The Power of SCI

What is cooperation?

Merriam-Webster.com says “cooperation” is: “(a) a situation in which people work together to do something, (b) the actions of someone who is being helpful by doing what is wanted or asked for.”

I hear disheartening reports of unmotivated SCIs, bitter about their circumstances, making life miserable for their families/caregivers. Not only are they unwilling and uncooperative to “work together” to get with the program—exercise, dressing, bowel and bladder, etc.—they resentfully and begrudgingly battle self-improvement, as well.

Because this character quality is lacking in so many able-bodied and disabled adults, I began explaining, talking about, and demonstrating lessons in cooperation to my grandniece when she was three years old. Teaching her skills for successful relationships is part of my contribution to her personal growth.

How is it that man is born with the reasoning capacity and capability for concerted cooperation, but it’s most often witnessed in the animal kingdom? It makes no sense; unlike the band of three bottlenose dolphins around Savannah, Georgia who work as a tactical unit.

The dolphin’s operation is to swim into the shallow tidal marshes. With their bodies, they patiently and strategically flush the herded fish onto shore. It’s life-threatening if one were to become marooned, but they risk it for food. They not only feed themselves, but also the egrets and gulls who have learned to rely on the dolphins.
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From this example, I’m comparing the ministry of caregivers who daily sacrifice their health for ours to that of the dolphin’s risk, and how we SCIs benefit from caregiving, to the egrets and gulls reliance on the dolphins.

Come on, SCIs. Let’s get with the program! Yes, it’s tough to lose physical independence. It’s the biggest bummer I know! No matter how hard you try to deny it, close your eyes to your needs, and barricade your heart from the disappointment, the situation remains. It’s time to accept the new reality of being dependent on others for things we took for granted prior to disability.

It doesn’t mean you’ve lost control of your life! (Look for the upcoming series on how to increase the power in your life for the New Year.) It just means that others may have to serve as your backbone, legs, and hands. You have control over the energy in the room, negative or positive.

For everyone’s health and happiness, make the decision to cooperate, “to work together to do something” beneficial for all. Become an enthusiastic member of the loving team working toward your rehabilitation and well-being. It’s within your power.

Christmas Gift Rush and Crazy’s Prediction

After each Christmas, I always say, “Spring will be here before we know it.” Then, when the first hot spring day summons summer, I predict, “Christmas will be here before we know it.” It happens with 100% accuracy. I’m a regular Jean Dixon!

Again, it’s that time. Stores have already announced that their manic rush-to-buy-Christmas-gifts-midnight-madness sales will begin this year after Thanksgiving dinner! The traditional Thanksgiving overindulgences followed with horizontal bemoaning of over-stuffed bellies has been sold out to bemoaning over-crowded stores, rude people, and traffic, traffic, traffic.

Yes, “crazy” has fulfilled itself again: doing the same thing over and over, expecting different results…which drives me crazy. And, I know people consider me crazy because I already have Christmas planned and gifts purchased, as well as for Christmas of 2014. Let me explain:

Considering the wear-and-tear of years living with SCI and the difficulty of outings, I host an internationally-themed Christmas Eve meal each year for my family in my home. I celebrate Christmas and exchange gifts with them here. (These pictures show a little from last year’s trip to The North Pole.)

blurry Elf tree
blurry Elf tree
HO! HO! HO!
HO! HO! HO!

 

 

 

 

 

 

 

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On Christmas Day, they host their own in their homes and/or with in-laws. I enjoy their exchanges via videos and pictures. (You can vicariously enjoy my past celebrations, or get ideas for your own, in the chapter, “Homemade Memories” of Views From My Chariot: A Wheelchair Oddity http://booklocker.com/books/6235.html purchased right here off my website, the perfect Christmas gift!)

favorite candy served as "name card" for seating
favorite candy served as “name card” for seating

I choose a country (or heritage), research its populous, geography, outstanding characteristics, famous people, and holiday menus. I decorate my home accordingly, and give gifts from that country or symbolic of the country. This all takes time and thought, not to mention being disabled, and a non-driver. But, it can be done with ease, excitement, and joyful anticipation of the season if you don’t wait. The only thing left for me to do is prepare, purchase or cater the meal. I can peace out.

What I’m saying is: You still have time. Save yourself the stress. Stop the crazy holiday madness. Everything can be done on-line or over-the-phone. No hassles, anxiety- and annoyance-free. And, if you’re disabled, disability is no excuse.

I’m predicting that a handful of you will get it, yet the majority will prove, again, that c-ra-zy is its own prediction!

FYI: Going with my “prediction” theme, the persimmon kernel is revealing 2013’s winter forecast.

When a persimmon seed is cut into, the inside of the kernel will be spoon-shaped forecasting heavy snow (spoon equals shovel), fork-shaped for light snow and a mild winter, or knife-shaped for “cut”-ting, icy winds.

This one is indicative of heavy snow—another reason not to procrastinate!

And, if you haven’t signed up for my newsletter, “Chariot Notes,” you’re missing out on some wonderful health tips and gift suggestions. December is the most fun yet! (After signing up, you’ll need to confirm that it’s you in an email I send you.)

 

 

Winning, Warnings, and Wheelchairs

As with any of you living with a disability, my journey toward independence has been showered with ubiquitous “ups” and, at times, littered with dubious “downs.” One of the downers is shopping.

Just like the able-bodied, I use earth-friendly bags, paper bags and, less often, the plastic bag. Unlike an able-bodied person, I do the stack-on-my-lap, carry-with-my-teeth, and hang-around-my-neck tricks transporting my haul. In the “FYI” chapter of Views From My Chariot http://booklocker.com/books/6235.html , I proudly share some of my inventive uses of plastic grocery bags for you other chariot (wheelchair) riders…even catching chipmunks. Yes, it’s a fascinating read and an excellent gift!

But, here’s one proven not so ingenious use. DO NOT try this at home, at work, or anywhere else.

I wanted to check my mail. From the street, my driveway slopes down to my house. My mailbox is halfway down my driveway, equidistant from the street and my house. (The P.O. approved my putting it off the street since I’m disabled.)

The wind was whipping as it began to rain. Being a SCI quadriplegic, I don’t have the dexterity to hold an umbrella and wheel uphill, so I thought I’d use an opaque plastic bag over my head as a rain hat; you know, like the clear plastic ‘rain hats’ your grandmother used after leaving the beauty shop on rainy days. It would keep my hair dry, and I could safely see through it.

ill-boding bag
ill-boding bag

I put it over my head and face, its handles hanging down over my ears like earmuffs. To secure it, I held the handles with my teeth and began my grind up to the box. Of course, to prevent a runaway wheelchair from sabotaging my errand in the rain, I had to brake my chair at the mailbox.

Once all my mail and catalogs were safely balanced on my lap, I unlocked my brakes. Again, to prevent a “runaway wheelchair” from skidding off the back of my covered carport, I held them in tension against my wet tires; yet, speedily grinding downhill.

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Instantly, the wind’s pressure swooshed the plastic bag airtight against my face. My hands otherwise occupied, I couldn’t remove it…and I couldn’t breathe!

Although I could clearly see my carport, it seemed an eternity away. With bulging eyes, I finally screeched to a frantic halt on its level pavement, snatched off the suffocation bag, and gratefully gasped in depleted air. Whew! I didn’t pass out!

Lesson learned: The “Warning: To avoid danger of suffocation, keep this plastic bag away from babies and children….” lacks clarity.

I still use the multi-purpose opaque plastic bags. But now, on rainy, windy days—not only as a creative solution, but also representative of my winning attitude, I stick my tongue out against the bag. This gives me an air pocket when it tries to suffocate me.

Is my disability the result of oxygen deprivation, you wonder? It’s up for debate.

 

 

“The Fifth Element”-Love’s Surrender, Will Power, and SCI

Today, I’m correlating the similarity of a fictitious character’s hesitation to change to those of us living with a disability, disease, or illness who do the same.

In “The Fifth Element,” a sci-fi movie set in the 23rd century, in order to defeat a great evil, there were four stones and a sarcophagus, containing a ‘fifth element,’ left for safe-keeping in an Egyptian temple. This fifth element was DNA representing the “Divine Light.” The stones represented the four elements—earth, wind, fire, and water.

The DNA is turned into the “state” lab where it is transformed into human form, Leeloo. She escapes, is rescued by Dallas, a former special forces Major who is now a taxicab driver. Soon, he presents her to a priest who recognizes her as earth’s savior. The battle to save earth ensues.

After battling the opposing evils to confiscate the stones, Dallas, Leeloo, and the priest return to the Egyptian temple to arrange the captured stones and release Leeloo’s ’Divine Light.’ When their efforts to unite the elements appear hopeless and Leeloo is slipping away from discouragement, a confession of love from Dallas causes Leeloo to surrender her love to him. As she yields, the power of ‘The Light’ melds with the other elements, explodes, and destroys the Great Evil.

Like-kind, how often do we, living with a disability, resist change, something new or unfamiliar, due to fear and discouragement? Whether it’s the uncertain territory of SCI or a life interruption that has overwhelmed you; being uprooted for a job promotion to face the unknown; a financial decision or business investment that could lead you into economic ruin; even the uncertainty of commitment to a new relationship. Fear can hold us back, blinding us to the light of opportunity, robbing us of purpose and fulfillment.

I try to stay positive and open-minded to change. “Flexibility” is my middle name. Both my books espouse the benefits of embracing change. But, I also have a “Someday” wish/fear. It’s an entrepreneurial venture that, ever so often, peaks its scary face into my consciousness.
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I’m not inexperienced in business. I’ve been invested in several. But, this “wish/fear” is a larger-than-my-past-business-venture budgets. It’s a BIG BUT-get!

But, I will get it! The chapter, “Facing Fears,” in Views From My Chariot http://booklocker.com/books/6235.html is about facing three of my past fears, all ramifications of my SCI. I’m forthright about other fears and failures in HOW TO BE THE BEST YOU http://booklocker.com/books/6811.html . I totally understand using denial and rationalizations to avoid the unpredictable. In time, after using these excuses over and over and over, they’re stretched so thinly that I can finally see through them to the ‘Divine light of possibility.’

Just as Leeloo’s surrender to Dallas’ love released the power to defeat The Great Evil, conquering “the great evil” of whatever fear (disability-related, or not) is causing you worry, anxiety, and trepidation will release your power, as well.

 

SCI Bonus Serendipities

In the SCI community, we’re familiar with most professional’s prognosis for expected return: Whatever return you’re going to have, you’ll have by the second year. Anything else is a bonus. “Bonus” is the optional—left to personal choice—word.

For many, this is a disappointing truth. But for a large majority, serendipitous bonuses continue to surprise us for many years post injury!

Until I joined Apparelyzed http://www.apparelyzed.com/disability-directory/disability-forums-chat/, I had no idea of the number of happy, productive wheelchair warriors there were like me. I’m a young whippersnapper of 37 years post-injury compared to some 45, 50, and 60+ years post-injury; most of them, still happily and positively contributing to society.

I didn’t know the importance of SCI like-mindedness: the nonjudgmental acceptance of normal depression, grief, and denial following a life trauma; an understanding sounding board to rant—to cleanse the emotions in a safe environment; to learn from others’ similar or like experiences, and how-to cope with such.

I didn’t know the importance of annual evaluations by my spinal cord injury and rehabilitation doctor, or even wheelchair and cushion evaluations from a SCI-specialized PT.

Late in the game, I’ve learned a lot from those contributing on this forum. I’ve learned that many others have also earned bonuses of increased muscular strength, movement, and sensation (my sensation continues to improve after this long!); urinary and bowel control or a maintenance program; having children and grandchildren; achieving professional/financial success; living a wonderful life.

No matter the circumstance, the best medicine for long-lasting mental and physical health, as well as productivity is: having an empathetic and understanding ear to talk to, a sunny outlook, a full calendar, and faithful maintenance of our body and lifestyle.

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We’re not the creators of our bodies, but I believe the more we know about them, understand their hints and hitches, envision and profess our hopes for them/our future, and optimistically work toward their fulfillment, the greater our bonuses!

Yes. In time, we will face one or more repercussions of SCI. Meantime, what we do with our abilities—imagination, determination, hope, and faith—assuredly makes a difference.

I wish a long life of serendipitous bonuses to you all!

Would you like to share a few of yours?

http://booklocker.com/books/6235.html (Views From My Chariot) 

http://booklocker.com/books/6811.html (HOW TO BE THE BEST YOU)

SCI and The Law of Possibility

At one time or another, most of us have used a crutch or have used something as a ‘crutch.’ Whether as a prop or for support, I think when our lives are newly interrupted by disability, denial is as good a crutch as a crutch.

In the beginning—the first ten years—I used it (denial) to my advantage. I wasn’t going to be in a wheelchair the rest of my life and tried to live as if I were still able-bodied; but, obviously, needed help because of my disability. Others telling me how I inspired them wasn’t a help. My wake-up call, out of denial’s slumber, was realizing my pride and stubbornness.

Yes, I charged back into work, and being independent, but I look back at the foolishness of thinking I was more capable than I was, putting myself, and others, at risk.

There were several falls: a back flip off the toilet, a nose-plant onto my pantry floor, a “…tilt me over and pour me out” in my carport, and a semi-twirl off my back porch. The law of universal gravitation is especially cruel to those of us with effected muscular function/responses. Dead weight falls hard. Why hasn’t someone invented an ‘Iron Man’-like rocket boost for wheelchairs?

Anyway, the most dangerous denial was ignoring signs of autonomic dysreflexia (also known as hyperreflexia). http://calder.med.miami.edu/pointis/automatic.html

Autonomic dysreflexia in the SCI has numerous stimuli but most commonly results from an extended bladder or UTI (urinary tract infection), over-exposure in hot weather, constipation, and pain. I would ignore symptoms until a rocketing blood pressure-induced migraine escalated into distorted s-l-o-w m-o-t-i-o-n speech, always requiring emergency assistance. If not treated, stroke, coma, and death can result.

Time, experience, and gained confidence work out the need for ‘crutches,’ but facing the truth on the wings of hope deals with denial.

Whether we improve physically or not, emotionally we can get better, day by day. If you lean on a crutch in the transition, that’s okay. If you’re honestly seeking to fit the puzzle pieces together for adjustment, this fellow SCI even recommends it. A little propping up, a little assistive support, goes a long way on the flight of optimism.
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After all these years, those initial ailments have either changed or improved. More importantly, I’ve become wiser dealing with new ones.

I’ve learned: that opportunities are peeking out from under every weight of limitation, and that some things are “in our head:” Possibilities.

“The Law of Possibility:” the unaffected space of weightlessness in the aerodynamic mind where possibilities abound, and gravity has no influence!

 

 

 

Proportional Relationships

You’ve all heard of, know someone who has, or have experienced sleep walking antics (in my dreams!), even the Ambien-induced zombie driving, cooking, eating, or whatever activity undertaken during/after the drug’s kick-in. Well, pathetically, I have no excuse. I was awake!

It had been a l-o-n-g day in my wheelchair: my back hurt, my boo-tā needed relief, my feet felt like stuffed sausages, and my face screamed, “Nourish me!” If a CSI quadriplegic can hurry, I was trying to!

Whether or not you’re living with a life interruption (my coined expression for SCI, a prolonged illness, injury, or disease), you know the urgency of a getting horizontal reprieve. It’s more expedient than a need; more urgent than a must; more demanding than a have-to. It’s an emergency!

In the throes of discomfort, after tending to the boys, turning back my sheets, preparing my bed with my nightly supplies (if you’re SCI, you know what I mean), and turning off all slumber-robbing lights and electronics, I remembered seeing a white tube of face cream next to my stash of Young Living’s medicinal, therapeutic essential oils on my kitchen table.

Okay, I’m on that side of sixty. Get a grip! You’ll be there in the blink of an eye.

Anyway, assuming it to be my anti-wrinkle-undo-sun-damage-of-my-youth cream, I squeezed its emulsion into my palm, and slathered it generously upon my face—around my lips, cheeks, eyes, eyelids, eyebrows, and forehead.

Instantly, I was distracted from its odd, but vaguely familiar, scent. OMG, did it burn!

Still in the dark, I wheeled to the bathroom to administer a soothing gel. After a couple of minutes of no soothing, I smeared on a hefty portion of hydrating lotion. Still, no relief. Hmmm.

I reasoned that my face was extra sensitive after washing my hair, head down, in the sink, rather than in the shower. I figured, “Oh, well; overnight, my skin’s pH will balance.”

In the night, I had a rememory of something work-related I had forgotten to do. In the morning, in spite of a tight, itchy face, my feet hit the floor running (in a manner of speaking) to my office. After a while, a growling stomach reminded me I hadn’t eaten.

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Back to the kitchen table in daylight, I noticed the writing on the tube of “face cream:” Sally Hansen® Crème Hair Remover for face. OH, NO!

YES, I do have facial hair…it’s peach fuzz…and is only noticeable in sunlight…if you’re using a magnifying glass…sort of.

In horror, envisioning the hikimayu practice—shaved eyebrows, I skidded to a screeching halt in front of my bathroom mirror to see if I still had eyebrows, or eyelashes. Disability is one thing but a bald face is another.

Amidst scattered red splotches and snake skin scales were two brows. Below, circling both eyes, there were lashes.

Through extreme gratitude, I can’t explain why those hairs defied removal, but it did explain the pain! Oh, and yeah, “…the vaguely familiar scent.”

I believe my oft’ recurring missteps are directly proportional to the air in my wheelchair tires, not to the air in my head.

Are there any mathematical geniuses out there that would agree?

(“In pre-modern Japan, hikimayu was the practice of removing the natural eyebrows and painting smudge-like eyebrows on the forehead. Hiki means “pull” and mayu means “eyebrows.” -Wikipedia.org)

 

SCI and Holes of Inadequacy

In the “Excuses” chapter of HOW TO BE THE BEST YOU, I told you the story of beginning a weeknight toddy habit with my mother, and how I was coerced into giving it up. It was after the fact that I realized its significance.

The initial teetotaler stage was hard; it got my attention. I wondered if I could have become an alcoholic if I hadn’t cut it out. I’d never been a “dependent” personality (even during my first couple of years of disability, I was working toward independence), but it made me ponder my feelings on the matter.

In order to get to my point…Some will say that I’m a little weird…maybe alotta’ weird, with what, when, how little, and how often I eat. I may eat lunch for breakfast then, lunch at 10:30am and again at 1:00 or 2:00pm, and even breakfast for dinner—which can be between 4:00 and 6:00pm.

I eat when I’m hungry which is pretty often; but I eat small portions because I feel satiated very quickly—another reason people think I’m weird: I don’t gorge. I detest that uncomfortable feeling!

The twain meet here. My toddy had to be around 4:00 or 5:00 while preparing dinner or waiting for its delivery. Once I eat, that’s it. Nada. Unless it’s water.

The significance of continuing our toddy habit after Mother passed away was my attempt to fill a social void. Mother was gone. After years of disability many friends have fallen by the wayside; those that have endured have families of their own and businesses to run. It was my “happy hour.”

The effect of SCI affects us differently. Whether it’s a loss of movement, a loss of freedom, or a loss of spontaneity, we’re dealing with the common denominator of loss.

Know this: the feeling of powerlessness can initiate addiction.

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In the moment you feel something is out of your control, what do you gravitate toward—think about, want to do, or physically need? That longing is an emotional, even physical, craving for worthiness. Subconsciously, we are trying to adjust to something that has slipped from our grasp.

Gary Zukav, The Seat of the Soul, says you can stop the cycle of addiction by feeling your pain, lack, or loss. Each time you challenge your inadequacy—own it, face up to it, readjust, seek help—you get your control back, little by little.

It doesn’t have to be SCI loss. It can be habits of gossip, jealousy, anger, sex, alcohol, drugs, pornography, shopping, gambling, loneliness…whatever. The situation you are trying to change may never change, but you can take control to change your thoughts and responses to them!

Be brave enough to ask yourself: When I…what hole of inadequacy am I trying to fill? What am I longing for?

Whatever unhealthy thing you’re doing to feel like you’re getting your power back is a smoke screen and a procrastination of truly taking back your control? Every temptation is an opportunity for a dress rehearsal for a life change OR a repeat of consequences. Make a responsible choice.

You’re worth it.

YOU CAN!

SCI Grenades: Weapons of Mass Distraction

For you fellow SCIs, or other involved, animal lovers who have one trouble-making “alpha,” this is my harmless, but effective, ammunition for breaking up pet fights. (I was bullied into its invention because I can’t squeeze a spray bottle to interrupt unwanted behaviors.) Before I get to it, everyone else has to hear my short spiel:

Becoming a pet owner is a big responsibility, and research is tantamount before adopting.

I’m a proponent of adopting from shelters. Even though most are Heinz 57 varieties, you can identify a predominant breed characteristic. Thus said, breed types, temperaments, longevity, veterinary bills (annuals, neutering or spaying, health issues), must be taken into consideration. Too many pets are chosen on looks alone, then rejected because they’re destructive (meaning bored with no exercise), require too much attention, need veterinary care, and/or aren’t suited for the owner/family’s lifestyle.

Please, know that animals should be an integral part of your life, not a possession you tire of, ignore, or abuse. As He did us, God created them on the sixth day and saw that “…it is very good.”

Fred Astaire-the debonair
Fred Astaire-the debonair

Now, to my feline “boys,” Fred Astaire and Laptop. (I dedicated the chapter, “A Little Bit of Heaven,” in Views From My Chariot http://booklocker.com/books/6235.html  to my pets. You know they’re exceptional!)

Fred was a feral I tamed. Two years later, I saved Laptop from being euthanized. All went well until Laptop turned three or four; I can’t remember exactly.

Initially, the skirmishes were tame. They would start out as brotherly grooming—Laptop ministering to Fred. Things were copasetic for a time…until Laptop (a head taller and five pounds heavier) began exercising his alpha-ness.

Laptop begins lovingly grooming Fred’s head and ears then, atypically, body slams Fred to the floor, deceptively licking all the while.

Laptop's deceptive "come hither"
Laptop’s deceptive “come hither”

Fred’s a lover not a fighter, so he complies. But somehow, during the body slam, Laptop maneuvers into a tactical spooning position over Fred as he licks. Fred complains ever so slightly until…with all four paws embracing Fred in a body hold, Laptop goes for the jugular.

If you could feel it, Fred’s screeching would send chills up your spine! The aftermath of cat fur looks like evidence of a feather pillow fight.
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Here’s my SCI-approved device for interrupting an all-out fight, equivalent to the ding-ding-ding of the boxing round timer: an empty 16 oz. plastic water bottle loaded with 5-10 pennies.

Normally, a rigorous shake is enough to send them running in opposite directions. But, when the battle has reached a screeching fever pitch, it’s expedient to hurl the device into their midst.

Since I can’t hop out of bed to break up night skirmishes, I’m armed with three in my bed; otherwise, one is in my kitchen and one, in my office. There have also been surprise attacks when I have thrown whatever liquid was in my hand. Clean-ups suck!

I digress. This morning, Laptop had two of his “Submit!” demonstrations over Fred. I was semi-armed for the second.

The skirmish erupted in the kitchen at the east end of my six foot long table. I was at the opposite end without a grenade, but my vitamin bottles were out for my week’s daily dosages. I grabbed the nearest, shook it for all it was worth, like pulling the pin, and hurled it into the battlefield.

Well, this one wrought a triple whammy of distraction: the warning rattle, the explosive landing, and the shrapnel of 60 vitamins ricocheting everywhere.

It worked! But, instead of running for cover, they acted like drug-sniffing cats.

As penance for not screwing the cap on tightly, I picked up each capsule, one by one; and some, over and over and over. Sort of like writing on the blackboard: “I will tighten my vitamin bottle caps. I will tighten my vitamin bottle caps. I will tighten my vitamin bottle caps…”

I will not soon forget!

 

SCI Wish List: Helping Hands

It’s my birthday. It’s my birthday! Today!

As the Girl Scout motto encourages, “Always be prepared.” I used to always prepare a written or mental wish list of suggested gifts for my birthday and Christmas. Although I love giving gifts, to a fault, at this point in my life, I prefer no gifts. After our family tended to my mother’s things after her death, it gave me a whole new perspective on stuff.

First of all, what we surround ourselves with are our own personal preferences. They aren’t necessarily another’s taste. Who will want them after we’re gone?

Secondly, I have acquired all that I need. It’s time to begin passing on those things that I know my loved ones like. Why wait? I’ve enjoyed them. It’s their turn.

Now, when asked what I would like, it’s a service that I request. Living with a SCI, it’s usually something I can’t do for myself, like: planting flowers that brighten my yard and light-up my days, arrange a bouquet from those that already bloom, pull dastardly weeds, make a favorite dish, a ‘drop in’ for a visit, or a transport and accompaniment to an appointment or errand.

Daily, life presents its demanding schedules and impromptu requirements. Expediency takes precedence in our busy-ness. Quality time is at a premium and my greatest treasure. For my birthday this year, with my deceased mother in mind, I requested some of her favorite food fare and helping hands from my sister and youngest niece.

For our lunch, (control your gag reflex, or your appalled, “WHAT!” response) I asked for Mother’s garlic sandwiches, her cottage cheese side dish, Zoe’s pimento cheese, and tea.

Because my sister knows how I love flowers, she picked Zenias from her neighbor’s prolific garden. (She says Jan can “spit” on a seed and it produces an orchard.)

For Mother’s garlic sandwich recipe, she rolled de-crusted whole wheat bread flat, spread a thin layer of softened butter and freshly pressed garlic on each slice then, rolled them into “shotgun slugs.” MY FAVORITE! Mother used to bring me a dozen or so to keep frozen until I needed one…or two.

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For Mother’s cottage cheese side dish, she combined cottage cheese, onion, and cucumber with a generous portion of coarsely ground pepper. OMG!

On my “3-seeded” wheat bread, we spread Zoe’s cayenne pimento cheese, and sliced some plump, juicy vine-ripened tomatoes, also from Jan’s garden. YUM!

After lunch, Candace acted as my hands to help me place a very special symbolic collection of items into a shadowbox to hang in my bedroom. See!

Calling to my heart
Calling to my heart

Its contents are: a small Indian doll, I have kept since childhood, and an arrowhead. With hair braids, dressed in white leather, the doll represents my Native American Cherokee roots; an antique china picanniney baby with bushy hair plaits representing mixed children that I love and never got to adopt; a small map of Ethiopia, and a charcoal sketch of an Ethiopian woman sent to me from a ministry I support in Addis Ababa. I’ve had a heart for Ethiopia since my early teens after reading about Solomon and the Queen of Sheba; and a colorful silk embroidery of a Chinese woman dressed in the traditional Cheongsam, a piece of their currency, and a hand-carved wood elephant representing my love for Asia.

Happy Birthday, to me!

P.S. Don’t expect others to read your mind. When I told my sister what I wanted, she was totally surprised, but selflessly giving.

I hope your birthday is as special!