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Nancy

Partner of sepsis victim

In February 2023, my husband's battle with sepsis began. My husband was admitted in emergency with a severe kidney infection. However, blood tests revealed that a dangerous bacterium - Staphylococcus - had entered his bloodstream. The infection spread throughout his body and affected several organs. It was only days later that I first heard the word sepsis - a life-threatening reaction of the body to infection.

He ended up in intensive care, underwent major heart surgery, and experienced numerous complications: pneumonia, thrombosis, new infections. Yet he fought back bravely, even after countless weeks in hospital. Together, we rebuilt his life step by step - sometimes literally, electricity pole by electricity pole - during short walks in our street.

But sepsis returned. Another infection followed in 2024, a second sepsis, and finally a severe stroke that deprived him of his speech and independence. From then on, I became his voice. After two years of struggle and additional complications, he died on 5 February 2025.

Sepsis changed our lives forever. I learned how quickly a common infection can threaten a life, and how severe the consequences are when it is recognised too late or not taken seriously enough.

That is why I am telling his story today. Not just for him, but for all patients and families. Sepsis is not rare. It can happen to anyone. It needs to be recognised faster, treated better, and the consequences really recognised.

No family should go through what we went through.

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Personal stories

Sylvie

Septic shock - cause unknown

I was born in 1966 and live in Schoten (north of Antwerp). Together with my husband, I had two sons: the youngest still lives at home while the oldest has built his life in Amsterdam. My days have long been filled with taking care of my family, running the household and cherishing the warmth of our daily life. Beyond that familiar rhythm, I have always had a desire to explore the world. Travelling opens my eyes, gives me new energy and makes me feel how vast and multifaceted life is. I also chaired the school council at the school where my children took their first steps in learning, and found it a joy to make time for my girlfriends.

Wednesday, 9 March 2022, disaster struck unexpectedly. What started as an ordinary day turned into a nightmare when I was struck by septic shock with multi-organ failure caused by streptococcus aureus bacteria. Suddenly, everything stood still: my body, my future, my certainties.

What happened. It actually started on Monday. I was not feeling well - nauseous, very high fever - and slept almost all day. On Tuesday, the GP came. She examined me and took blood. Meanwhile, the fever continued to rise above 40°C. Wednesday in the afternoon, the GP called to tell me I had to go to the emergency department at Klina to get a dose of antibiotics intravenously. Once there, things suddenly went very quickly: several catheters were immediately placed, and in no time I was in the Intensive Care Unit. My husband was told that my condition was very critical and that if he had arrived two hours later, it would have been fatal. Fluid resuscitation was started, vasopression with Noradrenaline, Amukin and Augmentin. This was then Floxapen via a PICC catheter. The doctor who was called in to emergency was literally my salvation. Pretty soon the term septic shock with multi-organ failure (DIC, acute renal failure, shock liver) fell. For me, that period is largely a black hole. All I vaguely remember of this period is walking through fields, endless fields of flowers... On Friday, I was transferred to the ICU of the UZA. Saturday followed emergency surgery: my ICD and leads were removed. This was followed by weeks in ICU, Mid Care and cardiology, first in the UZA and later again in Klina.

The period in the clinic was not easy and very lonely. There was a lot of time for brooding and thinking. I was only allowed (limited) visits from my husband and children - someone came every day - as special rules still applied due to the coronavirus. In mid-May, I was allowed to leave the clinic. But the struggle did not end there. A whole rehabilitation track was completed and unfortunately the implantation of a new device was necessary.

To this day, I still experience the effects: fatigue, severe pain symptoms, concentration problems, brainfog, poor sleep, moodswings and overstimulation. My world has become small and finding understanding is often difficult. Aftercare after such an experience is a big problem. There is basically no plan, no info and too little understanding. Sepsis survivors are not “fakers”. There are plenty of doctors I visited with whom you feel you are not taken seriously. You are sent from pillar to post... this is very painful. Fortunately, I have a cardiologist who does listen, helps me look for solutions, follows up my file and discusses it with colleagues. A doctor who is ‘human’, empathetic and dares to look beyond his speciality. I am extremely grateful and have endless respect for him.

This is who I am today. No longer the old me, but someone who fights every day and hopes for more understanding and for a future where there will be some space for ‘life’ again.

One more thing - not unimportant - I cannot say it enough, a heartfelt ‘thank you’ to my family and friends for your support and understanding. I am sorry that I am no longer who I once was, and I fervently hope that step by step I can get closer to myself again. For those who know me less well: what you see on the outside often does not tell the whole story. You mostly meet me in the moments when things are going just a little bit better, but the struggles I face inside every day usually remain hidden. I hope the day will come when I can say again that I am really doing well!

Sylvie

Categories
General

By trial and error

How do you actually...
get back on track after immense trauma?

How do you do it... get back on track after an immense trauma? And why do some people succeed, but not others? Is it just a matter of "making the click", Or is something more fundamental needed?

🌀 In her new book, Liesbeth Claeys dives deep into the topic of resilience. She asks the questions we all sometimes ask ourselves after a heavy blow:

➡️ Can train your resilience
➡️ Does it come in different forms?
➡️ What about children - are they actually more resilient than adults?

With an open mind, Liesbeth consulted experts and strong women who, each in their own way, braved the storms of life: Petra De Sutter, Uus Knops, Geena Peeters,... but also with Cindy Verthé, sepsis survivor, board member of Sepsibel Vzw and the epitome of resilience.

🎤 The result? A series of honest, powerful testimonies full of recognition, hope and inspiration.

👉 This book is for anyone who wavers, but knows deep inside that there is still strength. For those who want to learn to fall, but also to get up again. For anyone looking for a foothold, and perhaps above all: for themselves.

Categories
Personal stories

Robert

My sepsis episode

Retired but still active, I was struck by sepsis in 2006, without really being aware of the severity of what was happening to me. Apart from chills, which I attributed to a slight fever (38.4°C), I felt no pain. Although I experienced intense fatigue from the first few days, I did not worry too much about it and attributed it to a neurological condition I had been suffering from for several years.

At the time, I was volunteering at a palliative care clinic. I did notice that the wound on my tibia, which I had sustained at the clinic after contact with one of the wheels of a patient's bed, was not healing. It was only after four or five days, and at the insistence of the nursing staff, that I decided to have blood drawn the following Wednesday. The results came in that afternoon and were not good. The doctor therefore decided to take a blood sample, a urine sample and some culture tests on Friday, during my visits.

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