Epic Staffing Group’s Post

"Never stop trying. Never stop believing. Never give up.  Your day will come." - Mandy Hale 💙 It is so important to celebrate the small steps in life.  Small steps can open the doors to change just so long as we keep moving.  For the first time - EVER - a major medical organization, The American College of Obstetricians and Gynecologists, has created clinical practice guidelines for PMDD!  It may be just one step, but what an important step for PMDD awareness! @acog_org We are so proud to be a reference and hope that many more sufferers will find their way to our IAPMD resources because of these new guidelines. We appreciate all of you who share our social posts and web links, make donations, organize fundraisers, provide IAPMD resources to local dr offices and on bulletin boards, talk to your peers about us, sign petitions, lobby, etc. And so, IAPMD celebrates our AMAZING community! Thanks to all of you who have so passionately contributed to bringing about change for those with premenstrual disorders!  🎉 And if you haven't already, take a moment to donate the cost of one cup of coffee. Our donation link for Giving Tuesday is still open through the weekend, and we could really use your help to reach our goal of $2000. We're not quite halfway there. iapmd.org/links ☕️ Here's to more research, education, advocacy, and treatment options!  Remember - you deserve to feel good! #feelgoodfriday 💙 #pmdd #pme #pms #change #friday #pmddpeeps #networkforgood #pmddresearch #research #myperiod #givingtuesday #premenstrualhealth #premenstrual #treatment #awareness #pmddawareness #nevergiveup #moods #mentalhealth #thefutureisbright #trackyourcycle #grateful #suicideprevention #Gynecologists #Obstetricians #menstrual

Eleven years ago, I was diagnosed with Crohn's disease. As a young person with IBD, I struggled to find resources and support. But I wasn't alone. Millions of young people around the world are living with IBD, and many of them feel isolated and misunderstood. That's why I started IBD Hero, a student-led organization dedicated to supporting young people with IBD. We believe that everyone with IBD deserves to live a full and happy life, and we're working to create a world where IBD is no longer a mystery and where everyone with IBD has the support they need to thrive. We are planning to offer a variety of programs and services for young people with IBD, including the following: - Connect with other young people with IBD from all over the world - Participate in support groups and mentorship programs - Access educational resources about IBD - Help to raise awareness of IBD But we can't do it alone. We need your help to reach more young people with IBD and provide them with the support they need. Here are two ways you can help: - Join our mailing list to stay up-to-date on our latest news and events: https://ibdhero.me/ - Interact with this post by reposting, liking, commenting, or sharing it. The more people who see this post, the more young people we can reach. Together, we can make a difference in the lives of young people with IBD. Thank you for your support! Hashtags: #IBDHero #CrohnsDisease #UlcerativeColitis #IBD #Nonprofit #YoungAdults #CollegeStudents #Support #Community #Students

Share this as a reminder for all the Warriors you know! Nothing can stop you from thriving, not even RA! On rheumatoid arthritis awareness day we raise awareness for RA, but let's talk about what the facts don't say about autoimmune disease. That's why I started my non-profit, Inflamed Sisters Thriving. To provide a community where women, no matter their health journey, can aspire to achieve their goals in health and business goals together while supporting diversity and inclusion in medical research. We may be inflamed, but we are still here! And as long as we are here, we might as well thrive together. Join a community that thrives and is not defined by chronic illness. Follow Inflamed Sisters Thriving Inc. and become a founding member of our community. DM me THRIVE to learn more! Link in bio. https://lnkd.in/e-9Ffiwb #thrive #inflamedsistersthriving #rheumatoidarthritisday #rheumatoidarthritisawarenessday #inflamed #communityforwomen #nonprofitcommunity #foundingmember #aspire #diversityandinclusion #dei #medicalresearch #raawarenessday #rawarrior #autoimmunediseaseawareness #autoimmunediseaseadvocacy

Education is a powerful tool for empowering rare disease patients and caregivers. MSU provides a variety of resources to help you navigate your myositis journey, from our detailed "Simply Put" series to video education sessions with expert insights. You'll also find education, awareness, and self-advocacy tips on our social media platforms. But there's more! Learning from the experiences of others can offer a relatable and personal perspective. Through our online support groups and patient-led video education sessions, you can connect with peers to share knowledge and find support. We're committed to helping myositis patients and caregivers gain the knowledge they need to advocate for their health effectively. Visit our education hub at https://lnkd.in/e7t4VNMJ to learn more about myositis. Join us in our mission to support myositis patients, caregivers, and care partners. Whether you donate, volunteer, or spread awareness, every action makes a difference. Together, #SupportStartsHere for everyone in our community. Visit https://lnkd.in/eP6XRqhd to take part in our fundraising campaign. Your contribution will immediately impact our efforts to combat isolation, improve mental health, and offer vital education and support programs. Let's lift the burden of this disease together! #MyositisAwareness #SupportStartsHere

#DysautonomiaAdvocacyDay - March 12th The focus of Dysautonomia Advocacy Day 2024 will be raising awareness about #autonomic disorders, and advocating for a $10M federal investment in physician education on autonomic disorders. #dysautonomia #dei #inclusion #awareness #noisefortorquoise

Discover how charities bridge the gap between patients and innovators . . .   In this episode, I am joined by Caroline Morrice, CEO of GAIN (Guillain-Barré & Associated Inflammatory Neuropathies).   We explore the profound impact of working with technology to support patients facing neurological conditions.   Dive into the most critical issues that demand our attention when it comes to enhancing the patient experience and driving innovation.   Listen here >> https://lnkd.in/expiNaKh   #MedTechForBeginners #PymsConsultancy #PymsPodcast #NHS #Medtech #PatientSupport #InnovativeSolutions #HealthTechImpact

World MS Day, a day of global solidarity, collective action and hope. The international awareness day aims to bring the global Multiple Sclerosis community together to share stories, raise awareness and campaign for change. The theme for this year is 𝗠𝘆 𝗠𝗦 𝗗𝗶𝗮𝗴𝗻𝗼𝘀𝗶𝘀: 𝗡𝗮𝘃𝗶𝗴𝗮𝘁𝗶𝗻𝗴 𝗠𝗦 𝘁𝗼𝗴𝗲𝘁𝗵𝗲𝗿. We want to be talking about accurate and early diagnosis, overcoming global barriers to diagnosing and better training for healthcare professionals. Multiple sclerosis (MS) is one of the most common neurological diseases. Today, an estimated 2.9 million people around the world have MS. So do what you can to get informed and show your support - visit: https://bit.ly/3R1ZGRz for some ideas! As for us, we support MS clients daily and we invest in our clinicians' expertise in this area through professional development and mentoring. Additionally, a few keen walkers in our team have done the May 50K challenge to raise funds and awareness for crucial MS research! So far, we've clocked over 1000kms and raised over $500 - and we're still going!🚶 #MyMSDiagnosis #WorldMSDay #May50K

It all started 20 years ago when a conversation between two Australian friends, Travis Garone and Luke Slattery, sparked a worldwide phenomenon. They didn't just grow mustaches for fun - they ignited a movement for a vital cause. Today, Movember is more than just about mustaches; it's a global movement for men's health, addressing prostate and testicular cancer, mental health and suicide prevention. Since launching its website in 2004, Movember has grown into a community of over 6 million people. Together, they participate in the campaign, funding over 1,200 innovative health projects related to men's health in over 20 countries. Every November, men let their facial hair grow, not merely as a style statement, but to spark conversations, drive donations and fund life-saving research. It's a month where mustaches become a symbol of hope and solidarity. Movember and No-Shave November, often intertwined, represent more than just forgoing the razor. They symbolize a commitment to creating lasting change in the face of men's most significant health challenges. #Movember #MensHealth #ProstateCancerAwareness #MentalHealth #NoShaveNovember #OncologyCompass

Managing Alzheimer’s disease can be stressful for patients, caregivers and loved ones. Organizations such as Alzheimer’s Society are doing wonders to raise awareness and rally support.   But what can you do?   🌼 Share a social media post today - September 21 - using the hashtag #WorldAlzheimersDay 🌼 Register to volunteer at a local Memory Walk 🌼 Organize or take part in a fundraising event 🌼 Make a donation to support people living with dementia   For more information, head to: www.alzheimers.org.uk    #WorldAlzheimersDay #dementiacare #innovation #healthcareinnovation

Advocacy Matters! Let your voice be heard!