know, and maybe you’ll inspire them to contribute, too.
Thank you,
Lisa Genova
I have enjoyed Still Alice and Love Anthony. I am about half way through Left Neglected and really enjoying it too.
ReplyDeleteLoved meeting you at Advocates in Framingham last Saturday.
Just made a donation to Autism Speaks.
Thanks for your contribution to knowledge, understanding,and empathy. We are all connected!
Jan Krause Greene
I wanted to say that your fiction is very worthwhile/needed! You literally saved my life, I believe! Because of STILL ALICE, I was diagnosed very early with early-onset dementia (too early to know if it will progress to AD) and then I recognized the symptoms in my husband and he, too, has the same diagnosis only it is EOAD. I have given several copies away, including one to my neurologist and her practice, and the nursing staff of my doc. Thank you! My 25 yr old has PDD so this new book is important to me, too!
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