EmPower_Hart

EmPower_Hart

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Advocating, educating and providing community support for chronic and rare disease patients. IG @Empower_hart

Photos from EmPower_Hart's post 05/18/2024

Hey Warrior Fam! Exciting news alert! 🚨 Introducing the Diagnosis Dilemma Podcast 🎙️ 🙌🏻 Get ready for a weekly dose of LIVE episodes every Monday. Drawing inspiration from the gripping Netflix series "Diagnosis," we're here to tackle the challenges of obtaining a proper diagnosis for rare symptoms. Each week, individuals share their stories, and we'll help compile and share them on our website for crowdsourcing. Our mission? Connecting those with similar symptoms worldwide, aided by guest medical professionals steering the conversation in the right direction. While we won't diagnose, we aim to unite patients and experts, fostering support and guidance. Plus, delve into the realities of living with rare/chronic/invisible illnesses: from nutrition's impact to combating medical gaslighting. Need advice on migraine pillows? We've got you covered! If you're part of the chronic illness community, let's rally together. Tune in live, and join the conversation by calling us at 855-931-4747, or reach out to Emily (me) via email at: [email protected]. If you'd like to submit your story, please send an email with your name, best phone number to reach you, as many details as you feel relevant. **Please only submit if your comfortable sharing this with the public**

Join us on this journey of support and empowerment! Scan the QR code, hit the link, in bio, or visit bit.ly/4aXVeeO to join the Podcast. Let's make a difference, one story at a time. 🎗️🙏🏻 See you Monday! 🦓 💜

07/17/2023

Treatment day! It's important for me to stop and give a dose (pun intended 😂) of reality and look into my real life. While I try to remain a constant ball of positivity on social media, the fact remains I'm still dealing with serious medical issues in real life. I'm extremely proud of the fact I continue to work everyday and push myself sometimes beyond what I'm supposed to, but I don't want to give a false sense reality either. I know there are others who struggle with similar conditions and situations, and it's extremely important to me that I don't cause them to feel like they should be doing more because they see me running around in my posts - I have PLENTY of moments where I curl up in a ball and have a total breakdown. There's a fine line between making people aware of what you're going through to try to motivate and inspire others, and saying too much to where they think you're complaining and don't want to listen to your 💩 So thank you for allowing me to share this vulnerable and not so "pretty" side of me today, I just feel it's very important the world sees both. 🙏

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