Disclaimer: I may have been financially compensated or be gifted products from the companies mentioned in this post, unless otherwise stated. Posts on LouiseRoseRailton.com may contain items which have been gifted from a company, are a PR sample or paid for with a gift voucher. LouiseRoseRailton.com also contains sponsored posts, in which I have received paid compensation. All opinions and thoughts are genuinely my own. If you wish to find out more, please see my DISCLAIMER page for more information.
In 2013, everything changed for me and my family. Luke passed away from Sepsis in September 2013 at the young age of 22 years old. I was in my final year of university and really struggled to cope with the loss of Luke, who was like my brother. Grief has no time limit. It is suffocating. December 2017 marked our 5th Christmas without our lovely Luke. Christmas was his favourite time of year and it is always a very hard time for my family. I miss him every single day and think about him all the time. Even though there was only a months age difference between us, Luke was technically my nephew. I had grown up with my dad and step mum caring for Luke through his whole life. We used to go camping as a family, Luke loved the seaside so we would go on regular trips to the seaside for fish and chips. He would get me in trouble if I changed the TV channel from one of his favourite shows, and then be in absolute hysterics afterwards laughing to himself because he’d got me told off! That’s the kind of cheeky character he was and which is also why we used to call him a cheeky monkey.
Although Luke was diagnosed with Cerebral Palsy from just after birth, he was the bubbliest and loveliest lad ever. Due to Cerebral Palsy, Luke was unable to walk and talk but he could still express when he was sad, upset, happy, found something funny, etc. He just couldn’t actually communicate with words. He did normal things like any other person would do such as going to school, going swimming, had favourite meals, favourite TV shows, favourite music, etc.
“44,000 people in the UK lose their lives to sepsis every year.” The UK Sepsis Trust
It was sepsis which took my amazing nephews life. I will always remember when my incredibly strong step mum looked me directly in the eyes on the day of Luke’s funeral and said to me, “How am I going to get through life without my boy?” It broke my heart. Luke was unwell for a month(ish) with diarrhoea, vomiting, not drinking or eating, crying in pain, etc. My step mum sought out medical advice on a number of occasions from 111, Luke’s nurses who visited regularly and the on-duty GP multiple times. No one suspected sepsis, at all. There was no mention of it even being a possibility. The advice the GP kept giving was to keep up with regular water and paracetomol for temperature control, blaming Luke’s symptoms on “a nasty stomach bug”. My step mum knew something wasn’t right and kept asking for medical advice, but continued getting the same responses. It wasn’t until the middle of the night one particular evening where Luke was screaming in pain, so an ambulance was instantly called. Luke was taken into hospital and my family were told he had a matter of hours left. We lost him that night.
We need to treat sepsis the same as a heart attack. Sepsis kills, quickly, which is why sepsis awareness is so important and vital. Anyone can develop sepsis after an injury or minor infection, although some people are more vulnerable. Awareness of the symptoms (these differ depending on the individuals age) needs to be a priority. Sepsis needs to be one of the first things medical professionals consider. Even by just suggesting sepsis to the medical professionals who are treating the individual, could be the thing which alerts them and saves a life.
“There are around 123,000 cases of sepsis a year in England.” NHS Choices
Early symptoms of Sepsis in older children and adults may include:
Symptoms of severe Sepsis or septic shock can include:
There definitely needs to be more sepsis awareness, although things are already improving as I’ve seen a lot of campaigns in both my personal life and through work in recent years. The UK Government are definitely starting to work on sepsis awareness. We definitely didn’t think we would have to say goodbye to Luke so soon. Sepsis instantly took Luke away from us and our lives haven’t been the same since. All I can say is, we all need to realise how lucky we are and treasure moments with our families/the people we love. Don’t waste a single second that you have with them while they’re still here. You never know what could happen. I love you and miss you Luke x
“Although it’s difficult today to see beyond the sorrow, may looking back in memory help comfort you tomorrow.”
You can find out more information about Sepsis from the following resources:
Disclaimer: I may have been financially compensated or be gifted products from the companies mentioned throughout my blog, unless otherwise stated. Posts on LouiseRoseRailton.com may contain items which have been gifted from a company, are a PR sample or paid for with a gift voucher. LouiseRoseRailton.com also contains sponsored posts, in which I have received paid compensation. All opinions and thoughts are genuinely my own. If you wish to find out more, please see my DISCLAIMER page for more information.
I'm Louise, a 28 year old blogger living in York. I also work as a medical receptionist and I'm currently a trainee teaching assistant. This is my corner of the internet, in which I cover topics such as mental health, travel, fashion, lifestyle and so much more!
February 2019 – Leeds
March 2019 – Manchester
April 2019 – Harrogate & Hull
May 2019 – Yorkshire Spa Break
June 2019 – Disney Land Paris
August 2019 – Leeds