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Posts by Angela Wright

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Female sterilization: What are your thoughts? in Women's Health ·
Lisa Myers said:So, basically, if women over 35 haven't had kids yet and don't have some medical condition preventing it—they just aren't allowed to get sterilized?

From what I've gathered, they can, but they have to provide specific reasons, and then a hospital review board decides whether or not to approve the procedure.

Thanks for the advice and the info, ladies. As far as the Holy Spirit goes, I know where I'm headed. I spent 74 days in that place and made it through. I know the doctors, and specifically, I know their neonatal unit is top-tier. They saved my baby, so if God forbid we need them again, I know we're in good hands.
Casey Booth3 said:Hey—I’m reaching out because I’ve been exactly where you are right now. I feel for you. You're looking at your mother, trying everything to help her, breaking your own heart in the process... but maybe this is just how God intended it. You have to stay positive, especially when you're sitting there by a sickbed.

That was a long time ago. I saw her off peacefully.
Female sterilization: What are your thoughts? in Women's Health ·
Susan Diaz91 said:From what I know, they actually do that. I know a woman who had it done while she was having her second baby via C-section. She met all the criteria—over 35, two kids already—and just went for it.
I don't see why people are making such a big deal out of this; if you meet the requirements and give consent, that's that.
If you aren't looking to have more kids but still want safe sex, then why not? 🙂
Just talk to your doctor (if I recall correctly, you had your first one via C-section, so you'll probably have the next one the same way) and see if they can perform the procedure during the C-section so you can just have peace of mind in America. 🙂

Good luck. Honestly, I don't know what it's like to deal with a high-risk pregnancy (I'm a terrible incubator myself), so 🙂 I'm sending plenty of good vibes your way so this whole thing wraps up quickly.

Why would you assume the second one would be a C-section too? Is there even a rule about that? My first one was a C-section because my condition became an emergency, not because natural birth wasn't an option. I've thought about the possibility, but it feels like hospitals push for natural birth until the very last second unless I end up crashing into HELLP again. If it ends up being a C-section, I guess that's just how it'll be.
I can't keep gambling with my life or my health, let alone the lives of my children, because they need me around.
I'm also wondering if endometriosis creates any specific hurdles in this situation, since I'm "blessed" with that, too.
Female sterilization: What are your thoughts? in Women's Health ·
I couldn't find an existing thread on this before starting my own, so if one already exists, please merge this one.

As the title suggests, I’m looking to hear from women here who have gone through with sterilization.

I'm over 35 now, and after dealing with major complications during my last pregnancy, I'm just done. Between those health scares and the fact that I really don't want to deal with more hormone therapy for my own wellbeing, I'm seriously considering this option.
I've read that doctors like Dr. Miller are pretty strict about it—apparently, you have to be over 35 and meet specific medical criteria to get approved by a review board. Honestly, it caught me off guard; it seems like way more red tape than what you see with abortion discussions.
Andrew Cruz3 said:@dunjaranka
My sincere condolences
😢

She hasn't had a PET scan yet.
The doctor insists it isn't necessary, but my mom refuses to let us organize one at a different facility.

I'm not entirely sure which specific medications she was put on 🙈
All I know is she completed two cycles (6+3) of chemo—a mix of oral pills and IV—and this is her first check-up after a break.

I'll grab the paperwork from my mom and type out the details.
The latest report indicates significant progression of secondary tumors 🙂 (I didn't catch the medical terminology immediately)

Look, my strongest advice is to seek treatment somewhere else. In any decent American hospital, if a doctor claims they can't find the primary tumor and refuses to order a PET scan based on standard protocols, they'd be lucky to keep their license!
It sounds like your mom’s condition is widespread, and honestly, it seems like this doctor just doesn't want the headache. He's acting more like a bureaucrat trying to balance a hospital budget than a physician. If he actually found the primary tumor, it would trigger a much longer, likely more expensive treatment plan with high-end drugs, and since the outcome is uncertain anyway, he'd rather just play it safe and save the money.
Amy Torres4 said:ruggedpuma47, Angela Wright.... I feel like an orphan now..😢

😢 Please accept my deepest condolences... unfortunately, we are all such fragile, fleeting beings, but the love we receive and give is the only true meaning in this life. Hang in there, dear; she will always be right there with you.
Nathan Martinez9 said:I’m looking for anyone who has any kind of insight or experience regarding that herbalist, unknown. I don't care if it's positive or negative. Specifically, I'm interested in treating multiple sclerosis, because his website claims he can cure it in 30 to 60 days using herbal teas. To be honest, I'm not necessarily expecting a total cure, but any improvement in my health would give me a fresh sense of hope and momentum. Since these teas are $1333, I want to know if anyone has actually seen progress from them. Please send me a private message with your experiences; I'm living in Mexico and don't have much free time for forums due to work. I want everyone to overcome their illness and come out on top.

This forum doesn't cover alternative medicine; there is a specialized sub-forum dedicated to Alternatives, so take your question over there.
When it comes to MS, my own experience and a bit of common sense tell me right away that we are dealing with a top-tier charlatan and a criminal who preys on desperate people searching for a shred of hope just to line his pockets. If even a tiny fraction of what he claims were true, those "cured" patients would be all over the news by now, and the guy would probably be walking away with a Nobel Prize for discovering a cure that thousands of highly trained scientists using the best technology and expertise in the world haven't been able to find.
Stay far away from this stuff.
Kimberly Cox58 said:Thanks so much for the advice; it really helps while I'm going through this mess. I’m still wondering, though—how bad is it that my CEA tumor marker jumped from 6.9 to 7.9 in less than 15 days?

Look, markers aren't some foolproof diagnostic tool. They're just one piece of the puzzle used to track progress alongside things like imaging. A tiny fluctuation over a two-week window isn't worth losing sleep over. What actually matters is getting that surgery scheduled.
Kimberly Cox58 said:Guys, please help, I am in complete shock. We found out yesterday that my husband has colon cancer. He’s only 43. His surgery is already scheduled for Monday. I have no idea what comes next. Do they know the results immediately after surgery, or is there a long wait? I feel like I'm losing it, though I'm trying to stay strong for him (but honestly, I'm struggling). Most importantly, he hasn't lost his spirit yet.

After the surgery, you have to wait for the pathology report on the removed tissue samples. That’s what will pinpoint exactly how malignant the tumor is and determine the stage of the disease. It usually takes about 7 to 10 days to get those results, and everything regarding the subsequent oncological treatment plan depends on that report. The surgeon might be able to give you a rough idea right after the procedure, but take everything they say with a grain of salt until the lab confirms it.
Look, it is what it is. This shock you're feeling right now is actually the worst part; once the actual treatment begins, you'll likely find a better mental footing. You have to accept the reality and just take it one day at a time, dealing with things as they hit you. Right now, the surgery is the priority—focus entirely on that and then on the recovery process. Any more spiraling beyond that is useless and actively works against you. There are also a few critical rules both of you need to live by:
0. A man with a diagnosis doesn't suddenly become an alien or a different person. He is still the same guy; he just happens to have a diagnosis. As terrifying as that sounds, it’s just one medical condition among many people face every single day.
1. This diagnosis is primarily happening to your husband, and he's the one bearing the brunt of it. You are caught in the crossfire, but don't ever let yourself crumble in front of him or turn your emotions into a bigger drama than the situation warrants. It’s a very slippery slope, and it happens all the time—it ends up feeling like an unjustified psychological burden to the patient.
2. Let him make his own decisions, even when you disagree with them. This is vital because it gives him back a sense of agency over his own life, which is often the first thing stripped away during illness. Feel free to offer suggestions and voice your opinion, but never pressure or force him. Use this experience as a way to deepen your bond and strengthen your relationship. Be his rock; he needs someone steady and focused.
3. Don't let the illness run your lives. You are the ones in control, not the disease. Keep your daily routines, social life, hobbies, and work as normal as possible—assuming, of course, that treatment obligations and his physical condition allow for it.

Everything I've said here is, quite frankly, the best and most essential advice I can give anyone looking to navigate successful treatment.
Andrew Cruz3 said:@Angela Wright/">@@Angela Wright

Thanks a ton for putting in the effort and getting back to me.
We're going to go out and hunt for some more opinions.
What really stings is knowing my mother can't stomach even the best chemotherapy, and this situation—at its absolute best—definitely means facing piles of it.

When you've got the right therapy, you at least know what you're signing up for.

Honestly, I think it’s entirely possible we're looking at cancer somewhere in the large intestine. Because of how twisted things get during a colonoscopy, doctors often miss it or just can't reach it, and sometimes it even manages to hide from a PET scan. Plus, that type usually hits the liver first.

What specific treatment protocol is being used right now, or which drugs is she on? Do you have any official findings from an MD Anderson Cancer Center specialist that you could share? Maybe I or one of the doctors in this group could give you some better direction or point you toward the next steps.
wiredcanyon39 said:The PET scan results are in, and there are no signs of metabolic disease.😁

😍😍😍
Absolutely incredible news—huge congrats to a true fighter! Keep doing exactly what you're doing.🙂
Andrew Cruz3 said:Look, I need you to clear two things up for me:

What exactly keeps this status quo from shifting?
If I’m reading this right, "neither better nor worse" isn't exactly a victory lap, is it? Does that mean the disease is just steadily progressing at its own pace? Because if things aren't improving, that doesn't exactly sound like good news to me.

Our doctor told us they wouldn't be able to find the lesion at all, and that this is actually completely normal.
Also, if I've got this right, he didn't think finding it was actually that big of a deal, and now...
Do you think I’m going to start talking like someone else? No. My style isn't something you can just flip a switch on.

Look, let’s get one thing straight: not all cancer diagnoses are created equal, and you certainly don't treat them all with the same cocktail of drugs. If we're talking about potential colon cancer that has spread to the liver, you aren't going to approach that treatment plan the same way you would for breast cancer with liver metastasis. It’s a completely different beast.
Since they haven't pinpointed exactly where the primary tumor is located, they’re basically just treating based on some professional hunch that might not even be right. To actually pull off a successful treatment, you need a specific set of established parameters—data points they clearly lack—which means they're essentially just fumbling around in the dark. Otherwise, the medical term for a malignant metastatic disease without a known primary site is "occult carcinoma."
The reality is that dealing with metastatic disease is a massive uphill battle from day one. It complicates every single aspect of treatment when you're already fighting a moving target, but it’s an absolute nightmare when you don't even know where the primary tumor is hiding. 😢 So, they’re pumping them full of certain cytostatics designed to slow down the disease's momentum, but let’s be real—with that kind of therapy, you're usually just waiting for the inevitable relapse.
When a doctor claims that the primary tumor will never be found, I think it’s an outright absurd statement. It’s one of those reckless assertions our doctors love to throw around—especially the ones over at MD Anderson Cancer Center. 🙄...refusing to admit what is clearly a massive embarrassment. 🙄It’s pretty obvious they don't have the experience or the right gear to handle a situation like this. There are clinics around the world—places like MD Anderson Cancer Center—that deal with this kind of thing constantly, meaning they have way more hands-on expertise and much better technical setups. Since they didn't provide the kind of answers you actually need to get top-tier treatment, I think it is absolutely vital to go out and get at least two more opinions from people who actually know what they're doing. Sure, there's a chance you might get bad news, because sometimes it really is impossible to find the primary site—you know, when those tiny malignant micro-formations release metastases that end up being larger than the original tumor itself. But there is also a huge chance that specialists who have seen it all and actually know where to look will be able to track it down. Honestly, it would be a massive mistake and a total injustice to the patient to just sit there and treat one person's opinion like it's some kind of holy scripture. You can't just blindly trust one doctor's professional abilities and call it a day.

I remember a case involving an occult carcinoma that doctors in Washington, D.C. just couldn't pin down. It wasn't until the patient saw specialists over in Philadelphia that they finally caught it—it was a deeply hidden colon cancer. Because they actually found it, the patient was able to get the right targeted therapy specifically designed for colon cancer, which significantly boosted their chances of maintaining a decent quality of life. My point is this: you don't always need to fly halfway across the globe to find answers. Sometimes, you just need to head to the next town over and find someone willing to actually do the legwork and look a little closer.

Look, I’m no doctor, but I’ve spent years working alongside oncology patients, and I’m speaking strictly from that frontline experience. I’m sorry if my bluntness hits a nerve, but this is just how things work based on everything I’ve seen and learned. If this were someone close to me—my own flesh and blood—I wouldn't hesitate for a second; I would pull every possible lever to pinpoint that primary site as fast as humanly possible.
Andrew Cruz3 said:My mom has liver metastases, but they haven't been able to locate the primary tumor yet.
We just got her latest results back after two rounds of chemo and a three-month break. Her bloodwork looks incredible, but the CT scan shows the lesions have actually increased in number.
On the last scan, the lesions in the right lobe had vanished, and the ones in the left were smaller.
Now, they're back. 😢

What does this mean?
Is everything just getting worse and coming back?
Last time, the doctor was happy with the progress, even though we felt uneasy about the numbers, so I’m still trying to hold onto some hope. 🙂

It means things are stalling out. Unfortunately, without identifying where that primary tumor started, you're fighting a ghost, and successful treatment becomes an uphill battle. My honest advice? Go get a second opinion. Not every oncologist or radiologist at a major hospital has the same level of expertise.
Jamie Howard3 said:It’s basically a glorified placeholder—it doesn't do any harm, but don't expect it to actually move the needle.

☕

Maybe we should just stick to what the actual studies say. If you’re looking for some actual science on this, check out the research on beta-glucan over at PubMed. It’s all there if you want to dig into the data yourself.

I don't have any personal experience with this myself, but from what I’ve heard from people I know who have used it, they say it really helps bolster their immune systems and provides that much-needed boost between chemo cycles.

I think it all boils down to what we actually expect from it. If you’re looking for some kind of miracle cure that’s going to wipe out cancer overnight, you’re probably going to end up deeply disappointed. Look at it this way: it’s an excellent immune booster. It's designed to help bridge the gap during oncology treatments, keeping your immune system strong enough to handle the heavy lifting while shielding you from those nasty infections that become such a massive risk during this stage of treatment.
Amy Torres4 said:These are such brutal days for me; my mom is so weak and just can't seem to bounce back from this pneumonia. She's coughing constantly and can't get a wink of sleep at night... man, it's just hard, really hard... God, please help her...🙂🙂

It takes time. Go pick up some Apisirup. My kid was a preemie with super sensitive lungs and bronchi—spent a long time on a ventilator—and whenever they get sick, we usually knock it out in a few days with this syrup. It’s made from propolis, honey, marshmallow root, and mullein. Honestly, no other syrup we've tried has cleared up a cough that fast.
It’s also vital that the air in her room stays humidified. If you don't own a humidifier, go buy one; it's a lifesaver to have running in the bedroom. You can also light an aromatherapy lamp next to it with some inhalation oils. All of that helps. You can even mix those oils into a body cream and massage it onto her chest and back.
Need advice: Sestrin's boyfriend is couchsurfing at our place in Psychology & Therapy ·
Regarding what you wrote, I think the old folks are handling it their way. They know exactly what kind of personality your sister has, which is probably why they aren't making a scene. They're likely just letting things play out. On the flip side, your sister is clearly exploiting that, doing whatever she wants as far as she can get away with. Don't sweat it too much; she isn't going anywhere. Maybe she'll crash at her boyfriend's place, but let's be real—it's rare for parents that age to be flexible.
As for your situation, sorry to be blunt, but no matter how much you claim to be "at home," you aren't really. You're essentially living off the kindness of your parents. They helped you finish school, they landed you a job—even if it’s just minimum wage—but you have it. You don't actually have much ground to stand on to complain; you're basically a tenant. Your best move is to sit down with them, have a mature conversation, and tell them what's going on. Express your genuine concern for your sister because, from where I'm sitting, this whole dynamic is pretty dysfunctional.
You’re probably talking about calcification 😁
You really need to see a physiatrist. The treatment options are pretty broad, but they usually kick things off with ultrasound therapy, electrical stimulation, and stuff like that. If those don't cut it, they might try nerve blocks. There are plenty of other modern approaches available too, and surgery is strictly a last resort if nothing else manages to move the needle.
Larry Rivera6 said:Hey everyone, I’m spiraling a bit here and really need some perspective. My arms and shoulders have been aching constantly for about six months now, but every single scan I've had comes back totally clear. I started doomscrolling and now I'm convinced it might be lung cancer. I had a chest X-ray three years ago and everything looked fine then. Am I just being paranoid? I've got an MRI for my heart and lungs scheduled, but besides this pain, I don't have any other symptoms. Thanks in advance.

I don't buy it; you'd be dealing with a whole different set of symptoms if that were the case. It's way more likely that you're looking at issues with your cervical spine or maybe some chronic back problems.
Amy Torres4 said:Oh man, I am feeling absolutely terrible today... I'm having a total meltdown over my mom. She’s just completely checked out, constantly saying she doesn't want to live anymore... and nothing seems to be changing her state of mind at all...😢

Look, it’s just a rough patch; it'll pass. I'm currently pregnant with my second child and I felt like giving up yesterday too.
Amy Torres4 said:Mom is doing better today, thank God. She’s lucid, though she's still incredibly weak. Is it okay for me to hold onto hope?

Always