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When My Son Needed Hospital

  • Feb 23
  • 5 min read

"There is no such thing as a perfect parent. So just be a real one,"

Sue Atkins


I was still unwell when the phone rang Tuesday morning. My son had spiked a 40°C fever overnight at boarding school. The medical centre was monitoring him, they said. Probably just a bad sore throat. They'd keep an eye on it. But by Wednesday, something in my gut screamed that this wasn't just a sore throat. Fever that high, that persistent, in someone who's never really sick. I couldn't shake the feeling. So I took him out of the school and straight to the hospital.


Wednesday night: Admission

The A&E admitted him just after midnight. Upper respiratory tract infection (URTI), they said. Started him on broad-spectrum IV antibiotics immediately. The kind that covers everything whilst you're still figuring out what you're actually fighting.


I sat in that chair beside his bed, my own illness making everything feel slightly unreal, and watched the IV drip. They hadn't taken any cultures yet. This was being treated like a lousy spell of sore throat that had gotten out of hand. Pump him full of antibiotics, wait for the fever to break, send him home. Standard protocol. Nothing to worry about. Except I'd been the patient thirteen times. And I knew that sometimes standard protocol misses things.


Thursday: Too soon

The ENT doctor reviewed him Thursday morning. Looked at his charts, checked his vitals, nodded approvingly at the IV antibiotics doing their work. He was responding well to treatment, they said. Probably looking at discharge Friday.


I felt a tension in my chest. My doctor was always careful and meticulous. After a couple of rushed discharged that I insisted, which turned out badly, I learned my lesson. He'd been on IV antibiotics for barely a day. They still didn't know what they were treating. Just broad coverage and hope.


But what could I say? My gut says wait? This feels rushed? I was the anxious mother who'd brought him to the hospital herself instead of trusting the medical centre's monitoring. The one currently fighting her own illness and probably not thinking clearly. So I said nothing. And spent Thursday night watching him sleep, counting his breaths, checking his temperature every hour.


Friday: The cough

Both the IV broad spectrum antibiotics and paracetamol were removed, replaced with targeted oral ones. He started coughing overnight. Not the dry irritated throat kind. Something deeper. Something that came from his chest. And his temperature, which had been stable under the IV antibiotics and paracetamol, started climbing again.


The morning rounds came. The ENT doctor reviewed his progress, made approving noises about his response to treatment. Still on track for discharge, they said. Maybe even today if he continued improving.


I watched them prepare to leave and felt that same gut punch I'd felt dozens of times before. The one that says something's not right here. The one that knows responding to treatment and actually being treated aren't the same thing.


This time, I didn't stay quiet, "Could we do a chest X-ray before discharge? Just to be sure?"


The doctor hesitated, "He was responding well to the antibiotics. The fever will still be there for a couple of days more. His vitals are stable. An X-ray seemed unnecessary at this point."


"But he'd started coughing," I said. "And his fever was climbing again despite the medication. Could we just check before sending him home?"


The pause felt eternal. Then the nod. Alright. They'd order one.


The image that changed everything

Pneumonia.


The infection had moved into his lungs whilst everyone was congratulating themselves on how well he was responding to treatment.


I sat there staring at the nurse as she came in to take another blood sample, announcing the need for it due to this recent development, feeling relief and rage in equal measure. Relief that I'd pushed for the X-ray. Rage that I'd needed to push at all.


This was the moment everything shifted. Suddenly it wasn't just a bad sore throat anymore. The respiratory doctor was called. Suddenly they needed to know exactly what bacteria they were fighting. They finally took a sputum sample for culture. Now we wait 48 to 72 hours for results. However, they were still treating him very delicately. No broad spectrum antibiotics, oral paracetamol only on demand.


I thought about Thursday's planned discharge. About what would have happened if he'd gone home with the wrong antibiotics and pneumonia no one knew he had. About how far we lived from the hospital. About how sick I was myself, how little capacity I had to bring him back in an emergency.


That one question. That one X-ray. That's what stood between a routine discharge and a potential disaster.


Saturday: The spike

His fever spiked again overnight. 40°C. This time, the oral paracetamol no longer suffice. Only then, did the respiratory doctor escalated treatment. I couldn't understand why he was made to suffer when this could be prevented.


My thirteen hospital stays had taught me that you cannot rush cultures. That 48 to 72 hours is standard because that's how long bacteria takes to grow in a lab. That treating broadly first whilst you wait for targeted results is necessary, not negligent.


But knowing the reasoning didn't make watching your child burn with fever any easier. When broad spectrum antibiotics could be started early, yet didn't.


Sunday: Temperature stabilised

The respiratory doctor came by. Checked his temperature, listened to his chest, reviewed his charts. No fever without paracetamol drip. That was the marker they'd been waiting for. His body controlling the temperature on its own meant the antibiotics were winning.


They didn't rush to discharge him this time. His discharge pending the culture results, of course. Once those came back, they'd know exactly which antibiotic to send him home with.


I asked for another X-ray to check if the pneumonia was clearing. Apparently, according to the doctor, it was too soon. Radiological changes take time to show on imaging. Even when a patient was clinically improving, the X-ray might not reflect that for days. A follow-up appointment was scheduled in one week. That was the appropriate timeline to see progress.


Tuesday: Targeted treatment

The culture results finally came back. They knew exactly what bacteria had caused the pneumonia. The targeted antibiotic was prescribed. We were discharged that afternoon with a week's worth of antibiotics, a follow-up appointment scheduled, and instructions to watch out for returning fever, breathing difficulties, worsening cough.


I knew what to watch for. I'd been watching for days. But this time I was watching him heal instead of watching him suffer whilst medical timelines dictated patience.


Maybe this was the thing about being a caregiver when you had been a patient. About carrying medical trauma into moments when someone you love needed hospital. Your experience wasn't just scars. It was knowledge. It was instinct. It was the ability to distinguish between necessary protocols and dangerous shortcuts. It was armour.


But it was also exhausting. Using everything those thirteen stays taught me whilst also unwell. Being the voice, the advocate, the safety net, when I barely had the strength to sit upright.


If you had been the patient, you know things other parents don't. Use that knowledge. Trust those instincts. Push when something feels wrong. But also forgive yourself for how hard it is. For how much it takes. For the fact that being right doesn't feel like victory, just relief mixed with rage that you had to fight for it at all.


If this story resonated with you, please share it. Every parent deserves to know their instinct matters. That one question can change everything. That medical experience, however painful, can become the armour that protects someone you love.

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