What the heck are the “Twisties”

GETTING THE “TWISTIES” – Just like Simone Biles in the Olympics

You may remember that in 2021, one of America’s most loved gymnasts suddenly faltered in a dismount from her balance beam routine.

Simone Biles startled the world by withdrawing from several events to prioritize her mental and physical well-being.

Known as ‘the Twisties,’ this mental block causes gymnasts to lose their spatial awareness while performing aerial maneuvers, making it difficult to control their bodies and land safely.

Biles described the sensation as feeling “lost in the air” and likened it to losing control of a familiar car. The Twisties can be triggered by various factors, including environmental changes, stress, and psychological pressures.

In Biles’ case, she mentioned feeling stressed even before arriving in Tokyo, which may have contributed to the onset of the Twisties. Biles’ experience with the Twisties sparked essential conversations about mental health in sports and the pressures faced by elite athletes.

She recovered and will participate in the 2024 Olympics demonstrating resilience and a continued passion for the sport.

I had a similar condition.   I had a stroke in 2021 and lost my sense of balance.  I would fall for no reason, feel unsafe, and need help managing steps and simple walking.

I learned balance therapy is big business now due to its effectiveness in addressing balance disorders, especially among older adults.

It focuses on retraining the brain to process sensory information from the vestibular system, vision, and proprioception to improve stability and reduce fall risk.

I’ve had seven physical therapists in four different physical therapy clinics help me re-learn my balance. I learned it is not in my feet and legs but in my brain. Those neuropathways automatically telling me which way to step, turn, or lift a foot had to be “re-grooved” in my brain.

The only way that happens is through repetition. My favorite therapist used to say, “Now do it one more time—the first time is for muscle memory, the second time is for the brain.”

Wow, what a learning experience.  Do I have my balance back?  Yes, for the most part, but I still have trouble stepping backward, raising my arms while  moving my feet simultaneously, and going in a circle.

When I tell my friends I can’t do these things, they say, “Well, now that I think of it, neither can I!”  It makes me feel better. ❤️

How to say NO with grace and ease

Why is it so hard to say NO?

I credit learning to say NO to my recovery after a heart attack.  It’s the main thing I did to dramatically change my life after surviving a brush with death.

Many survivors will tell you that changing the way they live is their key to finding true peace and clarity after any life changing illness, trauma, or event.

For me, surviving a heart attack required plenty of physical changes like diet, exercise, daily naps, and taking all those pills! Those things were easy compared to changing my lifestyle of an energetic gal always on the run taking care of everything and everybody.

It was my ingrained belief  – it was the way each day should be – you know “filled to the brim” with fun exciting things.

To change that paradigm meant setting boundaries, giving myself grace, doing fewer things in a day (like ONE),  and most importantly learning to SAY NO.

Luckily,  I learned the words to say “NO” so I didn’t feel guilty and disappoint the person asking. After saying NO a few times and feeling successful doing it, I finally feel comfortable saying NO.

❤️Here’s a good list of things to say – copy it and use it freely – I did!

TEN WAYS TO SAY NO

  1. Sadly, I have something else to do.
  2. I have another commitment.
  3. I wish I were able to.
  4. I’m afraid I can’t.
  5. I don’t have the bandwidth for that right now.
  6. I’m honored you asked me, but I simply can’t.
  7. Thanks for thinking of me. However, I’m not able to.
  8. I’m sorry, I’m not able to fit this in.
  9. Unfortunately, I already have plans. Maybe next time!
  10. No, thank you, but it sounds lovely.

Lastly, here’s a great article  from Forbes packed with the reasons why we feel so stressed over it and some great tips on learning to say NO.  I hope you enjoy it as much as I did.  Here’s the link –

https://www.betterup.com/blog/how-to-say-no

You’re welcome.  ❤️

You Can’t Do Anything if You’re Dead (Read the first chapter of my book)

You Can’t Do Anything If You’re Dead

Women experience heart attacks differently than men. Men have the “Hollywood” attacks we see in movies: pain in the left arm, clutching the chest, collapsing.

I had none of those signs.

But I did have signs.

I was scheduled to be the spotlight speaker for one of my networking groups. Because I’d done this compelling talk before, I knew it would convince people to sign up for my writing class.

At six-thirty that morning, I began preparing for my talk. My fingers and toes were icy cold. I was tired and hadn’t been sleeping well, but I’d been chalking it up to any number of things: a poor dinner choice the night before, a case of nerves, or maybe sleep apnea.

I began packing up my handouts and props. I still needed to make copies and find business cards. I also needed to gather crayons and drawing paper for the coloring exercise. As I wrote my speech notes onto blue index cards, I was breathless. My collarbone ached as if it were being pinched.

I planned to arrive at the lunch meeting at eleven o’clock to set up my props. While loading the supplies into my SUV, I noticed I was winded even from that level of effort.

The meeting was being held at a local restaurant. At the restaurant, tables were set up in a hollow square formation to accommodate forty or more people. I took an end seat so I could get up easily to do my presentation. I heard the buzz of conversation around me and noticed my mouth was dry. I asked the waiter for some water.

The microphone came out. The leader explained it wasn’t working well. He instructed us to hold it tightly and put it directly in front of our mouths when we spoke. I watched as others struggled to get through their 30-second elevator speeches without the mic crackling or cutting out.

It was my turn. I stood at the front—all eyes were on me—and laid out my note cards in front of me. Then I grasped the microphone for dear life.

Despite the static coming from the mic, I talked easily for ten minutes, though I realized I was getting short of breath. I dismissed it as speaking too quickly or forgetting to breathe between sentences.

My heart started pounding. This was (I thought) probably because I was holding my breath—until it pounded faster, and I mean really pounded. It took everything I had to appear calm and composed. After all, I was giving a speech!

I started feeling lightheaded, to the point of dizziness. While the group got busy on the crayon exercise, I clutched the back of a chair to steady myself. I relaxed my tight grip on the microphone, breathed deeply, and tried to regain my composure. I walked around the square of tables, looking at the drawings people were making. This seemed to calm my heart.

At the end of my time, I took a few questions and sat down just before the room started to spin. Immediately, sweat formed at my hairline and trickled down my forehead, like a menopausal hot flash. I dabbed at my forehead with a napkin, desperate to be “fine.”

A friend noticed that all the color had drained from my face. She brought me more water. The waiter brought me Sprite. They wanted to call 911, but I resisted.

“No! I’m fine. Just feeling a bit woozy. . . .”

I figured I’d been standing for too long, hadn’t eaten my lunch—a hundred excuses!

I sensed I might pass out, and I wanted to lie down, but there was nowhere I could do that.

I kept saying, “I’m fine. Honest, I’m fine.” Finally, after drinking lots of water and using more napkins to mop up the cold sweat pouring from my scalp, I felt somewhat recovered.

Knowing I couldn’t drive in this condition, I called my husband to come and take me home. There, I lay on the couch, very still, and googled my symptoms. Anxiety attack. That explained everything! Somehow, this made me feel better, even though I couldn’t imagine what I might have been anxious about. But anxiety had to be it.

I rested, ate dinner, and went to bed, confident I’d be fine the next day.

– – – –

Friday, February 9, 2018.

I awoke with a head full of plans and a long to-do list. Among other things, I needed to go to the grocery store to buy food and snacks for my writing class on Saturday.

First, though, I wanted to get cleaned up. In the shower, raising my arms to wash my hair felt like such an effort. I was quickly out of breath. With a towel wrapped around my head, I put on my fuzzy robe and lay down on the bed until my breathing returned to normal.

Blow-drying my hair caused the same effect. So, back to bed I went, lying down for the second time that morning—and it wasn’t even eight o’clock. My thoughts raced.

This is unacceptable. I have too much to do to be lying down every five minutes!

Determined to push through and prepare for my Saturday writing class, I charged off to the grocery store. I knew exactly where to find all my favorite foods for the class. Veggie tray, crackers, cheese, fruit . . . but in the cookie aisle, it hit me. I reached for a pack of gourmet cookies, and they fell to the floor. As I bent down to retrieve them, I knew I’d faint if I leaned all the way down.

I left the cookies on the floor and retreated to the register to check out.

My legs felt so heavy, I could barely move. Thinking a jolt of sugar and caffeine would pick me up, I grabbed a cold soda and gulped it down.

As if moving through syrup, I slowly loaded my bags of groceries into the back of the SUV. I was short of breath again, and the pain in my collarbone was now constant.

After I got home, I finally gave in and called my primary care doctor.

“Sorry, he’s out of town,” said the nurse who answered the phone.

“Is someone covering for him? Who can I see?”

Her answer was short.

“Call your cardiologist. Or go to the nearest emergency room.”

“I can’t go to the ER,” I wailed. “I have too much to do!”

Her reply haunted me for months.

“You can’t do anything if you’re dead.”

 

Feeling the Breeze on My Face

Thankfully, I did have a cardiologist to call. It had been ten years since my last visit, but the receptionist found my file. She told me the doctor could work me in at one o’clock that day. I called my husband Tomas and we drove there together.

Soon I was hooked up to an EKG. The tech shook his head as he watched the needle move. The associate doctor came in, looked at the machine, and frowned. Dr. Marshall, the head doctor, entered the room. As they all stared at the machine, I knew something was up.

Dr. Marshall looked at me. “Susan, you’re having a heart attack.”

What?

It can’t be.

I thought he would just give me blood pressure pills and send me on my way.

Terrified, I looked over at my husband. Tomas looked terrified, too.

“You need to go to the ER—NOW.”

Things happened fast.

The tech gave me a baby aspirin, and the associate doctor gave me nitroglycerin under my tongue. I heard Dr. Marshall on the phone swiftly making arrangements for me.

Oh, God, I prayed silently.

DAY ONE

Tomas drove me to Tucson Medical Center’s ER entrance, which was only four blocks from the doctor’s office. I was whisked inside and placed on a gurney. I winced as the attendant peeled off my brand-new black leggings and my underwear. I was allowed to take off my top and bra myself. The hospital gown went on so quickly that nobody saw me naked.

The cardiac team swarmed around me.

Doctors, nurses, and techs each announced their names and what they would be doing to me. Calmly, they took my blood, put in a needle for an IV, asked about my health history and medications—and my nail polish.

Yes, my nail polish. They wanted to remove it so they could clip an oxygen monitor onto my finger. They said the polish would interfere, but I knew it wouldn’t come off because it was made of shellac. I tried to explain this but to no avail. Instead, they quickly attached the monitor to my ear.

I felt a breeze on my face from the speed of the moving gurney. As they rolled me to somewhere called the cardiac catheterization laboratory, one of the nurses explained what that meant. “It’s an exam room where doctors will use tiny flexible tubes called catheters to look at the arteries of your heart.” Having received anesthesia, I didn’t care.

In the cath lab, I was surrounded by nurses, equipment, and blinking monitors. The doctor threaded a tiny wire with a balloon on the end through a catheter tube in my groin. From there, he inserted a stent into my circumflex artery. It was 95 percent blocked and resistant to opening but, with the stent in place, my blood flow improved to 60 percent.

Less than twenty minutes had passed since arriving in the ER.

 

Sleeping While Praying

 When I woke up from the anesthesia, I found myself in a private room with nurses, techs, and orderlies coming in and out. My husband was there, and so was my son Tim.

I was starving, but I couldn’t eat until another round of tests had been run. That night was a blur of fitful sleep, bad dreams, a dinner tray at ten o’clock, and a constant struggle to get comfortable.

DAY TWO

The early morning ushered in more nurses, who got busy drawing blood, bringing pills, and taking my vitals. My breathing was still labored, and my collarbone pain had moved to my chest.

Three doctors visited and determined I wasn’t better, so they ordered a few tests. They gave me something for the pain, and to get the fluid off my lungs, then sent me off for a chest x-ray. After that, I was wheeled out on yet another gurney for an echocardiogram, a test that uses ultrasound to evaluate one’s heart muscle and valves.

Hours later, Dr. Waggoner, the hospital’s cardiologist, told me he was taking me back to the cath lab to fix another artery with a stent. I trusted him. I knew something had to be done because I felt so bad—constant chest pains, shortness of breath, fitful sleep, and non-stop sweating. I had also noticed the nurses’ frowns of concern whenever they took my blood pressure and checked my monitors.

After receiving a second stent, I improved dramatically.

The second stent opened up the right coronary artery, improving the blood flow along with oxygen to my body. My test results improved. Everyone noticed!

This fix marked the beginning of a slow recovery as my heart began to grow stronger.

DAY THREE

By the third day after my heart attack, my brain was on overload, trying to take in every face, test result, and procedure explanation. I had three cardiologists, four nurses, a dietician, a pharmacist, a physiologist, and a hospitalist who managed my case. One nurse was a counselor who had a soothing voice and wore a fuzzy cardigan.

Dr. Peña, my hospitalist, visited me every day. He’d squat down to look me in the eye, hold my hand, and ask if I knew what had been happening to me. His soft voice calmed me. He made sure I knew I’d had a heart attack and then stent surgery procedures. Whatever the circumstance, he took care to explain the details to me.

Sarah, the nurse with the fuzzy cardigan, told me, “Because you almost died, you’ll find yourself feeling depressed. Just expect this to happen at some point.”

A kid in blue scrubs—a cardiac rehab intern—said he’d walk me down the hall to see how far I could go. This excited me! I wanted to prove I was strong enough to be released. He offered his arm, and we started our walk. I made it a few steps out the door of my room before I was so winded I had to stop. My ankles felt wobbly, and my legs felt weak.

Then came Debbie, a manufacturer’s rep dressed in a slim skirt and peplum jacket. I wanted her to meet my bachelor son, she was that cute. Her job was to explain how to use a contraption I was supposed to wear 24/7 for six weeks. She opened a color brochure and showed me a defibrillator vest.

The vest was like a fabric sports bra with metal paddles in the back. Debbie explained that if a dangerous arrhythmia were to be detected by the sensors, the device would sound an alarm. If I failed to respond to the alarm within one minute, the paddles would deliver a shock, restoring normal rhythm to my heart.

Because it was Sunday, I wouldn’t get the actual vest until Monday.

The dietician lady wearing red scrubs was sweet as she launched into long explanations of what I should be eating for the rest of my life. Her visual of the desired salt intake mesmerized me. “Just make a little mound about the size of a dime in the palm of your hand,” she said. “That’s how much salt you can have in a day. Not just from the salt shaker but from everything you eat.” Then she showed me how to read labels on food products, especially the sodium content.

Cradling the stack of brochures she’d given me, I felt woozy and my eyelids were drooping. “This is a lot to take in,” I murmured.

Before I drifted off, I heard my doctor speaking with Tomas about the “ejection fraction,” or EF numbers. EF is a measure of how well the left ventricle is pumping blood. With a normal heart putting out 50 to 70 percent, mine was very low at 15 percent. This explained the need for a defibrillator vest.

I ordered heart-healthy chicken soup for dinner, but it tasted like dishwater. Yuck, no salt. I craved salt badly, so I ate the saltine crackers. I dozed off again and later heard the clicking of heels in my room. Opening my eyes, I saw my best friend bearing a vase of flowers.

“Happy birthday,” she said.

“Diana,” I blurted. “I told you not to come!”

“I had to see you with my own eyes to make sure you were okay.”

That’s when I started to cry. I didn’t want anyone to see me looking so debilitated—oxygen tube, catheter bag, tubes and needles in both arms, bruises on every visible surface.

I wanted to tell her I had almost died and how scared I was, but my breathing was so labored I couldn’t get the words out. We simply hugged.

DAY FOUR

Finally, Monday morning came, and so did a flurry of activity.

A young man in gray scrubs went through my discharge paperwork. One by one, he explained what the points meant so I could knowledgeably sign the papers. Most important was understanding the long list of drugs, their names, dosages, and what they would do for me.

It felt like a barrage: Do this, do that, make an appointment for this doctor, that blood test.

A chipper nurse dressed in brown corduroy came next, carrying my new defibrillator vest. With great enthusiasm, she showed me the first step for how to put it together, by inserting the electrodes, also known as paddles, into their proper slots. Then the skinny black cords were to be threaded through the waistband so that the sensors—all eight of them—would touch my body through the thin fabric.

“Put it on and get me out of here!” I wanted to shout. But no, I’d have to prove to her that I could put it together. Like a puzzle, she disconnected the parts, then made me put them back in place while she watched.

Despite my resistance, I knew that any slacking off on my part would be unwise. Wearing this vest was serious, life-saving stuff.

The kid in scrubs came to walk with me again. This time I made it farther than before. I wanted to jump for joy, but I couldn’t let go of his arm.

DAY FIVE: FIRST NIGHT AT HOME

Tomas and I decided I should sleep in the guest room and keep the walker nearby. I would need it when I got up to go to the bathroom. I wasn’t strong enough to make it there on my own.

That night, I had a nightmare, awoke with a start, and began to hyperventilate. My breath wouldn’t come. I was terrified. I made my way to the family room, got into the recliner, and covered myself with an afghan. I could breathe better sitting up.

While in that chair, I had a long talk with God.

“Please help me breathe better right now!” I wheezed.

My eyelids fluttered open. I kept them at slits and saw fuzzy shapes in the room. My breathing felt slow and steady.

“God, thank you for hearing my prayer!”

I touched my forehead with two fingers as if to stave off a headache. I felt softer and looser.

“And thank you for sparing my life. What can I do to repay you for saving me?”

I fell asleep mid-prayer.

Squinting in the Winter Sun

Do you ever notice the sun is so much brighter in January and February? Especially in Arizona! I’m really feeling it this year.  I live in Arizona so I’m used to plenty of sunshine.  But this winter sun is different.

One of my favorite winter morning rituals is to wake up while it’s dark, then when dawn breaks, go to the three tall living room windows and open the blinds to let the sun in.

“It will help warm up the room,” I explain to the walls.

Our winters here in the desert are dry and cold. I mean get out your puffy jacket kind of cold.  When the temperatures begin to drop below 60 Arizonans start pulling out their cold weather clothes. Give us a few mornings in the upper 20s and you’ll find a fire in the fireplace all day!

I know, I know. I hear from my friends in the Midwest and eastern parts of the country about their blizzards and closed roads and my heart goes out to them but I can’t help it – I AM COLD!

Besides being chilled all day long, I can hardly get out the door before that bright sun is hitting me right in the face. When I’m driving, it blasts through my driver’s side window making my skin feel like it is cooking on a hot skillet.

The only relief is to make a right turn and the sun goes behind me. Whew.

It’s not just the sun, it’s the sky! It’s so darn blue, so clear, not a cloud to be seen. That blue is nearly indescribable – certainly not royal or aqua or baby blue. It is not azure, cobalt or sapphire.

Most blues are considered calm and serene but not this cold winter Arizona sky color – it is bright, bold, intense, and powerful. I finally googled cerulean blue and this is the color swatch that came up.  Yup that’s it! Doesn’t it just hit you in the face?  Are you squinting right now?

My 8-year-old nephew bounced down his sidewalk to our car as we prepared to drive to a movie.  He’s wearing full size adult ski googles – the kind with a single lens tinted orange.

They barely fit on his small face.  I told him how cool he looked and he said, “I know.  We got them at a yard sale.”

I went on to tell him it was smart to wear eye protection on this exceptionally bright day.

Showing off, I explained, “The sun is high this time of year and its angle to the earth make it really bright! I’ll bet none of the other kids will have those kind of sunglasses.”

He says, “but it’s to keep the snow out of my eyes”.

Me, “Oh. I didn’t know you were a snow skier.”

He’s serious now, “Oh no, I don’t ski. I just go sledding on Mt. Lemmon. But now I won’t get snow in my eyes.”

“Well, you might want to take those off when the movie starts so you can see.”

“Oh yeah.”

Driving to the theater, I feel the skin on the side of my face start to sunburn through the car window. I put my hand on my cheek and feel the heat.

“Darn you, winter sun.”

The Real Reel

The REAL REELlooking back at 2023

Why am I struggling with all the hype around the new year. I feel pressure from what I see out there.  It looks like this:

“Have you selected your word for the year yet?”

“What are your goals for the new year?”

“Have you done your review of last year?”

“Look at the pictures of my 2023!”

You all know what a highlight reel is – you know the wonderful pictures on social media showing others having the best time, doing the coolest things, with all the wonderful people.  We all do it, show the highlights and not the lowlights.

Why am I so stuck?  Here’s my take on why.  My 2023 paper calendar had all squares filled in with the things I did – from the mundane dental appointments to the most exciting life events. But it also brought back a flood of memories.  Like losing one of my best friends to a little-known cancer; losing one of our best Oregon buddies to a better-known cancer; and a pretty dramatic search and rescue incident to find my grandson in August.

That calendar reminds me of all the trips I made to the small town library to get good WiFi while trying to finish the million details to publish my first book.  It also shows me all the great times I spent with Tomas in our summer spot on the Oregon coast.

I can’t even begin to tell you the greatest joy and love I felt all December from the days surrounding my mega book launch party and rolling right into the best Christmas holiday I’ve ever had. When I finally took a few minutes to realize that being human means living ups and downs every day, winning some and losing some, I said, “Highlights – Shmighlights! Not for me.”

I read my favorite author/blogger Carol Thomas at Heart Sisters and her new year’s blog was spot on. We women who suffer heart disease (or any other chronic disease) struggling with new year’s resolutions should make “self-care promises” instead.  (Link to read at end of my blog)

I really like that idea! She reminds us to make these promises doable for our level of strength. These are likely small but meaningful goals. She also mentioned a project she’s done called “52 small things”. Oh again, I love this idea. I figure it’s a small weekly goal instead of one giant year’s objective.

After all my own introspecting, I remembered to talk with my heart (I tell how I learned to do this in my book -pg 159 in the paperback) and she was so helpful!

She said, “it’s okay to #JUSTBE while you re-live those glorious memories from December.  You don’t HAVE TO do anything now, especially since you’re so happy.  There’s no need to change. You can take on the next change when it feels right.”

I felt encouraged to stay on the path I’m on feeling grateful every day and sharing the message of self-care and freedom from stress.

As I bid her farewell, she said, “You be you. Trust yourself to know what feels right.”

I realized I have brilliant ideas that become huge goals ALL the time, not just necessarily on January first. So why not keep riding the wave I’m on – I don’t really want to disrupt this happy place I’m in. So, I’m just going to keep enjoying the moment, living in my beautiful space with my best friend, and writing and working everyday towards living my passion.

Oh, and that pesky word of the year decision? I got it! Like a lightbulb! It is FAITH. Faith works as my word of the year on so many levels. Faith in myself to keep focused on the things that really matter. Faith in God to give me one new day every morning.  Faith in the human race to start behaving like decent people practicing kindness.

Signing off now on this first blog of the year. Thanks for letting me share my “real reel” with you.

P.S. Read Carol Thomas’ Heart Sisters blog post – https://myheartsisters.org/2024/01/07/new-years-resolutions-for-those-who-hate-resolutions-2/

The New Normal

Giving up my BUSY BUZZ

When the doctors released me from the hospital I had stacks of papers with instructions for diet and exercise and ALL the new medications I had to take for the rest of my life.

But, the hardest instruction to follow was from dear Dr. Marshall, he looked into my eyes intently and said, “Susan, you have to remove stress from your life.” That’s it. No explanation as to what exactly that meant.

My mind started to flip-flop. “What?! When I think of stress, I think of a terrible car accident, or being ‘stressed out’ over a sick loved one. Here’s what I learned.

Stress comes in many forms.  There is even a type of “good” stress (called Eustress).  It’s when we are excited or happy about an upcoming event.  Imagine you are excited about going on vacation – it’s that kind of feeling.

I had to admit I thrived on that kind of low-level stress, it gave me a buzz, and a certain amount of energy to get me going on my packing or preparing for the flight. Or if I was facilitating a meeting or hosting a party – I would be happy and excited with that Eustress working in the background.

That’s what the doctor was talking about – I had to stop those feelings, avoid those times and always be cool calm and collected.

Darn it!  I liked that feeling, I called it my busy buzz.

Here’s a clip from my book recalling my life in 2016.

One time I decided to list all my groups, meetings, classes, and clubs, along with the meeting days, in the back of my day planner. In my organized manner, I divided them by type: women’s groups, networking clubs, charity organizations, lunch groups with friends, online courses, and mastermind groups. There were easily 20 items on the list.

My calendar was packed with weekly and monthly meetings and a few quarterly gatherings. Some days I’d have a lunch meeting and an evening event. No problem!

Then there was my digital world.

By the time Zoom became the norm during the COVID-19 shutdown, I’d been attending Zoom meetings for several years. Some women hated them, but I was plenty comfortable with meetings conducted on Zoom. It allowed me to attend meetings of my favorite professional women’s group anywhere in the country. There’s a chapter in nearly every state.

I also became connected to a teacher who offered women sure-fire ways to become entrepreneurs working from anywhere in the world. It didn’t matter what your business was—or even whether you had a business yet. Her name was Monica, and she taught us her tips for getting customers and doing business online.

My product was an online course centered around writing one’s life story. I had developed a method to get a writer thinking, remembering, and creating pieces from her lifetime. This would become a memoir.

I learned from Monica about the “best” software to use to set up an online course. I learned about marketing in an “automatic” way. I was posting every day on Instagram, Facebook, and LinkedIn. Everything had a schedule.

Before I knew it, people were asking me to do anything but help them write their life story.

First there was Deanne, a petite brunette who owned and ran a preschool. “I’ve already written the story of my unique childhood,” she said. “Will you read it and tell me what you think?” I asked Deanne to send me a chapter so I could assess her project. Oh my, it was so disjointed. Too many storylines and characters.

Next was Lorna. An elegant 60-something dressed in Chanel, she approached me at a meeting. “I have a beautiful love story in my head. It’s the story of how I met my husband. I think it would make a great screenplay. Can you help me put my idea together and find a producer?”

Another off-target request came from a serious, dark-haired young woman named Connie. “I don’t want to follow a system. Can you just coach me through writing my book and finding a publisher?”

I said yes to all comers and let them know my hourly rate was fifty dollars. Even though I knew I was in over my head, I found myself creating services for editing, screenwriting, and book coaching—including publishing.

About a week after the heart attack, my son Tim helped me announce to my circles that I was out of commission. We canceled two writing workshops and refunded the fees. I closed two private Facebook groups where I’d been offering a weekly writing prompt. I stopped posting on social media. We let everyone know I didn’t have the energy for phone calls.

No more networking; no more crazy posting schedules; no more drained energy. I took two naps per day and went to cardiac rehab for a workout.

I gave up every group except for my women’s networking group. This filled my cup, offering a talented national speaker, a wonderful lunch, and some much-needed camaraderie. For these outings, I asked a good friend to sit with me, to make sure I ate and stayed hydrated, and to keep me from lingering too long. We joked that she was my “handler.”

Apart from this tiny oasis of freedom, I dutifully stayed home and rested. Like a prisoner with a ball and chain, I faithfully wore the life vest.

But this wasn’t the real me. And so, my journey began. It was more of a struggle than a journey because making those changes was one of the hardest things I’ve ever done!

Doesn’t this sound like a perfect description of a Type A personality?

Here’s a quote from one of my favorite actors.

“I have to admit, I was dismayed when I found out “Type A” refers to the risk of heart disease. I thought it was just a nickname my mom gave me!
—Reese Witherspoon