Friday, May 15, 2026

A Cautionary Tale: Of the Medical Kind

Yesterday I sat sideways on a chair in my dining room as a homecare nurse named Emily pulled 40 staples from the incision running down my spine.

Every few seconds there was a stinging sensation and then the sound of a staple landing in the metal dish.

Sting-plink, sting-plink, sting-plink.

And Now equiped with a zipper!


I absently tried to keep track of how many she had pulled, and when I had counted 34 and she suddenly announced only 6 left to go, I silently congratulated myself, I was bang on.

What an accomplishment!

Counting staples aside— it was indeed an accomplishment to be here, in my own home, spinal surgery completed, staples out, and looking towards the next steps in the treatment plan.

My mind abruptly shifted gears as I thought back to the journey that had begun more than six months ago, and what I had learned over that tumultuous time.

Go to the doctor, they said.

Be your own advocate, they said.

Speak up and tell your doctor exactly what you are experiencing, they said.

Get a second opinion, they said.

Well in this case, it turns out that they were 100% correct!

And yet...

It turns out that even if you take all of these common sense, proactive steps to safeguard your health, you may still end up being under the care of a doctor who fails you.

Doctors are just people, after all.

And over time, they may fall into a sort of daze, caused by the routine of similar ailments, if I can put it that way. In which case they may become unable to see beyond those common cases, to what could be a rare, unexpected cause for the symptoms their unfortunate patient complains of.

In my case, I believe this is what I experienced with my family doctor.

In October of 2025, I first experienced the beginnings of the symptoms that eventually progressed to the point where I could barely walk without experiencing excruciating pain.

When my symptoms first appeared, I expected my hip and knee pain to get better over time, but after a few weeks without improvement, I went to see my doctor.

I explained the symptoms and asked about some of the serious possibilities that worried me.

"I've had cancer before, and I'm worried about bone cancer."

Our discussion went back and forth. Where exactly is the pain? And eventually as he motioned to my leg, I was informed, bone cancer in your leg wouldn't cause pain here, or here, where you say you are experiencing pain.

He was indeed right — IF bone cancer was in the leg, it would have presented differently.

So that possibility was dismissed and we spent the next several months getting x-rays of my back and hips and knees and his eventual recommendation was physiotherapy for some mild arthritis.

I dutifully tried that with no improvement.

Then there were cortisone injections, first the SI joint and there was blessed relief for about a week.

Then it was another injection in the hip, and this time relief lasted 2 or 3 days.

Meanwhile I was experiencing more and more pain while walking and it was March and I had completely run out of patience.

March 30th, I went to my doctor one last time.

His final recommendation: take the GLAD program; an eight-week, group exercise therapy session for sufferers of osteoarthritis.

When I suggested he order an MRI, which I would gladly pay for, I was told no, it wasn't needed.

When I arrived home, my lovely wife saw I didn't have the MRI requisition that we were hoping for.

She was, shall I say, livid.

Did you tell him how you have declined so rapidly? Yes, I did.

Did you tell him you would pay for the MRI? Yes, I did.

"That's it, we need a new doctor!"

It was agreed, and we decided to seek out a second opinion.

But new doctors are hard to find right now in Alberta.

That was when we remembered that my sister had recently been seen by a doctor at a new clinic in St. Albert and she was very, very happy with how well he had looked after her.

He wasn't taking new patients, as far as they knew, but it was apparently possible to make an appointment with the clinic and request to be seen by a specific doctor.

So, Rose called and worked her charm and just like that, I had an appointment to see the doctor in one week.

In the meantime, it was the Easter weekend and because their church didn't have a Good Friday service and ours did, our friends decided to join us for the service, bringing along their daughter, a nurse practitioner in the city.

When she saw how I moved and how much pain I was in, she was shocked.

We talked for ten minutes after the service, and she was very glad that I was seeing a new doctor and was planning to seek an MRI as soon as possible.

Of course, there are many kinds of MRI, and we weren't sure which one would pinpoint the source of my illness; but the one that she recommended I ask my new doctor about, was a lumbar spine MRI.

A few days later we saw the new doctor and that's exactly what he ordered, along with a bone scan and a CT scan.

When we left the doctor’s office on April 13, we were clutching a fist full of scan requisitions and prescriptions and we finally felt we were on the way to diagnosing my illness.

As soon as the results came in from the MRI, three days later, ($540 at Insight) we knew we had done the right thing. Yes, the system may have eventually gotten around to scheduling a hospital MRI in a few weeks, but having it done so soon after all the interminable delays I had already experienced, was very much worth it.

A few days later we saw the doctor again and he explained the seriousness of the results to us, and we made an appointment for the following week, after all of the tests were going to be complete.

We listened carefully as he explained the likely diagnosis, but we had of course already Googled the heck out of it and had made some progress wading through the technical jargon of the scan reports.

Later, while the nurse practitioner helped us apply for a handicapped placard for the car, the doctor left the room to make some calls and get me a referral to the Cross Cancer Institute as soon as possible.

The next day was the bone scan and a couple of days later, the CT scan with contrast.

They all confirmed the same bad news; some sort of tumor that had damaged the bones in my spine causing all the nerve pain I had been experiencing.

The Cross didn't call me until the following Wednesday, after all of the tests were complete, but then I received the call from a friendly young woman who apparently works on "The Lung Cancer Desk".

From the first time I heard that voice on the phone, things began to happen at a speed that was hard to believe.

As I write this, two weeks later, I find it impossible to think of the enormous impact this young woman’s actions on my behalf have had on my life and my family’s lives, without being completely overwhelmed with profound gratitude.

I've tried time and time again to talk about it, and each time tears flood my eyes, and I am quick to lose the power to speak as I sit there, helplessly mute, looking for a tissue as I remember what she did for me.

Barely an hour after our first brief chat, she called back with a firm course of action.

She told me she had sent my file to the spinal surgeon, and I needed to go directly to the emergency room at the Royal Alex Hospital and tell them that and they would be expecting me.

Apparently, the oncologist at the Cross had looked at the scans and told her he wouldn't be able to do anything for me until my spine stabilized and they had taken a biopsy.

I wasn't thrilled at the prospect of waiting in the emergency room at the Alex, but she reassured me the spinal team was expecting me, and they would send someone to bring me through and get me admitted.

So Rose and I packed a little bag and headed down to the hospital as quickly as we could go.

There, due to the usual bureaucratic nonsense, my name had disappeared from their system, and I was shuffled off to wait with the other unfortunate souls.

But my benefactor had given me her direct phone number at the Cross, and I called and left a message.

Not too much later, she called back with the news we were hoping to hear. The NP (nurse practitioner) for the spinal team was now on her way down to meet us.

This NP became a key member of the wonderful team of people that gathered around and cared for me so well over the next few days.

I felt so blessed to be under their care.

She led us past the curtained cubicles of the ER that we are all familiar with, to a small private room, tucked behind the nurse’s station, and there the ponderous admitting process began.

At first, our questions went unanswered (there is always a certain amount of confusion in these circumstances). Am I going to be admitted? Can I have something to eat?

But of course, because I came to be there through the bureaucracy of the Emergency Department, I would have to be seen by one of the doctors on duty.

"Oh, oh," my mind screamed, "if this is going to go sideways, this is probably where it will happen."

When he did finally arrive, he didn't seem to be fully informed of my status or circumstances, and we had to convince him that what I needed was not more pain meds and then to be sent home.

Rose was adamant, "NO morphine!".

But all credit to him, he seemed more than happy to turn me over to the spinal surgery team and before long I had my blood taken and was gifted with an IV line and several wristbands before being moved upstairs to the surgical ward #34.

Once there, I was finally able to eat something and was told that my surgery would likely be the next day, so after midnight, no more food or drink until after it was complete, so make the most of it.

Finally, at 4 pm on Thursday, April 30th, I was informed they would be coming for me at 5 pm.

7 hours later, at 11 pm, I was back in my room, groggily talking to Rose, learning that my daughters, Kait and April had just been sent home at 9:30 after spending time being with their mom, comforting each other in the family waiting room.

I loved hearing that the girls had been there for their mom, they were both so sweet and considerate, leaving me flowers and stuffies and sweet treats and a very special card from my granddaughter Juniper.

It is a wonderful thing to have family and friends around you in times like this.

I learned also that Rose was getting a ride home around midnight from some friends who had volunteered to both come down and take her and her car home (Rose had let slip that she was contemplating sleeping in her car at the Royal Alex parking lot). For some reason they were aghast at the thought, and I'm glad they looked after her the way they did.

Finally in a chair and out of bed


Poor Rose had already had to listen to me woozily praising the recovery room nurse.

I've had a few surgeries now and each time I wake up from the anesthetic afterwards, whoever is there to greet me and welcome me back into the world, temporarily takes on a very large place in my recovery.

They have news of how it went; they may know something of where my wife is, they talk in a kind, comforting voice and the very normalcy of the interaction makes you feel good.

I am invariably chatty, a little goofy, and quite happy to be alive.

And then there's Rose.

While the recovery room nurse is important, hers is a bit part; just one small scene in a lifetime.

Seeing Rose again after surgery like this is something else again.

I don't remember if I cried at seeing her, but I may have, and if I didn't... I probably should have.

She is incredibly important to me.

Her steadfast love: her constant encouragement and support, her utter belief that I will recover and her patience with me along with her iron will and strong resolve that together we can get through any challenge.

All of these qualities lift me up and enable me to face whatever is coming.

But most important to me is her faith in God

Because faith in God is at the very heart of any strength I have.

On my own, I know that I am weak and powerless in this situation. At the mercy of a bureaucratic system where I am represented by a number.

Bed 22-1.

And I am treated exactly the same as any other occupant of bed 22-1.

But when faith and prayer and love come together to focus God's power on the resident of bed 22-1, something special happens.

Sam happens.

And the impersonal system throws open its doors and makes a place for me.

Simran happens.

And I am whisked through the emergency department and admitted to the surgical ward.

Dr. Raj happens.

And the next day I am operated on in a long and grueling, but successful surgery.

Rose happens.

My beautiful, loving, kind, patient wife, waiting to welcome me back after hours in surgery.

Dr. Naidoo, and Ruth, and of course, nurse Sophia happens. Wonderful, attentive nurses who cared for me. (Sophia now has a car named after her).

And before I had met any of these wonderful medical people, my coincidental meeting with Angelle, my NP friend, on Good Friday happened, and helped set off the sequence of events that led directly to the surgery and beyond to the recovery and treatment.

I know that all these people do their jobs every day in much the same way as they cared for me, and I know that their other patients are lucky to have them as part of their own medical team.

But in this case, I choose to believe that they came together as my team, as an answer to prayer.

I am incredibly grateful to each and every person who has been and who will in the future, be part of this group of willing people who looked after me.

It starts of course with family and friends nearby who are able to physically be there for us, but there are literally hundreds of people who have come together to pray for us as well.

Friends and family who live far away, and our Pastors and church family, faithfully lifting us up in prayer, and strangers who are part of the Christian community who somehow heard of my illness. All of these wonderful people are integral to this story.

Without prayer I am just the occupant of a bed, in a ward, in a hospital, where the staff is tired and overworked, just trying to do the best they can.

I can't explain it very well, but with prayer, something special happens. I am not alone, even when no-one else is nearby. I truly feel that there is something happening on another level.

Don't get me wrong, there was pain and discomfort and sometimes I did feel very much alone. 

Not every member of the nursing staff was part of my team, some were very much not.

But always, there was the thought of shift change and the prospect of the return of a favorite nurse.

Prayer is a wonderful thing, and now that I am home recovering, I pray for every member of my medical team, and for my roommate in the hospital, suffering with his own serious medical condition.

Lately, a new chapter in my story has opened up and the second part of my journey through this illness has begun.

On May 13th, exactly one month after I first saw my new doctor, and 2 weeks since my surgery, we had our first, in person interaction with the Cross Cancer Institute

My initial consultation with a radiation oncologist.

As we talked, Rose tried hard to pin him down as he explained my prognosis and the likely outcome of treatment.

"How much time does he have left?" She asked in her no-nonsense way.

We both liked the doctor and felt as reassured as it was possible to feel under the circumstances.

He explained that there was actually some good news. Even though they still needed to do a PET scan and a brain scan, the bone scan, MRI and CT already completed had not revealed cancer anywhere else in my body.

The biopsy results had shown that the cancer was an offshoot of the lung cancer from four years ago and it was common for it to turn up in the spine and that was what we were now dealing with.

After digesting this news, I tried in my own way to summarize my understanding of what he was saying.

"So I have an awful diagnosis, but with the best possible prognosis— providing these next scans are clear of any cancer?"

He nodded.

So now we know.

The first battle is over, but the war is not yet won.

Thank you all for your prayers and kind wishes.

Thank you to those of you who have been able to be those "boots on the ground" that we so desperately need as we prepare to move, and we deal with all that comes along with that.

Downsizing in the midst of a health crisis is not something I recommend.

Thank you, to all of you who have been there for Rose especially, and who continue to shower us both with love and kindness throughout this struggle.

Thank you Jesus for being there for us, for me; for strength, hope, comfort and healing and also for the wonderful team of people who made the occupant of bed 22-1 feel very special indeed.

May the Lord bless and comfort you all, in your own time of need.