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    Debunking Myths About GLP-1 Medications

    Debunking Myths About GLP-1 Medications

    February 16, 2026
    The Future of LLMs in Healthcare

    The Future of LLMs in Healthcare

    January 26, 2026
    The Future of Healthcare Consumerism

    The Future of Healthcare Consumerism

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    Your Body, Your Health Care: A Conversation with Dr. Jeffrey Singer

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    The Fight Against Healthcare Fraud: Dr. Rafai’s Story

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My Struggles with Imposter Syndrome

Writing Burden of Pain was a fight against myself.

Daily Remedy by Daily Remedy
January 15, 2023
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My Struggles with Imposter Syndrome

Eddi van W.

It tightens your jaw so the words can’t come out. Then it presses down on your chest so your breathing is labored. Finally, it dulls your mind so the thoughts grind to a halt.

It’s imposter syndrome, that insidious snake of a condition. It begins as a whisper and grows into a maddening screech, all while wreaking havoc throughout your body.

It’s what I felt when I began to tell my story. It’s what I still feel to a lesser degree when I tell my story today. Maybe it’ll never go away. But each time I tell my story, it feels easier.

“A lie gets halfway around the world before the truth has a chance to get its pants on”, said Winston Churchill. What he didn’t say was why. The truth has been inflicted by imposter syndrome, so of course it’ll be delayed.

But slow as it may be, the truth has a way of coming out. Much like those affected by imposter syndrome have a way of overcoming it. It’s difficult. Maybe it’ll take everything you got. But it can be done.

That’s what I tell myself. After I’ve whispered it to myself enough times, I’m actually starting to believe it. This seems to be the Achilles’ heel of imposter syndrome.

With the upcoming release of Burden of Pain, I hope to shed the remaining symptoms of this affliction. Looking back, I’ve come a long way. When I first began to write, I would suffer from intense, paroxysmal bouts of imposter syndrome.

I would go from writing coherent sentences to struggling to even spell out words. Sometimes I would just freeze, so it would look like I’m writing, but nothing would move and my eyes would simply stare ahead, empty and lifeless – like my very essence had been removed.

After a few days and more than a few rewrites, the symptoms began appearing more mildly. Sure, they would still come. And sure enough, my writing would be affected – but it wouldn’t die. The words would still be written. They would still come to life.

After enough writing and laboring, the words began to support me. They gave me life. Together, we built a relationship, sustaining one another. I would write the words, and the words would give me the strength to overcome imposter syndrome. The more I wrote, the less severe the symptoms became.

The result is my first book, Burden of Pain. When I look at the book now, in its entirety, I see a celebration of my resilience, my dedication to the truth. But when the pages were forming, I saw an imposter. I had little to no faith in myself or in my abilities. Yet I persisted. And through that persistence, I grew a sense of confidence out of the lingering emptiness.

I may never be free of imposter syndrome, but at least I know I can overcome it. You can read about my triumph in my concluding words in Burden of Pain:

Some say prison made me a writer. They would be wrong. Shame and humiliation made me a writer. By putting letters on paper, I display my scars of shame. By forming words from letters, I create an impression of my humiliation. By creating meaning out of words, I transform the alchemy of writing into the science of knowledge framed as solutions to the opioid epidemic.

Burden of Pain
Cover of Burden of Pain
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Daily Remedy

Dr. Jay K Joshi serves as the editor-in-chief of Daily Remedy. He is a serial entrepreneur and sought after thought-leader for matters related to healthcare innovation and medical jurisprudence. He has published articles on a variety of healthcare topics in both peer-reviewed journals and trade publications. His legal writings include amicus curiae briefs prepared for prominent federal healthcare cases.

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Videos

This conversation focuses on debunking myths surrounding GLP-1 medications, particularly the misinformation about their association with pancreatic cancer. The speaker emphasizes the importance of understanding clinical study designs, especially the distinction between observational studies and randomized controlled trials. The discussion highlights the need for patients to critically evaluate the sources of information regarding medication side effects and to empower themselves in their healthcare decisions.

Takeaways
GLP-1 medications are not linked to pancreatic cancer.
Peer-reviewed studies debunk misinformation about GLP-1s.
Anecdotal evidence is not reliable for general conclusions.
Observational studies have limitations in generalizability.
Understanding study design is crucial for evaluating claims.
Symptoms should be discussed in the context of clinical conditions.
Not all side effects reported are relevant to every patient.
Observational studies can provide valuable insights but are context-specific.
Patients should critically assess the relevance of studies to their own experiences.
Engagement in discussions about specific studies can enhance understanding

Chapters
00:00
Debunking GLP-1 Medication Myths
02:56
Understanding Clinical Study Designs
05:54
The Role of Observational Studies in Healthcare
Debunking Myths About GLP-1 Medications
YouTube Video DM9Do_V6_sU
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2027 Medicare Advantage & Part D Advance Notice

Clinical Reads

BIIB080 in Mild Alzheimer’s Disease: What a Phase 1b Exploratory Clinical Analysis Can—and Cannot—Tell Us

BIIB080 in Mild Alzheimer’s Disease: What a Phase 1b Exploratory Clinical Analysis Can—and Cannot—Tell Us

by Daily Remedy
February 15, 2026
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Can lowering tau biology translate into a clinically meaningful slowing of decline in people with early symptomatic Alzheimer’s disease? That is the practical question behind BIIB080, an intrathecal antisense therapy designed to reduce production of tau protein by targeting the tau gene transcript. In a phase 1b program originally designed for safety and dosing, investigators later examined cognitive, functional, and global outcomes as exploratory endpoints. The clinical question matters because current disease-modifying options primarily target amyloid, while tau pathology tracks...

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