Last year Gloria visited Karla and her school children in Missouri. Zeb, Karla’s lovie, visited the Aqua Roomers. It was wonderful.
Zeb is not only Karla’s lovie, he is the mascot for the rare form of cancer she has. Karla is always the bright light, the giver, the one who sees the good in everyone and everything.
Mitch Teemley just posted an update on Karla. Thank you, Mitch.
Meet My Dear Friend Karla
From left to right: Karla – Sharing with school children – With her beloved dog – “Stay kind and curious!”
Love With a Capital C for Cancer
Meet my dear friend Karla. When she was first diagnosed with stage-4 NETs (Neuroendocrine Tumors), Karla learned that this rare disease was incurable. It was however, treatable. But few clinics were prepared to do so. Then she discovered that the NCI, the government-sponsored National Cancer Institute, was equipped to treat her fully-metastasized cancer.
The NCI has extended Karla’s life-expectancy by several years. Years she’s using to bless untold numbers of others: through her wonderful, life-affirming blog Flannel With Faith, and through her live readings to school children from her memoir (when health allows) about adventuring in the Ozarks with her beloved dog.
Ironically, however, even though the NCI recognizes Karla’s disease as one of the most serious forms of cancer, it is not well-known enough to make Medicaid’s list of fully-covered conditions. Hence, she’s required to pay at least $3800 a month before receiving any additional aid.
As a result, she’s filed a chapter 13 bankruptcy, which will buy her time to pay back her growing medical debts. And, in order to further reduce her cost of living, she’s moving to a small 55+ community.
“I’m not bitter or angry at God or doctors or anyone,” Karla writes, “(but) my family does get angry. My mom cries a lot and is losing her memory, so it’s hard on my family to watch. (Nevertheless), they have grown in their faith, and I have joy in my heart!!”
Karla’s treatments can be extreme, the most recent she’s labelled her “worst nightmare.” Still, with 9 tumors in her skull, 6 in her spine, 5 in her kidneys, and dozens of others throughout her body, these treatments are the key to her surviving another five+ years.
Years Karla will use to bring her irresistable spirit of hope and love to others!
Note: Karla’s sister has created a GoFundMe page to help cover medical costs. I encourage you to visit and follow her blog and, if you feel so led, to consider making a contribution here!




We walked to the post office.










I hope that makes Gloria an ‘Honorary Brit’.




























Talking With Owen, the High School Student
I can’t get the conversation out of my mind.
Owen was one of the high school students who interviewed our kindergarteners and wrote their stories, turning them into a book.
Today I got a lovely card signed by the students.
Owen’s comment was strong, in a good way. “Thank you for helping us and bringing passion to our Winterim.”
That’s Owen. There’s more.
This isn’t about that time I spent with the students at all. I had a conversation with Owen; this conversation is one I just can’t let go.
It happened like this…
Owen: “You have an accent. Not a big one, but I hear one. Where are you from?
Jennie: “I’m from West Virginia, the south.”
Owen: “I’m from Alabama.”
As we talked about the south, we both agreed it is very different. We talked about accents, family, the heat… and then the conversation became deeper – about people.
Owen: “People don’t mix. They stay with their own group. Everybody mixes up here, but not back home.”
Jennie: “That’s true!”
WOW! I’m talking to a 17-year-old who sees the difference. Nobody else in his world ‘up here’, outside of Alabama, sees or understands. Clearly he wanted to connect with someone else who sees it, too. Me! It bothers him, and it bothers me, too.
I talked with his advisor, telling her of this conversation, but that was a grain of sand on the beach. I knew I had to reach out and do more, so I wrote a letter to Owen.
I hope it helps. I hope Owen sees I was in the same situation. I hope Owen feels like he can do something.
Jennie