🌟 The AusME Registry is making a real impact! 🌟 Thanks to our incredible community, the AusME Registry is now supporting 25 research projects across Australia - helping scientists unlock the biology behind #MECFS and #LongCOVID. Join us today - zurl.co/ZfQIv

If you are an Aboriginal and/or Torres Strait Islander person living with or caring for someone with #mecfs or #longcovid , we invite you to share your experiences to guide us in making our services more inclusive and community-led. Take the survey: zurl.co/P92Z8

Healthy volunteers signing up to the #AusMERegistry & donating blood to the #ausmebiobank give researchers the vital comparison data they need to uncover the biology behind #mecfs & #longcovid and discover effective treatments 👉 zurl.co/W6BsH zurl.co/YEf22

If you're a Culturally & Linguistically Diverse (#CALD) person living with or caring for someone with #MECFS or #longCOVID, we invite you to share your experiences to guide us in making our services more inclusive and community-led. Take the survey: zurl.co/O28dI

Reminder: The 2025 #MECFS & #LongCOVID #MediaAwards are now open for nominations! Let's celebrate reporting that amplifies patient voices, dismantles stigma, and deepens public understanding. Learn more about eligibility and submit your nominations here: zurl.co/zw6QQ

We are delighted to announce Lily Schubert as an Ambassador for Emerge Australia. Lily is a Sydney-based content creator and chronic illness advocate known for her candid storytelling on TikTok (@lilygschubert). Read more 👉 zurl.co/LjjYC

Virtual Support Groups for Carers & Supporters 🌿 Are you supporting someone living with #MECFS or #longcovid? Emerge Australia’s virtual #supportgroups offer a safe space to connect with others Next groups start October 2025 – zurl.co/VYsjh

If you’re living with #MECFS, #LongCOVID, or want to volunteer as a ‘healthy control’ for medical research studies, becoming an AusME Registry participant is the simplest way to get involved in research! Sign up today and make a difference! zurl.co/FE9c2

🩺 Join our Live Education Session w/ our Nurse at 2 PM (AEST) today! Topic: Post-exertional malaise (PEM). Get answers and personalised guidance. Complements our self-paced learning module. Register now: zurl.co/33MLA #MECFS #PEM #EmergeAustralia

Speak up for CALD communities. If you're part of the CALD Community combating ME/CFS or long COVID, we need your help. Share your experiences through our survey to help improve our services. Take the survey: vist.ly/44xtt

Improve your clinical knowledge with our free online modules on ME/CFS & long COVID. Enhance your skills & patient outcomes. Missed our webinars? Visit vist.ly/44x6x. Support for patients & carers at vist.ly/44x6v.

Aboriginal or Torres Strait Islander with ME/CFS or long COVID? We invite you to share your experiences. Your voice can help us make our services more inclusive. If able, kindly take our survey: vist.ly/44tx8

Supporting someone with ME/CFS or long COVID? Connect with Emerge Australia’s virtual support groups. Get emotional support, share experiences, learn coping strategies. Next groups start October 2025: vist.ly/44tqw

Stay updated with Emerge Australia's Research Digest on ME/CFS and long COVID. • Summarized • Easy-to-read • Convenient • Accessible Subscribe for monthly delivery! Browse past issues or listen on our website: vist.ly/44t5w

Healthcare professionals supporting individuals with chronic conditions like #MECFS & #longCOVID, join Emerge Australia! Stay informed about new learning opportunities. Sign up here: vist.ly/44nyh

AusME Biobank has 200 donors resulting in 20 litres of blood & 7,429 research samples. Your donations support 20+ studies! To further ME/CFS and long COVID research, we need more donors. Join us today!

Speak up for CALD communities. If you're part of the CALD Community combating ME/CFS or long COVID, we need your help. Share your experiences through our survey to help improve our services. Take the survey: vist.ly/447ju

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! Sign up today! vist.ly/446w4 vist.ly/446w5

Aboriginal or Torres Strait Islander with ME/CFS or long COVID? We invite you to share your experiences. Your voice can help us make our services more inclusive. If able, kindly take our survey: vist.ly/443jr

✨Create Your Legacy✨ Support ME/CFS & Long COVID research & care with a will bequest to Emerge Australia. 2% makes a huge difference. Set it up for free at gatheredhere.com.au/c/emerge-au or add us to an existing will at emerge.org.au/gift-in-will/. Start impacting lives today.

🩺 Tune in LIVE at 2 PM AEST for Emerge Australia's Education Session with our Nurse focused on Sleep. Improve your understanding with personalized guidance. Complements our self-paced learning module. Register now: vist.ly/43sh6 💡📅✨

Help list ME/CFS and long COVID aware GPs on our directory. Confirm their consent, then fill this form: vist.ly/43njh. GPs can find more info at: vist.ly/43njj

Sarah Vizer discusses her book "Too Tied to Think" and personal experiences in the new Imagine podcast series. Tune in here vist.ly/43fdr

Learn about Post-Exertional Malaise (PEM), a condition common in ME/CFS and long COVID, causing symptoms to worsen after minor activity. Join our free course to understand more. vist.ly/43erw 💡

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! Sign up today! vist.ly/43au8

Join our Virtual Support Groups for Carers & Supporters 🌿 supporting those with ME/CFS or long COVID. Share experiences, get emotional support, and learn practical strategies. Next groups start October 2025. Learn more: vist.ly/436t3

Nominations for the 2025 ME/CFS & Long COVID Media Awards are now open! Nominate pieces that are reshaping the perception of long COVID, from articles to podcasts. Open to Australian and international entries. Nominate here: vist.ly/436sn

🎥 Revisit the Severe ME Day Symposium via available replay! Audio-only & standard versions accessible. Hear from our CEO Anne Wilson, joined by individuals with and caring for those with #severeME. Watch here: vist.ly/433as Your engagement helps spread awareness! 🗣

Join us in advancing research for ME/CFS & long COVID. Help transform lives, improve treatments & quality of life. Sign up now: vist.ly/322qj or visit vist.ly/322qk for more details.

Last Friday, CEO Anne Wilson talked about DecodeME's ME/CFS genetic study on ABC Radio's Nightlife. Listen here: [link]. Read Emerge Australia's summary on DecodeME's results & how to participate in research: vist.ly/32wx2

The Thompson Institute/USC (QLD) is seeking participants aged 18-65 for a vital study! If you're healthy or living with ME/CFS, fibromyalgia, or other similar illnesses & can travel to us, you may qualify. More info: vist.ly/32wws

Recent changes to NDIS Supports Rules are adversely affecting people with ME/CFS and long COVID. We've submitted our concerns to the NDIA, calling for clearer rules, more flexibility and less red tape. Read our submission: vist.ly/32wqu

Join our free online course for improved ME/CFS and long COVID diagnosis & management. Module 1: Assessment & Diagnosis Module 2: Management of Common Symptoms 💻Clinician portal: vist.ly/32wjj Patients or Carers, find support at: vist.ly/32wji

Emerge Australia advanced GP and Allied Health training in FY24-25. Supported by John James Foundation and Moderna Australia, 600+ professionals were educated on ME/CFS at our national Clinical Education events. Check our summary of achievements in the tiles.

Exciting update! Our Community Advisory Panel, chosen from numerous quality nominations, is now live! Learn about its focus on Emerge Australia's advocacy priorities here: vist.ly/32sbe

Welcome to our #SevereMEDay2025 online symposium! Join us on Zoom now, or here where we will be live posting the event. #severeME #mecfs

Join us on #severeMEDay2025 to hear Shiloh Moore's podcast on living with severe #MECFS and Fibromyalgia for 35 years. Listen here: vist.ly/32nsy

Join us for an online symposium on #SevereMEDay2025, 8 Aug, 2pm (AEST). We'll discuss living with & caring for people with #severeME. Recording available post-event to address accessibility issues. Register here: vist.ly/32ndw 🎤💙🎥

Acknowledging #SevereME Day with Emerge Australia & World ME Alliance. We urge community to share their video, shining light on the everyday struggle.

Tune in to Chris Quill's podcast with Emerge Australia CEO, Anne Wilson, discussing his journey from disability support expert to suffering with #MECFS after contracting COVID. Link: vist.ly/32iez #severeMEDay2025 .

Join Emerge Australia for #SevereMEDay2025 Symposium on August 8, 2pm (AEST), focusing on Invisible Lives, Visible Care. Hear real-life experiences of those living with Severe ME. Register here: vist.ly/32i4k #SevereMECFS #InvisibleLivesVisibleCare

Join Amelia discussing issues of #SevereMECFS, support needed & ways to be mindful. As part of #SevereMEDay2025, Emerge Australia shares experiences in the series, Invisible Lives, Visible Care. Attend our Symposium, 8th August, 2pm (AEST) to hear more. vist.ly/32g2u

Join us for a Symposium on Severe ME Day, Aug 8 at 2pm AEST. Hear lived experiences & insights about handling Severe ME. Register here: vist.ly/32egs #SevereMEDay2025 #EmergeAustralia

Amelia shares how in-home medical care could impact those with #SevereMECFS. Join Emerge Australia for a Symposium on #SevereMEDay2025, presenting experiences and insights on 'Invisible Lives, Visible Care'. Register here: vist.ly/32eag

Join the powerful conversation with Simone Eyssen & Anne Wilson on the severity of ME, available on this podcast. Listen here: vist.ly/32dum #severeMEDay2025

Ahead of #severeMEDay2025, hear Dr. Steven Sommer discuss his transition from doctor to patient and Tori Sommer share her experience as his full-time carer on Emerge Australia's podcast. Listen now: vist.ly/32af8

Stacey shares the impact of in-home medical care for #SevereMECFS ahead of Emerge Australia's #SevereMEDay2025 Symposium. Join us on 8 August, 2pm AEST, for insights from those living with Severe ME and their carers - Invisible Lives, Visible Care.

🩺 Live Education Session with our Nurse @ 2 PM (AEST) today! Orthostatic Intolerance - managing upright hours Complements self-paced module, with live support for your pacing strategy Connect, learn, feel supported. We're here for you. 📅 Register now: vist.ly/329hi

Join us leading to #severeMEDay2025 and listen to Kate Baychek's podcast on #MECFS’ reality for caregivers, featuring Emerge Australia CEO, Anne Wilson. Listen here - vist.ly/325wx

Join Emerge Australia's Symposium on #SevereMEDay2025 to hear from Amelia & others about their experiences with Severe ME. Learn about the fluctuating nature of the illness and carers' insights on Aug 8, 2pm (AEST). Register & read more: [link] #InvisibleLivesVisibleCare