These results confirm that #ME is a deeply polygenic & biologically heterogeneous condition with @ least 4 major disease mechanisms implicated by genetic signals
Neurological dysregulation🧠
Inflammation🔥
Cellular stress response⚠️
Calcium signalling🚥
https://t.co/4022Ht3jlJ
WEBINAR TODAY:
Our researchers are unpacking the new ME genetics study today - join the live webinar to hear the findings first-hand and get your questions answered.
📅 Today
🕑 2PM GMT
🔗 Register: https://t.co/JyMcGneEBb
#pwME#MECFS#longCOVID#MissingMillions
Our genetic analysis of ME is now live. The new study identifies 250+ core ME genes, shared biology with long COVID, and dozens of drug repurposing opportunities for precision trials.
Huge thanks to our partners and the @DecodeMEstudy participants.
#pwME#longCOVID#MECFS
@CortJohnson Thank you for taking time out to speak with us, @CortJohnson - we look forward to sharing our progress as we advance our programs in #longCOVID and #MECFS.
For anyone interested in reading our published research, please visit https://t.co/kjlM3aUE7K.
Thanks for your support!
We’re excited to share a recently release preprint from our collaborative work with @PrecisionLife - identifying and validating 75 novel genes associated with endometriosis.
#Endometriosis#PatientsCantWait
🎥 As part of today’s recognition of #SevereME, we’re sharing this recent presentation by our Co-founder, Rowan Gardner, given at International ME Conference: 𝗣𝗿𝗲𝗰𝗶𝘀𝗶𝗼𝗻 𝗗𝗶𝗮𝗴𝗻𝗼𝘀𝘁𝗶𝗰 𝗧𝗲𝘀𝘁𝘀 𝗮𝗻𝗱 𝗣𝗲𝗿𝘀𝗼𝗻𝗮𝗹𝗶𝘇𝗲𝗱 𝗧𝗿𝗲𝗮𝘁𝗺𝗲𝗻𝘁𝘀 𝗳𝗼𝗿 𝗠𝗘.
𝗧𝗼𝗱𝗮𝘆 𝗶𝘀 𝗦𝗲𝘃𝗲𝗿𝗲 𝗠𝗘 𝗗𝗮𝘆 – a moment to acknowledge the strength, resilience, and determination of those living with the most debilitating forms of Myalgic Encephalomyelitis.
We are now running 𝗰𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝘁𝗿𝗶𝗮𝗹𝘀 𝗶𝗻 𝘁𝗵𝗲 𝗨𝗦 to validate new non-invasive diagnostic and therapeutic options – a major step toward faster diagnosis, targeted care, and hope for millions of patients.
𝗧𝗼𝗱𝗮𝘆 𝗶𝘀 𝗦𝗲𝘃𝗲𝗿𝗲 𝗠𝗘 𝗗𝗮𝘆 – a moment to acknowledge the strength, resilience, and determination of those living with the most debilitating forms of Myalgic Encephalomyelitis.
Thanks to you, we’ve:
✔️ Confirmed the 𝗳𝗶𝗿𝘀𝘁-𝗲𝘃𝗲𝗿 𝗴𝗲𝗻𝗲𝘁𝗶𝗰 𝗲𝘃𝗶𝗱𝗲𝗻𝗰𝗲 for ME/CFS and long COVID
✔️ Identified 𝘀𝗵𝗮𝗿𝗲𝗱 𝗱𝗶𝘀𝗲𝗮𝘀𝗲 𝗺𝗲𝗰𝗵𝗮𝗻𝗶𝘀𝗺𝘀 between both conditions
✔️ Discovered genes that 𝗿𝗲𝘀𝗶𝘀𝘁 𝗮𝗻𝗱 𝗽𝗿𝗼𝘁𝗲𝗰𝘁 against ME
@JackHadfield14 We hope that the research here if of interest: Identifying and Validating Genetic Risk Factors for ME/CFS and Long COVID - https://t.co/kjlM3aU6ic
Millions are still waiting for answers. Ahead of #SevereMEAwarenessDay, we’re reaffirming our support and using genetic insights to develop the first non-invasive mechanostic tests to accelerate diagnosis and improve care.
🔗 https://t.co/xBA9VITLxl
#MECFS#LongCOVID
On this Global MND Awareness Day, we're sharing our latest work uncovering the mechanisms behind ALS, new protective biology, and a path to non-invasive, personalized diagnosis and treatment.
Read more: https://t.co/GW3Tpc1yVf
#ALS#MND
⏰ Last chance to register!
Our webinar on #MECFS & #LongCOVID is tomorrow. Join for the latest research insights and their implications for the prediction, treatment and prevention of the conditions.
🔗 Register: https://t.co/hMsPJjnawx
#pwME#MyalgicE#MillionsMissing
Join the free webinar hosted by @actionforme on 6 June to hear the latest genetic research on ME/CFS & Long COVID and what it means for patients, clinical practice, and the future of precision medicine.
🔗 https://t.co/hMsPJjnawx
#MECFS#LongCOVID
🎥 𝗘𝘅𝗽𝗲𝗿𝘁 𝗣𝗿𝗲𝘀𝗲𝗻𝘁𝗮𝘁𝗶𝗼𝗻:
We highly recommend watching Dr. Sayoni Das' presentation, #PrecisionMedicine for Long COVID and ME/CFS.
👉 𝗪𝗮𝘁𝗰𝗵 𝗵𝗲𝗿𝗲: https://t.co/N24YKDYjXN