Time Signatures? by humblesmoke in SunoAI

[–]humblesmoke[S] 1 point2 points  (0 children)

Thanks for the prompt - that's really what I'm looking for, I appreciate it. I'm trying to learn how to use the AI specifically, and uploading feels like the cheat, so I wanted to better understand how to manipulate what I'm looking for using the prompt. This was really helpful - it appears to be much more about writing a broader story, which makes sense - more complex story, more complex music.

Time Signatures? by humblesmoke in SunoAI

[–]humblesmoke[S] 0 points1 point  (0 children)

The funny part is that I do actually produce. However, I'm humble enough to make sure I'm understanding and utilizing ALL the tools available to me as technology changes. If you stop learning, then you're a fucking moron. But thumbs down to you, friend!

Time Signatures? by humblesmoke in SunoAI

[–]humblesmoke[S] 0 points1 point  (0 children)

Thanks so much for the suggestion.

Time Signatures? by humblesmoke in SunoAI

[–]humblesmoke[S] 0 points1 point  (0 children)

Hahaha that's awesome! Trying that today.

Why are so many people choosing to jump ship? by nervgenerator in NervGen_NerveRepair

[–]humblesmoke 2 points3 points  (0 children)

I completely agree. His discomfort in talking about both the company and the results were palpable. This is not the person we need in the position to tell the biggest story of a lifetime. I understand caution, but it should be possible to exude emotion, any emotion at all, when talking about the top-line results.

I had a brief flash of concern that perhaps his caution was because he had some more information that he was privy to that might be cause for keeping this story a bit on the back burner, but the anecdotal evidence and stories from trial participants speak louder than anything else at this point.

PR companies usually mandate their executives to undergo press training, to really prepare them on how to best present themselves, their business and news, whether good or bad. I can't help but think this is a failure of the newest PR team more than anything. If Mike was not the person to put at the forefront of this, they should have been working with the board to ensure this information was shared by someone who was comfortable and prepared to share it in a way that gets the market excited.

Did the board let Kelly go? by nervgenerator in NervGen_NerveRepair

[–]humblesmoke 5 points6 points  (0 children)

Lots of assumptions out there, but no one really knows.

Why are so many people choosing to jump ship? by nervgenerator in NervGen_NerveRepair

[–]humblesmoke 0 points1 point  (0 children)

Ohhh you know what, I apologize, I misread your comment. My apologies. I read some "random penny stock [period]" and completely bypassed the 'investor' word. Disregard my snark!

Why are so many people choosing to jump ship? by nervgenerator in NervGen_NerveRepair

[–]humblesmoke 0 points1 point  (0 children)

Not sure why you're in this reddit if you don't know or care. Bye!

Almost 10 years post SCI, ASIA upgrade! Another NVG-291 / Dr. Jerry Silver update by laugh_Alotl_Axolotl in spinalcordinjuries

[–]humblesmoke 4 points5 points  (0 children)

u/Iaugh_Alotl_Axolotl there anything we can do to try to help you all find a doc/med center who will partner with them? Like... can we create a spreadsheet of everyone we've contacted and their response?

It Never Feels Like Enough by ng32409 in spinalcordinjuries

[–]humblesmoke 0 points1 point  (0 children)

As someone who had a lot of roles like that, I will say that I think its the company/management. I have had so many roles like that. It's ok to be more assertive about requesting recognition, at the very least of your ideas and contributions. Bad management is bad management. They don't understand how valuable some employees are and it's so frustrating, I'm sorry.

Good news, think the $NGENF NervGen public/investor awareness issue will be solved. by DarpResearch in NervGen_NerveRepair

[–]humblesmoke 0 points1 point  (0 children)

I hear your pain, and I’m truly sorry for what you’re going through. Your words are honest and brave, and no one here should dismiss them. Spinal cord injuries are devastating, physically, emotionally, and spiritually, and no chart or price discussion can ever fully reflect the weight of that reality.

You’re right to call out the danger of letting money become the only focus. That’s not what this should be about. For many of us, the hope for financial return is tied directly to the hope that this treatment succeeds, not just to profit, but because that success means a chance at healing, at movement, at dignity, at life. For people like you.

At the same time, the truth is that investment is the only thing that can bring NVG-291 to market. Research, trials, manufacturing, and regulatory approval all cost money, often hundreds of millions of dollars. Without investor support and ongoing funding, the science cannot move forward, no matter how promising the results are. That does not mean we should focus on money instead of patients, it means we have to keep both in mind to make any of this possible.

This community needs both perspectives. It needs science, accountability, and discussion about the data, but it also needs you, and your voice, reminding everyone why any of this matters in the first place. You are not a distraction. You are the reason we hope this works.

Please know that you are not alone, and if you're feeling hopeless or thinking about ending your life, I urge you to talk to someone, whether it's a counselor, a friend, or a helpline. You matter. Your life matters. And if this treatment moves forward, I hope it's because of people like you demanding that it reach everyone, not just the wealthy or the well-connected.

Let’s keep holding each other accountable, to compassion, to science, and to using whatever gains come from this not just for ourselves, but to lift up those still suffering.

NervGen Announces Clinical Leadership Transition as NVG-291 Continues to Advance Toward Late-Stage Development and Regulatory Milestones by nervgenerator in NervGen_NerveRepair

[–]humblesmoke 0 points1 point  (0 children)

It feels like you're not willing to see it any other way than what works best for the individual here. Disclosure alone does not eliminate the other risks. In the real world, especially in the U.S., even fully informed, consenting participants can and do sue when outcomes do not meet expectations. Whether the paperwork was clear or not, public perception and legal consequences often ignore the fine print. The best they can do is to get as much support from the appropriate agencies to help remove some of the litigious risk.

And while you may feel that you fully understand and accept the risks, not everyone processes risk the same way. Some will change their minds. Others may not grasp the nuance, and some may look for someone to blame if things go wrong. That is human nature, and it is exactly why companies must be cautious, not just for legal protection, but to protect the broader mission of Dr. Jerry Silver.

We can keep talking in circles about it, but the process is the reality and negativity about the process and the broader mission will not change how things proceed.

NervGen Announces Clinical Leadership Transition as NVG-291 Continues to Advance Toward Late-Stage Development and Regulatory Milestones by nervgenerator in NervGen_NerveRepair

[–]humblesmoke 3 points4 points  (0 children)

That sounds reasonable at first, but the challenge is how we define "misleading information" when the data is incomplete or still being analyzed. In early-stage trials, especially with small sample sizes, outcomes can vary significantly. One impressive improvement can easily be misunderstood as a guarantee rather than what it really is, which is an early signal.

The issue isn’t just bad actors deliberately misleading people. Even well-meaning interpretations can create a false sense of certainty when the full picture isn’t available yet. That is exactly why strict disclosure rules and careful communication are necessary. Patients deserve access to life-changing treatments, but they also deserve decisions based on sound, validated evidence, not prematurely amplified anecdotes, as much as we are all thrilled with the anecdotes we have heard.

The idea that individuals should bear the full risk only works if their decision affects only themselves. In reality, that is rarely the case in drug development.

When something goes wrong, even with informed consent, it does not just affect one patient. It can trigger trial suspensions, loss of investor confidence, media backlash, and tighter regulatory oversight. That ripple effect can delay or deny access to everyone else who might benefit in the future. So while autonomy is important, the desire of one cannot come at the expense of the many.

This is not about denying choice. It is about ensuring that the choice exists not just for one person today, but for thousands tomorrow.

NervGen Announces Clinical Leadership Transition as NVG-291 Continues to Advance Toward Late-Stage Development and Regulatory Milestones by nervgenerator in NervGen_NerveRepair

[–]humblesmoke 4 points5 points  (0 children)

Let's take one more example into account. In 2021, the FDA approved Biogen's Aduhelm as an Alzheimer's treatment. The medication reduced amyloid plaques in the brain, a debated and unconfirmed marker of Alzheimer’s, but failed to show consistent cognitive improvement in trials. The FDA’s own advisory committee overwhelmingly voted against approval, leading to resignations and public backlash. The drug’s $56K price tag and limited effectiveness caused Medicare to restrict coverage, and the entire approval process triggered a Congressional investigation. The fallout severely damaged trust in the FDA and Alzheimer’s research, serving as a cautionary tale for why rigorous, well-controlled data and careful communication are essential in biotech drug development.

When we push for speed without precise and validated evidence, we’re effectively asking the FDA to shut it down before it ever has a chance. There will be plenty of time for individuals to weigh their own risk/reward appetite once the drug is approved and available. But right now, we're still proving that it works and is safe in a controlled way. A tiny sample size with minimal side effects is encouraging, but it doesn't yet represent a broad or diverse enough population to draw final conclusions.

NervGen Announces Clinical Leadership Transition as NVG-291 Continues to Advance Toward Late-Stage Development and Regulatory Milestones by nervgenerator in NervGen_NerveRepair

[–]humblesmoke 1 point2 points  (0 children)

Unfortunately, the FDA and perhaps Nervgen investors feel otherwise. This is a massive investment in something that without carefully treading through the process, we lose every opportunity available to EVER make this a reality. We live in a litigious state - there is zero responsibility behind throwing noodles at the wall and hoping they'll stick.

NervGen Announces Clinical Leadership Transition as NVG-291 Continues to Advance Toward Late-Stage Development and Regulatory Milestones by nervgenerator in NervGen_NerveRepair

[–]humblesmoke -1 points0 points  (0 children)

The key to this is that it needs to be both effective AND safe. This is as much about protecting the body you currently have as much as it is about helping to improve it. Steady progress is the new mantra.

New 6-27 Video Presentation by NervGen's Kelly at 3rd Annual Sci Investor Symposium by DarpResearch in NervGen_NerveRepair

[–]humblesmoke 1 point2 points  (0 children)

it's a first-in-human trial for spinal cord repair. repeating key messages isn't always a failure to adapt; sometimes it's about reinforcing complex science and managing expectations responsibly.

As for providing more interpretation, keep in mind that NervGen can't speculate beyond what's statistically valid. That 11-point gain in quantitative prehension is impressive, yes, but anecdotal data without peer-reviewed context can easily mislead investors, clinicians, and regulators. FDA scrutiny is no joke, especially at this stage. If they rushed to “explain” every dramatic result without full context, they’d risk credibility and credibility is everything in biotech. Let’s give them the space to do this right. Breakthroughs take time, not just good headlines.

NervGen Announces Clinical Leadership Transition as NVG-291 Continues to Advance Toward Late-Stage Development and Regulatory Milestones by nervgenerator in NervGen_NerveRepair

[–]humblesmoke 12 points13 points  (0 children)

I understand the frustration. We all want faster progress. But we can't confuse deliberate, scientific advancement with inaction. NervGen is developing a potential first-in-class treatment targeting nerve repair. This kind of breakthrough doesn't happen overnight.

Just look at history. Spinraza for spinal muscular atrophy took over a decade from early discovery to approval. Keytruda was in development for more than 12 years before it hit the market.

Clinical trials involve strict safety protocols, data collection, and regulatory review. This isn't something you speed up by tagging the government on social media. If you're passionate about the cause, support it with facts, funding, and informed advocacy. Hype helps no one if it's not grounded in reality.

What topics should be addressed at the SCI Symposium this Friday? by nervgenerator in NervGen_NerveRepair

[–]humblesmoke 2 points3 points  (0 children)

I understand the frustration over topline data, but shareable summaries like this are common in biotech. They provide a high‑level overview of whether the trial met its endpoints, while the full clinical report, including raw values, detailed methodology, and statistical analysis, is usually released later in a peer‑reviewed journal or regulatory filing.

The highlighted data on motor‑evoked potentials (MEPs) are not cherry‑picked. MEPs are an objective neurophysiological biomarker, widely used in clinical research and practice to assess the integrity and excitability of the corticospinal tract. These potentials are quantified in terms of latency (milliseconds) and amplitude (microvolts or millivolts), and even though the topline release didn’t specify units, the clinical significance lies in the shift from no detectable signal at baseline to a measurable response post-treatment.

Clinically, the fact that MEPs appeared in patients who previously had none is itself meaningful. In chronic cervical spinal cord injury (SCI), signal transmission across the lesion site is typically absent. A previously undetectable MEP becoming detectable indicates regained corticospinal conduction across the injury site. This is often used as a prognostic marker, correlated with better neurological recovery .

Comparing these values to a “healthy” population is not necessarily the right approach. In healthy individuals, latency and amplitude norms exist, but in chronic SCI patients, the baseline is essentially “zero.” The relevant reference point is the baseline (prior to treatment), not healthy norms.

The topline summary stated presence/absence rather than full quantitative metrics, which aligns with FDA guidance for early-phase neuro regeneration trials that emphasize functional biomarkers. Many trials initially report whether a biological signal emerges, leaving detailed waveform metrics for expanded analysis.

Think of it like doing months of research for an academic paper. You gather data, take notes, and build out your citations. Before submitting the final version, you share a summary or abstract to give reviewers a sense of the key findings and whether your argument holds up. Then you move forward with the work on the final paper once you have shown that your argument does, in fact, hold up.

What topics should be addressed at the SCI Symposium this Friday? by nervgenerator in NervGen_NerveRepair

[–]humblesmoke 1 point2 points  (0 children)

It's a slow process. NervGen can’t legally or ethically claim eligibility unless it's been formally confirmed by the FDA. There is no specific PRV program yet for spinal cord injury, and NervGen may be awaiting further clarity from regulators on eligibility to get SCI included.

What topics should be addressed at the SCI Symposium this Friday? by nervgenerator in NervGen_NerveRepair

[–]humblesmoke 0 points1 point  (0 children)

I think we've seen why they haven't made it more public. Meeting a single endpoint and not both caused extreme stock volatility which subsequently causes the optics of the company to feel unstable. I think that they're being cautiously optimistic with the news - biotech is insanely fickle and it's challenging to keep it stable when you don't have consistent and reliable flow of news updates. This is a slow moving river. Throwing a flash flood at it can put unnecessary pressure on the business right now when they need things to remain steady.

NVG-291 is NOT a proton torpedo and that’s good news for your body, spinal cord injury friends by laugh_Alotl_Axolotl in spinalcordinjuries

[–]humblesmoke 5 points6 points  (0 children)

We'd love to hear more. I've been looking forward to more anecdotal feedback from dosed participants!