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Posts by Angela Wright

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Olivia Martinez98 said:Hi everyone. I really need some help finding information here. My grandfather has prostate cancer that has already spread to his bones and liver. Right now, his liver situation has improved, but things are getting worse with the bone metastases. He hasn't used any hormone pills or gone through chemotherapy yet, and he’s been on a new experimental drug called Xtandi for about 10 days now. His appetite is terrible, his digestion is a mess, and the pain is intense. On top of that, he started radiation again a few days ago. Does anyone know if it's safe for him to combine cannabis oil with these experimental drugs? Where can we look into this? I'm honestly not sure if it's even appropriate to ask the doctors.
Any bit of info would be a huge help. Thanks in advance.

The radiation should definitely help manage those bone metastases and take some of that pain away.
As for the cannabis oil, I don't have any firsthand experience with it, but I doubt there would be a major interaction. If you were to hypothetically ask an anesthesiologist, they could probably give you a straight answer on that.
Also, your grandfather is entitled to Durogesic patches, which make it much easier to manage his dosage.
Brain tumor - Grade III meningioma in Health ·
Gregory Ramirez2 said:Does anyone have a rough idea about the medical success rates for this kind of tumor? Like, what are the roughly min/max timelines we're looking at? I mean, how long does someone typically live after surgery and getting a diagnosis like this?
In your experience—or just from what you’ve heard—what’s the reality of those timeframes? I’m not looking for exact numbers, just a general ballpark so we know how much time there is to act, get treatment, or... you know, say our goodbyes...

Also, does anyone know if those Dren-Trogrlić Žepče herbal blends from Canada actually do anything for brain tumors (alongside whatever the doctors prescribed, obviously)?

So, the patient is a woman, 55 years old, and she just went through her third brain surgery.
The first two scans showed it wasn't malignant, but this latest one confirmed it's an anaplastic Meningioma Grade III according to the WHO.
The report also mentions: "Bone structure and brain tissue infiltration identified, IM 33/3 HPF."

If anyone knows of any other solutions or help—maybe from a different herbalist or some other alternative route—please, please shoot me a PM.

I would be incredibly grateful for any info at all. This is for a colleague of mine—she's such a wonderful, kindhearted woman and a great mom.

Everything you need to know has pretty much already been laid out right here:
The research presented here regarding meningiomas is a heavy lift, but it’s essential reading if you want to understand the actual mechanics behind tumor progression. We aren't just looking at surface-level statistics; we are digging into the cellular architecture that dictates how these things behave. It’s one thing to read a general summary, but it's an entirely different beast when you start parsing through the specific molecular pathways that drive malignancy. When you look at Grade III cases, the complexity spikes significantly. You can't just apply a blanket logic to everything; the biological reality is much more volatile. It’s like trying to predict the path of a storm based solely on the wind speed—you have to account for the pressure changes and the underlying temperature shifts too. In this case, those "shifts" are the genetic mutations and protein expressions that turn a manageable growth into something aggressive. If you aren't paying attention to these granular details, you're essentially flying blind.

Look, here’s the deal: we're dealing with a rare brain tumor that typically starts out as benign before mutating into a malignant, anaplastic type—which is exactly what happened in your case. It also has a nasty tendency to recur.
We’re dealing with a rare disease here—the kind that hits fewer than five people out of every 10,000. Just like most other orphan diseases, it suffers from a massive lack of fundamental research and a glaring shortage of effective treatments. For the most part, medical options are stuck in a loop of surgical removal and radiation. There isn't any chemotherapy out there that actually works for this. From a purely statistical standpoint, the prognosis is grim. This study published in the journal examines how certain types of meningiomas respond to radiation therapy. It’s a deep dive into the specifics of Grade III tumors—those aggressive ones that don't play by the rules. Essentially, the researchers looked at how we can better predict which patients are going to see actual progress after treatment and which ones might need a different approach entirely. It’s the kind of data that shifts the needle from "let's try this" to "we know this works."
Look, when people start obsessively staring at statistics, they have this annoying habit of trying to force every single individual case into a neat little average. It’s a fallacy. No one can predict an outcome for a specific person with absolute certainty because life isn't a math equation—it's a chaotic mess of infinite variables all pulling at once. Statistics work by creating a bell curve—you've got your left tail, your center, and your right tail. But let's get one thing straight: nobody can tell you exactly where any one person is going to land on that curve.
My best advice, coming from someone who has stared down an incredibly aggressive and hopeless diagnosis, is this: don't let it consume you. Every single one of us has an expiration date written somewhere, and frankly, most of us don't know when it is—which is exactly how it should be. People who think they "know" their timeline usually just spend their remaining days paralyzed by that knowledge, which only serves to strip away their quality of life. Patients and their families need to grab every possible second they can. Focus on the mundane, everyday stuff and those tiny, simple pleasures; just soak up high-quality time for as long as it lasts. You have to live day by day and deal with things as they land on your plate. I’ve seen plenty of people take such an assertive, defiant approach to life that they actually defy the odds, sometimes even sliding right back into remission.

When my mother first got her diagnosis, a few of her close friends dropped everything to come by one last time just to say goodbye. They left in absolute tears. It’s wild, though—they all passed away unexpectedly shortly after her. No one saw any of it coming.
Life is a shot in the arm, and you’ve got to grab it by the throat and fight for every inch while you're still standing—whatever comes, comes. There aren't any guarantees in this life, nothing at all, except for the fact that we’re all just passing through. All we really get to do is choose how we decide to face that inevitable fade-out.
Groin pain in Health ·
Tyler Bennett73 said:So I can just go to a private clinic instead of an ER?

If we're talking about a lump, does it have to be palpable? Is this kind of condition one where a lump is an absolute requirement for a diagnosis, or could it stay hidden? I’ve been feeling around and haven't found anything, though I'm obviously just a layman—there isn't anything visible on the surface either.

Is there any chance those pains were actually just kidney stones or some grit in my system?

What you're describing sounds like a hernia, where there's a gap in the muscle wall that allows the intestine to poke through. You don't necessarily need to feel a distinct lump for it to be real; a surgeon will be able to feel that defect during a physical exam. They'll also determine if there's a risk of the bowel becoming trapped or strangulated, which is when it can't be pushed back in.

There are plenty of surgeons in private practice. Honestly, I don't see why you couldn't just schedule an appointment with a specialist at a local hospital rather than rushing to the emergency room right this second.
Larry Baker67 said:Hi everyone. I’ve been following this thread for a while now, and after doing a ton of digging, I have a question for anyone who has dealt with this before...
The results show lung cancer with metastases in the liver... however, the patient has gained a few pounds in the meantime, and their condition fluctuates wildly from day to day. One day they seem fine and have energy, then the next day the pain returns... the tumor size itself isn't huge. So, I'm wondering—is it normal for a doctor to say with total certainty that chemotherapy won't work and that we should just prepare for the worst...
Thanks, everyone.

If the disease progresses while on a specific treatment, it means the medication has failed and there’s no point in sticking with it. There are other lines of therapy out there, so you need to look into those options.
Lung cancer with liver metastases is a pretty brutal diagnosis, and the prognosis generally isn't great.
Regardless, go get a second opinion—either privately or at a different hospital. Honestly, doing both is your best bet.
Groin pain in Health ·
Tyler Bennett73 said:Thanks.

Do I have to see my primary care doctor first before I can get an appointment with a surgeon?
Also, do you know what the exam is actually like—do they check the prostate and the testicles?

You hit up your regular doctor for a referral, unless you're planning on paying out of pocket at a private clinic.
No, they just have you lie down so they can feel your abdomen and groin area; they might check the testicles too, just to rule out a hydrocele.
Groin pain in Health ·
Tyler Bennett73 said:I had a feeling that might be the case. Just wanted to update everyone—everything felt fine last night; I could move around without much trouble, except for lying on my back, which was painful. Since I was studying for up to three hours, I tried lying on my stomach instead, and while lying on my back still felt uncomfortable, it was way better than it was a few hours earlier, so I just slept on my side. I actually woke up in the middle of the night, rolled onto my back to test things out, and didn't feel any pain at all. This morning, I got up feeling totally normal, like nothing even happened. If this is a hernia, I read somewhere that they don't always require surgery if the case is mild—is that true? Also, I read that prevention usually involves strengthening the abdominal wall, so I'm wondering if I can get back to doing sit-ups?

Only a surgeon can give you a definitive answer on that path. You need to find out if it’s actually a hernia and, if it is, how large the opening is. There are scenarios where the gap isn't massive, yet it's just wide enough for a loop of bowel to slip through and get trapped, which turns into a life-threatening emergency very quickly.
Go see a doctor and get this settled once and for all. Until then, stay away from sit-ups and stop pushing yourself with heavy physical exertion. Stick to a high-fiber diet to keep things moving smoothly.
Groin pain in Health ·
Based on how you’re describing this, it sounds like you might have a real issue on your hands, man. Seriously, go see your primary care doctor, get an exam, and grab a referral for a surgeon just to be safe and get some actual answers.
Sarah Wells23 said:I’m looking for a little help here! I know this has been discussed quite a bit in this thread, but I can’t seem to find which page the info was on.
My grandmother is in the terminal stage of colon cancer. She’s immobile, hasn't eaten in months, and stopped chemo three months ago.
Her salivary glands are basically shot. She has no saliva, no sores yet, but her tongue is terribly red, she’s struggling to swallow, and she can barely speak because it hurts so much. I bought some artificial saliva and she rinses her mouth with chamomile, plus she drinks water, but it doesn't help much.
Is there anything else that could ease this tongue issue or help keep her mouth hydrated?
We aren't living with her; my grandfather is the primary caregiver, and he’s not exactly the most organized person in the world, so I’d love to find something myself. I want to avoid stressing them out with doctor visits and prescriptions, and I don't want them wasting money. She can't suck on lozenges, even though I know menthol helps. Sage? Is Hexoral okay, or would that burn? Any ideas or experiences would be greatly appreciated.

Your grandmother likely has oral thrush due to the lack of saliva. Go to the pharmacy and pick up some Rojazol gel for oral use.
Forget about Hexoral or anything like that—don't even consider it. It will just further irritate her oral mucosa.
Try giving her water infused with ground flaxseed.
Take some ground flaxseed, dissolve it in a glass of lukewarm water, and let it sit for half an hour. Flax releases a mucilage that does an excellent job of coating the mucosal lining and protecting it. She can drink it too, as it's actually good for the stomach and esophagus.
You definitely need to introduce some strong probiotics. You can get them in powder form and mix them into water.
One more thing: insist that her primary care physician makes a home visit and prescribes home health nursing. In the US, she should be entitled to full coverage for a visiting nurse who can come by 7 days a week for up to 45 minutes per visit. A nurse will recognize issues like the tongue problem immediately. They can handle the daily cleaning and changing, and even a weekly bath, so you don't have to shoulder all of it. It was a massive help for me, even though I still handled my mom's baths on weekends once we had a solid routine established.
Rebecca Perez4 said:...

Reading what you wrote feels like looking at a mirror of myself from ten years ago. Yeah, it’ll be ten years this November since she passed, and twelve years since that initial diagnosis back in July.

A whole decade has slipped by, yet my thoughts haven't shifted one bit—if anything, they've just become heavier with everything I've learned since then...

I really hope you find more peace than I have. Honestly, I still haven't found that sense of calm I'm searching for, largely because the system itself hasn't changed an inch.
We still don't have real palliative care or decent hospices here in the States. As a society, we've completely failed. I can't find any peace.
Kate Morgan66 said:Hi there,

I'm cross-posting my "looking for a doctor..." thread here too. Any leads would be much appreciated. 🙂

I’m looking for a private clinic where I can get a high-quality abdominal and pelvic ultrasound. I really need a recommendation for a solid doctor who will actually take their time to examine me thoroughly (that's why I want to go through a hospital setting—I feel like they just kick me out after five minutes elsewhere).
I'm an oncology patient (gynecological cancer) and have undergone radical surgery (removal of all gynecological organs and surrounding tissue, plus lymph nodes), radiation, and chemotherapy. This is my first ultrasound since finishing treatment, so it would be ideal if the doctor has specific experience in oncology...

Oh man, I just saw this post.
I actually had an abdominal ultrasound done right here in the States two weeks ago with Dr. Kapetanović. He’s an older, highly experienced physician. He also did my breast and thyroid ultrasounds. I found him incredibly precise. He’s quiet during the actual exam, but he explains everything clearly afterward.

I used to work at Novamed two years ago. I can't recall her name specifically, but she was another excellent, seasoned doctor. She actually comments on everything while she examines you and shows you what she sees. She’s incredibly kind and warm, too.
Grace Ross20 said:Dear Minnie, I honestly can't wrap my head around the fact that your boyfriend has three primary tumors. If I'm understanding you right, they aren't metastases?
Huge respect to you both; you've stepped into an incredibly brutal fight, and I am sending you all the luck in the world. He's young, which means there's real hope—keep focusing everything on strengthening his body.

My Dad is currently stable, though he's immobile and non-verbal, but stable nonetheless. We aren't pursuing surgery because they could probably only remove half the tumor, and even then, it would just grow back even larger immediately.
I don't know anymore; I've already made peace with the absolute worst.
I'm just trying to find a way to live, to keep from falling into a pit of despair and dragging everyone else down with me. When things get too heavy, I just curl up on the bathroom floor and cry and cry. It helps.
I try my best to cheer Dad up, even though I think he's understanding less and less of what's happening around him. I'm just glad he isn't in pain—that's a thin comfort, but it's something.

If he has to go, I just hope it's in the spring. I know how much he loves the spring. 🙂

Oh honey, I'm sitting here reading through my own past.
No matter how hard this gets, or how many broken pieces you feel like you'll be left with when this is over, you will survive it all in the end and somehow find a way to keep moving forward.
I think I mentioned before that being unaware of the full gravity of the situation is actually the kindest thing during all this agony.
Hang in there and cherish every single moment you can with him. It’s never enough. ❤️
Donna Brooks20 said:Hey there!
I just can't seem to sit down and write out everything that's been happening with us while things are calm. My partner and I have been going through a total whirlwind lately.
Back at the end of November 2016, he was diagnosed with three different tumors, like I mentioned before. A testicular tumor, melanoma, and a brain tumor.
We moved fast to get in touch with the Mayo Clinic, and after seeing Dr. Melada, we managed to secure a room in neurosurgery.
They removed the brain tumor, and the pathology report confirmed it’s a high-grade anaplastic glioma. We were still fighting tooth and nail at the Mayo Clinic
to make sure they didn't discharge him until all the necessary surgeries were wrapped up. We finally pushed to have the melanoma removed too (pathology confirmed it was indeed melanoma),
and the surgery on his testicle was performed. After that, they let him come home, but within about ten days, we already had his next two procedures scheduled at the Mayo Clinic:
a sentinel lymph node biopsy and a re-excision of the melanoma site.
Once that was settled, we consulted with oncologist Juretić, who suggested radiation for the head along with Temodal therapy. We also reached out to Dr. Gamulin,
who advised monitoring markers for the testicular tumor (the markers have dropped) and emphasized how critical it is to stabilize the brain issue first.
After scouring thousands of pages online, I realize this might be the only path they could offer, but we still sought a second opinion from Avian.
We went there, they reviewed all the files, and they actually recommended the exact same treatment plan. They told us there was no point in trying
to seek treatment at Avian right now and that we should stick with the plan in Washington, D.C. The medical board approved my partner's treatment, so at the end of January 2017, we’re heading to Washington, D.C. to finalize the planning.
Looking back at everything that's happened over the last month and a half, I honestly don't know where we found the strength to organize this chaos. Just keep in mind, we live
out in California. But I took some advice from Ivanica; I made sure to be assertive in every single conversation, refusing to back down until I had ironed out every detail with the doctors.
I don't know what the future holds. I'm terrified—for him and for myself.
This forum has helped me wrap my head around this nightmare, so thank you all for being here.
Best to everyone,
Minnie

Man, I honestly don't know what else I could tell you; this is such an extreme situation to deal with mid-week.
A few days ago, I was watching an episode of House about a woman dealing with two cancers simultaneously, where one was kept under control by the other. I'm not sure how much of that is TV drama versus actual medical possibility.
My gut feeling is that they’ll focus on stabilizing the brain first.
Hang in there and just take it one day at a time. Who knows, maybe the Temodal will have some kind of effect on the testicular tumor and the melanoma too—maybe it'll set a precedent for some off-label clinical use in cases like this.
mellowharbor84 said:I’m not so sure about the allergy angle, especially right now. There just aren't any seasonal allergens floating around—and I’m not talking about dust mites or whatever. It’s pretty rare for an adult to suddenly develop an allergy out of nowhere just a few times a year, particularly when everyone else is busy dealing with the flu season.

Look, the reality is that the underlying allergy is always there; it's just that once your mucous membranes are irritated and compromised by a viral infection, they overreact to things that a healthy, mucus-protected system would have ignored entirely.
Take mold spores, for example. They’re thriving right now in those overly insulated, airtight, heated suburban homes. So many people are drying their laundry indoors, which basically acts like fertilizer for mold growth.
So yeah, it's not really that black and white.
Brandon Brown35 said:It’s possible this happens because I catch these bugs pretty frequently, but when I had my lung scan two years ago, everything came back clean—no obstructions, nothing, just healthy lungs. And it’s not like I can’t cough it up; it’s more that the mucus is just too thick for me to clear out easily. I’ve never dealt with extreme symptoms like shortness of breath or feeling like I'm suffocating; I mostly just get a fever, though it actually dropped quite a bit last night after that message, so I didn't have it all evening. I doubt it's allergies since I don't get sick during any specific season. The last time I was under the weather was early summer.

melloworca6, you’ve actually calmed me down a bit, haha. It just felt weird because I don't usually run a fever when I get sick, so my first thought was that it was the bronchitis I had a few years back, especially since the doctor mentioned it might be viral pneumonia.

Allergens are everywhere. Dust mites, mold spores, pollen, food—it doesn't matter what time of year it is, and it doesn't always show up as the typical runny nose, watery eyes, or sneezing.
I’m suggesting this based on my own firsthand experience with my daughter, because she fights off every single virus with thick mucus and a lingering cough about twice a month, so that’s why I’m bringing it up. If this keeps happening to you, make sure you get a spirometry test. An X-ray won't catch everything. As for the choking sensation, she was just breathing rapidly, and her oxygen saturation was dropping to 84%. She was breathing, but there was so much mucus blocking the way that oxygen couldn't reach her lungs. She ended up straight in the ICU on oxygen, where they spent four days aggressively draining her lungs and running nebulizers.
Brandon Brown35 said:You totally misunderstood me. I haven't been coughing for five years straight; I just have chronic lung issues. Every single year, I get sick at least once—either a cough or a sore throat—and over those last five years (according to my doctor), she hasn't actually managed to pin down a diagnosis. She just keeps sending me for blood work. The only reason I’m posting here is that, unlike my other symptoms, I've had this persistent fever for three days now, and she mentioned she suspects pneumonia. What do you guys suggest: should I go get my blood drawn or just wait it out for a few more days?

Get a referral for a pulmonologist. You really ought to get a spirometry test and some allergy testing done. Honestly, it sounds like you might be an asthmatic where an infection triggers a reaction to allergens because your membranes are so irritated.
My daughter deals with the exact same thing. In just ten months, she fought off atypical pneumonia twice, even though her inflammatory markers were barely elevated. Her bronchi tighten up, she can't clear the mucus, and then that gunk settles deep in her lungs and everything goes south.
If things take a turn for the worse—like if you're gasping for air or the fever spikes—get to the ER immediately. If you're in the city, head straight to Mount Sinai.
Ask your doctor about Ventolin or a steroid aerosol. Fluimukan works wonders. Pick up a compressor or ultrasonic nebulizer and use it 3 to 4 times a day. Also, rinse your nasal passages with a saline spray 2 or 3 times daily. Look up how to do that properly on YouTube.
If you aren't planning on doing full allergy panels anytime soon, ask your doctor for an antihistamine like Aerius. It'll give you a very quick indication of whether allergens are the culprit or not.
placidcobra7 said:Thank you for everything. My Dad passed away on Thursday. Once I get past this initial shock and grief, I’m going to start looking into what actually happened at the hospital. It’s honestly mind-blowing—one minute he was walking around on his own and functioning just fine, and within eight days, he's completely immobile and hooked up to a feeding tube. People were dropping like flies in that ward, and the records office told me they couldn't even keep up with processing all the death certificates. It’s horrific.

Mark Ruiz4, I am sending you all the strength and courage in the world.

Oh man, please accept my deepest condolences... I am so incredibly sorry 😢
Hang in there. I truly hope you find some peace.
placidcobra7 said:I’m heading out tomorrow to talk to the doctor. Mom found out today that it’s likely a primary liver tumor, and they’re basically playing it by ear regarding next steps since things have progressed quite a bit. They were planning on a colonoscopy and endoscopy, but he’s just too weak right now. He’s always had heart issues, and right now they’re trying to stabilize him with transfusions because he’s likely bleeding from the tumor. That’s just my gut feeling, though—honestly, given his age, it feels like they’ve already written him off. I don't know why they stopped mentioning the MRI. He isn't in pain, but he went from being an independent man to needing diapers within two days of being hospitalized, which is a lot for him to swallow. Visits are banned due to the flu, and I’m worried his mental state is going to kill him physically before the tumor does.
I’m doing some quick Googling and saw that sometimes drugs can shrink a tumor down to a size where surgery becomes an option. In that light, everyone seems to be raving about the team at Mercury. Who should we go to at the Mayo Clinic?
Who actually handles the referrals for further hospital treatment? Is it the people where he is currently staying, or his primary care physician? There are so many questions, and today they practically brushed Mom off when she tried to get a consultation. She was exhausted, so they finally showed her some mercy, but even then, it wasn't the doctor actually managing Dad.

A hospital specialist is the one who refers a patient to oncology. Liver surgery is on the table if her tissue isn't too scarred and if the tumor is localized in one spot.
Even a metastasis on the spine could potentially be treated with radiation.
Mercury has a top-tier transplant team, which is why they get such high marks.
The Mayo Clinic is a major medical center with the best resources available, so in that sense, it’s a solid place for oncological treatment.
placidcobra7 said:Forgive me for not scrolling through everything first; I didn't have the patience to hunt through the forum archives. I really need some help here. My Dad has been stuck in a local hospital for seven days now with a liver tumor diagnosis and what looks like metastases in his spine. His condition has taken a massive dive since he was admitted—they won't let him move, he isn't eating, and he's incredibly depressed because nobody seems to have any patience for a 76-year-old man who’s a bit slower after suffering two mild strokes.

What I really want to know is: at what point does an oncologist actually enter the picture? When does the actual cancer treatment start?

The facility he's at doesn't even have an oncologist on staff, so I want to get him transferred somewhere in Washington, D.C. (where specifically?)
It's impossible to catch a doctor or get any decent information...

You need to push your way in to see a doctor right when they're busy and demand thorough, clear information. Don't take "we don't know" for an answer.
An oncologist usually gets involved once the patient's general condition is stable enough to actually handle the rigors of oncology treatment.
Go to the Mayo Clinic.
Donna Brooks20 said:Believe me, I haven't spent my time deep-diving into the PhDs' research because, honestly, I was too terrified. I don't know if that makes sense, but that's just how it is. Doctors won't give you any kind of prognosis.
The only specific detail I can recall regarding the brain is that it was a high-grade anaplastic glial tumor.

What he actually went through was years of intense workplace stress and constant bullying. After about ten years of that, he finally snapped, switched companies, and completely turned his life around—now he’s at a place where he works hard and is actually respected and valued. And now, out of nowhere, this happens.

Yeah, I get it.
But you need to face the whole situation head-on as soon as possible. Once the diagnosis gets a first and last name, you'll be able to react properly and make informed choices when it comes time to make big decisions.
Donna Brooks20 said:Hi everyone,
I first reached out about twenty days ago when we found out my husband has testicular cancer with possible brain metastases.
Since that discovery, everything has moved at lightning speed.
We got in touch with neurosurgeon Melada, and my husband ended up being admitted to the Mayo Clinic. They identified three tumors: melanoma, testicular cancer, and a brain tumor. We handled all the surgeries at the Mayo Clinic, and according to the PhDs, all three tumors are primary.
We went from having a healthy 48-year-old man to someone fighting three different cancers in just one month.
At home, we’re in shock—terrified and heartbroken. But despite everything, we’ve stayed incredibly organized, and so far, things are moving according to plan as much as they can in a situation like this.

What I really wanted to say is this:
- These support forums are hands-down the best resource you can find when you're thrown into a crisis like this.
- I spent 48 hours straight reading page after page, jotting down questions and answers, which helped me wrap my head around this nightmare.

Thank you all for being here, and a huge thank you to Angela Wright from California.

Best,
Minnie

I have to admit, I haven't come across a case involving three simultaneous primary tumors before. My gut tells me there has to be some common environmental trigger involved.
Please, keep us posted on how things develop.
What specifically are the diagnoses for the tumors? I'm particularly interested in the one on the brain.
Hang in there; we're here for whatever questions or support you need.