Breaking: CMS drops $50B for Rural Health (and what it means for Tech)

December 30, 2025

Just as we were closing the books on 2025, the Centers for Medicare & Medicaid Services(CMS) made a historic announcement that fundamentally shifts the landscape for the coming year. Yesterday, they unveiled the $50 Billion Rural Health Transformation Program.


In my article earlier this month, 2025 Was a Year of Correction, 2026 Will Be the Year of Construction, I predicted that the industry would be forced to pivot from flashy AI pilots to serious infrastructure building.


I did not expect the federal government to prove me right this quickly!! :)


This new program is the largest single investment in rural healthcare infrastructure since the Hill-Burton Act. For health tech leaders, founders, and clinicians, this is not just a policy update. It is a signal that the market for 2026 will be defined by those who can solve the "last mile" problem in healthcare delivery.


The News: What CMS Announced


Late Monday afternoon, CMS Administrator Dr. Mehmet Oz announced the finalized rule and funding allocation for the Rural Health Transformation Program (RHTP). The program earmarks $50 billion over the next five years.


Crucially, the funding is distributed via block grants with a 50/50 split formula: 50% is distributed equally among states to ensure a baseline, while the remaining 50% is allocated based on specific rurality and need metrics.


Here are the three mandates that directly impact the technology sector:


1. The "Digital Infrastructure" Mandate While there is no hard cap, the rule mandates that states must allocate a significant portion of their grant specifically to "Digital Infrastructure Modernization" to qualify for the full award. This effectively unlocks billions for hardware and connectivity upgrades at Critical Access Hospitals (CAHs). As I noted in my "Construction" piece, you cannot run 2026 software on 2015 hardware. This funding finally addresses that technical debt.


2. Telehealth Parity Permanency The program codifies the "hospital at home" waivers that were set to expire this week, making reimbursement for rural remote monitoring permanent at the facility rate. This removes the "regulatory overhang" that has kept many investors on the sidelines regarding rural telehealth.


3. The "Tech-First" Workforce Grant A dedicated portion of the fund is reserved for training rural clinicians on advanced diagnostic tools. The rule specifically rewards systems that implement AI-assisted triage to extend the reach of limited staff.


You can verify the allocation formula and "allowable use" definitions here CMS Press Release: CMS Announces $50 Billion in Awards to Strengthen Rural Health.


Why This Matters Now


We have spent much of 2025 discussing the potential of Agentic AI and predictive analytics. However, the adoption of these tools has been uneven. While academic medical centers are piloting fully autonomous coding agents, hospitals in rural America are often struggling to keep their Wi-Fi running during storms.


This funding bridges that gap.


It acknowledges that high-tech software cannot function without high-tech infrastructure. By subsidizing the hardware and connectivity layer, CMS is effectively building the highway that our health tech vehicles need to drive on. This validates the "Construction" thesis entirely. We are done correcting the over-hype of previous years. We are now pouring the concrete for the next decade of digital health.


The Opportunity for Startups and Innovators


For the founders and product leaders reading this, the RHTP changes the calculus for your 2026 Go-To-Market strategy. The "Blue Ocean" is no longer in optimizing billing for urban centers. It is in bringing parity to rural zip codes.


1. Pivot to "Hybrid" Hardware Pure software plays have struggled in rural markets due to hardware incompatibility. This funding opens a massive procurement cycle for improved diagnostic devices. If your software can integrate directly with the new wave of CMS-subsidized connected devices (digital stethoscopes, handheld ultrasounds, remote vitals monitors), you have a distinct advantage.


2. Focus on Workflow, Not Just Diagnosis The "Tech-First" workforce grants are designed to combat burnout. Rural systems do not just need better diagnostics. They need tools that reduce administrative burden. The winners in this space will be platforms that automate scheduling, billing, and triage. This empowers the limited number of physicians and nurses to focus entirely on patient care rather than paperwork.


3. The Rise of Asynchronous Care With the new reimbursement rules for remote monitoring, asynchronous telemedicine (store-and-forward) becomes a viable business model for rural areas. Patients in remote locations can upload data or images which are reviewed later by a specialist. This model respects the time constraints of both the patient and the provider.


Dr. Matt’s Take: Empowerment Through Access


I want to be clear about what this means for our profession.


For too long, we have accepted a two-tier system where cutting-edge technology was reserved for high-volume urban centers. We assumed that rural healthcare had to be "low tech" by necessity. This investment challenges that assumption.


This is about empowerment.


It empowers the rural family physician to consult with world-class specialists in real time without the connection dropping.


It empowers the patient living three hours from a hospital to receive hospital-level monitoring in their own living room.


It empowers the health tech industry to look beyond the saturated urban markets and build solutions for the communities that arguably need them the most.


What You Should Do This Week



If you are leading a health tech organization, I recommend three immediate actions:


  1. Review the State-Level Allocation: Since 50% of the funds are need-based, you need to know which states are receiving the largest injections of capital. Look up the specific allocation for your target markets here HHS: Rural Health Transformation State Allocation Map.

  2. Audit Your Bandwidth Requirements: Can your platform run on the improved but still variable connections found in rural areas? If you require 5G speeds for your app to function, you may miss the initial wave of adoption.

  3. Reach Out to Rural Partners: Do not wait for the RFP. Connect with rural hospital administrators now. Ask them how they plan to utilize the RHTP funds and offer to help them draft the technical requirements for their "modernization plans."


Looking Ahead to 2026


We are entering 2026 with a clear directive. The resources are there. The policy is set. The technology is ready.


The question for the next twelve months is execution. Can we take this capital and translate it into meaningful outcomes? Can we build tools that actually work for the doctor in Wyoming as well as they do for the doctor in New York?


I believe we can.


Happy New Year. Let’s get to work.


— Dr. Matt

Breaking: CMS drops $50B for Rural Health (and what it means for Tech)
By Sarah Matt February 23, 2026
The Moral Injury of Being a Liability Sponge Let me be direct with you. Healthcare AI has had its honeymoon phase. The conference keynotes. The breathless press releases. The "transformative potential" slide decks. We all sat through them. Some of us gave them. That era is over. 2026 is the year where every AI tool, every vendor, and every health system strategy gets measured against a single question: Does this actually work at scale, and can we prove it? If the answer is no, the budget is gone. The pilot is dead. The vendor is off the approved list. Welcome to the proving ground. But as we enter this phase of accountability, we’ve stumbled into a dangerous trap. We keep talking about the "Human in the Loop" (HITL) as a design gold standard. In reality, HITL has become a legal strategy used to offload 100% of the malpractice risk onto the provider, while the system captures 100% of the efficiency gains. I’m all for AI, heck I've built a career on it! But the current implementation doesn't feel right. The providers are exhausted, and we aren't the ones getting the benefit. 1. The Liability Sponge: All the Risk, None of the Shield In the current legal landscape, the clinician is in a double-bind. If you follow the AI’s suggestion and it leads to a "hallucination" or error, you are liable for failing to exercise independent clinical judgment. If you override the AI and your intuition is wrong, you are liable for ignoring a "validated" clinical decision support tool. We are being used as a "Liability Sponge." Vendors often use "click-wrap" agreements to disclaim responsibility, leaving the person with the MD or RN after their name to hold the bag. According to Bell Law Firm’s 2026 analysis , technology is no longer a neutral tool; it is a causal chain of injury, and yet the "Human in the Loop" is the only one who answers for it in court. To derisk this, we must advocate for Statutory Safe Harbors . If a provider uses a certified, validated tool as intended, they should not face higher standards than the machine itself. We need shared liability, where vendors put their balance sheets behind their 99% accuracy claims. 2. The Productivity Trap: The "15-Minute" Repossession Ambient listening (AI scribing) was the great hope for 2026. It was supposed to let us look patients in the eye again. And it does save time, roughly 30 to 45 minutes of documentation a day . But here’s the catch: In many health systems, that "gift of time" is immediately repossessed by administration to increase RVU targets. We’ve automated the clerical task of writing a note, only to replace it with 2–3 more high-stakes human interactions. We are trading clerical fatigue for emotional exhaustion. The "Human in the Loop" isn't just a safety net; they’ve become an accelerator for the system’s bottom line. We aren't getting a break; we're just being asked to run a faster race. 3. The Vendor’s Dilemma: Finding the Middle Ground I’ve been on the vendor side. I know the fear. If a tech company takes on unlimited clinical liability, they effectively become an insurance company. Most wouldn't survive their first major malpractice suit. So, how do we break the standoff? Clinical Accuracy Warranties: Forward-thinking vendors are beginning to offer performance guarantees. They aren't promising perfection, but they are guaranteeing their model stays within a specific "standard of care" band. The Registry Solution: We need a National AI Incident Reporting System, like the FAA’s "black box" for aviation. If a model fails in a specific clinical scenario, that data should be shared immediately so every other "Human in the Loop" knows to watch for it. Check the Epstein Becker Green Checklist for the five critical points your 2026 vendor agreement must cover to ensure you aren't the only one at risk. Get the "Clinical Reality Check" Before Everyone Else. I send these briefings to my private list 24 hours before they hit social media. Join other healthcare leaders who get the raw, uncensored analysis first. [Join the Clinical Realist List] The Bottom Line In 2026, the "cool factor" is dead. We are entering the era of Clinical Pragmatism . I want AI to win. I want it to help us. But a system where the provider is the "Liability Sponge" and the vendor is a "Ghost" is unsustainable. We don't need faster AI; we need a fairer contract. If the system wants us to be the final authority, it needs to give us the authority to slow down. Stay Real, -Dr. Matt
By Sarah Matt February 16, 2026
The Moral Injury of Being a Liability Sponge Let me be direct with you. Healthcare AI has had its honeymoon phase. The conference keynotes. The breathless press releases. The "transformative potential" slide decks. We all sat through them. Some of us gave them. That era is over. 2026 is the year where every AI tool, every vendor, and every health system strategy gets measured against a single question: Does this actually work at scale, and can we prove it? If the answer is no, the budget is gone. The pilot is dead. The vendor is off the approved list. Welcome to the proving ground. But as we enter this phase of accountability, we’ve stumbled into a dangerous trap. We keep talking about the "Human in the Loop" (HITL) as a design gold standard. In reality, HITL has become a legal strategy used to offload 100% of the malpractice risk onto the provider, while the system captures 100% of the efficiency gains. I’m all for AI, heck I've built a career on it! But the current implementation doesn't feel right. The providers are exhausted, and we aren't the ones getting the benefit. 1. The Liability Sponge: All the Risk, None of the Shield In the current legal landscape, the clinician is in a double-bind. If you follow the AI’s suggestion and it leads to a "hallucination" or error, you are liable for failing to exercise independent clinical judgment. If you override the AI and your intuition is wrong, you are liable for ignoring a "validated" clinical decision support tool. We are being used as a "Liability Sponge." Vendors often use "click-wrap" agreements to disclaim responsibility, leaving the person with the MD or RN after their name to hold the bag. According to Bell Law Firm’s 2026 analysis , technology is no longer a neutral tool; it is a causal chain of injury, and yet the "Human in the Loop" is the only one who answers for it in court. To derisk this, we must advocate for Statutory Safe Harbors . If a provider uses a certified, validated tool as intended, they should not face higher standards than the machine itself. We need shared liability, where vendors put their balance sheets behind their 99% accuracy claims. 2. The Productivity Trap: The "15-Minute" Repossession Ambient listening (AI scribing) was the great hope for 2026. It was supposed to let us look patients in the eye again. And it does save time, roughly 30 to 45 minutes of documentation a day . But here’s the catch: In many health systems, that "gift of time" is immediately repossessed by administration to increase RVU targets. We’ve automated the clerical task of writing a note, only to replace it with 2–3 more high-stakes human interactions. We are trading clerical fatigue for emotional exhaustion. The "Human in the Loop" isn't just a safety net; they’ve become an accelerator for the system’s bottom line. We aren't getting a break; we're just being asked to run a faster race. 3. The Vendor’s Dilemma: Finding the Middle Ground I’ve been on the vendor side. I know the fear. If a tech company takes on unlimited clinical liability, they effectively become an insurance company. Most wouldn't survive their first major malpractice suit. So, how do we break the standoff? Clinical Accuracy Warranties: Forward-thinking vendors are beginning to offer performance guarantees. They aren't promising perfection, but they are guaranteeing their model stays within a specific "standard of care" band. The Registry Solution: We need a National AI Incident Reporting System, like the FAA’s "black box" for aviation. If a model fails in a specific clinical scenario, that data should be shared immediately so every other "Human in the Loop" knows to watch for it. Check the Epstein Becker Green Checklist for the five critical points your 2026 vendor agreement must cover to ensure you aren't the only one at risk. Get the "Clinical Reality Check" Before Everyone Else. I send these briefings to my private list 24 hours before they hit social media. Join other healthcare leaders who get the raw, uncensored analysis first. [Join the Clinical Realist List] The Bottom Line In 2026, the "cool factor" is dead. We are entering the era of Clinical Pragmatism . I want AI to win. I want it to help us. But a system where the provider is the "Liability Sponge" and the vendor is a "Ghost" is unsustainable. We don't need faster AI; we need a fairer contract. If the system wants us to be the final authority, it needs to give us the authority to slow down. Stay Real, -Dr. Matt
By Sarah Matt February 9, 2026
On February 5, the White House launched TrumpRx.gov , a direct-to-consumer platform connecting Americans to discounted prices on 43 brand-name prescription drugs. The site runs on GoodRx-style coupon technology and allows cash-paying patients to access manufacturer discount programs through most favored nation pricing agreements with 13 pharmaceutical companies, including Eli Lilly, Novo Nordisk, Pfizer, and Amgen. The next day, Mark Cuban sat on stage at the Silicon Slopes Summit with U.S. Medicare Director Chris Klomp and said the quiet part out loud: "Of the drugs we both carry, we are cheaper on 90%." Two platforms. Two approaches. Same promise: lower drug prices for Americans. But which patients actually benefit? And which ones are, once again, invisible? I wrote The Borderless Healthcare Revolution to make a simple argument: access is not a widget. It is a system. And any system that ignores the infrastructure underneath it will fail. This week, I want to apply that framework to both platforms and expose what the headlines are missing. TrumpRx: The Headlines vs. The Reality The headline numbers are real. Eli Lilly's Zepbound starts at $299 per month (down from roughly $1,060). Novo Nordisk's Wegovy pill drops to $149 per month. AstraZeneca's Bevespi inhaler falls to $51. For uninsured patients paying cash for GLP-1 medications or fertility drugs, these discounts are meaningful. But headlines do not treat patients. Systems do. So let me run TrumpRx through the Five-Pillar Access Audit from my book and see where the roof caves in. Pillar 1: Physical Access TrumpRx is a website. It requires an internet connection, a device, and the ability to navigate a government platform. According to the FCC, roughly 24 million Americans lack broadband access. Many are rural patients who also happen to live in communities where independent pharmacies are closing at record rates . Some of the listed drugs ship direct-to-consumer from manufacturer fulfillment centers. That assumes the patient has a reliable mailing address and someone available to receive temperature-sensitive medications like injectable GLP-1 drugs. For the tech executive in Manhattan, this is seamless. For the patient in rural Kentucky whose nearest pharmacy just closed and whose mail comes to a PO box, this is a wall. Pillar 2: Financial Access This is where it gets uncomfortable. TrumpRx.gov is designed strictly for cash-paying patients—a group that includes roughly 27 million uninsured Americans . However, for the 85% of Americans with health insurance, the math rarely works. Most insured patients will likely find that their existing pharmacy benefit offers a lower price than the "discounted" rates on the government portal. The "Cash Only" Barrier for Medicare & Medicaid A major point of confusion surrounds Medicare and Medicaid patients . While they are not technically "banned," they can only use the platform if they bypass their government benefits entirely and pay 100% out-of-pocket. See the Cultural Pillar below. The HHS Office of Inspector General (OIG) recently issued a Special Advisory Bulletin attempting to create a "low-risk" roadmap for manufacturers to sell directly to these patients. This guidance is a workaround for the federal Anti-Kickback Statute , which criminalizes offering incentives for items reimbursable by federal programs. For now, this pathway remains narrow and untested; many manufacturers may still avoid it to mitigate legal risk. The Deductible "Invisible Man" There is a hidden cost to using this portal: TrumpRx payments do not count toward your insurance deductible. . If an insured patient uses the platform for even one medication, every dollar they spend remains invisible to their insurance plan . For those with high-deductible plans, this means they aren't making any progress toward their annual out-of-pocket maximum. The Generic Problem Finally, there is the issue of brand-name bias . TrumpRx lists the brand-name drug Protonix for approximately $200 . Meanwhile, the generic version, pantoprazole , is widely available for as little as $6 through services like GoodRx or Mark Cuban’s Cost Plus Drugs . Analysis shows that about half of the drugs currently on TrumpRx have significantly cheaper generics available elsewhere. Without a pharmacist to guide them, a patient could easily pay six times more for a brand-name "deal" on the government site than they would for the generic at their local pharmacy. Pillar 3: Cultural Access The TrumpRx website launched in English. For the roughly 25 million Americans with limited English proficiency, this is not a minor inconvenience. It is a barrier. The coupon redemption process requires a level of pharmacy literacy that many patients do not have. The "Shadow Exclusion" of Federal Beneficiaries Perhaps the most confusing cultural signal comes from the HHS Office of Inspector General’s (OIG) January 27, 2026, Special Advisory Bulletin . In a move designed to "clear the path" for the platform's launch, the OIG provided a low-risk roadmap for manufacturers to sell directly to Medicare and Medicaid patients who choose to pay cash. However, a cultural disconnect remains at the point of entry: the TrumpRx.gov attestation form . To access these "deals," users must still check a box confirming they are not enrolled in any government-funded program. This creates a "shadow exclusion"; where the legal theory says yes, but the government’s own digital interface says no. For a clinician, this is the ultimate red flag: we are asking the most vulnerable, high-utilization patients to either misrepresent their status or forfeit their hard-earned federal benefits just to participate in a "revolution" that wasn't actually built for them.The attestation form asks users to confirm they are not enrolled in government health coverage. For immigrant patients, entering personal information on a .gov website carries real fear, real risk, and real consequences that the platform designers clearly did not consider. Pillar 4: Digital Access This pillar is where TrumpRx collapses most visibly. The platform creates what pharmacists call a "dangerous information vacuum." A patient buying blood pressure medication through TrumpRx, a cholesterol medication at a retail pharmacy, and a diabetes medication through a different direct-to-consumer program has effectively fragmented their own medication record. No single pharmacist sees the full picture. The risk of drug interactions, duplicate therapies, and dosing errors multiplies. There is no integration with electronic health records. No pharmacy claims data flows back to the care team. We spent two decades and billions of dollars building EHR infrastructure specifically so clinicians could see the whole patient. TrumpRx routes around that infrastructure entirely. Get the "Clinical Reality Check" Before Everyone Else. I send these briefings to my private list 24 hours before they hit social media. Join other healthcare leaders who get the raw, uncensored analysis first. [Join the Clinical Realist List] Pillar 5: Trust and Knowledge Trust is the currency of healthcare. TrumpRx has a trust problem on multiple fronts. First, sustainability. What happens to these prices when the current administration ends? Patients who restructure their medication access around TrumpRx have no guarantee these deals survive a change in government. Starting a patient on a medication they can afford today but not tomorrow is not access. It is a setup for medication abandonment . Second, data. When patients bypass their insurance plan to buy through TrumpRx, the plan loses utilization and adherence data. This sounds bureaucratic until you realize that data drives formulary decisions, drug coverage, and cost forecasting. We are trading short-term savings for long-term blindness. Third, the pharmacist relationship. If direct-to-consumer platforms pull even modest volume away from pharmacies, we lose the most accessible healthcare professional most Americans have. The pharmacist is often the last line of defense against a prescribing error. Removing them from the equation to save a few dollars is a clinical risk disguised as a consumer benefit. Now Enter Mark Cuban Cuban's Cost Plus Drug Company launched in 2022 with a radically different model: sell generic medications at acquisition cost plus a flat 15% markup and a $5 pharmacist fee. No coupons. No middlemen. No opaque pricing. Just transparent math. The contrast with TrumpRx is stark. Drug selection: TrumpRx offers 43 brand-name drugs. Cost Plus Drugs offers over 6,000 medications, overwhelmingly generics. Cuban pointed out that TrumpRx added many brands that have generic equivalents , and Cost Plus beats them on price "usually by a lot." Pricing model: TrumpRx uses manufacturer coupons and discount cards, meaning the underlying list price stays high and the "discount" is a marketing decision. Cost Plus Drugs publishes the actual cost of the drug and adds a transparent markup. One model obscures the economics. The other exposes them. Insurance compatibility: Cost Plus Drugs accepts coverage from more than two dozen insurance providers. TrumpRx is cash-only and explicitly excludes government insurance. The partnership twist: Cuban confirmed that Cost Plus Drugs is sharing its API with TrumpRx so the government platform can pull pricing data. Cuban's bet is that displaying Cost Plus prices alongside brand-name TrumpRx prices will drive patients toward the cheaper generic option. It is a shrewd move: use the government's marketing budget to grow your own customer base. The Medicare and Medicaid Problem Nobody Wants to Talk About Here is the uncomfortable reality that both platforms share: neither one adequately serves the patients who need the most help. TrumpRx explicitly excludes Medicare and Medicaid patients from using its coupons. That is over 150 million Americans on government-funded health coverage. The anti-kickback statute creates a legal wall that TrumpRx has not figured out how to climb, despite HHS guidance attempting to create a narrow pathway. Cost Plus Drugs does not accept Medicare. Its transparent cost-plus model does not fit cleanly into the Medicare Part D rebate structure. Research from the Journal of Urology estimated Medicare could save $1.29 billion annually if generic drug prices matched Cost Plus levels. A separate PharmacoEconomics study put potential Part D savings at $8.6 billion. The savings are there. The regulatory framework to capture them is not. The government is making moves on the margins. Medicare recently negotiated lower prices on key GLP-1 medications : $245 per month for Ozempic, Wegovy, Mounjaro, and Zepbound, with a $50 monthly copay for beneficiaries. State Medicaid programs can access the same rates. For the first time, Medicare will cover Wegovy and Zepbound for patients with obesity. (This starts in 2027) But these are individual drug deals, not systemic reform. They do not address the structural problem: the pharmacy benefit manager (PBM) layer that sits between manufacturers and patients, extracting value at every turn. Cuban said it clearly at the Silicon Slopes Summit: "Those big insurance companies are too big to care." His prescription? Break them up. The Five-Pillar Scorecard If I run both platforms through my Five-Pillar Access Audit, neither one passes: Physical: Both are online-only platforms. Neither solves the broadband gap or pharmacy desert problem. TrumpRx adds a direct-to-consumer shipping layer that assumes stable housing. Cost Plus ships to homes but also partners with a mail-order pharmacy. Neither has a walk-in option for patients without internet. Financial: TrumpRx helps a narrow slice of uninsured, cash-paying patients and excludes government insurance. Cost Plus Drugs is cheaper on most overlapping medications and accepts some insurance, but does not accept Medicare. Both leave the 150+ million Americans on government coverage largely untouched. Cultural: TrumpRx launched English-only with an attestation form that deters immigrant populations. Cost Plus Drugs has a cleaner interface but still assumes English literacy and digital fluency. Neither platform has invested meaningfully in multilingual access or community health worker integration. Digital: TrumpRx creates a fragmented medication record with no EHR integration. Cost Plus Drugs shares prescription data with its partner pharmacy (Truepill/pharmacy network), but does not integrate with a patient's primary care EHR either. Neither platform solves the information vacuum problem. Trust: TrumpRx's sustainability depends on who occupies the White House. Cost Plus Drugs is a private company with a transparent model, which is more durable but still subject to market forces. Neither platform has built the community-level trust infrastructure (local champions, clinic partnerships, navigator programs) that my book identifies as the foundation of lasting access. The Bottom Line TrumpRx is not a bad idea. Neither is Cost Plus Drugs. Lowering drug prices for Americans is a legitimate goal, and both platforms deliver real savings for specific populations. But both are 'Castle' solutions. They were designed for people with broadband, health literacy, and English fluency. TrumpRx does not account for the grandmother in Appalachia without broadband. Cost Plus Drugs does not account for the Medicare patient in a food desert who cannot afford the bus fare to a pharmacy, let alone a monthly subscription. Neither accounts for the immigrant mother who is afraid to enter her name on any website, government or otherwise. If you are a health system leader reading this, run your own Five-Pillar Audit before recommending either platform to patients. Ask: which of my patients does this actually reach? And which does it leave behind? The answer will tell you everything about where the real work still needs to be done. What to Do Next Audit Your Medicine Cabinet: Before your next refill, cross-check your brand-name prescriptions against TrumpRx.gov and Mark Cuban’s Cost Plus Drugs . If you find a massive price gap that doesn't make sense, let’s talk about it. Subscribe to The Clinical Realist: If you want more "no-filter" breakdowns of how policy actually hits the pavement in your clinic or boardroom, join the community on Buzzsprout so you never miss an episode. Drop Me a Note: I want to hear from the front lines. Are your patients actually asking about TrumpRx, or is this just more "health tech theater"? Reply to this email or DM me, I read every single message.  -Dr. Matt