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Resources and support for families dealing with cancer and serious illness

Started by Angela Wright · · 👁 20 views · 3K replies

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Participants Angela WrightChristian Wilson16Morgan Williams4Jeremy Nelson3John Chase6steelbadger83hiddentiger80urbanjackal3silentviper30mistyranger4ruggednomad182placidfalconJerry Morales4frozenviper492velvetgull9Joshua Flores48Frank Ramirez23Roger Hall15Walter Cox5mellowlynx8boldjackal70northernfox9ALaura Gomez10 …
Charles Edwards8 Charles Edwards8 Member
46 messages
joined Feb 2007
#301 ·
Regarding the press stuff, Mary and I are currently hashing things out with the New York Times and Metro (everyone else just ghosted my emails, by the way), so we're being pretty cautious with them.😉
When it comes to Noni and Propolis, I'm totally with you on what you wrote here:👍you can definitely take them together, but if you have to pick just one, go with the Propolis.
Now, Noni is definitely good, but like I mentioned before, it's become such a massive industry that you really have to watch your back and be super careful about where you buy it and what quality you're actually getting.
In the States, there's basically only one company importing the real deal Noni.
ruggednomad182 ruggednomad182 Newcomer
4 messages
joined Mar 2007
#302 ·
I had a tumor removed from my large intestine back in April 2004. Post-surgery, I was feeling pretty rough, so I started taking Noni. My wound just wouldn't heal—it dragged on for about two and a half months. Nothing seemed to touch it until I cooked up my own juice blend: Echinacea purpurea (which I’d actually planted before I even knew this little beast was living inside me), nettle, lemon juice, and chestnut honey. I’d prep enough for just one or two days at a time. I didn't read about this anywhere; I just threw it together based on what felt right. The only thing I ever actually read was that Native Americans used Echinacea to help wounds heal. This is just my experience, and I'm not suggesting it'll work for everyone.
George Palmer7 George Palmer7 Newcomer
2 messages
joined Apr 2007
#303 ·
You guys are truly wonderful, sending love to you all, George Palmer7. Here, let me share this one with you😘 . I’m going to suggest to my mother-in-law that she takes Noni and Native Propolis together. She starts chemotherapy tomorrow, so I’m keeping everything crossed for her.
Angela Wright, I didn't mean anything by it; calling her a maniac was just a figure of speech, and I know you caught that nuance.
But when you say that it's just part of being human... well, unfortunately, that's been the experience for many, including my mother-in-law and her sisters, and my wife too. It's true that when it comes to doctors and specialists in our hospitals, humanity is a rare commodity. They have so little of it that they practically sweat from the effort of trying to show it; it becomes an exhausting burden for them just to act human. (Maybe I'm being a bit too heated. Everything is still so raw right now. It will get better.)
Angela Wright Angela Wright RegularOP
731 messages
joined Feb 2007
#304 ·
George Palmer7 said:l
Angela Wright, I didn't mean anything by it. Using the word "maniac" was just a figure of speech—I know you caught my drift.
But when you talk about how people act, it’s just human nature... unfortunately, it's an experience shared by my sister-in-law, her sisters, and even my wife. Honestly, in our hospitals, doctors and nurses have so much humanity they practically sweat from it; it makes their lives difficult just trying to deal with it. (Maybe I'm just a little heated. It's still too early in the day. Things will settle down.)

🙂 I wasn't offended. I just wanted you to know there are actually people out there who do good deeds without any hidden agendas... As for the doctors, you'll get used to them. You find all sorts, but I think most of them act that way because they're working under impossible conditions. To function "normally," they have to shut down emotionally just to get through the shift. It's a shame, really, because to me, medicine is this unique science where humanism and natural science should be perfectly intertwined.
Ethan Garcia Ethan Garcia Newcomer
5 messages
joined Apr 2007
#305 ·
Angela Wright said:We haven't done anything yet😳. These holidays have slowed things down a bit. I’ve been thinking about what you suggested—it probably makes the most sense to find a journalist to sit down with, lay out the whole situation, and see if they can help get the ball rolling somehow.


What’s the situation? I'm actually a journalist myself—I work for EPH, though mostly on the weekly side rather than dailies... I can at least keep an ear out for what kind of press coverage you're looking for...
Angela Wright Angela Wright RegularOP
731 messages
joined Feb 2007
#306 ·
Ethan Garcia said:What’s this about? I’m a journalist working for EPH, but for the weekly editions rather than the dailies... At least I might know why you're looking for a reporter...

Look, all this info you're digging for should be handed to you through printed bulletins the moment you receive a diagnosis. I think I laid out exactly what the deal is quite clearly in my opening post. Please, just go back and read vpavi16's posts on the forum here —specifically the one where she describes how they lied straight to her face. It's the same story for everyone fighting a brain tumor in the US: they tell you that the medication her husband was on (Temodal) won't work for a recurrence because it's ineffective. But once she produced that email from Dr. Young in Houston, they finally admitted it *could* be used—it's just that Medicare refuses to foot the bill. They essentially shut down her ability to self-fund her husband's treatment before she even had a chance. That is just a tiny slice of the bullshit we have to deal with.
Personally, I am absolutely livid with the local cancer league, which seems more interested in lining their own pockets than actually helping people. You don't see them anywhere when it matters; instead, it was the late Ana Rukavina, speaking from her deathbed, who had to spearhead the initiative for the stem cell bank. Seriously, do a little digging and you'll find a mountain of irregularities that everyone keeps quiet about, while those "rights activists" are busy locking themselves in cages over on Ban Jelačić Square.
Brenda Richardson33 Brenda Richardson33 Member
12 messages
joined Apr 2007
#307 ·
Betty Allen65 said:dreamers......
I've already posted about this here.
Hope is a strange thing....it can be both a blessing and a curse.
When they were driving my Dearest to the hospital for the last time, clinically dead..... I was CERTAIN she would come home.

You can't just accept it like that, honey.
I certainly haven't.
Easter without my Dearest is, quite frankly, hell.

Don't be too hard on yourself....allow yourself to feel sad, angry, and furious.
Try, however, not to cry in front of him..... believe me, he would cry too if he could.
Try to coax out even a small smile.
Say something warm to him.
Steal a kiss...... I say steal because by the end, my Dearest was in so much pain that even the slightest touch was sensitive, so whenever I turned her or lifted her, I’d kiss her shoulder, her head, her foot..... something.

You'll eventually learn there are no guarantees in life and some things simply cannot be changed.
Cherish the love..... it's the only thing that stays with you and with him forever.

I am proud and happy to have been the mother of such a beautiful human being who touched so many people with their beauty, kindness, and charisma.

And you..... let yourself be overwhelmed by pride and remember those wonderful days spent with your dad.

And... one more thing... I hope I don't sound too blunt saying this, but..... I wish so much that IT had been ME who left before my Dearest did...... that is the natural order of things.
(If such an order even exists anymore.)

It is better when children bury their parents.

Wishing you strength and faith.😘

You aren't being too harsh... everything you wrote is the absolute truth... and what you're going through with your child is the exact same situation as with my dear dad... when we touch him, everything hurts, and even the gentlest touch is painful... I find myself hoping, too, but I'm also trying to make peace with the situation.

I only realize how much strength I actually have when the whole family shows up, and I don't cry; I just want to hear even two or three words from my daddy to brighten my day and, as you said, steal a smile from him.

And I don't cry... especially not in front of him; instead, I just want to enjoy the moment when he reaches for me with his weak hand.... but yeah, it's hard.

I always think of you and all the people who have had to endure the death of their own child, and it truly breaks my heart that you have to live through a pain that I believe is incomparable to anything else... so I wish you nothing but the best, and thank you so much for your words of support, even though you're the one who needs them. Hugs... and so on.😘
James Stewart8 James Stewart8 Newcomer
3 messages
joined Mar 2007
#308 ·
lung cancer
Well, I suppose it is finally my turn to chime in with our struggle... I have been reading through every single post here, and I just want to send my warmest greetings to everyone who posted before me—especially to the one running this whole show, you know who I mean😘.
So, back on February 28th, we received the news that my father has lung cancer—malignant—and it’s spreading fast. It was such a shock... I honestly don't know whether to believe it or not... just endless tears and this constant, heavy weight on my heart thinking about losing someone so dear and close to me. And if you're wondering why I've been in such a dark headspace, it's because the doctors had such an incredibly negative attitude regarding my father's condition. They gave him this prognosis... they said he has maybe a year left at most, can you imagine?😈 Honestly, people, I refuse to think that way! If that's how you feel, please, just keep those thoughts to yourselves. It was absolutely horrific to hear... and then they claimed he wasn't even a candidate for surgery or chemotherapy, which turned out to be complete nonsense, because he actually did go ahead with chemo after all.
He handled the first round relatively well, though he lost quite a bit of weight... but this second round—which wrapped up last Thursday—has been brutal. He couldn't eat anything for four days, he was vomiting, he couldn't even go to the bathroom... The hardest part of everything we're dealing with is that the doctors... well, nobody ever gave us any real specifics about this chemotherapy or what the side effects would be like. Seeing him today, seeing how much he has withered away... he's down to only 60 kg now, he speaks so slowly, he can barely move... part of me almost regretted him being on chemo, even though I know there's no other choice. We ended up taking him for an IV drip, and then in the afternoon, an enema—poor man, he's having to suffer through all of this—and still, he wouldn't eat until we explained the risk of a bowel obstruction and potentially needing surgery. Only then did he force himself to eat.
As for his medications, he's currently using: - Noni /he's been taking two different kinds for ages/
- Aloe Vera
- Beta Glucan tablets
- Some American anti-nausea meds
- Tramadol for the pain
- Zofran—God knows how much that costs!
- And today he was given some syrup with propylene glycol for
constipation.

It's just so hard... but I guess over time, we all learn (the whole family is learning) how to carry the burden of this terrible illness. We never stop hoping, though. I am a believer, truly, and I know that God has plans for all of us... I know what my father is facing is incurable, so I just pray to Him to extend his life, even if it's just five times longer than what those doctors predicted.🙂
HAPPY EASTER
George Palmer7 George Palmer7 Newcomer
2 messages
joined Apr 2007
#309 ·
So, I'm sitting here reading what Donna Fox48 has to say...
And honestly, the more I spend time lurking on this forum, the more convinced I am that there's this unspoken rule where doctors just refuse to share anything useful. Forget about being warm or empathetic—fine, even if their words are ice cold, let them be. But actual information? Details regarding the specific type of cancer, dietary needs, treatment protocols... that’s the fundamental stuff! If the patient can't have it, then at least the family deserves to know. And when they give a prognosis, for heaven's sake, could they just add a shred of compassion? Come on, Doc. Even my mechanic will actually sit down and talk to me before he breaks the news that my engine block is cracked!!!!
Angela Wright, look, I realize the conditions in our healthcare system are pretty impossible, but doctors spend their entire lives studying different approaches. Yet, they still treat these critically ill patients like they're nothing more than sacks of potatoes!! 😠
restlessmarlin6 restlessmarlin6 Active Member
219 messages
joined Oct 2003
#310 ·
Our experience dealing with lung cancer has been a bit different from the norm.
Reading through some of your posts, I’ve noticed that a lot of doctors seem to avoid telling people exactly what they're actually fighting.
In our case, we knew practically from day one—including the patient himself (though, honestly, it took us a little while to actually wrap our heads around the truth, but that's another story entirely).
The patient was actually in total shock because the doctor just dropped the news bluntly, without any sugarcoating whatsoever. But looking back, we eventually realized that being direct is actually better.

But man, those doctors... nobody would say anything concrete about the chemotherapy or the side effects. Today, seeing my dad so weakened—he's dropped down to 60 kg, speaks so slowly, can barely move—I almost regretted him being on chemo (even though there isn't really another way out). We took him for an IV drip, then an enema in the afternoon—poor guy has to go through all this—and he still couldn't bring himself to eat anything until we explained that he could end up with a bowel obstruction and need surgery. Only then did he force himself to eat.

We knew chemotherapy was going to be brutal, but witnessing it is a whole different beast. It is so much harder to watch it happen than it is to just know it's coming. I try to comfort myself (as much as possible) by thinking this is just how it has to be, and that everyone goes through this. I sort of get why doctors hold back on the specifics regarding side effects; I guess it's easier when you don't know exactly what's hitting you. Personally, I think giving someone a detailed roadmap of all their future suffering might actually be counterproductive.

As for the prognosis... it's terrible. You want to hear everything, you really do, but nobody is going to give you the full picture. I've done a bit of digging through various articles, and I'm painfully aware that the general outlooks aren't great, but since no one talks about the specific details, we just accepted things as they were. Still, curiosity is a killer, and now I find myself choosing to focus on every single positive sign rather than constantly reading nonsense or hunting through heavy articles for some kind of comfort (let's be real, the chances of finding actual solace in those things aren't that high anyway).

And please, don't be too hard on the doctors. Sure, there are some catastrophic ones out there, but there are plenty of excellent ones, too. 🙂
Charles Edwards8 Charles Edwards8 Member
46 messages
joined Feb 2007
#311 ·
I mentioned this earlier, but I really don't want to get into playing doctor and throwing around timelines like "you've got six months" or "maybe a year." I’m just not about that life.
Basically, according to the rules, we all have every right to know exactly what we're dealing with—the diagnosis, the treatment plan, the tests, all of it.
That said, doctors often feel they have the right to "dose" information, and there are a million reasons why they might do that. restlessmarlin6 made a great point that if doctors dumped every single detail on us at once, it could actually backfire.
At the end of the day, it’s up to us. We either have to be the "annoying" patient who asks a million questions, or we try to learn the science ourselves (though let’s be real, the internet can be super counterproductive too). It mostly comes down to our own initiative. It’s not fair to paint all doctors with the same brush, though. We definitely get blindsided by that "coldness" or lack of empathy sometimes, but let’s try to see where they're coming from. You can't exactly teach bedside manner in med school. We naturally gravitate toward the sweet, chatty doctors over the blunt ones, but just because someone isn't "warm" doesn't mean they aren't doing an amazing job.
To be fair, a lot of doctors do deal with "God complex" issues, and honestly, that needs to change, but it’s easier said than done.
There are so few doctors willing (mostly due to massive egos) to just say, "Look, I don't know," or "I don't want to give you info if I'm not 100% sure."
Some will hide behind fancy medical jargon to make things sound mysterious, but again, I’m not saying everyone does that.
restlessmarlin6 restlessmarlin6 Active Member
219 messages
joined Oct 2003
#312 ·
Charles Edwards8 said:I think I mentioned this somewhere before, regarding how doctors communicate about specific illnesses, but let me reiterate: I don't approve of anyone giving out prognosis timelines—whether it’s a month, six months, or a year.

Honestly, me neither.
On the flip side, I’m as healthy as can be, so a car could hit me tomorrow and that's just how it goes. We're all going to kick the bucket eventually, so why not just focus on living for "here and now" instead?
Laughing.
Enjoying life. 🙂
George Palmer7 George Palmer7 Newcomer
2 messages
joined Apr 2007
#313 ·
Angela Wright, please..... you said
>>If you decide to go with Noni, make sure you get the original Tahitian Noni, which can only be obtained through a direct distributor. With Noni, it’s vital that it doesn't grow on volcanic soil (like Hawaii), because then it might contain compounds that aren't exactly healthy. The lady I buy my Noni from is a biochemist who ran some analyses on it and says it’s all perfectly healthy, and now...

You know how messy things are with this Noni business, so I was wondering if you could please give me the name and phone number of that lady? I really need to track down that original Noni for my mother-in-law. She was supposed to start chemo today, but they found out she’s anemic. They’re going to give her a transfusion first, so it would be great if she could prepare herself during this time. We already picked up some Native Propolis (we’ll give her 3x5 capsules a day as you suggested... but should we drop back to a regular dose after chemo, or...? ), now we just need that original Noni. Thank you. Would it be okay if I sent you this: 😍 ????
Angela Wright Angela Wright RegularOP
731 messages
joined Feb 2007
#314 ·
George Palmer7 said:Angela Wright, please..... you're saying
>>If you decide to go with Noni, make sure you get the original Tahitian Noni, which you can only get through specific distributors. With Noni, it’s vital that it isn't grown in volcanic soil (like Hawaii), because then it might contain compounds that aren't exactly healthy. The lady I buy my Noni from is a biochemist who ran some analyses on it and says it's all perfectly healthy, and now...

You know how messy this whole Noni situation gets, so I’d ask you to send me her phone number and name. I need to track down that original Noni for my mother-in-law. She was supposed to start chemo today, but they found out she's anemic. They're going to give her a transfusion first, so it would be good if she could prepare herself for that period. We already picked up the Native Propolis (we'll give her 3x5 capsules a day as you suggested... and after chemo, should we drop back to a regular dose or...?), now we just need that original Noni. Thanks. Is it okay if I send you this: 😍 ????

No problem, I'll DM you her number.🙂
Just make sure she doesn't go overboard with the Propolis. Let her stick to those high doses for another month or two to really cleanse the system, then taper down to a maintenance dose. My mom took that high dose for a full year—maybe it was overkill, but honestly, putting that dosage in our daily pill organizer just became part of our routine. Now she takes 3x3 capsules. Take it about 30 minutes before meals. Once she gets the Noni, she can take it alongside the Propolis. For Noni, you start with a larger dose, about a deciliter before each meal for the first week, then gradually scale it down to about a deciliter a day—basically a shot glass before each meal. There are actually different protocols for how to best take Noni depending on the specific ailment. I'll dig up that paperwork and see what it says regarding colon cancer, and I'll either write it out here or email you a copy (?) we can figure that out later.😁
I hope you're feeling a bit better now that you've finally started tackling the problem head-on.
slyseal28 slyseal28 Member
11 messages
joined Mar 2007
#315 ·
Ethan Garcia said:What’s the situation here? I'm a journalist working for EPH, though specifically on the weekly editions rather than the dailies... At least I can understand why you might need a reporter...

My husband finished his last round of chemo on March 10th, 2007, and now he's just sitting there waiting for radiation.

The fact that we have to wait over a month just to start radiation—let me quote what my doctor told me: "If we went through the standard channels, you wouldn't even get a spot in the queue for radiation until July!"—is driving me absolutely insane. This is one of those things I really wish someone would actually report on in the news.

Because, apparently, if you want to actually get treated, you have to pull some strings (which is exactly what I've had to do), but then what about everyone else who was ahead of us in line? Are we supposed to just bump them out of their treatment? That isn't right, is it?

Chemotherapy and radiation therapy have to be continuous. What happens when a radiation machine breaks down? The treatment stops, and you just sit around waiting for repairs. Who can say for certain that these interruptions aren't actively sabotaging the treatment? When you take an antibiotic, you have to take it at precise intervals. Shouldn't treating a malignancy be approached with that same level of responsibility and clinical seriousness?

Another thing—once that final cycle of chemo is done and you move on to radiation, what is the absolute latest deadline to start that radiation? So far, I haven't been able to get a straight answer to that question.

In any case, I really feel like our voices need to be heard regarding these issues, because it seems to me that they are being overlooked far too often.
Jessica Taylor62 Jessica Taylor62 Member
10 messages
joined Mar 2007
#316 ·
Here are my thoughts on the doctors
I haven't actually talked to them much myself because my mom decided she wanted to handle things personally. She’s incredibly sharp, and she’s been extremely satisfied with everyone she’s dealt with. When she first arrived at the hospital for her exam, they told her exactly what was going on right away. Even before surgery, the surgeon came to her room to explain the entire procedure. She later told me she almost turned around and went home, but the doctor comforted her and explained there was nothing to fear. Honestly, thanks to him, everything was much easier to bear. Later, when we went in for follow-ups, we’d find ourselves waiting for him for up to four hours. I was starting to lose my patience, but she would just defend him, explaining he’s busy and that he’s an excellent doctor. It turns out she was right. She has total confidence in him, and when he tells her he’s happy with how the treatment is progressing, she’s genuinely happy.
The first time we were at the Cancer Institute, we waited about four hours just to see a radiologist. The doctor gave her a very brief look, took the data, grabbed all her paperwork, and said they’d mail the follow-up treatment plan to her house. We walked out, and I just stood there like a statue. He didn't really explain anything—just added a few bits here and there, I guess. It lasted a few minutes. When you arrive facing a diagnosis like that, being told "we'll send a notice" is totally jarring.
Around 12:30 the next day, the phone rang. It was that same doctor calling to say that during today's consultation, they decided she needed another CT scan, so to come back once that's done. Again, I was left speechless because I really wasn't expecting the call. To me, that shows a high level of responsibility toward the patient.
At the oncologist's office, our first wait was about two hours before they scheduled her for additional exams at the hospital. As we were leaving, the doctor pulled me into his office to explain everything regarding chemotherapy. Since she takes the medication at home, he warned me about all the side effects and what steps to take. He was patient and polite. When I asked about starting the medication immediately, he simply replied: this illness didn't appear overnight, and it won't vanish overnight either; a couple of days don't make a difference.
I forgot to mention that before she was discharged after surgery, the head nurse called us over to show me how to manage the stoma. She warned me about what to watch for and gave me some informal advice to bring her into the ER in the afternoon if anything gets complicated. Fortunately, everything has been fine, which proves the surgeon who operated on her is a master at his craft.
I should also add that over the last ten months, only one nurse was rude, and only because she wouldn't tell me I could leave a deposit if I didn't have a referral until I insisted.
My humble opinion is that the doctors and the rest of the staff are doing the best they can. They aren't to blame for the lack of better hospital conditions or outdated equipment.
Also, not a single doctor recommended any dietary supplements to help with faster recovery.
James Stewart8 James Stewart8 Newcomer
3 messages
joined Mar 2007
#317 ·
So, today my father is doing much better, thank God... he can finally eat and even move around a bit! I realized after yesterday's post that I actually forgot to mention something important... if anyone knows of a similar lung cancer case where chemotherapy actually yielded positive results, please let me know.
James Stewart8 James Stewart8 Newcomer
3 messages
joined Mar 2007
#318 ·
...BTW-Još, I didn't mean to trash the doctors, I just meant to call out the whole damn situation...😠
Jessica Taylor62 Jessica Taylor62 Member
10 messages
joined Mar 2007
#319 ·
Donna Fox48
I completely hear you.
In a situation like this, it’s easy to feel angry at the entire world.
Personally, I think it’s pathetic when certain doctors dare to give prognoses, even if many claim they can do so based on experience.
To be honest, I don't know much about this specific type of colon cancer my mother has; frankly, it feels much easier not knowing. At first, I was terrified of running into a doctor or anyone else who might drop bad news on me, so I barely asked anything. Looking back, staying uninformed was actually the right move. It kept me from obsessing over a future that hasn't happened yet and crying constantly. Instead, I just focus on giving my mom the very best of me, day by day. I believe she needs that more than she needs me wasting my time and nerves studying a disease that even doctors don't fully grasp.
Have faith that things will improve. Just stay by your dad's side and somehow show him that you aren't afraid for him. Even if you are, it will make things much easier for him.
Try to help him maintain his dignity and show him how much you love and respect him. I assume he knows how sick he is, so if you can, talk to him about it. It helped my mother immensely to share her fears with someone.
Usually, older people don't have close friends to lean on, so they are willing to open up to their children—but they need to feel that their child is strong enough to handle it.
Whenever he needs something, or you think he might, just bring it to him, even if it means making several trips to the hospital a day. It won't be a burden, and you should ALWAYS make time for him. Believe me, it will mean more to him than anything else and will help him recover faster.
slyseal28 slyseal28 Member
11 messages
joined Mar 2007
#320 ·
Jessica Taylor62;8063710 said:Donna Fox48
I hear you completely
In a situation like yours, it’s easy to feel like you want to take it out on the whole world
Personally, I think it's nonsense when certain doctors dare to hand out prognoses, even if many claim they can do so based on their experience
To be honest, regarding this specific type of colon cancer my mother is dealing with, I don't know much about it either; sometimes it feels much, much easier just not knowing. At first, I was terrified of running into a doctor or anyone else who might drop some bad news on me, so I barely asked anything. Looking back, I realize that was actually a good approach because instead of obsessing over the future and drowning in tears, I can just focus on giving my mom the absolute best of me, day by day. I think she needs that more, and it means more to her, than me wasting my precious time and sanity studying a disease that even the doctors haven't fully mastered yet.
QUOTE]

(Just to add to that) My Pigeon and I haven't had negative experiences with doctors when it comes to them offering prognostications. Personally, I find giving prognoses to be a bit foolish. We are all unique individuals; everyone reacts differently to medications, to the illness itself, and so on. Similarly, there are people who want to know every single detail about the disease they're facing and every possible treatment option (which we certainly do), while others prefer not to (as you so beautifully illustrated). However, that choice belongs to the patient and their family. It isn't the doctor's call. That is one thing I truly resent. That said, if doctors weren't so overworked—if they had better working conditions and didn't have to be in five places at once (teaching, symposiums, clinics)—perhaps they would treat patients differently. I'd venture to say they would certainly be better, simply because they'd actually have the time to devote to their patients.
My grievances, my dissatisfaction, is primarily directed at those:
-who allow these kinds of working conditions to exist, especially in oncology,
-because of whom the waiting lists are unforgivably long,
-because of whom there aren't enough hospital beds, leading to situations where a patient who is ready for chemotherapy gets sent home instead,
-the lack of adequate equipment, such as PET/CT scanners,
-and the shortage of medical staff available to provide proper information or assistance when the doctor is away.

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