I’ve been lurking here for years, mostly following the stories of several cancer cases within my own family and various pre-cancerous scares.
Unfortunately, this time, I’m the one stepping into the spotlight. I noticed the cervical cancer thread has gone pretty stale, so I’m hoping it’s okay if I pop in from time to time to vent or maybe hunt for some actual decent advice or just a kind word.
I’m only 38—well, maybe a little older now—and last month I was hit with stage 3b squamous cell carcinoma of the cervix. It’s infiltrated the left side near the ureter, so they actually had to install a nephrostomy tube because of the obstruction and kidney dilation.
They mentioned there might be lymph nodes involved on the left, and potentially the right too, though the right side is only suspicious for now.
The silver lining here is that I haven't been in America for a while; this whole mess caught me while I was in the Netherlands, where the healthcare has been top-tier so far—though that might just be my bias talking since I’m comparing it to how things work back home.
As soon as things went south, after the usual runaround of ultrasounds, Pap smears, biopsies, MRIs, and CT scans, they sent me straight for a PET scan. Honestly, I feel like I caught a break because I didn't have to spend an eternity waiting for answers.
Now comes the hell part, or at least that’s how it feels after everything I’ve read, heard, and seen.
On December 28th, the fight against the beast begins: 25 radiation sessions from Monday to Friday, plus 6 cycles of 40mg Cisplatin administered via a 4-hour infusion on Mondays (plus the standard two hours before and after chemo, obviously)—so we're looking at eight hours of pure madness at the hospital. To top it all off, there’s brachytherapy, which I am absolutely dreading because I know how brutal it can be when they pull those applicators out. Luckily, they told me they’ll probably sedate me like a baby during the placement so I don't have to deal with the pain.
To make matters worse, the PET scan flagged a node in my lung. It’s not considered highly suspicious yet, but they want to keep a close eye on it. I’m just crossing my fingers that it’s just some leftover inflammation from the lung issues or asthma I dealt with since my teenage years.
There are also these tiny little nodules they say aren't active, but of course, the paranoia is already setting in, even though I know PET scans can throw false positives.
Specifically, I wanted to ask if anyone has experience with Cisplatin—what exactly should I be expecting? My oncologist insists my hair won't fall out, but every time I Google it, I find completely different stories.
I’m also wondering how much fatigue and nausea the Cisplatin actually hits you with, because I honestly can't wrap my head around what that's going to feel like. Are we talking "I might be bedridden and wanting to scream because I have zero strength" levels of exhaustion, or is it more like a really heavy flu?
They handed me a massive pile of pills to take during treatment, supposedly to ward off the nausea and other side effects, but the nagging thought in my head is: "God, what if these pills don't work and I'm still stuck screaming?"
They also let me know that if my blood counts tank during the process, they’ll go straight to a transfusion so they don't have to pause the treatment. That’s news to me; usually, I hear they just delay things if the labs look bad.🤔>
If anyone has any practical advice on how to survive all of this at once—besides just bracing myself with patience and grit—I would be incredibly grateful.
And most importantly, people, what on earth should I be eating?! 🙂🙂 I’m already a picky eater even without this whole ordeal making things complicated.
Thank you all, and if this post belongs somewhere else, I get it... but you guys have been my rock.
Unfortunately, this time, I’m the one stepping into the spotlight. I noticed the cervical cancer thread has gone pretty stale, so I’m hoping it’s okay if I pop in from time to time to vent or maybe hunt for some actual decent advice or just a kind word.
I’m only 38—well, maybe a little older now—and last month I was hit with stage 3b squamous cell carcinoma of the cervix. It’s infiltrated the left side near the ureter, so they actually had to install a nephrostomy tube because of the obstruction and kidney dilation.
They mentioned there might be lymph nodes involved on the left, and potentially the right too, though the right side is only suspicious for now.
The silver lining here is that I haven't been in America for a while; this whole mess caught me while I was in the Netherlands, where the healthcare has been top-tier so far—though that might just be my bias talking since I’m comparing it to how things work back home.
As soon as things went south, after the usual runaround of ultrasounds, Pap smears, biopsies, MRIs, and CT scans, they sent me straight for a PET scan. Honestly, I feel like I caught a break because I didn't have to spend an eternity waiting for answers.
Now comes the hell part, or at least that’s how it feels after everything I’ve read, heard, and seen.
On December 28th, the fight against the beast begins: 25 radiation sessions from Monday to Friday, plus 6 cycles of 40mg Cisplatin administered via a 4-hour infusion on Mondays (plus the standard two hours before and after chemo, obviously)—so we're looking at eight hours of pure madness at the hospital. To top it all off, there’s brachytherapy, which I am absolutely dreading because I know how brutal it can be when they pull those applicators out. Luckily, they told me they’ll probably sedate me like a baby during the placement so I don't have to deal with the pain.
To make matters worse, the PET scan flagged a node in my lung. It’s not considered highly suspicious yet, but they want to keep a close eye on it. I’m just crossing my fingers that it’s just some leftover inflammation from the lung issues or asthma I dealt with since my teenage years.
There are also these tiny little nodules they say aren't active, but of course, the paranoia is already setting in, even though I know PET scans can throw false positives.
Specifically, I wanted to ask if anyone has experience with Cisplatin—what exactly should I be expecting? My oncologist insists my hair won't fall out, but every time I Google it, I find completely different stories.
I’m also wondering how much fatigue and nausea the Cisplatin actually hits you with, because I honestly can't wrap my head around what that's going to feel like. Are we talking "I might be bedridden and wanting to scream because I have zero strength" levels of exhaustion, or is it more like a really heavy flu?
They handed me a massive pile of pills to take during treatment, supposedly to ward off the nausea and other side effects, but the nagging thought in my head is: "God, what if these pills don't work and I'm still stuck screaming?"
They also let me know that if my blood counts tank during the process, they’ll go straight to a transfusion so they don't have to pause the treatment. That’s news to me; usually, I hear they just delay things if the labs look bad.🤔>
If anyone has any practical advice on how to survive all of this at once—besides just bracing myself with patience and grit—I would be incredibly grateful.
And most importantly, people, what on earth should I be eating?! 🙂🙂 I’m already a picky eater even without this whole ordeal making things complicated.
Thank you all, and if this post belongs somewhere else, I get it... but you guys have been my rock.