what did YOU read in 2021?

I consume news in the form of two daily, hard copy newspapers (I know, I’m ancient), the Boston Globe and the New York Times. I also read online subscriptions of the Washington Post and the Wall Street Journal, as well as devour magazines, the New Yorker and New York Magazine (yes, in hard copy), and the online version of The Atlantic.

When I’m not busy reading all of that journalistic and literary goodness (I just added the literary magazine Creative Nonfiction to my subscription list), I’m reading books. Funny books. Serious books. Fiction. Nonfiction. New England-centric. Politically-oriented. My tastes run wide.

Halfway through the year I published a list on Instagram of the books I’d read starting in January 2021 through early June 2021:

Then, as 2021 drew to an ignominious close with lines for COVID-19 tests wrapping city blocks, I shared the second half of my 2021 reading list:

What did YOU read in 2021? Give the authors a shout-out. They’d appreciate some social media love.

new ms-related pieces: diagnosis story & chronic illness lit

Screenshot 2019-11-05 10.03.42I’ve written two new pieces about multiple sclerosis and chronic illness for your reading pleasure:

HealthCentral: Diagnosis story

How and why did it take two years from the initial onset of symptoms for the medical community to diagnose me with multiple sclerosis? This essay details my journey to learn something that would change the course of my life.

istock-846475966Chronic illness lit: Finding solace between two covers 

Over on the National Multiple Sclerosis Society’s MS Connection blog, I paid homage to writers who’ve shared their stories of strength and struggle while living with chronic illnesses. When you’re feeling down, reading about the experiences of others can provide an existential balm.

An excerpt:

Sometimes I just need to relate.

I need to see my experiences, my struggles confirmed instead of negated and misunderstood. I need to remind myself that I am not alone in my fatigue, in bouts of cognitive fuzziness, in my hair-pulling frustration.

I have been reading books written by those who are living with multiple sclerosis and other chronic illnesses. I’ve been quite voracious about it, collecting these tales as a way to see myself reflected, helping me feel seen and heard.

Works I noted as being inspirational include: the collection of stories Bodies of Truth: Personal Narratives on Illness, Disability, and Medicine; Sonya Huber’s Pain Woman Takes Your Keys, and Other Essays from a Nervous System, and Andrea J. Buchanan’s The Beginning of Everything: The Year I Lost My Mind and Found Myself. (My praise for Nicola Griffith’s So Lucky — a novel about a character with MS who solves a murder mystery — got edited out of the final piece.)

Read the rest of the essay here.

Image credits: HealthCentral and MS Connection.