🇦🇺 South Australia
🏳️🌈 Queer
👩⚕️ Retired doctor - ME/CFS & POTS advocate (Doctors with M.E. associate + Australian POTS foundation member)
🌏 Climate crisis advocate (Climate and Health Alliance member + Doctors for the Environment Australia member)
This week is the Big Give Christmas Challenge! Donate today and your donation will be DOUBLED! Improving lives and accelerating understanding for anyone affected by ME.
Charity number: 1036419 / SC040452
Physician. Recovered, Long Covid 2022. continues
John@100apples.com
Metformin, TLR4 quieting, microclot busting, NRF2 promoting, HIF1a limiting approach. “CORE” circ, oxygen, rebuild energy
Tx Long Covid & MECFS
Chief Med Officer Renegade Research
ME Research UK is a charity which funds scientific (biomedical) investigation into the causes, consequences and treatment of ME/CFS (charity number SC036942)
501(c)3 transforming how #LongCovid, #ME/CFS & Lyme+ are studied, diagnosed, and treated. Leading the #LongCovid Research Consortium.
Share your story / Amplifying the chronically ill / #MyalgicEncephalomyelitis #LongCovid et al / #MillionsMissing / Contact: millionsmissingpodcast@gmail.com / linktr.ee/millionsmissingpodcast
CrunchME is a patient-led organisation, creating the evidence and insight base needed to crunch infection-associated chronic conditions (IACCs), including #MECFS and #LongCovid.
📍 https://crunchme.org/
LongCovid & ME/CFS conference project. We’re a small group of affected people living with LC & ME/CFS, alongside dedicated supporters.
#UniteToFight2024
www.youtube.com/@unitetofight2024
Solve M.E. is a non-profit organization that serves as a catalyst for critical research into diagnostics, treatments, and cures for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), Long Covid, and other infection-associated chronic conditions.
A UK registered charity for people with #MECFS and Long Covid (and Post Covid ME/CFS). We inform, educate, raise awareness, fund medical research and campaign for positive change.
RPs do not necessarily mean endorsement.
https://linktr.ee/meassociation
2001 PVFS 'Recovered' to 90% by 2006. Sepsis 2013 resulted in M.E. / relapse. Brain/fitness not 'what it used to be'. Beloved Lisnakill Myles-Happy Hound himself 🌈
Former medical doctor | PhD | Living with moderate/severe Myalgic Encephalomyelitis (ME) | Dutch 🇳🇱 | Cat mom of two | #pwME #myalgicencephalomyelitis #myalgicE
News, interesting information and commentary on ME/CFS.
My passions: Lightsabers, tech, books, comics, graphic novels, and the sweet sound of a Penguins goal horn. 🚨 My not-so-secret villain: #LongCovid. Still here, still nerdy! #LetsGoPens
https://darthfoo.substack.com
Fully disabled mom of 4 disabled kids, married to my love, we battle ME/CFS, Long Covid, MCAS, POTS, Fibro & other chronic illnesses. Dog mom to 3 Pompsky pups, chaos coordinator, advocate, ally, crafter, decorator, survivor, supporter, etc.
Collection of news, resources, and discourse related to the ongoing COVID-19 pandemic & health advocacy. Occasional venting, hot-takes and memes.
Los Angeles, CA.
Composer who is currently working on a Song Cycle.
Posting about: Music, COVID safety, Clean Air, Climate Change & wildlife.
#Covidisairborne #FBCV
#Vaccinessavelives
#WearARespie ffp2/3
❌ to mask bans
#TransparencyCovid
Vote Green Party 💚
We are a 501(c)(3) sounding the alarm on ME/CFS through digestible, creative content. This is #NotJustFatigue. Visit www.notjustfatigue.org
Soccer, Politics
#Resistencia
#EpilepsyAwareness
#BlackLivesMatter
🇨🇦 🇵🇹 🇺🇸 🇮🇹 🇪🇺
#ElbowsUp
🐧 🐧 🐧
