Tuesday, December 10, 2024

“Letting All The Light In: Gracefully Surviving Illness, Injury, And Grief”

“Letting All The Light In: Gracefully Surviving Illness, Injury, And Grief”
Dax Meredith (daxmeredith.com), the pen name of a Chico area author, college instructor and counselor, wrote of her escape from the Camp Fire in "The Sound Of The Snow Geese." But she is also dealing with a years-long debilitating illness. 

“Both the illness and the fire almost killed me,” she writes in “Letting All The Light In: Gracefully Surviving Illness, Injury, And Grief” ($15.99 in paperback, independently published; also for Amazon Kindle). “Twice now I have been much closer to death than I like to consider. But I am a better person because of it. … I am more patient, more grateful, more present in the moment each day because of those events.”

This is not a story of “arrival” but an ongoing journey as Meredith navigates the health care system and returns with cautionary tales. 

The book’s three parts include the harrowing memoir of her mysterious illness where, she writes, “The left side of my face was numb for almost a year. … My spine was numb. I remember constant and continual migraine headaches. The pain was excruciating. I remember endless vomiting, blurred vision or partial and temporary blindness, and on several occasions, hallucinations.” She adds: “As a general rule of thumb, hallucinations are just not a good sign.”

The second part features short interviews with two dozen sufferers, of all ages, each presenting the biggest challenge (including grief at the loss of a son and wife, amputation, addiction, miscarriages, multiple cancers, depression), resources used, the person’s belief system (some are Christian, some “spiritual,” some have no professed religious commitment), what others need to know, the roughest parts, and what wisdom has emerged. The accounts are devastating, gut-wrenching, in part because this is you or someone you know.

The final section is practical advice; Meredith covers everything to be aware of, from how to talk with one’s children to fighting the judgment from others and oneself. “I don’t believe all the bad things that occur are a punishment from God. But there are lessons in the bad things that happen to us.”

With graceful kindness, Meredith may well change how you understand your very life.



Tuesday, December 03, 2024

“Even Broken-Winged Divas Can Fly”

“Even Broken-Winged Divas Can Fly”
Forty-something Chicoan Jennifer Kuhns (www.jenniferkuhns.net) has published more than a dozen books. “I write children’s books,” she tells readers in her latest memoir, “most of which have a disabled protagonist with a strong and positive character and attitude. Well, maybe a little bit of a snarky attitude … What can I say? I put a little bit of me into all of my characters.”

Her own story is told in “Little Diva On Wheels: Growing Up Differently-Abled” and now “Even Broken-Winged Divas Can Fly” ($16.95 in paperback from Shalako Press) which focuses on her high school and college days. Born ten weeks early, diagnosed with spastic quadriplegic cerebral palsy, Kuhns notes that while “my fine motor manual dexterity is basically non-existent,” she has “the ability to memorize like a freaking elephant.”

This “broken-winged diva” has a penchant for literary symbolism, “a strange sense of humor,” a competitive instinct, and self-advocacy.

Her cerebral palsy affects speech. “I can say the word. The problem is ‘saying’ and ‘enunciating’ a word are two absolutely, completely, different animals.” Most of her family members, friends, and those who have interacted with a disabled person understand what she calls her “CP-babblelistics.” She is “greeted, not ignored. I was spoken to, not at. I was not made to feel like I had leprosy. And I was verbally understood.”

Perhaps other adults lack the patience or are afraid, but there is no rancor in Kuhns’ description. Instead, she reveals a well-rounded life, including raising a sheep and an awkward relationship with her mother: Mom is the boss at home, but she is also hired as an aide by the Department of Rehabilitation and so Jennifer is her boss at school.

“I’ve not always been happy about my condition, my situation in life. I’ve been mad, and I’ve been sad, and I’ve hated the body I’m in.” And yet, “I know how to harp like nobody’s business to get what I need, want, or think I should have … not that it always works.” 

A color section at the end showing some of her tattoos (one for each book published), receiving her MA, and newspaper clippings, demonstrates that something very much worked.