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Posts by Angela Wright

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Jamie Sullivan4 said:Angela Wright, thank you 🙂 you really help everyone out with your advice. Unfortunately, I read that glioblastoma is the worst kind. With diseases like this, everything is so individual.
In cases involving tumors like this, is it possible for the tumor to spread—meaning, could things just get worse instead of better? With all the guesswork flying around, I honestly don't know what to think anymore.

Unfortunately, it’s a very aggressive tumor. If treatment doesn't start immediately, it spreads quite rapidly, though strictly within the brain, sometimes extending into the spinal cord where glial cells are located. At the end of the day, treatment is focused solely on trying to slow the progression and maximize quality time. 😢
wiredcanyon39 said:Thanks, that makes me feel way more confident—I've got over 90% certainty right now before I start my third round of treatment in a few days.

I can't figure out the schedule here. My doctor mentioned that the third round is just like the first one, while the second was different. Does it go 2-4-6 exactly like 1-3-5, or what?

I wouldn't know, honestly. You should try Googling it. There might be a specific treatment protocol listed on PubMed.
wiredcanyon39 said:Can anyone tell me more about the BFn-86 protocol?

However, the recent use of the BFN/NHL 90 protocol, introduced by Reiter and colleagues, has demonstrated a greater than 90% 3-year survival rate in children with advanced T-cell lymphoblastic lymphoma (see Table 138D.5).74

Basically, we're looking at a newer treatment protocol that’s yielding incredible results—we're talking a three-year survival rate north of 90% for the kids involved.
You can’t—and you absolutely shouldn't—base a diagnosis on nothing but guesswork, especially when dealing with neurological symptoms that aren't just minor glitches, but massive red flags. It doesn't matter what any of us personally thinks or feels about whether it's "real" or not. What matters is that urgent testing is required, and that's exactly where the first doctor failed. Instead of taking action, she just dumped a mountain of referrals on them and sent them packing. At this point, the parents are just as much to blame for their own negligence as she is for her lack of professionalism and sheer hesitation.
An EEG is going to provide answers to some critical questions and will finally determine if there's a need for more extensive testing or not.
Jamie Sullivan4, an astrocytoma generally carries a better prognosis than a glioblastoma. You see people who live for ten years or more, but that usually involves a constant cycle of surgeries to deal with recurrences. It isn't uncommon for it to progress into a glioblastoma. I am truly sorry to hear this. 😢
Prolonged lactation after weaning in Women's Health ·
I have to admit, reading through this thread has me feeling a little anxious. I finished breastfeeding over a year ago, yet if I apply any pressure to my nipples, milk still leaks out. I’ve tried expressing manually, but I can’t get more than a few drops to show up. My breasts feel completely normal to the touch and my period is regular and predictable; my only real struggle right now is the weight that just refuses to budge. When I saw my OB-GYN about nine months ago, she mentioned that this kind of prolonged lactation can actually stick around for quite a while. That said, since I’ve been feeling pretty sluggish and just generally "off" ever since I gave birth, I think I’m going to go see an endocrinologist and schedule a breast ultrasound very soon.
Sophia Davis4, the truth is, we’re never truly ready to say goodbye to our parents. It doesn't matter if it happens when you're young or in your twilight years—you'll feel that same gut-wrenching sense of loss. Regarding the gallbladder, it’s highly likely she’s been dealing with stones for years; those little things cause constant inflammation that slowly eats away at the tissue until everything just hits a breaking point. Honestly, that's the most common playbook with this type of cancer. Look, she’s coming to you to get treated, and you guys are going to do absolutely everything necessary. It is such a massive blessing that she’s staying optimistic. Having you all by her side will give her the emotional lift and stability she needs to maintain a semblance of a normal routine, which is absolutely critical during treatment. In my opinion, a positive atmosphere and solid family support can be just as vital as any medication. Right now, the primary mission is focusing on her quality of life and extending her time with you. You can still live a meaningful life even after a diagnosis like this.
@Sophia Davis4/">@@Sophia Davis4, I am incredibly sorry you’re dealing with all of this hitting you at once; I can only imagine how brutal this stretch is for you. You didn't mention which primary tumor we're actually talking about, so I can't give you a specific answer regarding that. Look, nobody can tell you exactly what to expect next. Given that we're dealing with cancer and the targets involved, the situation clearly isn't good—and I know you're already aware of that. What’s done is done, and neither you nor your mother can change the past. All you can do, and honestly all you *must* do, is fight. You need to dig deep, find every ounce of strength you have, and be her rock. You have to pull yourself together, because if you crack and let despair take over, nothing good will come of it. You have to take whatever chances are on the table, no matter how slim, and fight. I really hope you aren't facing this alone and that you have some support around you. Hang in there, dear, and don't let life win—unfortunately, this is just how life is built. 😢
@wiredcanyon39/">@@wiredcanyon39, the CT scan happens after the first line of treatment is finished.
@dustyjackal10/">@@dustyjackal10, I am in no position to make a decision like that, nor do I actually know who I would even give it to. You could put out an announcement, and someone might donate the medication based on the medical history provided.
Sorry for the typos, I'm typing this on my phone.
Michael Cruz28 said:Hello,
My mother-in-law is currently unconscious in neurosurgery at Washington, D.C. Memorial Hospital.

She was hospitalized on July 25th presenting with mild right-side weakness and dizziness.

The initial CT followed by an MRI showed shadows measuring 1.5 x 1.7 cm and a larger one at 2.5 x 3 cm.
She underwent an open biopsy and partial tumor reduction.
The diagnosis is Stage 4 glioblastoma, affecting almost the entire left hemisphere.
They mentioned edema and other issues.
She’s on medication to manage the swelling, but she’s too weak for intensive treatment. I'm not sure if she'll even receive any radiation or chemotherapy.
The doctors say she's too unstable for Gamma Knife or other therapies, so they're waiting for her condition to improve before potentially treating her. But her condition is just getting worse, and they've already prepared a ventilator.
They’re giving her a few months, but a few months of what???
I see people discussing tumor cases here, so I’m wondering if there is any clinic in the US or Europe where they could intervene to temporarily halt this progression.
Basically, my wife gave birth to a beautiful baby girl just 18 days ago—specifically, two days after her mother and my child's grandmother was hospitalized.
My wife is doing so poorly that I think it's affecting her breastfeeding, which is understandable given the circumstances. It's a tragedy because we can't fully celebrate the baby or truly grieve because we're caught between two extremely intense emotional events.
Our only wish is for Grandma to wake up and see her granddaughter. That would bring such peace to my wife and our whole family.
Is there any hope???
THANK YOU

Unfortunately, when it comes to glioblastoma, especially at this stage, medicine simply doesn't have an answer. Even in the best clinics in the world, she would receive the exact same treatment she’s getting now: anti-edema therapy (Mannitol and Dexamethasone). That edema creates massive intracranial pressure inside the skull, which pushes the brain to one side and keeps her in a coma. If there is hydrocephalus (fluid buildup), it might be possible to mechanically drain that fluid to reduce the pressure. This could stabilize her and allow her to wake up, potentially opening the door for radiation therapy combined with Temodal. My own mother was in a similar state at Rebro Hospital, and we fought hard just to get them to perform a stereotactic procedure and a fluid puncture. They took her away completely unresponsive, and brought her back to the room fully conscious after just 20 minutes. The doctors often won't do it, likely for pragmatic reasons. It is a palliative procedure, but for people in your situation, it can mean everything. Ask about it, and if you can, try to push for it.
As for the Gamma Knife, with a tumor that widespread, it unfortunately isn't an option😢. That's generally only considered for tumors under, I believe, 2cm.
The progression of this disease is inevitably horrific; the only thing you can do is try to slow it down slightly. I am so incredibly sorry, but I can't write anything positive or optimistic about this diagnosis, no matter how desperately or selfishly I might want to. Just like my mother, she ended up with the one type of tumor out of all possible ones that offers the bleakest outlook for recovery.
Hang in there.
dustyjackal10 said:Hey everyone,

this fight is over; my mother passed away this past Saturday, August 11th, 2012. 😢

Wishing you all nothing but luck, strength, and wisdom as you continue your own battles.

I am so sorry, please accept my deepest condolences. 😢

When you don't even know who the primary enemy is, trying to wage that kind of war and actually win it feels almost impossible. 😢
She’s in a much better place now, far away from this valley of tears. May your mother rest in peace and watch over you from above.
melloworca6 said:So, what was the final word from them? What did the results actually show?

Man, I’m really not digging how she hasn't reached out yet.😢
Medical clearance for working on a ship in Health ·
Anthony Nelson4 said:Well, yeah—but like I was saying before, that specialist my agency suggested I talk to—the one who told me I should clear up any questions I have with him directly—he mentioned that they wouldn't be checking specifically to see if the medication is present in my bloodstream. Instead, he explained that the whole reason they’re pulling blood is just to run those standard toxicology panels. It's funny how those things work sometimes, isn't it? You think they're looking for one thing, but then there's this whole other layer of testing happening behind the scenes... anyway, that was his take on it.

Your best bet is to check out this resource instead: http://www.epilepsy.com/?page_id=124
Medical clearance for working on a ship in Health ·
Anthony Nelson4 said:So, here’s the deal—I noticed that during the medical clearance for working on a merchant vessel, they do a full blood panel. Now, I’ve been dealing with epilepsy, though honestly, I haven't had a single issue or seizure in about seven years—it's been smooth sailing since then—but I am still on medication. This got me thinking... if they run these tests, is there any chance they'll pick up traces of my meds in my system? One doctor mentioned to me that when you're getting cleared for maritime work, the bloodwork is mostly focused on various toxicology screens to ensure everything is clean. He suggested that because I've been consistently taking my Depakote and Lamictal for the last seven or eight years, they wouldn't even register as "drugs" in the way people usually think. I'd love to hear your thoughts or if anyone else has navigated this kind of thing before.

They probably will.
Let's be real here: you're just trying to hide the fact that you have epilepsy, aren't you?
Smola 😢
Can I bring my medication on a plane? in Health ·
Larry Mitchell4 said:Hey, does anyone know if I can bring a full pack of 30 Xanax tablets on a plane? What’s the deal with having written documentation? I'm traveling within the European Union.
thanks

Get a doctor's note written in English. Honestly, your best bet is just calling the airline you're flying with directly to get the specifics.
Sam Roberts8 said:So, what's everyone's take on this?
By the way, I've been at this for 16 years.

Get outside, ride a bike, play some hoops, go out and hunt for some action. 🙂
Sam Roberts8 said:Is it actually possible to get cancer from using a computer?
I'm getting a bit paranoid because I've been spending about 5 to 7 hours a day glued to my PC for the last six months.

Look, sitting hunched over a computer or staring at a TV from sunrise to sunset, combined with stuffing your face with junk food and basically zero physical activity—that is a one-way ticket to health problems. You're looking at a massive increase in cancer risk, not to mention setting yourself up for a heart attack or a stroke.
copperraven53 said:Not in hospitals, but I think you could pull it off with the doppelganger if they use top-tier spinal anesthesia. 😁

Everything is "possible" and "happening" when you're dealing with the doppelganger. 😳
Chloe Gray5 said:The oncologist told us today that Dad has lung cancer, which is why he had the pulmonary embolism and the leg thrombosis..
Back in early April, the lung scan showed only one lesion—the same one from a year ago that they thought was just tuberculosis. But by the end of April, a new shadow popped up, and now they’re calling it cancer. The oncologist claims this was all found by pure chance because they were scanning his lungs to check for the embolism, and she says it's an early stage that won't cause major issues for a few years. She recommended small daily doses of radiation, just a few seconds at a time, saying if he were healthy, he wouldn't even feel it. Apparently, since it's such a tiny, localized spot, it's a preventative measure. She said the choice is ultimately his. Of course, he made his decision. According to her, it's curable.
This really hit me hard. After everything else, just when things were finally looking up and he started recovering, now there's this. How much more does my dad have to go through 😢.
What are the general prognoses? Is it actually curable? After everything we've been through, I'm skeptical of everything. How can my dad handle the radiation more easily?

Oncologists don't just throw statements like that around unless they truly mean them. So, he'll go ahead with the radiation, and at this stage, tumors are incredibly sensitive to it. Since his immune system took a hit, the malignancy clearly flared up. Up until now, his immunity was keeping it in check, but all this recent chaos provided the perfect trigger.
I'm so sorry he has to deal with this on top of everything else. You know what they say: "When it rains, it pours."
My life has been a non-stop series of disasters since my mom got sick. Ever since 2005, I haven't had a moment of peace; it feels like one nightmare just follows the next. Just when you think you've cleared a hurdle and can finally catch your breath, boom—another crisis hits. That's just how life works for some people. You either end up resigned, frustrated, or completely revolted. Personally, I'm a little bit of all three, hitting me all at once.
Sarcoma diagnosis/discussion in Health ·
Raymond Flores39 said:Hi everyone... I'm reaching out because we're going through a nightmare right now. Our two-year-old little boy has been fighting rhabdomyosarcoma for about a year now. It started in his arm, and after three surgeries and ten rounds of chemo, the tumor is just spreading... the doctors here honestly don't know how to help him anymore. We even sought specialized care at a clinic in Tübingen, Germany, where they handle these kinds of tumors, but there was no success there either. All they could suggest was an amputation—arm, shoulder, ribs—and even then, the chances of him actually recovering are so slim... I'm desperate for any information on treatment options. Does anyone know anything about using Vertex Pharmaceuticals drugs for children? Every doctor we've consulted so far says they haven't used that specific cytostatic on kids before. Since he needs to start the next phase of treatment immediately, we are willing to travel anywhere in the world to find help... money isn't the issue, it's just finding someone who can actually save him. Please, if you know anything at all, let us know... thank you.

I'm honestly not sure if Vertex Pharmaceuticals is even used for kids. 😢
You really ought to try reaching out to Dr. Paul Casali at the National Cancer Institute in Italy (National Cancer Institute). He's easily one of the top specialists globally when it comes to rare tumors.
Also, definitely get in touch with a pediatric cancer support group to see if they can point you toward more resources (www.example-support-org.org). You'll find contact info right on their homepage; don't hesitate to reach out to them.
vividcanyon13 said:Yesterday I was just sitting there by her bed, holding her hand and stroking it...

Reading this brings back a moment I shared with my own mother. We were lying just like that, and I found myself staring out the window at the clouds racing across the sky. I remember it so clearly—that sudden realization that I would carry this exact moment with me forever. Even now, when that memory resurfaces, the emotional weight feels just as heavy as it did then.
Time moves just like those clouds drifting overhead; eventually, everything turns into nothing more than a memory. All we can really do is try to make sure those memories are as beautiful as they can possibly be.

It breaks my heart that mothers have to endure this. It’s just not right that their departure has to look like this, even if this life is just a brief stopover on an infinite journey. They should be leaving us happy, peaceful, and content in the twilight of a long life, with smiles on their faces and a healthy glow in their cheeks. 😢