CheckEmoji Community · the emoji forum
🏠 Home 🆕 What's new ❓ Unanswered 🔥 Popular 📡 RSS Members 👥 0 online log in · register
Home › cosmiclynx14 › Posts

Posts by cosmiclynx14

47 posts shown.

I didn't even realize there was already a thread for this... I ended up posting my question under a completely different topic.

Anyway, I’m looking for some guidance here—does anyone know where I should even start when dealing with something like this?
feralsurfer72 said:My dad still doesn't have a definitive diagnosis. The abdominal CT showed stomach cancer, enlarged lymph nodes near the pancreas, and multiple liver metastases—the largest one is about 80mm. I tried to make sense of the reports while we were waiting over at the surgical wing, but... I can barely understand half of this medical jargon. All I could grasp was that his heart and kidneys are functioning okay...
They’ve been running us in circles through this hospital from 1:00 PM until 6:00 PM.
He had blood work done again on Monday, provided urine samples, another scan, and they’ve scheduled him for yet another endoscopy. And the last one was back on March 5th.
In the interim—between the CT, the colonoscopy, and the endoscopy and before we even got these results—he spent the weekend vomiting what looked like coffee grounds. Massive amounts of it. It wasn't until later that I realized it was actually blood.
At first, they didn't want to admit him, but since he lost so much blood, he's been stuck in the internal medicine ward since Monday.
He's on an IV drip and receiving transfusions... He can't eat, can't drink anything... I cornered the doctor today. She told me they still aren't certain where the primary tumor is located.
They initially thought it was the pancreas, then they thought it was the duodenum. But after that bleeding episode, nobody is sure anymore.
They took a biopsy during the endoscopy; we should have the results in a week.
I asked the doctor if surgery would even be an option if it turns out to be stomach cancer.
She said no, because of the multiple liver metastases.
Today marks exactly two months since my father fell on the ice. Since then, it’s just been one frantic dash from one department to another... And then they have the nerve to say, "Oh, if only you had come in a month earlier..."
Just when I thought I finally "wrapped my head around" everything regarding the pancreas, now they're bringing up the stomach (though they don't even know for sure if that's it, or if it's something else entirely, or maybe a perforated ulcer...).

I feel like I've stepped into some twisted, horror version of Alice in Wonderland. I honestly have no idea what to hope for.

It’s the exact same situation with my dad; it's inoperable because of the multiple liver metastases. The only thing we know for certain is that the primary site is the colon.

He went straight into chemo without surgery—12 cycles total. We've finished the fourth cycle and just did a CT scan, and the metastases have actually shrunk by half!!! And they were even larger than what your dad is dealing with...

The only issue is that the lymph nodes are enlarged and more numerous. I assume that's bad news?! Is that a really terrible sign??
And I don't get it—there isn't a single word mentioned about the primary tumor in the colon. How is that possible? Is it a doctor's oversight or what? My dad didn't have his previous records on him, but they claimed they had everything in the system. What are the odds they haven't even looked at them? I don't know...
Hey everyone... here I am again with another question. It probably looks like I only pop up when I need something, but that isn't true. I read everything here regularly and I feel for all of you—I’m going through the exact same thing. I’ve already lost three people very close to me, dear ones, and now, here we go again 🙂 .. 😢

Does anyone know anything about microwave therapy treatments over in Europe? Who should I contact about this? We are dealing with colon cancer with liver metastases, and I’m just hoping there’s some kind of option for the metastases specifically.. maybe they can be destroyed, or at least shrunk enough to make surgery possible, or even just slow down the growth for a little while...

I realize I might just be chasing shadows here, but I stumbled upon this one article, so
if anyone knows even a shred of information regarding this, please let me know..

edit: I was reading about radiofrequency ablation here in the States, but the article claims what they do in Europe is superior to that. I intend to ask my dad's oncologist as soon as the opportunity arises, but right now, things are just too hectic..
Angela Wright said:To start a non-profit, you only need three people. You can find more info here.
As someone who dove headfirst into this with nothing but pure altruism and massive enthusiasm—only to end up having a pretty miserable experience, to put it mildly—I have to warn you right now: this is an incredibly tricky and thankless game. You need a circle of people you can actually trust, a rock-solid legal foundation from day one, someone who knows how to handle the financial and bureaucratic nightmare, and someone capable of writing grants. Otherwise, the organization won't last a month. Unfortunately, when it comes to cancer support groups, people usually only show up when they have a crisis. They expect you to solve their problems for them, but the moment you need actual help with the organization—or even just ask them to show up for the annual meeting required to keep things running—they flake. Everyone screams for help when they need it, but once their issue is resolved, the noise stops completely. And don't even get me started on the sheer amount of stress you endure, only to have some member act entitled because they think membership gives them the right to harass you at all hours of the night... it’s endless. In reality, most non-profits end up being carried by two or three exhausted people while everyone else just offers "thoughts and prayers." On top of that, you're constantly being circled by corporate vultures from all sides. There are some organizations with legitimate strategies for partnering with non-profits, but there are others that will literally devour you and spit you out. You have to know how to handle them, but the problem is, you can't avoid them. There are even people who prey on brand-new non-profits; they join, worm their way into leadership, and then run everything for their own benefit or the benefit of some third party.
So, seriously, think long and hard before you jump in. For me, running an association brought almost nothing but grief. It cost me nearly the loss of my own child because of how much I stressed myself out, and it left me with a massive amount of disappointment in people in general, not to mention my own self-confidence. I swore off joining or running any organization ever again. There are other ways to help people, and posting here is one of them.

Okay, thanks... I looked up the requirements for starting a non-profit on Google and realized what it takes...
Part of the reason I'm thinking about this is because of my dad. When he first started his treatment, he was losing his mind—terrified about having to go to the hospital, being stuck in a room with strangers, hoping he wouldn't have to talk to anyone. But now, after his third round, he’s actually looking forward to it. He tells me it’s a whole new world, a community of people facing the exact same battles. He thinks it would be wonderful if, outside of the hospital walls, people could gather just to talk and share experiences... because every other family we know is dealing with similar struggles. We all know each other, and we know how important this is...
That's why I thought of you. I'm wondering if there's a way to organize something officially so people can volunteer themselves, rather than me having to hunt people down and drag them by the arm...
Maybe we wouldn't go as broad as your organization, but we might try to provide concrete help, like helping people navigate finding doctors...

I don't know, the desire is there, now I just have to figure out what the options are...

Grandpa, Grandma, my mother-in-law, and now Dad with cancer... it's terrifying. It feels like it's just a matter of time before someone else gets diagnosed. People just don't talk about it enough... some even hide that they're sick...
Hello, everyone... right now, my family and I are both fighting this disease head-on.
My father has colon cancer that has already metastasized to his liver. 😢

What I’m really trying to figure out is where to even begin if I want to start a non-profit association here in my hometown to support patients and their families. Who do I actually reach out to? Should I go through City Hall, the local health department, or somewhere else entirely? And does this have to be a major metropolitan area, or can it just be a small town or a county-level organization?
Wedding cakes and desserts in Weddings ·
Thanks, Chris Lopez4... I mean, if people are actually giving them praise, they probably aren't that bad. I ended up ordering from them myself.
Wedding cakes and desserts in Weddings ·
Hey... anyone here actually tried the pastries from Babić??