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Support resources for families dealing with cancer and other serious illnesses

Started by James Cox6 · · 👁 8 views · 3.9K replies

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Participants James Cox6Lisa White54shadowmason6Angela Wrightbrightgardener8Melissa Moore39James Martinez3Grace Stewart6Megan Fowler78Zachary Howard2Ashley Rodriguez41Douglas Lee13rowdyheron17placidheron24slyseal28jadesailor14Michael Newman3jadetinker42Benjamin Grant6wanderingharbor61cosmicviper76Dana Baker37Jason Torres5Peter Chavez6 …
Brenda Walker58 Brenda Walker58 Newcomer
8 messages
joined May 2008
#101 ·
Hey everyone, I haven't been around these forums in a while. Sadly, it's not because my parents' health improved—it was actually the exact opposite. My dad had renal cell carcinoma with metastasis in his spine and lungs, and my mom was battling breast cancer with lymph node involvement (3/14 axilla). Things just kept getting worse for my dad over this last year, and he finally lost his fight. He passed away on September 1st, leaving a massive hole in our lives... As for my mom, her checkups are looking good so far (thank God).
Anyway, we have 12 tablets of 50mg Sutent left over. It’s used for treating kidney cancer—one of those "smart drugs"—and we’d rather pass them on to someone who actually needs them. If this could help someone, please shoot me a private message or email me at tinnaos@net.hr and we can figure out the details. A full bottle holds 30 tablets and is taken in 4-week cycles (28 tablets total). My dad worked with his oncologist to complete 6 cycles, and it truly made a difference for him; it gave him more time, as much as he could get.
Hang in there, everyone.
Steven Ward25 Steven Ward25 Newcomer
1 message
joined Mar 2009
#102 ·
Hi everyone,
I’ve been following all your posts for quite a while now, and I finally decided it was time to jump in and register myself.
First off, I just want to say how much I admire everyone here for being so incredibly brave and staying so positive through it all. Sadly, this terrible disease has found its way into my family too. My mom is 50, and she’s fighting breast cancer. She just finished her first round of chemo.
I was wondering if you all could share what your experiences were like with chemo? Along with the chemo, my mom is also receiving immunotherapy. So far, she hasn't had any major side effects, though she does feel like she’s coming down with a bit of the flu, but nothing too overwhelming... I’m just curious if things can take a turn for the worse, meaning if new symptoms might pop up, or if we might be among those lucky enough to handle that first round of chemo pretty smoothly. Thank you.
Steven Ward25 Steven Ward25 Newcomer
1 message
joined Mar 2009
#103 ·
Is there anyone out there?😢
Zachary Howard2 Zachary Howard2 Newcomer
6 messages
joined Jan 2009
#104 ·
Linda Cox69 said:Hi everyone,
I’ve been lurking here for quite a while, but I finally decided it was time to actually register.
First off, I want to say how much I admire everyone's resilience and positive outlook. Unfortunately, this relentless disease has made its way into my family too. My mother is 50 and was diagnosed with breast cancer. She just finished her first round of chemo.
I’m curious to hear about your experiences with premedication for chemo. Along with the chemo, my mom is also undergoing immunotherapy. So far, she hasn't had any major side effects. She feels like she's coming down with a mild flu, but nothing too debilitating. Is it possible for things to take a turn for the worse—meaning, could new symptoms suddenly pop up—or are we just one of those lucky families who handled the first round well? Thanks.

Based on what my mother went through (ovarian cancer), she dealt with vomiting, diarrhea, an intense aversion to smells and food, bone pain, and exhaustion after every single session. It usually lasted anywhere from three to seven days. When it came to nausea, besides taking Reglan, she found that simple popcorn from Target and some menthol candies really helped manage it.
The side effects from oral chemotherapy were significantly milder, though, predictably, hair loss was unavoidable.
James Cox6 James Cox6 Active MemberOP
150 messages
joined Mar 2009
#105 ·
Hey everyone...

I’ve been MIA for about ten days because I was looking after my mother, who just got discharged from the hospital.
It’s confirmed—she has lung adenocarcinoma that has spread to her neck and lymph nodes... they even found a metastasis in her sternum...

To give you the full picture... she was sent home from the hospital looking completely wasted. She lost so much weight. I’ve been cooking for her, trying everything, and she finally started eating, which was a relief.

Her pulmonologist didn't sugarcoat it: "Your mother's condition isn't just serious, it's critical. You need to start chemo IMMEDIATELY." The issue is the oncology department in Washington, D.C.—they simply don't have any openings...

I just stood there and watched... (didn't pull any strings or use any connections) and the staff at oncology told me: "Your mother will get the Gemzar once we order it and Medicare approves it in about three weeks."
The drug isn't the bottleneck; it's the space. Because she's a cardiac patient, she won't be seen for inpatient care for at least two to two and a half months.

I didn't say a word to the oncologist... didn't argue or protest anything. I just said, "Fine, please put her on the list."
They scheduled her for inpatient admission and chemo starting in June. They mentioned that's actually fast, considering you might wait up to six months for radiation...😱

Luckily, I spent years working in law and collaborating closely with doctors—handling things like accident reconstructions, trauma, and autopsies, so I deal with forensic medicine quite a bit. Because of that, I managed to reach a high-ranking official at the Mayo Clinic to ask for the real truth about my mother's illness... (That raw truth that doctors tell one another as colleagues, but would never tell a patient or family member. I learned through my work that there are two truths: the one told to the patient, and the actual reality discussed between professionals when they comment on a case.)

When I went to his office the next day, he looked me right in the eye and said: "Get your mother out of here immediately. Forget the formalities and the paperwork... skip the waiting lists for Gemzar approval... she needs chemo literally tomorrow. If you wait, she might die between doses."

They shouldn't have even bothered with the CT scan of her thorax or the lung biopsy. They could have just taken fluid from the lymph node in her neck via aspiration and gotten the cancer cells then. If only my dear Luna had reached out sooner, we could have saved three weeks.😢

When it comes to cancer, honey, every single day counts. Take this seriously...

I was stunned. I asked if he could recommend someone in a major city like New York? A hospital... somewhere... anyone? I'm six and a half months pregnant and feeling completely lost. He said he could, but warned me that entering a major hospital is such a bureaucratic nightmare—admissions, connections, more tests, then being back at oncology because hospitals always want their own specific results. And then there are the priorities (keep in mind there will always be someone with better connections or a more advanced stage of illness who jumps ahead of your mother because she isn't dying *yet*... and there's still hope...) the waiting lists, the Medicare approvals, all of it.

Then he told me: "Unfortunately, our working conditions mean we don't have time to deal with the patient; we deal with the disease. A more advanced, aggressive disease is a bigger challenge for us than something that isn't quite as urgent." That's the reality.

So I asked... what am I supposed to do then?

He said, "If you have the money... take her to a private clinic. She can't wait."

And so, guys, here we are. My brother and I decided to take Mom across the border to a private clinic... and I have to say, they admitted her immediately on Sunday. They did an X-ray right away (nothing worsened; the pleural effusion is gone, no fluid in the lungs)... they even complimented her "star student" pulmonologist (that's my nickname for her). Her electrolytes were low, likely from losing them during her hospital stay, so they gave her four liters of IV fluids over two days.

They did a full consultation yesterday morning, and here’s the lineup:
1. A cardiologist (she has heart issues)
2. An oncologist,
3. A pulmonologist,
4. An internist, and
5. A pharmacologist... and she starts chemo this Thursday.

One dose of the standard chemo is about $275, plus $65 a day for the hospital stay...

They praised the Pulmonology department for being thorough, but they wouldn't say a word about Oncology (and honestly, I wouldn't either).

The point of this post isn't to trash our doctors—they deserve respect because they're working in conditions that are frankly beneath human dignity—the goal is to point out what's actually happening: we are becoming exactly like America... if you have the cash, you get treated; if you don't, you cross your fingers and wait.

Pathetic, truly pathetic.

To be clear, I don't have unrealistic expectations or insane demands (let's face it, nobody "cures" cancer—those who do usually reach out years later when it recurs, or they end up the subject of some documentary or science special), but
I perfectly understand what it means when one doctor tells another "treatment needs to happen NOW." I simply cannot live under that kind of weight. I want to help IMMEDIATELY (as they told me) because there is such a thing as fighting for your life—giving a person a chance to try and save themselves... all while maintaining some shred of human dignity.

If I can't save my mother, I'll be devastated because I failed, but at least I'll have a clear conscience knowing I did everything possible.
Steven Ward25 Steven Ward25 Newcomer
1 message
joined Mar 2009
#106 ·
Amanda Miller69 said:Based on what my mom went through with her ovarian cancer, she dealt with vomiting, diarrhea, being super sensitive to smells and food, bone pain, and just total exhaustion after every chemo session. It usually lasted anywhere from three to seven days. When it came to the nausea, besides sticking to a regular schedule, she found some relief with simple popcorn from a local grocery store and some menthol candies...
The side effects from oral chemotherapy were much more manageable, though of course, the hair loss is unavoidable

Thanks so much, Amanda Miller69😍

My mom is doing a bit better today, and I really feel like the worst part might be behind us now... although I have to say, the aches in her bones, muscles, and joints were quite intense...
Is your mom taking anything specific for the pain?
We were given some Tylenol, but it didn't seem to do much at all, so we ended up giving her some Voltaren, which actually helped ease the pain a little and made things a bit easier for her...😢
Steven Ward25 Steven Ward25 Newcomer
1 message
joined Mar 2009
#107 ·
Dear Lara.
I am so incredibly sorry about your mom and everything your family has been forced to endure lately.

To be honest, our own experience with the doctors wasn't exactly wonderful either, at least not until we finally made the switch to a private specialist.
I joke sometimes that they practically shaved five years off my life...
I really don't want to dwell on all our past struggles because rehashing it all just drains my energy and adds so much unnecessary weight to my shoulders, and there has always been unfairness, and there likely will be again... if we even started asking why this happened to her specifically, I don't think there would ever be an end to the questions.

We are just navigating this situation the best way we know how, though it certainly takes its toll, and sometimes I wonder where I find the strength to keep going... We are all standing right by Mom's side, doing everything possible because we refuse to let her fall.
It truly breaks my heart seeing her in pain when you feel so helpless and unable to do anything to take that suffering away...

But, deep down, I’ve always been an optimist. We have finished one round of chemo, and now we are waiting for the second, then another, and before we know it, we'll be halfway through the journey.🙂
I just really hope this next round does a better job of killing that monster (I'm usually not a violent person, but when I think about it, whew!)...

I just know that people who haven't walked through this kind of Calvary with someone they love can't truly understand what we are feeling right now. People can be sympathetic and full of empathy, but the moment it involves someone of your own blood, your entire world collapses in a heartbeat... The whole point of this story is to build a new world from the pieces, and we are building ours right now, and we aren't giving up, and we certainly aren't letting that monster win against Mom.
Our fight is going to be fierce and incredibly difficult, but I completely agree with what you said.
Even if the final outcome isn't exactly what we are praying for😢, we will know that we did absolutely everything within our power... that we fought with every last drop of blood we had, whether it was against the doctors, Medicare, that monster, or anyone else...
I won't ramble on too much longer.
I am sending nothing but positive energy to all of you as you continue your own battles.
I am right there with you...😍
Zachary Howard2 Zachary Howard2 Newcomer
6 messages
joined Jan 2009
#108 ·
Linda Cox69 said:Thanks so much, Amanda Miller69.😍

My mom is doing better today. I honestly think we've passed the worst of it. That said, the bone, muscle, and joint pain she was experiencing was pretty intense.
What kind of pain relief is your mom using?
The doctors gave us Tylenol, but it didn't do much, so we switched her over to Voltaren, which actually provided some relief and made things a little easier on her.😢


Unfortunately, my mother lost her battle; it's been almost a year now. She usually relied on ibuprofen for the pain. Tylenol is more suited for fevers or basic muscle aches. You might want to try ibuprofen—it’s a fairly strong analgesic and is typically used for rheumatic pain.
On top of that, she took Megamin, Brocolin, Bio Bran, shiitake mushrooms, and raw propolis (not all at once, obviously) to help support her immune system.
Steven Ward25 Steven Ward25 Newcomer
1 message
joined Mar 2009
#109 ·
Amanda Miller69 said:Unfortunately, my mom lost her battle, and it’s been almost a year now... She used to take ibuprofen for the pain. Tylenol is more for when you have a fever or muscle aches. You might want to try ibuprofen, though, since it's a pretty strong analgesic and is typically used for rheumatic pain...
Besides that, she took things like Megamin, Brocolin, Bio Bran, shiitake mushrooms, and raw propolis—not all at once, of course—to help boost her immune system...

😢I am so sorry to hear that.

Thanks for sharing this, you brave soul...🙂
Nicholas Hughes2 Nicholas Hughes2 Newcomer
2 messages
joined Oct 2008
#110 ·
Hey everyone, I really hope things are going okay in your own battles 🙂

I’m feeling so happy today—my mom finally got all her test results back and everything looks great. Her radiologist told her—well, he said it with a huge disclaimer, obviously, because he's technically not supposed to give definitive news like that—but he truly believes she's in the clear. Given where she is in her recovery and how good these scans look, he said the chance of the disease coming back is basically non-existent 👋 🙂🙂🙂

I really hope we get to read more good news like this more often... hang in there, everyone 🙂
Benjamin Grant6 Benjamin Grant6 Member
36 messages
joined Aug 2008
#111 ·
Susan Diaz91 said:My dear ones...

I haven't been around for about ten days because I was looking after my mother, who just returned home from the hospital.
It has been confirmed that she has lung adenocarcinoma which has spread from the lungs to her neck and lymph nodes... they even found a metastasis in her thoracic spine...

To build upon everything else... she was discharged from the hospital looking absolutely frail, having lost so much weight... I’ve been cooking for her, trying everything I can, and she finally started eating, which was a relief.

Her pulmonologist was brutally honest with me: "Your mother's condition isn't just serious; it is extremely critical, and she needs to begin chemo IMMEDIATELY." The issue is the oncology department here in the local area—they simply don't have any openings.....

I just stood there observing... (I wasn't pulling any strings or using any connections) and at the oncology ward, they tell me: "Your mother will receive the GEMZAR medication we ordered, but we have to wait three weeks for Medicare to approve it."
The medicine isn't the bottleneck; it's the space... she won't be seen for a minimum of two to two and a half months, and that's for inpatient care since she is considered a cardiac patient...

I didn't say anything to the oncologist, nor did I protest... I simply said, "Very well, please schedule her."
They scheduled her for inpatient admission and chemotherapy back in June. They told me that's actually fast, considering radiation can sometimes have a six-month wait...😱

I suppose I was lucky to have spent so many years working in law and collaborating closely with physicians—handling things like accident reconstructions, trauma assessments, autopsies, and forensic pathology—so I was able to approach a high-ranking official at the Mayo Clinic to ask for the unvarnished truth regarding my mother's illness... (that specific truth that doctors tend to share with one another as colleagues, but rarely reveal to a patient or a family member; I learned through my work with doctors that there are two truths—the one told to the patient, and the one shared between professionals when discussing a case).

When I visited his office the following day, he looked me straight in the face and said: "Get your mother out of here immediately. Forget the formalities and the referrals... skip the waiting lists for GEMZAR approval... your mother needs chemotherapy literally tomorrow... because it could very easily happen that while you are waiting, she passes away between doses."

There was no need for them to perform a CT scan of the thorax or put her through the agony of a lung puncture... if they had simply sampled the fluid from the lymph node in her neck, they would have identified the cancer cells instantly... oh, dear Susan Diaz91, if only you had reached out sooner, we could have saved those three weeks.😢

When dealing with cancer, darling, every single day matters, and you must take this seriously...

I was left stunned and asked if he could recommend someone in Washington, D.C.???.. A hospital... where, who... anywhere, because I am six and a half months pregnant and feeling completely lost... He told me he could help, but warned me that entering a major hospital is always a massive ordeal: the intake, then the connections, then the repeat tests in oncology because hospitals insist on their own findings, and then there are the infamous priorities (you have to understand there will always be someone with a stronger connection or a more advanced stage of disease who will jump ahead of your mother because she isn't dying yet... and because there is still hope... the waiting lists, the Medicare approvals, and so on...

Then he told me: "Unfortunately, our working conditions are such that we don't have time to focus on the individual patient; we deal with the disease itself, and a more aggressive, advanced disease presents a greater challenge to us than a condition that isn't quite as urgent." That is the reality.

Regarding what I said... what else am I supposed to do????

He told me that if there is money available... seek private treatment immediately... this cannot wait...

And so, my dear friends here, what can I even say... my brother and I decided to take Mom across the border to a private clinic... (just over the border from us) and I must say they admitted her immediately on Sunday, performed an examination right away, and did a chest X-ray (nothing has worsened, the pleural effusion has resolved, there is no fluid in the lungs)... they praised her pulmonologist, who was such a brilliant specialist (that is how I affectionately used to call her), her cardiac function is good, but they noted she lost a significant amount of electrolytes while in the hospital... they administered 4 liters of IV fluids over two days...

They held a consultative review yesterday morning, consisting of:
1. A cardiologist (since she is a heart patient)
2. An oncologist,
3. A pulmonologist,
4. An internist, and
5. A pharmacologist... and she begins chemotherapy this Thursday.

One dose of the primary chemotherapy costs 250 Dollars, and the daily rate for a hospital bed is 60 Dollars...

They spoke highly of the Pulmonology department for their work, but they declined to comment on anything regarding Oncology (and frankly, neither would I).

The purpose of this post is NOT to disparage our doctors—they deserve respect because they work under conditions that fall far below basic human dignity—the point of this post is to highlight a growing reality: we are becoming exactly like America... if you have the funds, you get treated; if you don't, you suffer and you wait.

Pitiful and utterly wretched

To be clear, I don't hold unrealistic expectations or make unreasonable demands (after all, no one is truly "cured" of cancer, and those who claim to be usually reach out years later facing a recurrence, or if someone actually does beat it, they become the subject of documentaries and science specials), but
I understand perfectly well when one professional tells another that treatment must happen IMMEDIATELY, and I simply cannot live under that kind of pressure; I want to help IMMEDIATELY (as we were advised) because there is such a thing as a fight for life, giving a Person a chance to try to save themselves... and doing all of this while maintaining some semblance of human dignity.

If I fail to save my mother, I will be profoundly saddened by my own perceived failure, but at least I will have a clear conscience knowing that I exhausted every single possibility.

We faced a similar situation with our mother during her initial diagnosis, which was repeatedly delayed, and the doctors offered neither certainty nor solutions nor timelines. Nothing.

As friends helping friends, we uncovered the truth and spent the middle of the night searching for an emergency discharge from the hospital, much like I mentioned before regarding that discharge summary stating (after a month and a half of biopsies and hospital stays): "patient is discharged pending new results, suspicion of cancerous cells"! By then, the stage was already IIIC.

In any case, from day one, we didn't hesitate so that she wouldn't be stuck waiting in line for surgery or chemo, which is why she is at Mayo Clinic now. According to my father, quite a few people from the local municipal hospitals end up going there.

Anyway, I hope that despite everything, the chemo goes well because you acted on accurate information immediately and provided her with an opportunity!

Stay strong!
Benjamin Grant6 Benjamin Grant6 Member
36 messages
joined Aug 2008
#112 ·
Linda Cox69 said:Dear Lara.
I am truly sorry for your mother and everything your family has been forced to endure...

Unfortunately, our experience with the doctors wasn't exactly stellar either, at least until we finally transitioned to a private specialist.
I sometimes joke that they effectively stole five years of my life...
I have no desire to recount all our specific struggles because it is simply too draining and places an unnecessary burden on my mind. Injustice exists, and it certainly will continue to exist. If we were to start asking why this happened to her specifically, I suspect there would be no end to the questioning...

We are navigating this situation as best we can. It drains one's energy, and sometimes I find myself wondering where it all goes... We are doing everything possible for Mom; we won't let her fall.
It broke my heart to witness her pain, knowing there is absolutely nothing you can do to alleviate it...

Still, I suppose I am an optimist at heart. She has completed one round of chemo. We are waiting for the second. Then comes another, and before we know it, we'll be halfway through...🙂
I just hope this next round manages to kill that monster more effectively (I'm not usually a violent person, but when I think about it, well...)

I only know that those who haven't walked this gauntlet alongside a loved one cannot possibly understand how we feel. People may offer sympathy or empathy, but once it involves someone of your own blood, your entire world collapses in a single second. The essence of this whole ordeal is to build a new world from the ruins. And we are building ours. We aren't giving up. We aren't letting that thing take Mom...
Our fight will be fierce and difficult, but I agree with what you said...
Even if the final outcome isn't what we are praying for😢, we will know that we did everything in our power. That we fought until the very last drop of blood. Against the doctors, against Medicare, against the monster, against everyone...
I won't dwell on it any longer...
Sending positive energy to all of you as you continue your struggle...
I am standing with you...😍

Regrettably, you have described the reality perfectly. Worlds collapse, and then new ones are forged. Anyone who experiences such cruelty emerges stronger and more courageous, gaining a new dimension to their character—though not everyone can grasp that, as everyone carries their burden in their own way...

Similarly, after reading many accounts here, browsing various sites, and listening to my own mother, I must say there is no rule stating that if one round of chemo goes well, the next one will follow suit. This isn't meant to discourage you, but one should certainly prepare for every possibility. During the first year, my mother bravely and heroically endured six rounds of chemo without major symptoms, despite the devastating psychological blow of losing her hair. Now, in this second year, she tackled the first round heroically, even though (perhaps out of sheer fear) she lost track of time regarding her appointment, which resulted in the doctors calling us with the shocking news that she had to arrive for therapy in just two days. She approached the second round with a fighting spirit, but a reaction occurred and she had to be admitted to the hospital. We were told to prepare for the worst, as complications can arise, especially since they will be changing the medication. Regardless, it seems like everything is so far away at the start, but then all the cycles pass, and you wonder where the time went so quickly...

From the very beginning, the doctor instructed my father to watch closely; if she complained of intense pain, he was to ask her to provide a small scale from 0 to 10 by moving a slider herself. If it wasn't higher than a 6, he was told not to give her anything. She regularly stayed around a 5, so she didn't require any pain medication. One must also keep in mind that ibuprofen can lead to dependency...

We are facing the fifth round this Monday! Apparently, there will be six in total, but if there need to be more, we are ready—and most importantly, she is ready. She copied an article for me where the core idea is this:

"A few brief reminders regarding certain scientific truths:
1. Desire is essentially a form of prayer. If you can visualize your desire being fulfilled—truly feeling it as an existing reality—you will experience the profound joy of having that prayer answered.

2. Through the focused application of thought, one can construct perfect health, success, and happiness.

3. One should permit oneself to feel both joy and tranquility by anticipating the certain realization of their intended goals.

4. A single mental image carries more weight than a thousand words. The subconscious mind will eventually materialize any image born within the consciousness that is firmly rooted in faith.

5. Avoid all forms of forceful effort or mental strain during prayer. Instead, allow a sense of drowsiness to wash over you, drifting into sleep with the absolute conviction that your prayer has already been heard.

6. Whatever you perceive as truth, command it to be fulfilled within your thoughts—and it shall manifest. Direct your focus toward harmony, health, peace, and abundance."


Let us all remain courageous and resilient, maintaining a positive outlook on life, for there is no tomorrow, only the present moment...
Benjamin Grant6 Benjamin Grant6 Member
36 messages
joined Aug 2008
#113 ·
Maria Fox said:Hello everyone, I hope your own battles are going well... 🙂

I am feeling quite happy today, as my mother finally received all her test results and everything looks perfect; even her radiologist told her—with that specific emphasis one uses when they aren't technically supposed to say it—that he considers her cured, noting that given her stage and these specific findings, the probability of a recurrence is virtually non-existent... 👋 🙂🙂 🙂

I truly hope we find ourselves reading news like this more frequently, so please, stay strong... 🙂

I also share the hope that we will be reading such wonderful news much more often! 👋
Steven Ward25 Steven Ward25 Newcomer
1 message
joined Mar 2009
#114 ·
Maria Fox said:Hi everyone, I really hope your own battles are going well...🙂

I am feeling so happy today because my mom finally got all her test results back, and everything looks wonderful; her radiologist actually told her—though he made sure to emphasize that he technically shouldn't be saying this—that he considers her fully recovered, and given her stage and these specific findings, the chances of the disease returning are incredibly minimal...👋 🙂🙂🙂

I truly hope we get to read more news like this more often, so please, everyone, stay strong...🙂

Heartfelt congratulations!!! I'm hoping we see much more good news like this very soon...🙂
Steven Ward25 Steven Ward25 Newcomer
1 message
joined Mar 2009
#115 ·
Nancy Hernandez43 said:Unfortunately, you really hit the nail on the head with what you wrote... It’s true that through struggle, entirely new worlds are forged. Anyone who endures this kind of hardship finds themselves becoming stronger and more courageous, gaining a whole new depth to their character—though I suppose not everyone can truly grasp that, since we all carry our burdens in such different ways...

From everything I’ve read on the forums here, all the websites out there, and just by listening to my own mother’s experience, I’ve come to realize that there really isn't any guarantee that because one round of chemo went smoothly, the next one will follow the same pattern... It’s certainly not meant to be discouraging, but I think it is important to mentally prepare yourself for every possible outcome. During that first year, my mom bravely powered through six rounds of chemo like a true hero, hardly showing any major side effects, though she did have to deal with the hardest part for anyone's mental state, which was losing her hair. Now that we are in this second year, she tackled that first round with such courage, even though she was understandably terrified—she actually had a bit of a breakdown thinking about having to go back, and then the doctors called and completely caught us off guard by telling us she had to start therapy in just two days. She headed into the second round ready to fight, but she had a reaction and ended up being admitted to the hospital... We were told to brace ourselves for the worst since things can take unexpected turns, especially when they decide to switch up the medication. But regardless of how it unfolds, I always feel like at the beginning, everything seems so far away, and then suddenly all the cycles pass by and you find yourself wondering where the time went so fast...

From the very beginning, the doctor advised her father to be extremely careful regarding how they managed her pain levels... he was told that if she started complaining about intense discomfort, he should first have her use a small 0-10 scale to indicate the intensity herself, and if she wasn't rating it higher than a 6, he shouldn't administer any medication at all. She was consistently rating her pain around a 5, so they decided it was best not to use any painkillers... it's also worth keeping in mind that things like ibuprofen can actually lead to dependency if you aren't careful...

We’re facing our fifth round of chemo this Monday! It looks like there might be six sessions in total, but honestly, if it turns out we need more than that, we’re ready to take it on—and most importantly, she is ready... She actually sent me an article that breaks down how the treatment plan is going to look...

Just a few little scientific reminders to keep in mind...
When you hold a deep desire in your heart, try treating that wish as a prayer... If you can truly visualize your wish being fulfilled—really seeing it happen and feeling the reality of it within yourself—you will eventually experience the pure joy of having your prayers answered...

By harnessing the power of your own thoughts, you can truly begin to construct a foundation of perfect health, lasting success, and genuine happiness...

Just take a moment to really lean into that feeling of joy and pure peace, knowing deep down that everything you’re working toward is already becoming your reality...

A single mental image truly is worth a thousand words... the subconscious has this incredible way of materializing every vision we hold within our consciousness, provided those images are firmly rooted in faith...

When you sit down to pray, try to let go of any sense of force or intense mental strain... just allow yourself to drift, letting that heavy, peaceful drowsiness wash over you, all while holding onto the quiet, steady conviction that God is truly listening to your heart...

Everything you hold to be true, everything you feel deep in your soul, just let those thoughts manifest into reality—because eventually, they will come to pass and you will find yourselves fully realized... Just focus your mind on harmony, on vibrant health, on peace, and on true abundance...


Let’s all try to stay brave and keep fighting together, looking at life with a positive outlook since there really is no tomorrow, only today...

Nancy Hernandez43, thank you so much for sharing all of those helpful tips and your own personal experiences with us...😘A special and heartfelt thank you for all the truths I've learned along the way...🙂
We really ought to focus on keeping our thoughts positive...🙏👍
Brenda Walker58 Brenda Walker58 Newcomer
8 messages
joined May 2008
#116 ·
My post about Sutent has been sitting there for a few days now. Is it actually possible that nobody needs this stuff?
(If that's the case, thank God!)
Benjamin Grant6 Benjamin Grant6 Member
36 messages
joined Aug 2008
#117 ·
Linda Cox69 said:Nancy Hernandez43, thank you for the advice and the experiences you’ve shared with us...😘especially for the hard truths we needed to hear🙂
we really need to keep our thoughts positive🙏👍

I found myself spiraling into anxiety over these circumstances, essentially manufacturing an impossible situation in other areas of my life just to chase an article that might offer some inspiration for my mother...

We keep fighting...👍
Grace Stewart6 Grace Stewart6 Member
37 messages
joined Mar 2009
#118 ·
Maria Fox said:Greetings to everyone; I trust your respective battles are progressing as expected. 🙂

I’m feeling quite relieved today. My mother finally received all her test results, and everything looks perfect. Her radiologist actually told her—though he made sure to emphasize that he wasn't technically supposed to say it—that he considers her fully cured. Given her specific stage and these current findings, isn't it a relief to know that the probability of the disease returning is practically non-existent? 👋 🙂🙂🙂

I truly hope we see more news like this from time to time; hang in there, everyone. 🙂

Simply wonderful. 🙂🙂🙂
Thank God, and may we see many more pieces of news like this.
feralridge3 feralridge3 Active Member
54 messages
joined Dec 2010
#119 ·
Susan Ruiz76;19339374 said:Dear Luna, I am so incredibly sorry to read this, but please know it isn't all hopeless. I truly hope that, even if you’re feeling physically drained from all the testing and chemo, your spirit remains strong and resilient—because having that mental toughness is honestly half the battle. I also hope you have your family right there by your side. If it's within your budget, consider picking up some beta-glucan 500 mg (it goes for about $223) which comes in a box of 60 tablets.


Is there any kind of limit on how long one can take glucan?
I stopped by the pharmacy to ask, and they told me it needs to be taken consistently over a long period, but they couldn't give me a straight answer regarding the duration.
I even asked my oncologist, and he just told me I was throwing my money away.
feralridge3 feralridge3 Active Member
54 messages
joined Dec 2010
#120 ·
Maria Lee54 said:Hello everyone! It’s been quite a while since I last posted here. Things have been incredibly complicated on my end regarding finding a way forward with my treatment. Since my health has taken a bit of a downward turn lately, I won't bore you all with the unpleasantness and the difficult situations I've had to endure—it's been deeply unsettling. Right now, I am focusing on just one thing: getting to the clinic where I was previously treated as soon as possible, so this second surgery can be a success. I would like to ask if anyone who knows their stuff could advise me on what to use to improve my appetite and strengthen my system? I am currently taking Medrol tablets, which I've heard can be quite hard on the body, but they have helped reduce the edema and I feel a bit better... sorry for such a long post. Thank you.

If I understand correctly, we are talking about a recurrence of a brain tumor?
I take beta-glucan for my immunity.
Ever since the surgery, I haven't had any appetite or even felt hungry, but I've forced myself into a routine of eating at specific times, four times a day. Often I eat by sheer force of will, and sometimes I find food completely nauseating. 😢
My oncologist prescribed the Medrol to me. It has side effects similar to the dexamethasone I used for three months. That was honestly pretty terrible for me, so when the oncologist said I could take the Medrol as needed, I stuck to that because I didn't really need it most of the time.
I truly want you to get well and hope your surgery goes smoothly.

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