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A little about us and how Cancer came to be.

A little about us and how Cancer came to be.

 Hey! Thanks for joining us and taking the time to read this. Long story short, if you're looking to read a blog about living with Oesophageal Cancer, you're in the right place! Short story long.... My name's Jo, I'm in my early 30's, live with Type 1 Diabetes and I'm partner to Tony. In November 2024 Tony was diagnosed with Stage 3 Oesophageal Cancer. We've started this blog to raise awareness, our experiences, tips and things we've learned along the way.  The highs and lows, good and bad. Oh and have a good vent every so often too! So how did we find ourselves here? - PS, there's going to be a lot of plurals in here, lots of ''We''. While it's Tony that has the Cancer, I promised him from the start that he won't face a single moment of this alone, and as a result ''we'' have Cancer. Tony has had acid reflux for a long time, years in fact. It's always been managed with over the counter tablets like Nexium ...
Recent posts

Surgery week tips for the carers.

 I will be posting an update on a what to expect day to day with all of this, both from the patient's and the other person's perspectives. Before i head into writing those though there's something i feel is really important to share. Maybe someone can learn from my mistakes. We felt reallly prepared going into surgery week, we had done lots of research on the procedure, recovery, medical terms used, what pipes ro expect post surgery, monitoring for issues or complications. I'm not taking anything away from the brilliant people who work in our NHS, or drawing a paralell between me on the good old google, and someone who had an education and career in this field. Tony and i are both very information driven and ready for pretty much anything. I felt prepared. I forgot one part of all of this... I approached Tony's operation clinically, I didn't approach it as the partner of someone who was about to undergo a life changing major operation. I'm very lucky in that...

The Difference Between Palliative and Curative Cancer Treatment

 A cancer diagnosis brings a wave of emotions—fear, hope, uncertainty—and one of the most important aspects of navigating treatment is understanding the options available. Two terms often discussed are curative and palliative treatment. While they serve different purposes, both play a vital role in improving quality of life and ensuring the best possible care for patients. Curative Treatment: Aiming for a Cure Curative cancer treatment is designed to eliminate cancer completely , giving a patient the best chance of long-term survival. The focus is on removing or destroying all cancer cells, preventing them from returning. This may involve: Surgery – Removing a tumor and surrounding affected tissue. Chemotherapy – Using powerful drugs to kill cancer cells. Radiotherapy – Targeted radiation to shrink or destroy tumors. Immunotherapy – Boosting the body's immune system to fight cancer. Curative treatment can be intense, with side effects such as fatigue, nausea, and a long recov...

Surgery Week & CCU

    As you'll have read in my last post, I made the mistake of being too clinical in my approach to this whole thing, and the emotional and mental impact of this whole thing hit me like a train. Just as a warning, images of Tony's wounds around 7 days after surgery are shown further down in this post, I will warn closer to the time in case anyone doesn't want to see. They will be at the very bottom of the blog with a huge warning before hand.  I'm going to compress the surgery week into one blog and break it down day by day. Tony's hospital stay was for a total of 9 days, the average is 10 to 14, but many get discharged as early as 7 days post op. It all depends on how well the patient is healing. Tony's brother and partner arrived over from abroad the night before surgery so the 24 hours pre op were pretty crazy too! A brilliant way to take our minds from what was coming next. They were staying with us for 2 weeks, which was good for me as I wasn't coming h...

Understanding the Ivor Lewis Esophagectomy: A Journey Through the Procedure

Embarking on the path of esophageal cancer treatment can be daunting, with surgical interventions often being central to the journey. One such procedure, the Ivor Lewis esophagectomy, stands out due to its complexity and significance. Let's delve into what this surgery entails, its purpose, and the road to recovery. What is an Ivor Lewis Esophagectomy? An Ivor Lewis esophagectomy is a surgical technique primarily used to treat cancer located in the middle or lower sections of the esophagus. This procedure involves the removal of the affected portion of the esophagus and the upper part of the stomach, followed by reconstructing the digestive tract to maintain its functionality. The Surgical Steps: Navigating the Procedure The surgery is typically performed in two main stages: Abdominal Phase : Surgeons begin by making an incision in the abdomen to access and mobilize the stomach. This step ensures that the stomach can be reshaped into a conduit to replace the removed esophagus. Thor...

Surgery Prep & Surgical Appointments

 Hey! It's been a while! So since we last posted we've been getting ready for surgery. I'll write another post shortly about the surgery and explore that in more detail. We've had 2 meetings with the surgical team since we got the go ahead for the surgery, one with the surgical team, and one with the surgeon who will be performing Tony's operation. I've mentioned in previous posts that compared to the Oncology side of things, the surgical team seem to be a lot less..... Fluffy, shall we say. We had been warned to leave surgical appoinments feeling like you've been hit by a train or swamped with negative stuff, and our first appointment certainly did! The Doctor we saw for the first appointment  seemed to be pushing us towards a palliative treatment plan, rather than the curative one our oncologist recommended. He wasnt happy that Tony hadn't had the prescribed 4 rounds of chemo pre op, and called the surgery ''sub-optimal''. We found this...

PICC line removal.

 If you’re reading this, you may be getting ready for a PICC (Peripherally Inserted Central Catheter) line removal, or perhaps you’re simply curious about the process. Either way, I want to walk you through what to expect so you can feel prepared. We know that even small procedures can stir up a mix of emotions – relief, anxiety, or maybe just a bit of uncertainty. A PICC line is commonly used for patients who need long-term intravenous (IV) access, whether for chemotherapy, antibiotics, or nutrition. It’s an incredibly useful tool, but eventually, when treatment is finished or no longer needed, it’s time for removal. Here’s our PICC line removal experience. When we arrived, we were taken to a treatment room where Tony was asked to lie down on an exam table with his arm positioned comfortably, as that’s where the PICC line is placed. The nurse  performing the removal explained what will happen in detail for us. The actual removal of the PICC line is a straightforward procedur...

MRI results and next steps.

Once again there was an MDT meeting today and a path to move forward. Mel started the call by saying ''I'm calling with what I think is a positive update for you. The surgeons are happy to proceed''  So, our next step is the Ivor Lewis Oesophagectomy we've written about in previous posts. Tony's MRI shows no lasting damage to his heart, no necrosis , (tissue death) no myocarditis (swelling), no blockages and both ventricles are working as they should. We now await a pre op meeting with the surgical team, an appointment to have the PICC line removed.  This part is a bit surreal really, we've always had surgery on the agenda, now that we know that's the next step it's both nerve wracking and really positive at the same time. The Ivor Lewis oesophagectomy can feel like a daunting experience. It’s a major surgery often used to treat esophageal cancer. The procedure involves removing part of the esophagus and sometimes part of the stomach, then reatt...

CT update.

 So following on from our last update, chemo was paused to allow the round Tony had been given to run it's full course. It wasn't safe to continue with that particular chemo reigme due to Tony's reaction to it. We had a CT scan on monday as the surgical team wanted to see if the chemo had shrunk the tumor any.  There was an MDT meeting this morning and our amazing nurse Mel has called with an update. Good news (bear with me, i'm always searching for the positives). We don't yet know if we're going for a different chemo, or if it's surgery. Now, that could be seen as frustrating or negative, and yes, it's a bit annoying..... BUT, both the chemo team and the surgery team are happy to go ahead with treatment. That means we still have two curative treatment options. Brilliant! The hold up is heart health. Both teams would like the cardiology guys to have a check on how Tony's heart is recovering and go from there. Yes it's another delay, but both tea...

Hair loss

 We were advised before chemo that hair loss was likely. Secretly we thought that because it's been so long since the chemo was given we may have escaped this particular side effect. It is something we've talked about, the idea of it can take a little getting used to. Tony's always said it didn't really bother him if it fell out, because he doesn't have to look at it! It's something I hoped didn't happen.  I know how that sounds. Hang on, i'm not being judgey allow me a sec to explain. I don't care what Tony does to his hair, clothes, it's irrelevant. I was scared of him looking ill, gaunt. That probably sounds really shallow, but it's true. Tony came into our bedroom from the bathroom this morning with a clump of hair is his hand. Clump sounds dramatic, I can't think of a better word though. 10 strands or so. I hugged him and cried fo a moment. He explained it was happening all over his head and he was certain it was falling out and not ...

Post chemo review.

 As we mentioned in our last post, the first chemo did not go well. A rare reaction the the 5FU resulted in a ''cardiac event''. As a result we had a meeting with the oncologist to explore how we will proceed with Tony's chemo treatment. It's another ''that didn't go as expected'' moment. We discussed what might happen next over the weekend and we expected they'd tone down the drugs used to minimise side effects, we pondered if they'd perhaps admit Tony for future treatments so that he would be in a safe environment should there be any further issues. Nope! The oncologist explained that waht we have experienced is very, very rare. She's only seen it happen 3 times in her career. She explained that treatment would temporarily stop. In that moment both Tony and I tensed. It was another moment in which the world stopped spinning. I asked Tony what he was thinking, I could see the gears in his mind turning. He simply replied '...

First Chemo.

 Our first chemo experience has been far from normal! As advised Tony started his steroids the day before chemo ( dexamethasone ). Steroids are given to take the day before, the day of, and the day after chemo. Our understanding is they help with the side effects and will giveTony a bit of a boost. It's advised to take them at breakfast and lunch as they can cause insomnia if you take them too late in the day. We arrived at the chemo ward nice and early. We took plenty of layers for Tony, aware that the chemo would cause an extreme sensitivity to cold, lots of snacks and a book to read as we were expecting to be at the hospital for up to 6 hours. We were taken into the chemo lounge which is a really bright and calming space, there's a tv on the wall playing relaxing music, the nurses are all upbeat and friendly. Tony got comfortable in one of the patient's chairs and one of the chemo nurses walked us through what to expect for the day. Tony's PICC line was flushed and h...

Straight into treatment - PICC Line.

 We landed back on the 29th and today we head to the hospital to get a PICC Line fit. A PICC line (Peripherally Inserted Central Catheter) is a long, thin, flexible tube inserted into a vein in the upper arm and guided to a large vein near the heart. It is used for delivering medications, chemotherapy, fluids, or nutrition over an extended period, reducing the need for repeated needle sticks. How is a PICC Line Inserted? A nurse or doctor numbs the upper arm and inserts the catheter into a vein. The tube is guided through the vein until it reaches a large vein near the heart. A chest X-ray confirms proper placement before use. The PICC line is secured and covered with a sterile dressing to prevent infection. The procedure to have the line fit was really quick, Tony was in and out in under 30 minutes. We entered the treatment room and the nurse explained how the line is put in and gave us some guidance on aftercare. Keep the dressing clean and dry to prevent infection. Avoid heavy ...

Managing Dysphagia on holiday

 Swallowing issues aren't easy to manage, though they are manageable with a little practice. Our advice is to work with food, not against it. Listen to your body. Experiment with food.  For Tony foods with sauces / gravy work best. At home things like cottage pie, rice pudding, ragu, are go to meals and cause little to no issue. That's at home, and we're in Fuerteventura! Thankfully with our break being all inclusive, there is plenty of choice and room to try different foods. For the first day or so, Tony had small portions and samples of the foods on offer. Breakfast isn't something we normally have, so that meal was easy! For both lunch and dinner there was always a selection of pasta and sauces. Tony was able to eat this with ease as he could pile on as much sauce as he wanted to. Soup was served daily while was also a great option for him, alongside sweet treats like rice pudding, ice cream and a selection of cakes. He experimented with other foods that were availab...

Positive updates.

 This will be our last post this year, as next week we're jetting off to Fuerteventure for a pre cancer treatment recharge. We have received a letter following on from the Staging Lap which confirms stage T3N1M0, Signet cell Adenocarcinoma. Now that all of the tests and results are in, everyone is happy and treatment can soon start. It's been a rollercoaster 2 months, but we're happy we have an accurate diagnosis, we know exactly what we are dealing with and have a plan moving forward. For now, we hope you're well, look after yourself, have a fab few weeks and we'll be back soon!

Staging Laparoscopy

 Staging laparoscopy is a minimally invasive surgical procedure used to determine the extent of esophageal cancer and whether it has spread beyond the esophagus. This procedure helps doctors decide on the most appropriate treatment plan by providing real-time insights into cancer staging. Esophageal cancer can spread to nearby lymph nodes, organs, or the lining of the abdomen ( peritoneum ). Imaging tests like CT scans and PET scans provide useful information, but they may miss very small cancer deposits. A staging laparoscopy offers a more accurate assessment by allowing direct visualization of the abdominal cavity. Heading into the procedure Tony's staging is T3N1M0. Why is Staging Laparoscopy Performed? The primary goals of staging laparoscopy in esophageal cancer include: Detecting metastases – Identifying whether the cancer has spread to areas not visible on scans. Assessing operability – Determining if the tumor is resectable (removable by surgery). Guiding treatment dec...