Hillcrest HealthCare System’s Post

A story of medical excellence & hope: Couple's journey from 9 miscarriages to a healthy baby, via @DeccanChronicle https://lnkd.in/gG7J-FNF

When I was 19, I visited my doctor, fed up after 5 years of putting up with a plethora of painful symptoms my friends never got with their periods. I left with: ❌ A prescription for the pill, ❌ (incorrect) advice about getting pregnant sooner rather than later to cure my symptoms (I was single, a teenager, and not at all interested in having children), ❌ a little bit of shame for seeking help. In my early 20s, a friend at university told me about endometriosis. By the time I was 24 — after a decade of missing events (including my own 21st birthday celebration) and struggling to keep up with work and uni while constantly in pain — I decided it was time to revisit my doctor armed with this new word. Since then, I have been diagnosed with endometriosis, had some emergency room visits due to ovarian torsion and internal bleeding, and had two surgeries, drastically different in levels of skill and post-surgery relief. In an article I wrote for Endometriosis Australia, I share some lessons I have learnt along the way that I hope may help someone newly navigating the disease. ✅ Listen to your body. ✅ Keep a journal of your symptoms and take this to medical appointments. ✅ Educate yourself.  ✅ Keep seeking until you find the right specialist for you. ✅ If possible, find a teaching endometriosis specialist. ✅ If it feels right to you, explore alternative therapies and treatment options You won’t uncover the magnitude of what I’ve been through in this article — that isn’t my focus. I hope that anyone who reads the article feels a bit more informed. There is power in knowledge — arm yourself with it. Link in comments. #Endometriosis #EndometriosisAwarenessMonth #PelvicPain #MentalHealth #Knowledge #WomensHealth

Seattle Children's is giving new hope to epilepsy patients with a cutting-edge procedure called responsive neurostimulation (RNS). This innovative treatment involves placing a battery-powered device in a patient’s skull to detect and stop seizures. Dr. Stephanie Randle and Dr. Jason Hauptman highlight that RNS is a game-changer for children who haven't found relief with other treatments. Seattle Children’s is the only center in the Northwest offering this advanced option, showing promising results with significant seizure reductions for many patients. [Image description: Image of a smiling epilepsy patient in a hospital bed. There is another woman smiling at her bedside.] #DaretoBeRare #PatientEmpowerment #HealthcareSolutions #PatientSafety #BeAnythingButOrdinary #LifeWithoutLimits #ChallengeWhatsPossible #PatientEmpowerment #DreamBigWithGusGear #GusGearAcrosstheGlobe https://bit.ly/4clqnta

For Heart Month's #HeartFailureAwarenessWeek, I want to re-share a pivotal chapter of my journey, not just as a physician but as a patient and advocate for people with heart failure. Five years ago, during my Emergency Medicine residency, my life took an unexpected turn. Despite enduring 12-hour shifts and maintaining a semblance of normalcy, a persistent cough and shortness of breath led me to the ER one day and the rest is history. I was suddenly battling severe end-stage heart failure. The diagnosis was a shock and threatened to steal everything I'd worked so hard for. My condition meant an inpatient stay in the cardiac ICU, clinging to life and the hope of a heart transplant. The situation was dire; I was placed on the transplant waiting list immediately. There was constantly a palpable sense of hope mingled with desperation. That’s what I remember the most. A couple of weeks later, my life was irrevocably changed thanks to a heart transplant. My organ donor had been a young woman named Lucy. She’d had aspirations in healthcare, much like myself. This second chance at life was not only a personal victory but a story of hope for those with heart failure. Discharged before the end of January 2019, I was reborn… armed with a new heart and a renewed purpose. The root of my heart failure-- familial dilated cardiomyopathy-- was something that I had unknowingly carried. Recovery was arduous, yet it was marked by determination and a HUGE commitment to return to medicine. Now, having completed my training in Emergency and Critical Care Medicine, I've dedicated my career to advocating for and managing critically ill patients, including many with heart failure. My experiences have given me a unique understanding of patient care and the healthcare system as a whole. My story is not just mine but belongs to every person facing heart failure AND to every clinician striving to make a difference in this field. It's a call to action, to advocate for policies that ensure no one is left behind in their fight against heart failure. Happy HF Awareness Week! #HeartFailureAwareness #NewBeginnings #Docswithdisabilities

Accompanied by insights from our Medical director, Dr. Dohadwala, Melissa Rudy for Fox News Media shares Cheryl Jordan Winston's #SurvivalStory after 25 minutes without pulse due to sudden cardiac arrest. Dr. Dohadwala underscores, 'Sudden cardiac arrest is common and often occurs without warning.' Winston's survival, attributed to CPR and swift medical intervention, highlights the critical need for awareness of proactive health measures. Read the full story below: https://lnkd.in/gD_cq3ZD #proactivehealthcare #suddencardiacarrest #healthawareness

Infantile Idiopathic Scoliosis (IIS) is a rare condition affecting children aged three or younger. 🧒 It represents only 1% of pediatric idiopathic scoliosis cases.  IIS causes a curvature of the spine, leading to deformities and impacting the child's quality of life.   Early detection is crucial for prompt intervention. 👍 Signs include uneven shoulders, prominent shoulder blades, or asymmetrical waistlines. 🏥 At Squareone Health, we follow SOSORT guidelines for IIS treatment. 🩺 Our screenings involve visual checks, physical assessments, and imaging to create personalized treatment plans. 💪 Early detection leads to better outcomes. 📋 Choose Square One Health for customized care and support.  Schedule a free scoliosis screening today to ensure a healthy future for your child. 📅 #NaturalPainRelief #PainFreeLiving #WellnessCare #PersonalizedMedicine #OptimizeYourHealth #FortCollinsColorado #ChiropracticCare #ChiropracticAdjustment #SpinalHealth #PhysicalTherapy #NeuropathyTreatment #HormoneReplacementTherapy #AdvancedTechniques #IntegratedHealthcare

CONGENITAL HEART DEFECT WEEK : 🎗️ During Congenital Heart Defect (CHD) Awareness Week, we unite to shed light on the impact of CHD and support individuals and families affected by this condition. From February 7th to February 14th, let's raise awareness, share resources, and celebrate the resilience of CHD warriors worldwide. I urge everyone to learn more about CHD, the most common birth defect affecting newborns globally. Despite advancements in diagnosis and treatment, CHD remains a significant health challenge for many individuals and families. Throughout this week, let's: Educate: Spread awareness about CHD by sharing accurate information, facts, and personal stories. By increasing understanding and empathy, we can help reduce stigma and support those living with CHD. Empower: Empower individuals with CHD and their families by connecting them with resources, support groups, and healthcare professionals. Together, we can navigate the challenges and triumphs of living with CHD. Advocate: Advocate for policies and initiatives that prioritize CHD research, early detection, access to quality healthcare, and support services. By raising our voices, we can drive positive change and improve outcomes for CHD patients worldwide. Celebrate: Celebrate the strength, courage, and resilience of CHD warriors, caregivers, and healthcare providers. Every milestone, big or small, deserves recognition and celebration. Let's come together as a community to raise awareness, offer support, and inspire hope during Congenital Heart Defect Awareness Week. Together, we can make a difference in the lives of those affected by CHD. 💙 #CHDAwarenessWeek #HeartWarriors #TogetherWeAreStronger

Get your eye exam!

An incredible survival story with some important takeaways: 1) CPR saves lives, 2) know the signs a cardiac emergency and take action, 3) women need to be aware of how symptoms may present differently for them, 4) miracles happen https://lnkd.in/gnw8Vvim

When you have a rare disease such as myasthenia gravis, it is critical that you make the most of your doctor appointments by asking the right questions and being prepared. Medical resources and time are so short these days, so having the right approach will help you better manage your #MG. Check out this informative blog and webinar from Dr. Heather Finlay-Morreale. #MGFA #myastheniagravis https://lnkd.in/e5PEgzS8