My apologies for being away lately.  My siren song has been the birds chirping and the sun shining.  I just can’t stand to stay inside on days like these.  I’ll have to figure a way to bring the laptop outside so I can post en plein air.

One of my recent time commitments that would be worthy of more than just a mention here, is my mother.  My mother hurt her hip.  One morning, about 3 weeks ago, she came in complaining that she couldn’t walk.  She was using my father’s hemi-walker.

I gave her some ibuprofen and told her to rest it.

The next morning it was worse.

Well, I took her to the doctor’s office to see the Physician’s Assistant.  Her doctor was not in that week.

From there I took her to a radiology lab to get x-rays and then a pathology lab for blood work.  (This was to rule out more serious problems it could have been.)

Thankfully, each of the worst case scenarios was false.  But after spending all day and a lot of expensive tests ruling out what it wasn’t, we never got a diagnosis of what it was!  The PA suggested it might be just a bruise or perhaps bursitis.

It couldn’t be the bruise, since it hasn’t ever darkened, nor has the pain abated in three weeks.

So, in my infinite medical wisdom, it’s probably a hip bursitis.  (Any suggestions or helpful advice would be very appreciated!)

From there I go to the internet.  I find that for hip bursitis you should:

  1. Rest
  2. Treat with an anti-inflammatory
  3. Ice the area
  4. After the pain starts to subside, start to exercise the hip.

As you can imagine, my mother has no problem with first 3 methods of treatment, except of course that she would forget to do #2 and #3.  But if I give her the medicine and bring her fresh ice packs, this treatment fits right into her normal day of activities:

Infidelic / flickr.com

Before breakfast nap

Breakfast

After breakfast a little “closing of my eyes”

Mid morning rest

Before lunch catnap

Lunch

Après lunch snooze

3:00 Her favorite TV show

Pre dinner sleep

Dinner

TV shows

Bedtime

It’s #4 on the list that she can’t grasp.  Start exercising the hip after the pain starts to subside.

With my mother’s stage of Alzheimer’s, I can’t rely on my mother’s mind to help me.  She doesn’t remember going to the doctor, let alone how it felt yesterday or last week comparatively. But after 3 weeks, the pain should have subsided a bit by now.  Right?

So I try to start her on a mild exercise program.

Ugh.

It requires a whole lot more exercise from me to get her to do some exercise!

After waking her, …nudging her, …waking her again,…cajoling her, …threatening her…finally after about 30 minutes of this tiring routine, she’ll come with me to exercise.

We go downstairs where I have our home exercise equipment:  an elliptical and an upright bicycle.

First hurdle of course, is the stairs.  My mother hasn’t had to tackle stairs in years.

Then on to the bike.  The seat isn’t comfortable.  She has to stop every few minutes to catch her breath.  (I have it set on Level 1 on a flat course.)  She’s able to make it 15 minutes.

Then we’ve got to get back up the stairs.    More than an hour of my day gone.

I give her a couple of days to rest, then, we go again.

Next time after the bike ride, I ask my mother to get down on the floor so she can stretch out her hip, lower back and legs.  And to do some exercises that isolate the hip muscles.

You’d have thought I’d have asked her to fly to the moon.  But after more cajoling, and a bunch of small steps and rests, she got down there.

This additional part of the exercise adds another 45 minutes.  I hear “Just let me lie here a while,” a lot.

Each time we’re done with this very minimal exercise, she comes away enthused.  Once she even went directly to the kitchen to feed the dogs.  She chose to remain standing longer!

She’s says her hip feels better after.

I believe it’s good for her.  I believe it’s good for her hip.  I believe it’s good for her mind.  The blood pumping in her heart must deliver more oxygen to her brain.  The endorphins must lift her mood.

Now, how can I get her to remember how good she feels after exercising?

I’m just hopeful that the routine of my actions will soon start to take root and she won’t fight me as much.  Then maybe she can let the memories of the good feelings after exercise blossom.

And there I go letting words that belong outdoors in the garden creep into my writing.  I hear the dirt calling.


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I think about my Papa a lot these days.  He and I have a lot more in common these days – both of us being caregivers of Alzheimer’s victims.  My grandfather cared for his wife until she passed away with pneumonia.  I am caring for my mother, right now in the moderate stage of Alzheimer’s.

My grandfather was a crusty, old man.  As a child I always equated him to a bear.  Not a welcoming teddy bear to cuddle into his lap and read a book with.  But a scary, imposing bear you’d keep your distance from.  He loomed above us grandkids and his voice, when he spoke, was a booming sound.  He lumbered about the house, filling the rooms.  Crossing into the next room he’d have to bend down slightly in the doorways and on the stairs.  We were always careful to keep a safe distance, or to keep one of my parents between him and us.  Thankfully we were quicker and could escape if needed.

I’m sure Papa viewed our visits with mixed emotions.  He probably loved the attention, energy and vitality of our young family.  But four nosy grandchildren getting into everything, hungry all the time and the incessant noise level almost certainly really upset his carefully planned routine.

A product of the Great Depression and life of hard knocks; he was a very frugal man.  My mom calls him stingy.  A container of frozen orange juice would last him a month, using just one teaspoon of the liquid gold to make a pitcher of orange juice.

I remember once we found a stash of hard candy he had hidden in the basement behind the laundry room.  You’ve got to understand, this was rare find.  There was nothing but the bare minimum in this man’s house.  To have found such a frivolous, yummy nugget his house was like discovering water on the moon.

It was probably Papa’s little retreat.  A little sweet needed to rejuvenate him. When we were discovered, we saw the bear’s anger!  From my mother’s accounts, he had softened with age.  She says I just knew the gentler side of him.  You couldn’t convince me that day he was soft or gentle!

My grandmother never saw a doctor.  Papa, most likely, didn’t want to pay for it.  He probably saw it as futile, since he had known Mama’s younger sister had already suffered through this disease and the doctors couldn’t prevent it.

Mama and Papa used to take long walks together.  Once the Alzheimer’s became more pronounced my grandmother walked by herself.  I imagine my grandfather relished the time by himself, as I do.

On one of our visits my mother noticed Mama was walking in a pair of house slippers that the tiny heels had been worn off.  My mom purchased a new pair of walking shoes for her.

One day Mama left for a walk and she didn’t come home.  The wandering had started.  My grandfather searched and searched the neighborhood and finally resorted to calling the police.  They found her sitting on someone’s step with a flower in her hand.

Papa began walking with her again, for safety.  His small reprieve was gone.

I recall stories of how my grandfather would go into the bank’s public restroom and take handfuls of their paper towels.  These he would use in my grandmother’s panties to stem the flow of urine when her incontinence set in.

Papa was all alone in dealing with this disease.

-     He didn’t have a wonderful husband who is there at the drop of a hat; someone to yell at in frustration, to cry on in pity or fear; someone to just say “Take me away”.

-     He also didn’t have a teenage son to laugh with; someone to lighten his day, take his mind off the end of life and focus on the fun, youthful years; someone that inexcusably gets hit with a lot of misdirected frustration.

-     He didn’t have a condo just hours away where he could escape to one weekend a month, just to get a breather.

-     He didn’t even have a pet, to give him unconditional licks of affection and the warmth of a loving lapful whenever it was needed.

Papa was all alone.

His neighbors were all shunned by disagreements or cold shoulders.  There were no sisters or brothers living nearby, not that he would have asked them for anything anyway.  My aunt, Sue, lived nearby and she helped as much as he would allow her.

This was his responsibility.  And he was never one to shirk responsibility.  He was stoic.

He cared for my grandmother during her entire ordeal with Alzheimer’s with love.  Not perhaps the most compassionate, warmest, huggable kind of love.  But with the love he was capable of giving.  Papa’s love was the independent, steadfast, take-care-of-everything kind of love.

And it was this exercise of caring for his wife through her Alzheimer’s that caused him to become softer and gentler.  That also allowed him to become closer to his own daughters.

I want to go back in time and will my little childhood frame the courage to go up to the imposing bear, reach out and give Papa a hug or a kiss.  Some sign of affection.  A sign of appreciation for the love he was showing in his own way.

Papa lived a few years by himself after my grandmother passed away from pneumonia.

He traveled out of state to my wedding – on a plane, no less. He was staying in a hotel in a downtown area, and the morning after the wedding, he got up, got dressed and went outside his hotel.  He sat down.  He had no idea where he was.  He was lost.

I can just imagine the fear that must have overcome him.

A bellhop found him and called my mother.  All was okay.  Mom got him where he needed to be and then flew home with him.

But the fear was still there.  It had gripped my Papa’s core.

Once home, he decided he’d had enough.

He didn’t eat or drink anything else.

He didn’t want to put anyone else through what he’d just gone through with Mama.

After I returned from my honeymoon, I found out what was happening.  I flew to visit him.  My brother had moved into his guest room to help him, to try and get him to change his mind.  No chance.  When I arrived he was bedridden.  He was no longer an imposing bear, just a mere man, hoping to die with his dignity.

For the better part of an hour I rubbed lotion on his feet, hoping it would feel good.  Hoping it would spark a sensory pleasure that would get him to want more, and thus sit up and drink.  Nope.  He was resolute.  It probably eased my conscience more than his.

My mother talked to him on the phone the night before he died.  She remembers him saying “I don’t want to walk by myself anymore.”

Below you’ll find some of my mother’s memories of her childhood.  She has Alzheimer’s and I’m asking her to put her thoughts on paper for a bit of mental exercise.  The unedited words of my mother, Terre, appear in green italics.

I grew up in an older neighborhood near Cheeseman Park.  Cheeseman is not a “child-catering” park – no swings and slides – but it does have three shallow “wading pools” in front of its elegant marble _________.

Marketing Punk / flickr.com

The greatest child attraction is the “sugar bowl,” a depression in one grassy area, with a small hill in the center, a perfect sledding spot for small children.  Another attraction of the park was the “summerhouse”, a rustic sitting area on the south side; a great place for climbing or meditation, depending on your age and inclination.  Mother and I frequently walked in this park, summer or winter.

My father was a civil engineer with the D & R G.  Needless to say, when we traveled it was by train!  He was a quiet man – very tall and dark – very intimidating for a young child.  He was very forbidding – mostly to Sue (her younger sister) and I, probably more to Sue then, because she was more defenseless.  If I was honest, I’d say he was a mean man, but softened up a bit later in life.  In reflection I see now this was mostly the result of a very difficult life.  By the time my Dad passed away we were pretty close.  But isn’t that a shame to have wasted all of those years.

He had emigrated from Canada into Detroit when he was about 20.  He continued his self-education, gradually and finally was able to work as a civil engineer.  He was very proud of Sue and me for going to college, although he never wrote a check to the college.  My mother went back to work to pay for my college.

He and my mother both lived into their 80’s, and are fondly remembered by my sister and me.

This is an interesting article I found relating to the genetic risk of Alzheimer’s being higher if carried by the maternal side of your parents.  This is an extremely small study, but it certainly holds true for my maternal family line.

Previous studies have shown that the incidence of Alzheimer’s is higher among those whose parents were diagnosed with the memory-robbing disease. Now, scientists have found the likely basis for this heightened familial risk—especially from the maternal side.

With the help of a new version of a brain scanning technique, an international collaboration led by NYU Langone Medical Center researchers discovered a far greater number of protein clumps linked to the disease among healthy adult children of parents with Alzheimer’s compared to counterparts with no family history of dementia.

The average increase in these clumps, called amyloid-beta plaques, was particularly striking among study volunteers whose mothers had been diagnosed with the disease. The plaques appeared throughout most regions of the brain.

The study examined 42 healthy individuals, including 14 whose mothers had Alzheimer’s, 14 whose fathers had Alzheimer’s, and 14 counterparts with no family history of the disease.

On average, the first group of volunteers showed a 15 per cent higher burden of amyloid-beta deposits than those with a paternal family history, and a 20 per cent higher burden of the protein clumps than those with no familial risk factors. The new findings may help explain why a family history is such a big risk factor for the brain disease—individuals with an affected parent have a four- to ten-fold greater risk than those with no family history.

The study has been published in the March 15, 2010, online early edition of Proceedings of the National Academy of Sciences.

http://timesofindia.indiatimes.com/life/health-fitness/health/Why-family-history-ups-Alzheimers-risk/articleshow/5690646.cms

According to many researchers today, there are various risk factors of Alzheimer’s.  I’ve listed the top twelve below.  Plus I’ve added a little of my personal motivation, so I can keep this dreaded disease at bay for as long as possible.

12. Brain exercise – If you participate in mentally stimulating activities that are ongoing and varied, you’ll be lowering your risk of Alzheimer’s.  Keep learning.

11.  Social activity – Those who remain socially active can ward off Alzheimer’s longer.  People who suffer from isolation and loneliness are at a significantly higher risk of succumbing to Alzheimer’s.  (Question: Is depression a risk factor or a symptom of the disease already at work?)

10.  Diet – There’s growing research that suggests eating an unbalanced diet and high-fat foods leads to a higher risk of Alzheimer’s.  Pass on the desserts.

9.  Smoking – Smoking raises the risk of Alzheimer’s.  Nonsmokers have a lower risk, along with those that have quit.  Snuff it out.

8.  Education – The greater educational level you’ve completed in your life, the better your brain will be able to fight off the debilitating affects of Alzheimer’s, probably because it has made more neural pathways.  Keep learning.

7.  Overweight – Carrying around those extra pounds, even as early as in your 40’s, isn’t good for your brain. Those that were classified as overweight or obese by body mass index were at an increased risk of Alzheimer’s.  Get moving.

6.  Exercise – Exercising regularly may reduce your Alzheimer’s risk by as much as 40% for adults 65years and older.  Again, get moving.

Raideres/flickr.com

5.  Diabetes – Type 2 Diabetics have a doubled risk of suffering from Alzheimer’s than those without diabetes.  Pass on the desserts and stay moving.

4.  Head injury – People that have had serious head injuries, especially after age 50, are at an increased risk of developing Alzheimer’s.  Wear a helmet.

3.  Family – If one of your parents and a grandparent on their side had Alzheimer’s or if one of your parents and a sibling has Alzheimer’s, then you are at greater risk of possibly developing it.  (See related post: Is Alzheimer’s inheritable?)

2.  Sex – You’re at greater risk if you’re a female, perhaps because women tend to live longer to the ages when Alzheimer’s becomes apparent.

And your number one risk of developing Alzheimer’s is…

1.  Age – Your risk of developing Alzheimer’s doubles every five years over the age of 65.

A new combination of drugs may provide relief from Alzheimer’s symptoms!  And it won’t cost half of your IRA savings!  And the drugs are actually naturally occurring substances!  And they’re in ample supply! And they’re side effects include a lower rate of developing cancer!

Unbelievable, right.

nickwheeleroz/flickr.com

Well, it’s true.  They are Vitamin D3 and Curcumin.  Curcumin, or turmeric, is the spice that gives the curry (a blend of spices) it’s heat and bright yellow color.

Much like aspirin is to our culture, curcumin has been called upon in Asia to treat pain, inflammation, jaundice, colic and even flatulence.  (Hmmm.  My dad would swear curry causes him flatulence!)

Curcumin has been used in traditional Indian (Ayruvedic) and Chinese medicine for thousands of years largely because of its proven efficacy in treating conditions with inflammation.

http://alzheimer.neurology.ucla.edu/Curcumin.html

The researchers of UCLA are finding studies “highly successful” in animals and are currently conducting many trials on humans.

These studies have shown that D3 and curcumin together have reduced the oxidized damage to the brain and also decreased the inflammation.

There is new hope that these two natural occurring substances may help boost the immune system and thus clear the brain of amloid-beta, which forms plaque, therefore giving hope and relief to Alzheimer`s patients.

http://www.naturalnews.com/026861_curcumin_vitamin_D3_disease.html

The researchers don’t give any recommended doses and they do clearly state that some people benefit from just one of these supplements and not the combination.

But what great news, to hopefully find a natural way to combat the devastation of Alzheimer’s.

Well, I’m off to Vitamin Cottage to stock up on some supplements of D3 and Curcumin for mom.

Check back in a couple months and I’ll report if I can detect a difference.

At least for now, I have more to be optimistic about.

The following was written by my mom, Terre.  I identify her words on this blog with green, italic type.

My parents were both born in Canada, but in different areas.  My mother’s father was a Church of England clergyman, leaving England for the city of Toronto, Ontario.  He and his wife, Jane, had eight children.  As I have mentioned before, all of these aunts and uncles of mine have developed Alzheimer’s.  I am no longer close enough to the many cousins to comment on their mental health.

My father’s family was from Austria, and in recent contact with these relatives, they all seem to be in good health – and mental stability.

One of the wonderful  benefits of this background, was an island on Lake Huron north of Toronto, Ontario near Parry Sound.  It was a long trip from the Denver area to Parry Sound, but the trip was well worth it.  Seven rustic wooded acres, with a scattering of “cottages” and welcoming relatives each summer we were able to go.  Our four children loved this wonderful place, and the relatives, as much as I did.

Whether this Alzheimer’s is a type of “British” Alzheimer’s, I do not know.  It would have been a questionable thing to import!

I think my mind is still pretty clear but my daughter might question that.  My husband and I sold our home in Colorado Springs last summer, and were invited to move in with our oldest daughter and her husband and family.  It has been wonderful for Tom and me, but probably challenging for them.

The last time I saw my mother, Tom and I were visiting Colorado from New York.  Mother was 81 and had lived with Alzheimer’s for about 20 years.  As we all sat in the living room, Mother asked if I was “waiting for my date”, obviously a memory from a previous time!  I have wonderful memories of her, and hope my children will have the same consideration for me!

My resolution for 2010 was for patience.

There’s one important thing I’ve learned from taking care of my mother and reading so much about this disease, Alzheimer’s.  It’s that you need to meet the person where the Alzheimer’s has taken him/her that day.  At least with my mother, you can’t force her into your time and place, or where the pressing concerns reside.  If you try, she’ll just get more anxious, more fretful.  Then she’ll spin further and further away from you.  Then she loses more and more of what you’re trying to bring to her.

It hasn’t been easy for me to come to this realization.  Of course, my first attempts to correct our disharmony were all focused on fixing Mom or her odd behaviors.

Sometimes I rushed to conclusions.  I would finish her thoughts so I could go about my day.  At times I moved quickly around her as if she were in my way.  When I would discover one of her many financial errors, yes, I admit I would yell at her.  Explaining over and over wasn’t making a difference.  Frustration was mounting in me.

Then at the end of those long days, when absolutely nothing I had planned to do had actually gotten done, I would snap.  Sometimes I would bark at my family, my dog, and just run through the rest of my day curtly, just looking forward to my pillow.

After a long and painful year of that, I tried to see if there were methods that worked for others and began reflecting on our own discord.

I noticed the more aggravated, curt, angry, annoyed, and forceful I became, my mother reacted by becoming more anxious, fretful, worrisome, forgetful and despondent.

Conversely, when I was happy, calm and easy-going, she reacted by also being happy, calm and easy-going.

It’s almost as if she was being fed by my emotions.

And the intensity of the emotions counted.  The more intense my emotions, the more intensely she reacted.

The challenges are still there.  We still have mishaps, forgotten phone messages, financial errors, forgotten names and events.

I knew then I needed to be able to approach each of these challenges calmly and not react with such intensity.  I needed to be able to look at them from the Alzheimer’s-induced perspective of my mother.  So I prayed for patience.

Sheeps Clothing/flickr.com

And my prayer was answered.  I’ve found a big dose of patience.  I think of it as a Patience Snuggly.  I’ve tried it on, and yes it works wonderfully.  It’s warm, comforting, easy-going.  I can tell my mother is so much happier and at ease when I’m wearing my Patience Snuggly.  Our conversations flow smoothly.  She’s free to communicate more, not worrying about the missteps.

Now I just need to learn to reach for it more quickly when working with my Mom.

I’m extremely thankful that I found more patience.  It has indeed made my life and my mother’s life easier.  And I’m certain that it has also improved the life of everyone else in my household.

“I know if mama ain’t happy, ain’t nobody happy,” or so says Jeff Foxworthy.

How did I get my mom, who has been diagnosed with early dementia/Alzheimer’s, to agree to a driver’s test?  I used her strengths and a whole lot of patience.

Memories of earlier times are something she has a very clear grasp of these days.  Why not use this strength to my benefit?  I asked her to recount stories of her father and his driving habits, particularly focusing on his later days.

I did this over several days, just listening to the old stories over and over.

Each time we would end up laughing at the picture of my grandfather trying to squeeze by a city bus, hop the curb, drive on the downtown sidewalk with pedestrians jumping out of his way.  Each time I would end with a phrase like, “Boy, I bet you worried every time he grabbed the keys, like all of his neighbors did!”

Then I one day, I nonchalantly slid it in.  “Can you imagine how much I worry when you grab the keys?”

Then we went into the “But I’m a good driver” argument again, but this time I had some ammunition.  “I’m sure your father thought he was a good driver too.”  Ahh.  She was silent.  Finally, she could follow my logic.

Then I began talking about how nice it would have been for an independent, objective body to measure her father’s effectiveness behind the wheel. Someone to ensure all elderly drivers had adequate reaction times and decision-making skills to maneuver 2,000-pound pieces of machinery down neighborhood roads where pedestrians walk and children play.

Davey Brown/flickr.com

She agreed that everyone once they reach a certain age should probably take a driving test.  Yes, the crumbs of logic must be there somewhere.

Then, I said, “Would you feel comfortable taking a driving test?”

Sure, I could pass a driving test.  I’m a good driver,” scoffed Terre.

“You’ll take one?”  I prod making sure my tone is so gentle, so sweet.

Yes.  I could.

“But will you?”  I almost whisper.

Yes.  I guess I should do it,” my mother relents.

Hurray!  One hurdle down.  Now my job will be to remind her of her agreement, gently.  If I push too hard, she’ll get indignant again.  Maybe the next time we recount the stories of her father’s driving, we’ll ask her to put her pledge in writing.

For now, the car sits idle.  She can see it out the picture window.  Perhaps it beckons to her, wishing for her to take it for a joy ride.

Perhaps it comforts her just knowing it’s there, a possible escape if needed.

Meanwhile I wait with patience for the day that she agrees to sell the car or give it to one of her grandchildren.  At least today, I’m not listening for the ambulance sirens.

My mother loves to drive.  She loves the freedom it gives her.  The problem is …she has Alzheimer’s.

Yes, she still has her keys.  Maybe it’s because of her emphatic insistence that she is still a good driver.

I would occasionally ride with her just to see, and to be honest, I’ve witnessed more than a few of the signs on the safety risk test for the past few years.  (Click for test: www.walkingintothefog.com/?page_id=91)

However, thank God, she hasn’t had a fender-bender or even a traffic ticket.  But then again, that just fortifies her defense.

I’m partially to blame too.  I let her go.  I have let her hurl herself down the street enclosed in a 2,000 pound metal capsule with a shiny, front grill.  At least she has succumbed to the slow speeds of old age.  You know the type of driver.  They drive white-knuckled, 40 miles per hour on the highway, never turning their head, with the blinker going the whole time.

It’s also my reluctance to admit her total dependence on me.  Help.  It’s hard.  I’m just not ready for that.  That was not something I was able to come to grips with easily either.

After she was diagnosed over a year ago with early dementia/possible Alzheimer’s, we began talking about her giving up driving.  I’ve been easing her into it, getting her used to the idea.  Meanwhile, I was getting used to the idea too.  Both of my parents would be soon be totally dependent on me.

I brought it up at the doctor’s office.  Boy, if looks could kill, the daggers shooting out of my mom’s eyes would have sliced me in two.  Her doctor recommended she stop driving.  He pointed out the risk to others on the road.  She protested by saying “But I’m a good driver.”

Then we had a horrific accident in the local papers where someone ran into a gas pump, a big explosion resulted and many people in the filling station were critically injured and one young woman was even killed.

We used that to point out the dangers.  That got Mom to agree that she would no longer drive on the highway.  She would just make short trips around our corner of town.

But she doesn’t remember this all the time.  Like when my sister flew in to the airport, my mother was the first to volunteer to go pick her up.  The airport is on the other side of town.  She’d have to use the highway to get there.

So then I thought the best way to handle this would be to make sure she never needed to drive anywhere.  For the past 6 months I have done all the shopping, all the drug store runs, and all the appointment runs.  I’d tell her everyday that I was going to this store or that one.  “Is there anything I can pick up for you?”

PhotoDu.de

Terre was still too proud to ask me for anything.  She’d just get it while she was out.  Yet, she’d forget it typically.  She’d go out again on another trip, and come home with armloads of impulse items, just to find out she’d forgotten what she needed again.  Eventually she found herself asking me to help.  Then over time, she found it made life easy, really easy.

And it worked, sort of.  She didn’t drive.  She was content just knowing she could if she had to.

(You could argue that by taking this task away from her, I’ve also robbed her of the brain’s stimulation of remembering how to drive, the items she needed to pick up or how to even get to the store.  But with the safety of others involved, I’m just going to have to live with that.)

Meanwhile, winter came and her battery died.  Maybe it’s a gift from God?

Violà.   Terre can’t drive.  Her car doesn’t start.  Problem solved.  Right?

Well, not really.  As you can read from her post, she still craves the freedom of driving.  And no, it’s not that she’s driving around the countryside lost.  She hasn’t shown signs of wandering, yet.  She just wants the ability to drive, just in case she needs to.

She holds it very dearly.  Now she tries to demonize me for not getting the battery fixed.

At some point I’ll guess I’ll have to fix the battery.  Maybe I can delay until after winter.  After the snowy, icy streets all melt away.

In the meantime, I’ll have to be the bad cop.

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