Many of us living with pain have experienced the challenge of no longer being able to see our familiar doctors. In my state of Rhode Island, along with those who are naturally retiring, many have also chosen to leave to receive the more reasonable pay that they deserve in a different state. Whatever the reason, this leaves us searching for a new doctor. However, for those of us living with a chronic condition, this process can be extremely challenging. Our mission is to find a new doctor who is willing to take us on despite our complications. Chronic pain sure puts a monkey wrench into the journey of searching. I live with Ehlers-Danlos syndrome, which is an incurable, painful, and complicated condition. Therefore, finding a doctor who is willing to add me to their practice is not so simple. When searching for a new physician, we must share the truth about our difficult journey, while also showing them that we are taking an active role in working to help ourselves. I have found that since it is hard to find an EDS-knowledgeable doctor, I instead search for one who is willing to listen to me, believe in me, and trust me—one who is willing to learn with me, to search for ways to improve the quality of my life with my condition. Framing my search in this way helps me find a match that is supportive and fulfilling for me. While it can be difficult to establish a doctor-patient relationship when you have chronic pain, your journey may help pave the way for the next patient who is also struggling with your condition. So what should you be prepared to share with a new doctor? I’ve found it helpful to bring the following: Medication list, including the dosage and date each was started Medication reaction list Any diagnoses you have been given, and the dates of diagnosis Dates and details of any body scans or imaging you’ve had done Dates and details of any surgeries or procedures you’ve had, and where they took place Insurance cards  Name and contact information of the pharmacy you use List of doctors who are presently working with you I am sure you have times of frustration living with your condition. And, as in my case, it’s possible a doctor won’t be able to cure you. But I have found that developing a kind and caring relationship with my doctors has made my visits pleasant, and the compassion they have shown me makes a difference in my care. Listening, believing, and caring for me means the world, and I have worked with each provider to create this type of relationship.  When you have found a good match with a provider who is willing to add you to their practice, consider, during your appointment, asking your doctor how they are doing. They tend to be initially shocked, but it brings on appreciation and a chance to get to know each other in a caring way that will help to nurture your relationship and mutual respect.  May life be kind to you… —by Ellen Lenox Smith Source link

What is menopause? Menopause occurs when you’ve gone 12 months without a period. Most women experience menopause between the ages of 45 and 58. The average age of menopause in the U.S. is 51 Natural menopause  The decline in female hormones that happens naturally with age.  Induced menopause When medical treatments like cancer treatments or surgery temporarily or permanently shut down the ovaries so they no longer make estrogen and progesterone.  Induced menopause happens quickly — within a few weeks or even overnight — and can cause early or premature menopause.  Premature menopause = Menopause before age 40 Early menopause = Menopause before age 45 Factors that cause or are associated with premature or early menopause Risks of early or premature menopause Living longer without the health benefits of higher estrogen levels may increase your risk for health problems like: Talk to your healthcare provider about your risk  If you think you may be at risk for early or premature menopause, talk to your healthcare provider. Together you can figure out a plan.  This educational resource was created with support from Bayer, a HealthyWomen Corporate Advisory Council member. Source link

Add topic to email alerts Receive an email when new articles are posted on Please provide your email address to receive an email when new articles are posted on . “ data-action=”subscribe”> Subscribe We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. Back to Healio Key takeaways: Martin Makary, MD, MPH, has reportedly resigned. Inconsistency was a major component of his tenure, an expert said. Martin Makary, MD, MPH, is resigning as FDA commissioner. Politico was first to report the news on Tuesday, citing an administration official who was granted anonymity. The official told Politico that HHS Secretary Robert F. Kennedy Jr. made a decision months ago to “move on from Makary,” but the president also had to sign off. Kyle Diamantas, JD, will now lead the FDA as an acting commissioner, according to Politico. Diamantas is currently the FDA’s deputy commissioner for human foods. The FDA has not yet responded to Healio’s request to confirm the reports. Arthur L. Caplan, PhD, a professor and founding head of the division of medical ethics at NYU Grossman School of Medicine, told Healio that “it’s clear there’s a lot of dissatisfaction with [Makary], and has been for some time.” “I think the main reason for that is he’s been inconsistent at times, trying to approve drugs or speed up pathways — at other times, hindering drugs or treatments for approval,” he said. “Patient groups don’t understand what the hang up is. They’ve been pushing hard against that. One thing the FDA needs is consistency. Manufacturers want it; they need to know where the goal posts are to enable them to get across the approval line. Patients want more and more to be allowed to take risks with things that look promising. He was very inconsistent in response to that wish.” The other issue, Caplan said, is that “other things have slowed down because of cuts in personnel. That makes the biotech and pharmaceutical industries very anxious. I think Trump himself has been for some time on the side of hurrying up drug approval processes. I’m expecting that’s what we’re going to see in the next nominee to be the commissioner: speed over, if you will, caution.” Editor’s Note: This is a developing story. Please check back soon for more details. For more information: Arthur L. Caplan, PhD, can be reached at primarycare@healio.com. Sources/Disclosures Source: Healio Interviews Reference: Disclosures: Caplan reports no relevant financial disclosures. Ask a clinical question and tap into Healio AI’s knowledge base. PubMed, enrolling/recruiting trials, guidelines Clinical Guidance, Healio CME, FDA news Healio’s exclusive daily news coverage of clinical data Learn more Add topic to email alerts Receive an email when new articles are posted on Please provide your email address to receive an email when new articles are posted on . “ data-action=”subscribe”> Subscribe We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. Back to Healio Source link

As life moves forward, many of us have dreams of the places and things we would like to see and experience through traveling. After our four sons grew up, my husband and I planned to visit every state in the United States, and then travel the world to see other countries and experience their cultures. But then life happened for us both, and those dreams had to be set aside. At the age of 54, as my health became complicated, it was determined that I had been born with Ehlers-Danlos syndrome. This led to over 28 corrective surgeries, four years in a wheelchair, many months of recovery, and continued daily work to cope with the condition as it progresses. Then, my husband started to experience his own health challenges about four years ago, which eventually led to his diagnosis of Parkinson’s disease. So he now also lives day to day, working to maintain the best quality of life possible as he copes with his progressive condition. We had never thought about having to add medical conditions to our lives, but here we were. So those dreams we’d always had of traveling became complicated—and, eventually, just not a reality. It’s natural to mourn certain losses when you have long-term, debilitating, and painful conditions. But when life throws you those lemons, you also have to learn to live with your new situation. It is not easy to watch others participate in simple activities in life that you once took for granted, but are no longer within your reach. But you also have to decide: Will you spend the rest of your life angry, hurt, frustrated, and feeling you were cheated? Or could you find ways to adjust and accept the new life you’re now facing? When we open our eyes and look at other lives, we can see there are so many forms of loss. Yours might be a medical condition to cope with. Someone else is coping with the loss of a parent at a young age, the loss of a dear friend, or a sudden loss of a job and housing. We are not the only ones trying to find our way in life on an unexpected journey. Since our dreams of traveling were no longer a reality for us, what I decided to do is to travel through others’ eyes. This may sound silly, but when someone I am connected with tells me they are traveling somewhere, I always ask them to share photos with me and to tell me about their adventures. I want to experience the world, and this seems to be the best way I can do it safely. My sister and her husband took a trip of a lifetime recently, and I “traveled with them” to Antarctica. I joked about finding a suitcase they could sneak me into so that I could tag along, but reality meant staying at home. Still, while I wasn’t there in person, hearing their stories and seeing their photos took me on this journey, too. You might be like us and also find traveling just too difficult with the progression of your condition. But give this a try: Find fun with the travels of a friend or family member, and allow yourself to dream you were there as you see the world through their eyes. Try to make the lemon into lemonade, as the old saying goes. Show others that despite your challenges in life, you can live, breathe, and travel in your own way! This may be one way to help you be identified not by your condition, but instead as you—the person you are. May life be kind to you… —by Ellen Lenox Smith Source link

Mujeres de todas las edades pueden contagiarse del VIH, incluyendo las de más de 50 años 1 de cada 4 personas que viven con VIH en Estados Unidos es mujer Más de 1 de cada 2 diagnósticos nuevos de VIH son para personas de más de 50 años Las mujeres mayores tienen más posibilidades que mujeres más jóvenes de recibir un diagnóstico de esta enfermedad en etapas posteriores , posiblemente porque no saben que tienen riesgo Recibir el diagnóstico en etapas posteriores incrementa el riesgo de enfermedades relacionadas con el VIH y de morir por este trastorno ¿Qué efecto tiene la menopausia en el riesgo del VIH? Las mujeres de más de 50 años siguen teniendo relaciones sexuales En un estudio reciente, 1 de cada 2 personas de más de 50 años reportó haber tenido relaciones sexuales la semana anterior. Puesto que el embarazo ya no es una preocupación para mujeres posmenopáusicas, ellas podrían no pensar en tener relaciones sexuales con protección o en hablar de eso con sus parejas o proveedores médicos. Esto significa que las mujeres podrían ser menos propensas a usar preservativos para protegerse del VIH y de otras infecciones de transmisión sexual después de la menopausia. Pero las mujeres en la perimenopausia y posmenopausia podrían tener más riesgo de infectarse con el VIH. Los cambios hormonales pueden hacer que la vagina se haga más estrecha y seca, lo cual hace que el tejido vaginal sea propenso a desgarres, y eso incrementa el riesgo de que el VIH ingrese al cuerpo durante relaciones sexuales. Algunas mujeres mayores (y sus proveedores de atención médica) atribuyen cambios de la salud a la menopausia cuando podrían causarlos algo más. Por ejemplo, los sudores nocturnos son un síntoma clásico de la menopausia, pero también son comunes para personas con VIH. La prevención del VIH durante la menopausia y años posteriores Ninguna edad es demasiado avanzada para protegerte del VIH. Empieza con estos pasos proactivos: Usa preservativos si no sabes si tu pareja tiene VIH o no Hazte pruebas de detección del VIH Habla con tu proveedor de atención médica acerca de PPrE (profilaxis previa a la exposición) , medicamento que puede prevenir el VIH. Este recurso educativo se preparó con el apoyo de Merck. Source link

by Dr Yuri Gorelik (Frontline Gastroenterology Global Taskforce 2025-6)   Since the introduction of ChatGPT 3.5 in November 2022, artificial intelligence (AI) and specifically large language models (LLMs) have been set to revolutionize our daily and work life. Multiple LLM based GI utilities have been developed and researched. In this blog post I will try to provide a mini review in the form of a description of a GI practitioner workday powered by such LLM based utilities and products. Many of the specific LLM applications and use-cases I mention below are discussed in Frontline Gastroenterology’s narrative review of generative AI in colorectal practice (Frontline Gastroenterology, 2025). Morning Clinic Upon arrival at the clinic all previous follow-ups and clinic referrals for the clinic patients on your list are already summarized by one of the multiple published tools for such tasks. Soon after, the patients start to come in, all history taking and patient communication is scribed by an LLM such as the Google health medical speech to text tools (Google cloud). This text is also transformed into a structured text with clinical terms and specific disease-centered classifications. In IBD, multiple sources of medical data (notes, endoscopy, imaging) contain abundant unstructured information and such tools showed high accuracy in the identification and structuring of these texts. The need for natural language processing of IBD patient data was previously highlighted in Frontline Gastroenterology’s review on AI in IBD (Frontline Gastroenterology, 2022). Finally, each clinic comes down to patient recommendations and these are derived with the assistance of multiple LLM based decision support tools that provide recommendations based on the summary of the structured visit in the context of the relevant guidelines. Such tools can be extremely useful across multiple fields of GI, often where guidelines are inconsistent or complex and where clinicians must integrate multiple data sources with the current patient’s clinical data. Even common clinic complaints such as functional dyspepsia require integrating multiple symptoms and clinical data for optimal work-up and treatment, as described in a recent Frontline Gastroenterology guidance (Frontline Gastroenterology, 2025). Care is extended as the patients leaves with a link to chatbots that can answer questions specific to his condition. Afternoon in the Endoscopy Suite On to the endoscopy suite. Your list allows open access endoscopy received from multiple referral sites. These referrals should be evaluated to decide on appropriate settings, medication management, and type of preparation. At your location the referrals are managed by an LLM based tool which already analyzed the referrals and identified the requested procedures, the indications, pre procedural medication management (anti-coagulants, GLP-1 receptor agonists, etc.) and type of bowel preparation. Patients who come in for a procedure are well informed since a chatbot already addressed multiple concerns and questions they had regarding their upcoming colonoscopy. Just like at the clinic, during colonoscopy, you narrate findings, while an AI tool transcribes the report with high accuracy, and as clinic notes these reports will include LLM generated, guidelines-based recommendations. The patient will get an automatically generated concise letter explaining the findings and forward recommendations. Of course, the entire endoscopy is AI powered with various pathology detection and diagnosis tools, but this is a subject for a different post. Prior to heading home, you can deidentify your clinic notes and endoscopy reports from the day to a research AI agent, which is provided by all large models to look up or summarize any patient specific evidence that was not covered in guidelines or large reviews and evaluate some additional possibilities for patients. Guideline preparation in gastroenterology was already shown to benefit from augmentation with LLM-powered systematic reviews (using deep research AI tools such as those provided by all the major LLMs). If you are in a hurry, you can convert the findings to an audio podcast, using tools such as NoteBookLLM, to listen to on your way home. In summary, AI and specifically LLMs are set to revolutionize and potentially improve every aspect of our daily work as gastroenterologists, and the possibilities keep expanding. Worth mentioning that LLMs can also enable us to perform research by providing statistical and epidemiological advice and implementation and empower us to create our own tools with models that can automatically convert your prompts to apps (see vibe coding). Now briefly go over the daily description above and consider “is a human gastroenterologist really needed here and where?”, and if you are thinking “clearly in the endoscopy part” then robotics also has some surprises coming. (Visited 227 times, 1 visits today) Source link

By Jennifer Hess and Samantha Wladich, Riemer Hess LLC Living with chronic pain usually means adapting—again and again. People adjust schedules, modify tasks, try new treatments, and push through symptoms over and over. Many continue working not because they are well, but because they are trying to hold things together. When work finally becomes unsustainable, the long-term disability (LTD) process can feel confusing and discouraging. Pain conditions are frequently misunderstood in insurance reviews, and the way claims are evaluated often fails to reflect what daily life with chronic pain actually looks like. This article offers a general, educational look at how long-term disability claims are commonly evaluated for people living with chronic pain—and why those claims can be so difficult. Important note: This article is for general educational purposes only. It is not legal advice and is not a substitute for guidance specific to an individual’s situation or insurance policy. Hear more from these experienced attorneys during a FREE webinar, “Preparing for Your Long-Term Disability Claim,” at 1 p.m. ET on Tuesday, March 10. Register today. Why Chronic Pain Disability Claims Are So Often Challenged One of the biggest problems in pain-related disability claims is that pain often does not behave the way insurers expect disability to behave. Chronic pain can: fluctuate worsen with activity improve briefly and then return limit endurance, not just strength Insurance reviews, however, often look for steady decline, clear-cut test results, or visible impairment. When those markers are missing or unclear, insurers may conclude—incorrectly—that someone is still able to work. This disconnect is one reason long-term disability claims involving chronic pain often face higher scrutiny. A Common Scenario: When Working Through Pain Stops Working Consider this example, which reflects a pattern many people with pain will recognize. A professional living with chronic spinal pain continues working while undergoing physical therapy, medication changes, and injections. At first, they shorten their workday and recover at night. Over time, therapy triggers flares instead of relief. Medication causes brain fog. Recovery stretches into the next day. Sleep deteriorates. From the outside, it looks like they are still “functioning.” On paper, treatment is ongoing. But behind the scenes, the effort required to work becomes unsustainable. When work finally stops, insurers often ask:Why now?Why stop work if treatment was ongoing? Without context, the timing can be misunderstood. Function Matters More Than Diagnosis in Long-Term Disability Claims In most long-term disability claims, the diagnosis itself is not the deciding factor. Insurers focus instead on function. For people living with chronic pain, that usually means questions like: How long can you sit, stand, or walk? How often do symptoms flare? What happens after physical or cognitive exertion? How much recovery time is needed? Can this be repeated day after day? Someone may be able to complete tasks in short bursts and still be unable to meet the demands of regular, full-time work. Disability evaluations do not always capture that distinction unless it is clearly documented. Why ‘Trying Harder’ Isn’t the Same as Capacity A recurring theme in pain-related claims is the assumption that effort equals ability. In reality, chronic pain often limits: duration frequency consistency recovery People may push through pain at work for many reasons—financial pressure, professional identity, fear of losing benefits. That effort can later be misread as proof that work was sustainable. Understanding the difference between what can be done briefly and what can be done reliably is central to understanding disability in chronic pain-related cases. Variability Is Normal in Chronic Pain — Not a Red Flag Many people with chronic pain have good days and bad days. That variability is often used against them. Insurance reviewers may interpret fluctuating symptoms as: inconsistency exaggeration improvement In reality, variability is often one of the defining features of chronic pain. Short periods of relief do not mean the condition has resolved, especially when those periods are followed by flares or prolonged recovery. Clear explanation of symptom patterns over time helps prevent this misunderstanding. Why Baseline Function Matters When Disability Follows Treatment For many people, disability does not begin at diagnosis, or at the onset of undiagnosed symptoms or pain. It begins later—after months or years of treatment attempts and symptom progression. A baseline helps show: what functioning looked like earlier how endurance declined how treatment affected symptoms over time This matters because insurers often assume that treatment leads to improvement. When work ends after treatment begins, baseline documentation helps explain that disability developed despite care, not because care was avoided. Objective Evidence and Chronic Pain: What Insurers Look For In the disability context, “objective evidence” generally means information beyond self-report alone, such as: imaging exam findings functional testing documented observations by providers This does not mean pain must show up clearly on a scan to be real. Many pain conditions do not lend themselves to definitive test results. Still, insurers often weigh claims more heavily when some objective support exists—especially when policies scrutinize conditions labeled as “subjective,” which is often the case for pain-related diagnoses. Objective evidence is most effective when paired with clinical explanation and functional context. Treatment Does Not Always Mean Recovery Many people living with chronic pain are deeply engaged in treatment long before disability becomes an issue. Insurers sometimes interpret continued treatment as proof that improvement should follow. In reality, chronic pain treatment often focuses on: management symptom reduction preventing decline Ongoing treatment does not guarantee restored work capacity. Modifying or stopping treatment can also be medically appropriate, particularly when side effects outweigh benefits or progress plateaus. The Question Disability Claims Are Really Asking: Sustainability Whether a policy applies an “own occupation” or “any occupation” standard, the real question is the same: Can this person work reliably and sustainably over time? For people living with chronic pain, the answer often hinges on endurance, recovery, and consistency—not whether isolated tasks are possible. Final Thoughts Long-term disability claims involving chronic pain are often difficult—not because pain is unclear or insignificant, but because the claims process does not easily account for

Women of all ages can get HIV — including those over 50 1 in 4 people living with HIV in the United States is a woman. More than 1 in 2 new HIV diagnoses are in people above age 50. Older women are more likely than younger women to be diagnosed at a late stage of the disease — possibly because they don’t know they’re at risk. Later diagnosis of the disease increases the risk of HIV-related illnesses and dying from the disease. How might menopause affect HIV risk? Women over 50 still have sex. In a recent study, 1 in 2 people over the age of 50 reported having sex in the last week. Since pregnancy is no longer an issue for post-menopausal women, they may not think about safe sex — or talk about it with their partners or providers. This means women may be less likely to use condoms to protect themselves from HIV and other sexually transmitted infections after menopause. But women in peri- and post-menopause may be extra vulnerable to HIV infection. Hormonal changes can cause vaginal thinning and dryness, leaving vaginal tissue prone to tearing — which increases the risk of HIV entering the body during sex. Some older women (and their healthcare providers) chalk health changes up to menopause when they could be something else For example, night sweats are a classic menopause symptom — but they’re also common in people with HIV. Preventing HIV through menopause and beyond You’re never too old to protect yourself from HIV. Start with these proactive steps: Use a condom if you’re not sure about your partner’s HIV status. Get tested for HIV. Ask your HCP about PrEP (pre-exposure prophylaxis), medication that can prevent HIV. This educational resource was created with support from Merck. Source link

Add topic to email alerts Receive an email when new articles are posted on Please provide your email address to receive an email when new articles are posted on . “ data-action=”subscribe”> Subscribe We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. Back to Healio Key takeaways: A “top-down” infliximab/immunomodulator therapy reduced long-term risk for abdominal surgery vs. a “step-up” approach in newly diagnosed Crohn’s. It also lowered risk for disease progression and hospitalization. CHICAGO — Early treatment with infliximab and an immunomodulator was associated with more than five times reduced risk for abdominal surgery at 5 years among patients with newly diagnosed Crohn’s disease, according to a presenter. Follow-up PROFILE trial data presented at Digestive Disease Week showed that early control of inflammation during a 48-week treatment period also lowered long-term risk for disease progression and hospitalization. Nurulamin “Nuru” Noor, MD, speaks at Digestive Disease Week. Image: Robert Stott. “Historically, there has been a reluctance among some clinicians to use a ‘top-down’ approach due to potential concerns about overtreatment,” Nurulamin “Nuru” Noor, MD, clinical lecturer in gastroenterology at University of Cambridge, said at the presentation. “Over 5 years follow-up, we found no difference in safety outcomes between the two groups, either for serious infections or malignancies. “Patients receiving ‘top-down’ infliximab from diagnosis had a more than five times lower risk of Crohn’s disease-related abdominal surgery.” Prior data from the randomized, controlled PROFILE trial showed improved clinical outcomes at 48 weeks for patients who received the “top-down” therapy approach with infliximab and an immunomodulator compared with an accelerated “step-up” strategy, or conventional treatment. Noor and colleagues followed 386 participants for a median 5 years after the 48-week visit to evaluate whether early treatment can impact long-term outcomes of Crohn’s disease. They reviewed medical records for abdominal surgeries, hospital admissions and disease progression. Follow-up data were available for 358 patients (93%), of whom 182 received top-down therapy and 176 received step-up therapy. Analysis showed 28 Crohn’s-related abdominal surgeries were required among patients who received step-up therapy compared with six surgeries among those who received top-down therapy (adjusted HR = 5.23: 95% CI, 1.99-13.76). Time to surgery also was earlier in the step-up group. Patients who received top-down therapy were about 2.5 times less likely to experience disease progression and two times less likely to be hospitalized. “Our data suggest that the course of Crohn’s disease can be modified with therapy and this should be considered the standard of care,” Noor said. Published by: Sources/Disclosures Source: Noor N, et al. Profile trial 5-year disease modification outcomes. Presented at: Digestive Disease Week; May 2-5, 2026; Chicago. Disclosures: Noor reports educational or travel grants and/or speaker fees from AbbVie, Bristol Myers Squibb, Celltrion, Falk, Ferring, Johnson & Johnson, Eli Lilly and Co., Medfyle, Pfizer, Pharmacosmos, Spyre, Takeda and Tillotts Pharma. Please see the study for all other authors’ relevant financial disclosures. Ask a clinical question and tap into Healio AI’s knowledge base. PubMed, enrolling/recruiting trials, guidelines Clinical Guidance, Healio CME, FDA news Healio’s exclusive daily news coverage of clinical data Learn more Add topic to email alerts Receive an email when new articles are posted on Please provide your email address to receive an email when new articles are posted on . “ data-action=”subscribe”> Subscribe We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. Back to Healio Source link

English + Infographic text Slide 2: VRS es la sigla del virus respiratorio sincitial. Es un virus común que causa infecciones en el pulmón y en las vías respiratorias. El VRS usualmente empieza a propagarse en el otoño y llega a su punto máximo en los meses invernales. Slide 3: La mayoría de personas experimentan síntomas moderados similares a los de la gripe y se recuperan en 1 o 2 semanas. Rinitis Congestión Tos Estornudos Sibilancia Fiebre Apetito reducido Slide 4: Pero algunas personas, especialmente bebés y adultos de edades avanzadas, pueden tener infecciones más graves y el VRS podría ser mortal. Las complicaciones que pueden causar dificultad para respirar incluyen: Infecciones de las vías respiratorias Bronquiolitis Neumonía Hipoxia (niveles bajos de oxígeno) Deshidratación Ataques cardíacos y accidentes cardiovasculares Slide 5: Puedes controlar los síntomas del VRS: Tomando antifebriles de venta sin receta Bebiendo muchos líquidos Descansando Si tienes hipertensión o si tomas medicamentos de venta con receta, asegúrate de hablar con tu proveedor de atención médica antes de tomar medicamentos de venta sin receta. Slide 6: El VRS puede empeorar trastornos pulmonares subyacentes tales como EPOC y asma. Las personas que tienen esos trastornos podrían requerir tratamientos para brotes si se contagian del VRS. Slide 7: Habla con tu proveedor de atención médica o ve a una sala de emergencias si: Tienes dificultad para respirar No puedes comer o beber Tienes dolor de pecho Slide 8: La prevención es la mejor medicina. Vacunarse es la mejor forma de protegerse de trastornos respiratorios graves. Slide 9: Las vacunas contra el VRS se recomiendan para: Bebés Adultos de 75 años o más Adultos entre las edades de 50 y 74 años que tienen un mayor riesgo de infecciones graves del VRS Slide 10: Logo Este recurso educativo se preparó con el apoyo de Moderna. Source link