🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

Pete McCluskey, ME/CFS advocate, discusses the issues of ME/CFS on the "Conditional Release Program" podcast. Join the conversation and raise awareness: redcircle.com/shows/tcrp.

Huge thanks to our #MECFS & #LongCOVID community for your support & generous donations. Big shout-out to Shiloh for sharing her journey, highlighting the importance of this cause. Stay tuned for upcoming events! #ThankYou #CampaignSuccess

Emerge Australia honours NAIDOC week, celebrating the endurance and contributions of Aboriginal and Torres Strait Islander people, aligning with our advocacy for complex hidden illnesses. Let's respect the world's oldest living cultures.

🩺 Join our Live Education Session w/ our Nurse at 2 PM (AEST) today! Topic: Post-exertional malaise (PEM). Get answers and personalised health guidance. Complements our self-paced learning module. Register now: vist.ly/3n8siuw 💡✨📅

Missed our webinars last year? Visit our free online clinical education space for ME/CFS and long COVID. The first two recordings are available now: 1. Assessment and Diagnosis 2. Managing Symptoms and Co-Morbidities For clinicians: education.emerge.org.au

Donate blood to AusME Biobank and accelerate ME/CFS and long COVID research! If in NSW/VIC and have these conditions or are a willing volunteer, join at vist.ly/3n8xtkr.

Explore our Accessibility Tools! Adapt for your needs: Text Size, Grayscale, High Contrast, Negative Contrast, Light Background, Underlined Links, & Readable Font. Available site-wide. Feedback? Email [email protected]. Let's make web accessible for all!

Share your experiences of living with or caring for someone with Severe ME for Severe ME Day (Aug 8). Contribute via video, text or image here - vist.ly/3n82fyr. Submissions close July 25th. Thank you!

Join us at #GPCEMelbourne! Visit Emerge Australia's booth D20 to learn how we can assist #MECFS and #longCOVID patients. Don't miss Prof. Bernard Shiu's session on diagnosing and managing these conditions. Saturday, July 12, 10-11am. vist.ly/3n82uec

Heading back to school with energy limiting conditions like #MECFS and #LongCOVID? Check out our guide to understanding rights, managing school life, and communicating effectively with the school. Find more here: vist.ly/3xrfv 🍎💪📚💬

Edith Cowan University needs 18-60-year-olds for a study. Suitable for healthy or long COVID individuals capable of basic hand contractions. Those with neurological or neuromuscular disorders, or pregnant women shouldn't apply. More info here: vist.ly/3xvix.

Nominate now for the 2025 ME/CFS & Long COVID Media Awards! Help honor journalism that correctly depicts these conditions and fights stigma. Open to all mediums, both Australian and international. More info: vist.ly/3y6pi

Help Needed! We aim to connect ME/CFS and long COVID sufferers to supportive GPs. Are you a patient with a supportive GP? Are you a GP treating ME/CFS or long COVID patients? Fill out this form to help us fill the gaps in our directory. Join today - vist.ly/3yap9.

Ahead of Severe ME day on Aug 8, share your experiences living with or caring for someone with Severe ME. Your stories will be shared & used in our advocacy efforts. Contribute video, writing or image: vist.ly/3ybbh. Submissions until 25 July. Thanks for your energy.

🩺 Join our Live Education Session w/ our Nurse at 2 PM (AEST) today! Topic: Post-exertional malaise (PEM). Get answers and personalised health guidance. Complements our self-paced learning module. Register now: vist.ly/3yp7a 💡✨📅

Help us shed light on Severe ME ahead of Severe ME day on Aug 8. We're collecting experiences of living with/caring for someone with this condition. Share your stories via video, writing or photo here: vist.ly/3ytas. Submissions end on Jul 25. Thanks for participating!

If you’re living with ME/CFS, long COVID or want to volunteer as a ‘healthy control’ for medical research studies, signing up and becoming an AusME Registry participant is the single easiest way to become involved in research! vist.ly/3yxm4

Kit stresses the importance of accessible, affordable home care after years of struggling with severe ME/CFS. Learn about their journey with Emerge Australia ahead of #SevereMEDay2025. Join our Symposium on 8 August: vist.ly/3yzbu.

No cure for ME/CFS or long COVID exists yet. Management includes pacing, rest, and treating symptoms. Emerge Australia offers 10 essential questions for safe treatment decisions. 👉 More info: vist.ly/3z46m

"Join Emerge Australia's Invisible Lives, Visible Care campaign, sharing stories from individuals like Stacey who is battling severe ME. Let’s discuss a brighter future at our Severe ME Day Symposium on 8th August, 2pm (AEST). Register at vist.ly/3z4p4 #SevereMEDay2025"