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Posts by gentlemoose62

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To my brave warriors out there,
Tinchi,
If I could have had a kid, I’d want them just like you... but don't sell yourself short, you're doing everything right. You two share a bond that some people
might never experience in their entire lives—she has the real YOU, and you have the real HER, and that connection stays ALIVE forever.🙂

Nancy Thomas18,
I am so happy you checked in and that you're fighting so hard without backing down! 🙂
We're all waiting for those test results and the new game plan!

Aranza (Lela)
Welcome to the group. I'm also an ovarian cancer survivor, and I'd love to hear your story, whether it's on the Zanovidan forum or right here... either way.

Sending love to everyone else, I'm reading ALL of you. I'm right here with you, hang in there!
Elizabeth Gonzalez55 said:Hey everyone,

Just wanted to share an update (for anyone following our fight against melanoma, or if someone ever wonders if you can take on Stage IV...) :

One year after the diagnosis, everything still looks clear. The next checkup is in six months. So far so good—we're feeling happy and satisfied, and the fight goes on!

I read this thread all the time and am sending positive vibes to all of you. Hang in there!

🙏That is so wonderful, thank you for sharing. Every checkup that comes back clean feels like being REBORN. People who haven't been through this can't even imagine the rush of emotion and strength that hits your whole body... suddenly, you're ready to fight even HARDER!
👍May it stay this way forever!
Nancy Hernandez43 said:Dear Muscle and everyone else,
It’s honestly wonderful to find some support when you're feeling angry, shocked, or just totally lost! Still, the most understanding people are always those true fighters who stay strong and full of optimism!

Maybe I didn't express myself right, mostly because I was just terrified. My parents had their checkups yesterday. I knew immediately something was wrong because usually, we at least get a quick text update, but yesterday they even turned off the phones. This morning, it was just waking up to juice. There might be a swollen lymph node in her left leg, but the oncologist couldn't feel it. Because of that, they need to perform surgery. However, looking at the PET scan images and the reports (I still don't know the actual values or if the markers are low—they're keeping me in the dark again), he wasn't satisfied. He thinks that if there's any malignant growth anywhere, especially in the abdomen where the previous tumor was centered, the PET scan might have missed it because even at its best, it won't catch anything smaller than 0.4mm (did I get that right? I don't know... but that call woke me right up). Anyway, an emergency surgery is scheduled to open up the abdominal cavity again.

In a way, I'm glad they're being so proactive and caring about the patient so nothing gets missed and treatment keeps moving forward. But on the other hand, until the surgery is over, I'm stuck in the same loop: wondering whether to believe or not, feeling just as helpless as the rest of the family. She sounds calm over the phone, but I know she isn't, because they're filling her head with all the things that could go wrong during surgery, or the oncologist saying stuff like, "I went through this too, and I ended up with sepsis..." 😢

From what I understand, a PET scan just shows activity—basically areas of intense uptake—rather than giving a definitive diagnosis, especially when a CT hasn't shown anything yet. It basically just points out where to focus next. That surgical procedure will give you the real answers and definitely needs to happen... but, dear God, without scaring the patient like that! I can't believe an oncologist would say something so reckless. If this is just an isolated recurrence, this surgery could actually mean a cure for your mom!
Tell your mom to clear those negative thoughts out of her head. Of course, there are always pros and cons, but you've gotta face things bravely and optimistically... that applies to everything in life, especially when life itself is on the line.
I had three abdominal surgeries myself, all with the same vertical incision from my sternum down, and everything went fine. I was always just counting down the days until they could get "that thing" out of me. After that, if chemo or whatever was needed, then so be it—just get it out. After one of those surgeries, when they removed some suspicious cysts, the pathology report came back completely clean—zero recurrence!

I know how hard this is for you all, but it's hardest for her. You need to find a way to be fully present and break through that fake calmness she's putting on so she can really open up to you... it'll be easier for both of you once she shares her fears. Let her talk, maybe gently talk her out of the scary stuff, and then cheer her up with real positive stories. This period of uncertainty will pass, and once the work begins, everything will settle into place. Only the person who is sick truly knows what it feels like to be "alone with their fears," which makes everything seem so much darker... that's where you come in. If you can ease even just one fear, you've done so much already...
Just keep pushing forward bravely...
Lisa White54 said:I really admire you. You're so brave, and I hope you never lose that infectious optimism of yours!

I was in such a bad mood today, but everything changed once my husband got home. The hospital just completely drained him. Now we're finally feeling like ourselves again. He's doing better (well, of course he is, since I'm right by his side!), and the pain is easing up.
He’s going to be O. K. Borac. He's a fighter.
Oh my God, I love him so much!

Bravo! See, both your optimism and your love are totally contagious.
Believe me, reading news this beautiful makes me so happy too.

Love and positivity are truly the best medicine for someone who's sick.
Nancy Hernandez43 said:The results came in this morning. They found some undefined mass in her left leg. Mom took it all in stride, saying, "After that terrifying diagnosis, this is nothing." They suspect an enlarged lymph node. She called her oncologist, and he scheduled an emergency appointment. I should hopefully know more tomorrow... honestly, I’m ready for anything, but deep down, I just don't believe everything is okay. I totally feel you, and I'm praying things get better for all of us soon! We're all fighters! Don't give up!...👍

Hey Nancy Hernandez43...

Please don't assume things are bad before we even know! We all just need to stay calm and wait to see what the oncologist says after the extra tests come back...
It’s happened more than once—Grace Fowler even wrote about her own experience... A PET scan shows something scary, but in the end, it turns out it wasn't even the worst part...
Her CA125 is low and hasn't gone up, right? They told me that as long as that marker stays low—or at least isn't spiking or doubling—there's really no reason to panic...
👍 Hope everything goes well! Let me know...
Grace Fowler said:Hi everyone!!!
Just a quick update on my recent test results.... My marker is actually starting to dip slightly after three weeks, which is so encouraging... I'm waiting until October 14th to get my CT and biopsy on that suspicious area... Until then, I'm supposed to be resting, hmm, that's the hard part because staying in bed is the absolute worst (though I do treat myself to a little walk with my Fitbit:-👍) AND I AM COOKING EVERY POSSIBLE DELICIOUS THING THAT COMES TO MIND😉.🙂The truth is, I can't eat most things (thank goodness for my husband! :-) but it still makes me happy.
I WANT TO SHARE SOME OF THIS OPTIMISM AND FAITH WITH ALL OF YOU—IT'S GOING TO BE OKAY Stay brave and don't give up...
Your Dina

Honey, this is better than good... the marker is dropping without even starting therapy! In every case
I've seen where a recurrence starts, once it begins to drop, it doesn't stop.
I really think you have a legitimate reason to hope that the suspicious spot was just an abscess all along. Dear God, please let it be true!

Until then, just keep cooking, keep gaining weight, and keep posting. Your optimism is totally contagious🙏👍
Hey everyone,
I know so many of you are right in the middle of waiting on tests or results, so I didn't want to leave
anyone out... I just want to wish you all 👍👍👍...just because, it feels right.

Hang in there, guys!
Nancy Hernandez43 said:My family and I are going through that same fear right now—wondering if we missed something or if we're just being too optimistic. We have a PET/CT scan scheduled in two days. My dad went over the recent test results, and honestly, it’s so hard watching him act like everything is fine while you can tell he's terrified inside. I totally get that shock and disbelief you're feeling. A couple of days ago, I finally stopped looking through rose-colored glasses and started bracing myself for whatever comes next.

Stay strong!

Waiting for results is absolutely brutal. It would be so perfect if they could just settle everything in one single day, but... sadly, that's just not how it works.
Still, I really feel like things are okay since the Ca125 looked good. Was it just that slightly elevated CEA that was bothering you guys? Or was there something else? Is the PET scan just a routine checkup?

Well, things have been worse before and they passed, and this will pass too.
Fingers crossed!
frozencobra25;16032173 said:My dad lost the hardest fight of his life this morning at 6:10 AM.

He finally fell asleep, exhausted and worn out, leaving behind a body that had struggled so much. In one word—he's free...

Like you said... he just drifted off and left that tired, hurting body behind. His soul and his memory will stay with you forever...
My deepest condolences.
Nancy Thomas18 said:Hey everyone, I haven't posted in a while because my CT scan results were pretty devastating. They say there aren't any metastases, but there's fluid in my abdomen and tucked between the loops of my small intestine... everyone is just shrugging their shoulders... my surgeon wants a PET scan, but the oncologist thinks it isn't necessary—they won't recommend it—and my stomach is basically being pushed out of place... I honestly don't know what to do... I'm losing heart...

I am so incredibly sorry, honey, but please insist on that PET scan, especially since your surgeon is asking for it. From what I've seen, I've come to realize that oncologists are often the first ones to throw up their hands... Hold onto your surgeon's recommendation and get that PET done ASAP; we have to find out what's causing that fluid in your abdomen.
Don't lose hope now... I know it's hard... and obviously, nobody knows exactly how you're feeling right now except you, but please don't stop... you have to keep pushing. Anyone can give up, but fighters like you... you know you always have to keep moving forward...
🙂
Susan Ruiz76 said:OK, we're heading to another city this Monday to see the oncologist. Since I've heard a few different things about premedication for Taxol, do you think it's smart to pack some hospital supplies? Some people stay a day or two, others longer. Should I take something for nausea a day early (like with other chemo treatments, e.g., what he did when he was on Cisplatin)?
I want to wish Rose and her husband nothing but the best—it doesn't have to be that scary! We met someone where they had to drain "gallons" of fluid from his body—it was intense, he was completely drained, kidneys were failing, he was getting albumin through an IV, and they had to tap his lungs... but now, after two months at home, he’s out every single morning for coffee! Good luck!

Personally, I never took anything a day early. I just ate lighter meals so my stomach wouldn't feel heavy. The premedication itself isn't hard; it actually helps calm everything down and protects your stomach lining. I didn't have any issues at all. It's always smart to bring a few things for the hospital just for practical reasons, but if everything goes smoothly, you can definitely head home the next day. I only stayed overnight the first time because I didn't know what to expect after chemo, but after that... I would have gone home the same day 186 miles times over!
The hardest part for me during chemo (when I was on the Day 21 schedule) was just lying there for so long... it has to drip slowly for about 6 hours... so you're constantly needing the bathroom, feeling dizzy, and just feeling totally stiff. A weekly Taxol therapy with smaller doses worked much better for me since it's automatically shorter, though you do deal with more poking and searching for veins and stuff like that.

But, my best advice right now is... don't overthink it! You have the weekend ahead of you, so enjoy it. Everything will go exactly how it needs to on Monday. We can't change our circumstances, right? So let's just make sure we enjoy ourselves as much as we possibly can...
Best wishes and good vibes!
Susan Ruiz76 said:In the short time I've been hanging out on this forum, I’ve noticed that—whether people want to admit it or not—it’s pretty much the same group of people constantly showing up because they're all dealing with serious illness. It feels like "newcomers" don't always get a warm welcome unless they speak the exact same language or fit a certain age bracket... if you don't vibe with the established crowd, you just get ignored. Take Rose, for example... she's 44 and shows up everywhere just like I do, but I bet she's feeling that same sense of being left out that I am...
Look, can we give us a break? Some of us just aren't great at using all those emojis and angry faces... We aren't actually mad at the healthcare system or the doctors—honestly, why would we be? It’s just the nature of the disease itself. They read our CT scans immediately today, just like they did during our checkup two months ago. They're doing everything humanly possible, so how can we blame them if the results aren't what we hoped for? Our oncologist tells us exactly what's happening, what we're entitled to, and what we aren't. We’re fighting just as hard as everyone else to deal with these massive drug costs, and our struggle doesn't have to be an "open wound" for everyone to see... even though we've been absolutely relentless with letters and inquiries to the authorities! Believe me, he’d be the first one wanting to provide the absolute best treatment without any hesitation—like what you'd get at the Anderson Clinic in Houston. But with the tools he has right now, he is doing his absolute best for us, and we truly believe that...
So, quick question—it looks like we’re starting Taxol on Monday... we’re totally in the dark about the side effects and how it's actually administered. Does anyone have experience with this? Any advice would be amazing...

I feel so bad that you’re feeling left out, but honestly, I don't think you have any reason to feel that way! I’m not exactly young myself, I'm definitely not a tech wizard, and I've only been on this forum for about ten months without meeting anyone in person... but believe me, I've never once felt rejected or ignored. On a forum as heavy as this one, I really doubt anyone would ever ignore someone on purpose...
It feels like people often stay silent because they aren't sure how to answer, or maybe they’re just afraid of saying the wrong thing... It always makes me sad when someone gets left hanging! But hey, this is just a community of everyday people where age and status don't mean a thing. You get out exactly what you put in...
You just share what you know and what you can... There aren't any "duty officers" here who have to answer everyone's questions. We're all in this together, at least that's how I see this forum... Right?

I have to share my own experience with Taxol... I took it as my first line of chemo alongside Cisplatin every 21 days, and then later used just Taxol as a second line—weekly, but with smaller doses...
He usually handles it pretty well! No vomiting at all... just a little bit of nausea for the first two or three days...
Honestly, I felt almost back to my old self after just the first round of treatment. I didn't even lose a single pound... Phew! But hey, no big deal, all things considered! During that first session, they watch you a little more closely just to make sure you don't have a heavy reaction to the chemo, but that rarely ever happens...
Anyway, like Angela Wright said, you should definitely check in with your oncologist about the most common side effects. It’s way better to be prepared so you don't get unnecessarily stressed out... This is just my own experience, though, since I dealt with metastatic ovarian cancer myself!
Hey there! I really hope you'll keep checking in with us...
Lisa White54 said:I felt so foolish thinking we had actually won, even though I’m so deep in this disease and feel like I know everything there is to know. But you just want to believe, right? And honestly, I had my reasons to be hopeful. My husband was doing so well.
He stayed overnight at the Jordan hospital this Wednesday. The cancer came back. It’s in the exact same spot as four years ago. They’re doing a bronchoscopy on Monday, so we’ll see what happens then. He’s getting some drainage today because of pleural effusion.
It’s just awful.
It totally knocked the wind out of me. And it’s not like four years ago... not even close. He isn't physically or mentally anywhere near where he was back then. I have no idea how he’ll react when he finds out, since they haven't told him yet.

Honey, I know things are heavy right now, but I’m certain you’ll find your footing again soon. It happens naturally... you just find that strength and start fighting for every single day, because you never know what tomorrow holds... maybe even a new medication? Who knows?! You can never be sure...
Where we pull this strength from, only God knows. But seeing the stories here, it’s truly incredible how much people can endure—both the patient and the one caring for them.
And... you aren't stupid for thinking you'd won. I feel just as foolish because that damn thing can come back whenever it wants. You have to keep believing in the good stuff and pass that hope on to him... I'm sure there are still options to try.
Stay strong, but please don't try to carry this whole weight by yourself...
Grace Fowler said:Hey everyone!!
Well, I just survived an absolutely insane week. I've been running all over town—literally bouncing from one hospital to the next—just trying to get my test results back ASAP. Thank God for the amazing people who helped me stay on top of everything... So, here's the deal: my chest X-ray is set, the abdominal ultrasound is done, and now the gynecological surgeon is pointing toward a supposed "abscess"—basically saying they might need to try an ultrasound biopsy... and then wait for them to call you back. That's it... :-(. To make matters worse, my wonderful abdominal surgeon got stuck in surgery all day today... and his assistant finally deigned to talk to me after a few hours just to say, "We'll contact you when there's an opening for the biopsy." But honestly, I'm not even sure if that's the right way to catch this thing... They basically told me to just go home... and wait. I left the hospital feeling pretty frustrated and just totally fed up with the whole situation. But as I was walking to my car, that crazy thought popped into my head again... I CAN'T CHANGE THIS BODY, BUT AT LEAST I'M DOING OK RIGHT WHERE I AM... I hopped in the car, blasted my favorite CD, and drove home with such a great vibe!
So, my friends, LET'S KEEP GOING.........
Warm regards from Dino :-)

Dina, we love you just the way you are... even when you're feeling down. God knows you have every right to feel that way sometimes!
And like you said, you can't change your skin... so you just keep moving and handle things however you can. THAT'S IT. You're staying active, you're involved, and you're making sure everyone else fights for YOUR life.
It's definitely a win that all your other results are steady, and I'm crossing my fingers👍that you get that biopsy appointment quickly and that it shows exactly what needs to happen next!
Take care.
Melissa Kim45, honey, I am so sorry. You gave her everything you possibly could, and I know you both felt that connection deep down. I'm certain she loved you just as much...

Dina, PLEASE, keep fighting! I'm positive that once they get these next tests and results back, they'll come up with a whole new game plan! Honestly, after everything you've been through, you've learned how to take those hits with grace—but staying tough, never giving in!
You have so much strength left for the fight, for every single new day, sweetie... and you know it too! What do you mean, goodbye?!
I'm so glad you're planning on immunotherapy, and I truly, truly hope it does the trick for you.

Hi everyone!
Nancy Thomas18 said:Thanks everyone for the support... but honestly, that yellow phase just hits you hard. I've got an abdominal CT scheduled for next week... fingers crossed for my little liver 🙂

I'm so glad you're through the worst of that yellow phase and moving forward!
Sending all the good vibes for next week xxxxxxxxxxxxx👍
Nancy Hernandez43 said:Thanks for such a quick and clear reply! My mom is battling ovarian cancer—it was surgically removed, and she just finished her chemo cycles about 10 months ago. Her markers and most blood work look okay, but her CEA keeps creeping up slightly every month (from 6.0 to about 6.3 now). I’m really hoping it's just lingering effects from the chemo? Unfortunately, I can't ask her or my dad for specific details on what the oncologist is saying...

I honestly don't think a tiny jump in CEA from 6 to 6.3 is a major red flag for a recurrence, especially if CA-125 isn't trending upward—assuming that's been her main indicator so far.
Also, just a heads up, CEA levels can run a little high in smokers too!
Best wishes!
Thomas Hill11 said:Hey there.
Can you actually tell from a blood test if someone has a benign or malignant tumor?
If so, which part of the results would show that??
Thanks

Man, I wish it were actually that easy!
My advice is, if you’re really worried about something, don't just rely on blood work. Sure, some levels or markers might shift, but that’s never enough to make a real diagnosis, especially when it comes to tumors. Plus, blood work can look totally normal even when something else is going on...
If you feel like something is off, you've got to push your doctor for more tests.
The main thing is to take action until you find the actual cause—which, luckily, is usually something else entirely instead of a tumor... then you can finally breathe easy...
Grace Fowler said:Hey everyone!!!
I was literally crawling out of the hospital... About two and a half weeks ago, my fever spiked through the roof, CRP shot up to 308 (ref range 0-5), and SE hit 125 (ref range 0-24). Long story short: emergency hospitalization with a diagnosis of clinical sepsis. To make things even more fun, a nasty case of sciatica hit my right hip, so I was actually crawling to the bathroom... it was awful... But I'm feeling better now! My labs have improved, and while I'm still on antibiotics, I am ALIVE, oh my goodness! :-) I missed my immunotherapy session in Germany, but once I'm back on my feet, I'm heading straight there...

MY HEART GOES OUT TO Alenka's family and friends!

Sweet friends, sending tons of positive vibes to everyone—please hang in there...
Your Dina

🙏 Oh man... what can I say besides admiring you for the hundredth time, dear Grace.
Did your Ca125 levels go down too?
I really hope you recover quickly so you can get back to your immunotherapy!
Nancy Hernandez43 said:So... whether they're strict or not, they head there with their blood work from San Diego, check in first thing in the morning, and then I'm not really sure what happens next. All I know is my dad usually calls once they've been discharged, which is around 2 PM. I'll ask him in a few days, since I can't exactly ask her... They definitely seem to put in more effort over there than we do here. This time, they'll probably decide if she needs a follow-up CT or PET scan, and if so, she'll be heading to Chicago for the imaging in about two weeks.

Thanks so much for the support, I'll check back in soon!

Thank you! I was actually wondering if they perform CT/PET scans as follow-ups once the markers look good. I'm asking because I have the exact same diagnosis as your mom, and I haven't had any imaging done in five years now...🤷
Please let me know!