Big Decision — Big Day

After considerable thought and discussion with Jon, I am scheduled to have a Gastrostomy (G) Tube (aka feeding tube) inserted via interventional radiology at French Hospital in San Luis Obispo this afternoon, November 21. Outpatient procedure. This past Monday morning, we became aware of a cautionary red flag involving the protocol utilized by our local interventional radiologists vs. protocol utilized by UCSF specifically for ALS patients with breathing and swallowing issues. The main issue of concern is general anesthesia v. less sedation and no utilization of oxygen. Late Monday afternoon, UCSF’s highly trained and knowledgeable respiratory care practitioner (RCP) phoned our local interventional radiologist and comprehensively reviewed UCSF’s recognized protocol. UCSF does not use general anesthesia for ALS patients when inserting feeding tubes nor do they administer oxygen.

We believe we’re “good to go” now. Your prayers for our peace of mind as well as care and skill for the interventional radiologist, anesthesiologist, nursing staff, etc. will be appreciated. Admitting time is 11:30 a.m., surgery set for 1:30 p.m., discharge anticipated at 4:30 p.m.

The purpose of the G Tube is to supplement my daily food intake. Eating is becoming more challenging by the day, exhausts me, and swallowing presents a possible choking hazard. 

Please be especially mindful of Jon. This is more difficult for him than it is for me. He’s walked through many phone calls, deliberations, some frustrating miscommunication and/or lack of communication between medical professionals and/or their staff, long periods of silence when we’ve been left wondering, etc. He is exhausted while being concerned for his wife’s well being. He’s a trooper but I know it’s taking its toll.

Thank you so much❣️

What’s with Hound by the Sea anyway?

A Young Girl’s Dream

My love affair with not just any hound—bloodhounds—started as a young, impressionable girl growing up in Sierra Madre. The small, charming community in southern California nestled beneath the San Gabriel Mountains is flanked by Pasadena on the west and Arcadia to the east. Every Fourth of July, the town hosted a festive parade on Sierra Madre Boulevard. Bloodhounds were always accompanied by the Sierra Madre Search & Rescue Team (SMSR). The high point for me!

While enrolled in third grade at Sierra Madre Elementary School, two classmates’ fathers served as volunteers with SMSR. One momentous day, both of those dads visited our classroom, magnificent bloodhound in tow. The men told us real stories involving their perilous work looking for missing hikers in the local mountains. Cell phones, GPS, and satellite communication weren’t even on the radar in the late 1950s. Bloodhounds, however, have been around for a very long time.

A concerned mother would call the police (no 911 dispatch in those days!) when her son and his friends failed to return home as anticipated from a day hike in the mountains. The SMSR would be deployed to search for the missing boys. A boy’s dirty sock, baseball hat, or other unlaundered piece of clothing could serve as a scent article—something having direct contact with the skin. Every person is created with a unique scent. No two alike. The handler strapped on the bloodhound’s work harness, simultaneously sending a message to the hound saying, “We’re going to work!” At the place the boy was last seen, the handler presented the scent article to the bloodhound. Once the hound connected the scent on the article with the matching scent on the ground, the bloodhound immediately shifted from neutral into high gear and instinctively began hunting for the lost boy. Amazing! It’s just a fun game to the bloodhound. For humans, it can mean the difference between being lost or found. Perhaps life or death.

Continue reading “What’s with Hound by the Sea anyway?”

Counting our many blessings . . .

Pity Parties

Have you ever had a pity party? defines pity party as “A way of experiencing grief, in which you spend your time feeling sorry for yourself and whining endlessly about how crappy your life is.” offers a slightly different twist: “A pity party is an instance of feeling self-indulgently sorry for yourself.”

You may have your own definition. Regardless, each one of us can experience hardship that elicits complex emotions. Life isn’t, as Mary Engelbreit suggested in 1992, “just a chair full of bowlies.” And pity parties accomplish nothing good.

You may have concerns about thieves breaking into your home and stealing precious things . . . family mementos, safeguarded coins, antiques, heirloom jewelry. Installing dusk-to-dawn, motion-detecting outdoor lighting; deadbolt locks; and security cams may thwart would-be burglars. But thieves come in many forms. Such uninvited pirates may show up at any time of the day or night to rob, bit by bit, our . . . health.   The nerve!   What have I hit on?! ALS ruins nerves! What does that look like for a victim of speech-onset ALS? A few personal glimpses:

Diminished ability to speak
Difficulty chewing
Swallowing—even liquids—can be hazardous
Excessive saliva results in drooling
Weakening diaphragm causes undue fatigue
Ordinary tasks take an unreasonable amount of time

Jon often reminds me to be thankful for what I still have left. Pivotal. Otherwise, it’s tempting to wallow in what I’ve lost.

Please thank God today for your many unearned blessings. And when you take a bite of that In-N-Out burger or turkey thigh or pumpkin pie, chew and swallow it, be grateful. Something as seemingly insignificant as that shouldn’t be taken for granted.


So glad you’re here! Heartfelt appreciation to our daughter and son-in-law, Laura and Jarrod, for sharing their expertise in designing this website from their home in Chattanooga, Tennessee.

Thank you for your concern expressed through emails, texts and cards and for your prayers. An appreciable decline in stamina makes it difficult for me to keep pace with individual emails and text messages. My hope is you’ll return here for current news and personal reflections. You’re welcome to email or text me but no promise you’ll receive an individual response.

Jon and Leslie Sands
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ALS Overview

Adapted from:

ALS Association Golden West Chapter
Health Communities
Mayo Clinic

Amyotrophic lateral sclerosis (ALS), also called Lou Gehrig’s disease, is a progressive neuromuscular disease that weakens and eventually destroys motor neurons— components of the nervous system that connect the brain with the skeletal muscles.

Upper motor neurons are located in the cerebral cortex of the brain and conduct impulses from the motor cortex to nerves in the brain or the spinal cord. Lower motor neurons are peripheral neurons that originate in the spinal cord and conduct impulses to the skeletal muscles. Skeletal muscles are involved with voluntary movements, such as walking and talking. The lower motor neurons transmit the command to move from the brain to the skeletal muscles, which respond by contracting.

A person with ALS usually presents with problems in dexterity or gait resulting from muscle weakness, or with difficulty speaking or swallowing. Sphincter control, sensory function, intellectual ability, and skin integrity are preserved. Patients become paralyzed and often require ventilation and surgery to provide a new opening in the stomach (gastrostomy). Loss of respiratory function is ultimately the cause of death for people who have ALS.

Incidence and Prevalence of ALS

Approximately 30,000 patients in the United States currently have ALS. The disease has no racial, socioeconomic, or ethnic boundaries. The life expectancy of ALS patients usually ranges from about 3 to 5 years after diagnosis.

ALS is 20 percent more common in men than in women. However, with increasing age, the incidence of ALS is more equal between men and women.

About 90 percent of ALS cases occur without family history. The remaining 10 percent of ALS cases are inherited through a mutated gene. On average, it takes about one year before a final ALS diagnosis is made.

ALS signs and symptoms

Once a motor neuron degenerates completely, the muscle that it controls no longer receives impulses from the brain. Approximately 60 percent of ALS patients experience muscle weakness and stiffness as the initial symptom.

Continue reading “ALS Overview”