Nix 🍀 (@KryptyPop) header
Nix 🍀 (@KryptyPop) profile picture

Deep value bio investor. KryptyPop and my wife Julia. 35 yr Financial Advisor. Christian. Music lover and part time bull shitter. Dog lover.

Lake Dallas, TX
Joined October 2021
Photo by Nix 🍀 (@KryptyPop)Photo by Nix 🍀 (@KryptyPop)Photo by Nix 🍀 (@KryptyPop)Photo by Nix 🍀 (@KryptyPop)Photo by Nix 🍀 (@KryptyPop)Photo by Nix 🍀 (@KryptyPop)Photo by Nix 🍀 (@KryptyPop)Photo by Nix 🍀 (@KryptyPop)Photo by Nix 🍀 (@KryptyPop)Photo by Nix 🍀 (@KryptyPop)
Replying to @Boomchrisy
Freeze the tumor. No pectin. $NWBO killing cancers DCVAX-L
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Market makers, hedge funds, and other manipulators know that upon MHRA approval the $NWBO order book will rise to the top. 📈 That explains the 24/7 noise. Ignore it and focus on the science and math. research.quackmaster.io/p/be…
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One of the Best Videos that I have seen that Destroys the arguments of the left. You can’t be for this if you are for that! 🔥
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Nix 🍀 retweeted
Idiot liberal moves from a blue state (because it sucks to live in) to a red state(because it’s great to live in) and then votes to turn it into a blue state. Incredible.
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🚨 TODAY, I submitted my public comment to the FDA regarding its proposed Rare Disease Framework. As the mother of a 19-year-old fighting an aggressive, deadly brain cancer, I have one urgent message: Patients don’t just need faster drug approvals. They need ACCESS to promising treatments while they’re still alive to benefit from them. My comment shares Braelyn’s extraordinary journey, the clinical evidence and long-term survivors associated with DCVax-L, and the enormous barriers American families face trying to access investigational treatments. I also outline Braelyn’s Bill, built around four fundamental patient rights: ❤️ The Right to Know ❤️ The Right to Preserve ❤️ The Right to Choose ❤️ The Right to Access My most urgent request is Braelyn’s Rule: Patients facing life-threatening diseases should be able to access investigational treatments through their physicians, with informed consent and manufacturer participation, without unnecessary regulatory obstacles. We should not have to fly across an ocean to access a promising cancer treatment developed right here in America. The FDA’s new framework must measure success not just by how quickly treatments are evaluated, but by whether patients can actually access them while there’s still time. I’m sharing my full four-page public comment because this fight is about far more than my daughter. It’s about every family who deserves the opportunity to fight for their loved one’s life. Please read and share. ❤️🙏 #BraelynsBill #DCVaxForBraelyn #RareDiseases
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If you see this, please, I am begging...please I have had 4 years of terrible chronic pain in a large portion of my ribs. I am supposed to be flying from AZ to NY in a week to visit my daughter who was diagnosed with brain cancer a year ago. My pain is nearly unbearable and I can't imagine being trapped on an airplane. I need to get to her. Please pray for me. The chronic pain community knows how hard it is to get pain relief, and how pain can keep them from seeing loved ones. My daughter needs me. Please pray🙏
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Nix 🍀 retweeted
@elonmusk please get the word out and make "right to try" and $NWBO cancer treatments including $DCVAX available in the United States. Thanks to @DrOz and @realDonaldTrump
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Replying to @thereal_rok
$NWBO @POTUS has been made aware of Braelyn’s situation through @greta. She also launched a GoFundMe campaign to help @HollensbeAmanda cover travel expenses to the United Kingdom, enabling @HollensbeBrae to receive treatment. @peterjkostis also played a pivotal role by raising public awareness through his large following on X. It would be wonderful to see @elonmusk support this promising advancement in the fight against cancer. It is unacceptable that an innovation developed in the 🇺🇸 should force patients with unmet medical needs to travel abroad to access treatment.
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Amanda never quits. She spoke w Dr. Oz this week about bringing a remarkable cancer vaccine made in the U.K. to the U.S. Her daughter Braelyn had a virulent tumor that once affected three lobes of her brain. Her latest scan? No evidence of tumor, thanks to surgery to de-bulk it & the vaccine, made in the U.K. from her tumor. Nothing is finalized, but after talking w Dr. Oz, Amanda sounds hopeful about bringing the technology to the U.S. ALSO: It's vital that when surgeons remove tumors they're correctly preserved so that vaccines like Braelyn's can be made. Hospitals do *not* routinely preserve tumors. It's the patients who have to make sure that it's done correctly. There needs to be a law for that, because sick patients & their families have enough to deal with. Maybe Amanda can tackle that next. @HollensbeAmanda @LoriMills4CA42
🇺🇸❤️ BIG NEWS & A LITTLE EXTRA HOPE! 🙏 We’re headed back to London for Braelyn’s next DCVax treatment, but this trip feels different! This past week, I had the incredible opportunity to speak personally with @DrOz! He’s been discussing Braelyn’s case with the FDA, and we’re exploring possible pathways to bring her ongoing DCVax treatments HOME to America! Could Braelyn’s next treatment in MARCH actually happen right here in the USA?! 🇺🇸 Nothing is finalized, but some very important doors may be opening! Please watch, share, and keep praying! ❤️🙏 #DCvaxForBraelyn #BraelynsFight @DrOzCMS
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Nix 🍀 retweeted
BREAKING 🚨: The hospital found out Gail Seiler was unvaccinated for COVID. Then they tried to MURDER her. They STARVED her for 12 days, denied her water for 7 days, and told her husband she was going to die. When her husband came to take her home, the hospital made her a PRISONER. They called the police, and a 6-hour standoff followed. When the hospital finally let them go, it wasn’t through the main entrance. It was through the freight elevator used to carry bodies to the morgue. On the way out, a nurse told her husband, Brad, “Mark my words, she’ll be dead tonight, or before you even get home.” Gail survived. Not because of a miracle, but because a caring physician stepped in and guided her home treatment: nebulized budesonide and ivermectin. BRAD SEILER: “Over the next 30 days, she was weaned completely off of oxygen. Within 60 days, she had recovered sufficiently to return to work. Today, Gail is alive, healthy, active, and enjoying life with our grandchildren and children.” Gail’s story is horrendous, but it’s not uncommon. Hospitals were rewarded with perverse bonuses during COVID, and the more interventions they ran, the more they made. As Attorney @RenzTom previously testified: “We have incentivized the MURDER of patients rather than incentivize TREATMENT.” “When you go to the hospital, you get tested. They get paid more. When you get admitted for COVID, they get paid more. When they put you on remdesivir, they get paid more. When you get ventilated, they get paid more. When you die, they get paid more. This is perverse.” W.H.G
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#DCVAX $NWBO Thank you, @HollensbeAmanda , for your tireless efforts. And thank you, @greta , for helping connect Amanda and Braelyn with @POTUS and @DrOzCMS You deserve tremendous respect for all the work you’ve done.
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Nix 🍀 retweeted
Replying to @thereal_rok
Relentless pursuit makes things happen. Amanda, Braelyn's mom, has been relentless. Dr Oz may or may not know it yet, but she's a force to be reckoned with. She will get DCVax-L made available in the US, where $NWBO, the company that makes it and those who invented it live.
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🇺🇸❤️ BIG NEWS & A LITTLE EXTRA HOPE! 🙏 We’re headed back to London for Braelyn’s next DCVax treatment, but this trip feels different! This past week, I had the incredible opportunity to speak personally with @DrOz! He’s been discussing Braelyn’s case with the FDA, and we’re exploring possible pathways to bring her ongoing DCVax treatments HOME to America! Could Braelyn’s next treatment in MARCH actually happen right here in the USA?! 🇺🇸 Nothing is finalized, but some very important doors may be opening! Please watch, share, and keep praying! ❤️🙏 #DCvaxForBraelyn #BraelynsFight @DrOzCMS
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Please share $NWBO Amazing cancer treatment made in USA but only available in the UK!
🚨 TODAY, I submitted my public comment to the FDA regarding its proposed Rare Disease Framework. As the mother of a 19-year-old fighting an aggressive, deadly brain cancer, I have one urgent message: Patients don’t just need faster drug approvals. They need ACCESS to promising treatments while they’re still alive to benefit from them. My comment shares Braelyn’s extraordinary journey, the clinical evidence and long-term survivors associated with DCVax-L, and the enormous barriers American families face trying to access investigational treatments. I also outline Braelyn’s Bill, built around four fundamental patient rights: ❤️ The Right to Know ❤️ The Right to Preserve ❤️ The Right to Choose ❤️ The Right to Access My most urgent request is Braelyn’s Rule: Patients facing life-threatening diseases should be able to access investigational treatments through their physicians, with informed consent and manufacturer participation, without unnecessary regulatory obstacles. We should not have to fly across an ocean to access a promising cancer treatment developed right here in America. The FDA’s new framework must measure success not just by how quickly treatments are evaluated, but by whether patients can actually access them while there’s still time. I’m sharing my full four-page public comment because this fight is about far more than my daughter. It’s about every family who deserves the opportunity to fight for their loved one’s life. Please read and share. ❤️🙏 #BraelynsBill #DCVaxForBraelyn #RareDiseases
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FDA has responded to my $NWBO #DCVax proposal. Today, the Rare Disease Innovation Hub confirmed that my submission "has been received and will be routed to the appropriate centers for consideration." I submitted a 21-page proposal advocating for DCVax-L and DCVax-Direct under the Rare Disease Framework, beginning with rare cancers. The future I am advocating is a system built to handle personalization from the start. DCVax-L uses a patient's tumor material to load their dendritic cells. DCVax-Direct places prepared dendritic cells into a tumor to acquire tumor material there. Each program has its own evidence requirements. Both make the same larger question impossible to ignore: how do we evaluate a treatment whose patient-specific inputs are supposed to vary? The framework should distinguish intentional personalization from manufacturing inconsistency. Define what must remain reliable, what changes with each patient, and how those differences affect safety and benefit. That distinction can shape the next generation of cancer treatment: 1. Preserve options before surgery. Plan consent, diagnostic allocation, tissue handling and storage while suitable material is still available. 2. Build on what has been learned. State which clinical and manufacturing evidence can be reused, where new evidence is essential, and how to test applications across rare cancer types. 3. Make every study answer a clear question. Connect mechanism, measured biological activity and meaningful patient outcomes. Use external controls and Bayesian methods when their assumptions can be justified and tested. 4. Plan for continuing care. Identify who is responsible for supply, qualified treatment sites, lawful access and financing. Beginning treatment and being able to continue it belong in the same plan. These are my recommendations as an independent physician and patient advocate. I do not speak for Northwest Biotherapeutics. FDA's reply gives us a clear next step: keep the evidence and patient experience in front of the people building this framework. Families can explain where the current system breaks down and what a workable path must provide. The measure of progress will be a family that knows what comes next, who is responsible, and how to reach them while there is still time. Read the proposal: drive.google.com/file/d/1qvB… Add your own comment by December 11, 2026: regulations.gov/commenton/FD… #RareDisease #RareCancer #Immunotherapy #PatientAdvocacy #GBM
$NWBO #DCVax #DCVaxForBraelyn #RareCancer #PatientAdvocacy #GBM 📣 𝗛𝗲𝗹𝗽 𝗽𝘂𝘁 𝗽𝗮𝘁𝗶𝗲𝗻𝘁𝘀 𝗶𝗻𝘁𝗼 𝘁𝗵𝗲 𝗿𝗲𝗰𝗼𝗿𝗱. FDA is taking public comment on its new Rare Disease Framework. A proposal for DCVax-L and DCVax-Direct is already in the docket, with the evidence, tissue and access questions laid out in one place. Supporting it is one way to speak with a unified voice. A hundred different asks scatter FDA’s attention. A hundred people behind one documented request give the agency something it can act on. 1️⃣ 𝗥𝗲𝗮𝗱 𝘁𝗵𝗲 𝗽𝗿𝗼𝗽𝗼𝘀𝗮𝗹. drive.google.com/file/d/1qvB… 2️⃣ 𝗖𝗼𝗺𝗺𝗲𝗻𝘁 𝘁𝗼 𝗙𝗗𝗔. regulations.gov/commenton/FD… Write it in your own words. Three things to cover: • Who you are: patient, caregiver, clinician, researcher or shareholder. • That you support the DCVax-L and DCVax-Direct proposal submitted October 29, 2026 (tracking number mvt-lzyl-zjmn), and want FDA to clarify evidence requirements, tissue preservation and a practical path to patient access. • What only you can say: what waiting has cost you or someone you love. Same ask, your own words. FDA weighs arguments, not counts, and a hundred copies of one letter count as one. 📅 𝗗𝗲𝗮𝗱𝗹𝗶𝗻𝗲: December 11, 2026, 11:59 p.m. Eastern. Comments are public. Use your name if you can, leave out private medical details, and save your confirmation number. 𝗢𝗻𝗲 𝗮𝘀𝗸. 𝗠𝗮𝗻𝘆 𝘃𝗼𝗶𝗰𝗲𝘀. 𝗬𝗼𝘂𝗿 𝗲𝘅𝗽𝗲𝗿𝗶𝗲𝗻𝗰𝗲 𝗯𝗲𝗹𝗼𝗻𝗴𝘀 𝗶𝗻 𝘁𝗵𝗲 𝗿𝗲𝗰𝗼𝗿𝗱.
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NorthWest Biotherapeutics Inc ( $NWBO ): Attached photo is a copy of my email I s... investorshub.advfn.com/board… via @Investors_Hub $nwbo. If you have been around for almost a decade, like I have, then you understand the parties involved and the implication of this response is as good as it’s gonna get prior to approval.
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🚨 TODAY, I submitted my public comment to the FDA regarding its proposed Rare Disease Framework. As the mother of a 19-year-old fighting an aggressive, deadly brain cancer, I have one urgent message: Patients don’t just need faster drug approvals. They need ACCESS to promising treatments while they’re still alive to benefit from them. My comment shares Braelyn’s extraordinary journey, the clinical evidence and long-term survivors associated with DCVax-L, and the enormous barriers American families face trying to access investigational treatments. I also outline Braelyn’s Bill, built around four fundamental patient rights: ❤️ The Right to Know ❤️ The Right to Preserve ❤️ The Right to Choose ❤️ The Right to Access My most urgent request is Braelyn’s Rule: Patients facing life-threatening diseases should be able to access investigational treatments through their physicians, with informed consent and manufacturer participation, without unnecessary regulatory obstacles. We should not have to fly across an ocean to access a promising cancer treatment developed right here in America. The FDA’s new framework must measure success not just by how quickly treatments are evaluated, but by whether patients can actually access them while there’s still time. I’m sharing my full four-page public comment because this fight is about far more than my daughter. It’s about every family who deserves the opportunity to fight for their loved one’s life. Please read and share. ❤️🙏 #BraelynsBill #DCVaxForBraelyn #RareDiseases
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Nix 🍀 retweeted
Replying to @elonmusk
@elonmusk surrounds himself with brilliant engineers. $NWBO ´s Linda Powers surrounds herself with brilliant scientists, clinicians, manufacturing experts and strategists. Different industries, same philosophy: build something extraordinary by bringing extraordinary people together. Linda Liau, Laura Posner, Annalisa Jenkins, Joanna Stanson, Marnix Bosch, Pawel Kalinski just to name a few
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Replying to @elonmusk
The company that gave this young girl a clear MRI and no evidence of disease has the ultimate Banger Treatment - check it out, hear her story. The cure to cancer has never been closer and it is not coming from Big Pharma
I have been waiting almost 3 years to write these words: NO EVIDENCE OF DISEASE. 🙏❤️ Today we met with Braelyn’s neurosurgeon, Dr. Linda Liau at UCLA (telehealth). When our local radiologist read Braelyn’s August 28 MRI as “no evidence of disease recurrence,” we were thrilled—but I was afraid to fully exhale. I knew Dr. Liau and the UCLA tumor board would scrutinize every millimeter of those images. What if they saw something the local radiologist missed? Today, Dr. Liau told us that she and the tumor board had thoroughly reviewed Braelyn’s MRI. They were amazed. There is NO VISIBLE TUMOR. Even the ~10% Dr. Liau had to leave behind during surgery because of its intimate involvement with critical structures is no longer visible. She emphasized how amazed and pleased the entire tumor board was by such a complete response at this point. Her assessment: the prior radiation and the ongoing DCVax appear to be working very well. Their recommendation after also reviewing the Keytruda regimen Braelyn recently started? KEEP DOING WHAT SHE’S DOING. 😭🙏 First and foremost, we give ALL thanks and glory to God. People all over the world have prayed for this girl. I cannot begin to express how humbled and grateful we are. But tonight I also cannot stop thinking about how close Braelyn came to never having this opportunity. Earlier this year, her tumor was enormous and growing rapidly. We sought help from multiple surgeons—including at prestigious institutions. We were told further surgery was too risky. We were offered the same old options: chemotherapy and photon radiation that would affect most of her brain, given the size of her tumor. Her tumor is MGMT-unmethylated, so for Braelyn, chemo was all risk with little to no benefit. And then a stranger I met here on X changed everything. @ThomasOwenMcCa1 connected us with Dr. Liau. After reviewing Braelyn’s case, one of the first things she said was: “This girl needs surgery right away.” I told her we knew that. We just couldn’t find anyone willing to do it. I asked if SHE would. “If you can get her to me, I will do her surgery.” We got Braelyn to UCLA. Within two weeks, Dr. Liau operated and removed ~90% of a massive tumor spanning three lobes, stopping where continuing would risk critical structures. And this time, her tumor tissue was PROPERLY PRESERVED. That tissue was ultimately sent to England and used to manufacture Braelyn’s personalized DCVax vaccine. She has now received 3 induction doses + her first booster. And today? The tumor that Dr. Liau had to leave behind is no longer visible on MRI. Think about that. And then think about what could have happened if we had simply accepted “there’s nothing else we can do.” THIS is why I will not stop advocating for reform. Patients should not have to find potentially life-saving treatment options accidentally through strangers on social media. Patients should be told about legitimate investigational options when standard treatment offers little hope. Patients undergoing tumor surgery should be informed BEFORE surgery about preservation of tissue that could potentially be used for personalized treatments. And patients should have the right to make informed decisions about which risks they are willing to take. Promising science means very little if the patients who need it cannot access it. Braelyn is living proof of why access matters. Tonight, though, advocacy can wait for just a moment. Tonight I’m her mom. And I finally get to say the words I have begged God to someday let me say: NO EVIDENCE OF DISEASE. Thank You, God. Thank you, Dr. Liau. Thank you to everyone who opened a door, donated, shared her story, fought for her and prayed for our girl. There is always light, even in the darkest places. Tonight that light is shining incredibly bright. ❤️🙏 #DCVaxForBraelyn #CureNotCovered @greta @kshaughnessy2 @andrewcaravello
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It is with the deepest ache in our souls that we share the passing of our baby girl, Laurel, on 10•27•26. Though her time on Earth was brief, she was endlessly loved. We are forever blessed to have held her, loved her, and been together as a family in her final moments.
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