I'm looking for someone to do some contract work promoting the emerge pacing app on social media. Good social media skills and knowledge of ME/CFS needed. Email me at [email protected]#pwME#MECFS
I've just released, in conjunction with Emerge Australia, the new improved version of my free Pacing app.This app is designed to help you better manage your energy and experience less Post Exertional Malaise (PEM). Available in apple and Google AppStores.
17K Followers 6K FollowingI tasted chronic illness in the form of Long Covid. It tasted horrible. But I was lucky & improved over 4 years. Now I’m here for those still struggling
3K Followers 2K FollowingCertified medical #writer, enthusiastic #journalist, cat mom, @UChicagoProEd, ME/CFS patient. Freelance journalist. Available for medical writing and editing.
4K Followers 1K FollowingOn medical leave due to a debilitating chronic illness. Surviving Not Living. Sick Not Tired. #MECFS We just want our lives back. Posts are not medical advice.
959 Followers 628 FollowingI have ME and Fibro since 2003. I run a support group for us with chronic fatigue conditions. We are based in |pswich, Suffolk. Follow us on our journey!
1K Followers 4K FollowingFND Warrior 💪🇬🇧 Down, but not out!
Bringing more awareness to the debilitating effects of Functional Neurological Disorder (FND)
Coffees warmly welcomed 👇
5K Followers 3K FollowingFundraising for @Invest_in_ME charity Centre of Excellence @CofEforME programme of biomedical research and medical education for M.E. #MyalgicEncephalomyelitis
2K Followers 1K FollowingSharing CFS and Long Covid recovery stories on my blog & YouTube @ Heal With Liz. Mom of toddlers and Her Majesty, Baby Sister. Mirror dancer.
56K Followers 43K FollowingAspiring Author ✍🏼📖 |Singer/Actress, Trainee Therapist on hold due to #MECFS ♿️ for 6 years | #POTS / #IST✨Spiritual Awakening. Lessons from the void. 💖
3K Followers 1K Following#Nonprofit #research laboratory providing #disability evaluations, #education, and #resources for #MECFS, #LongCOVID, and other #fatigue related illnesses.
8K Followers 9K Following#MyalgicEncephalomyelitis #MECFS
@ME_CFS Many think caused by chemical poisoning/chlorine #ChronicFatigueSyndrome is severe muscle/nerve pain
Like #LongCovid
2K Followers 2K FollowingCBME is a support group based in #Cambridge UK for people with #MECFS, #MyalgicE , #CFS, #PostViralFatigue, #Fibromyalgia, including #pwME caused by #LongCovid
569 Followers 2K FollowingI am a cat with a purpose! I am here to help my human friends advocate and bring awareness to TMJ disorders. We need scientific research! No DM 🚫. 🐈🐱
911 Followers 5K FollowingNon-Profit. We magnify your health journey to help others. https://t.co/7VLiqMV99u Sharing your story can heal: [email protected].
226 Followers 718 FollowingPatient advocate. Founder of https://t.co/UKbDeLXQM0. Sharing individual health stories to inform and empower all those living with illness.
867 Followers 4K FollowingPodcast amplifying voices of people with Multiple Chemical Sensitivity (MCS) and research about the illness. Subscribe where you get your podcasts! 🎙️🎧✨
383 Followers 2K FollowingA documentary that seeks to shine a light on and tell the stories of those suffering with myalgic encephalomyelitis and Long COVID.
1K Followers 791 FollowingFormer musician mostly housebound with #ME. BA in Music. BA in Theatre. 3/4 of a MA in Theatre, had to stop due to MECFS. I write. Languages. Genealogy.
2K Followers 2K Following#MyalgicE Patient Advocacy 4 better treatment & cure. UR life/dreams are gone before ur eyes! Federal Advocacy Research Education & Funding #Dysautonomia
15K Followers 65 FollowingA passionate molecular virologist who believe in patient oriented scientific research. Using viruses to understand human existence. Science is for society.
17K Followers 6K FollowingI tasted chronic illness in the form of Long Covid. It tasted horrible. But I was lucky & improved over 4 years. Now I’m here for those still struggling
15K Followers 622 FollowingWith ME 36 years (31 yrs severe). 95% of posts on #MEcfs/#LongCovid/#chronicillness. 26 publications in peer-reviewed journals. @IrishMECFSAssoc trustee 28 yrs
16K Followers 224 FollowingCaregiver for very severe ME/CFS son, advocate and fundraiser for End ME/CFS PROJECT at OMF and CFSRC at Stanford. The rest of my life is on hold...
7K Followers 190 FollowingPh.D. in physics, also interested in mathematics and science theory. Loves to apply general knowledge of science to other fields, for example ME/CFS.
7K Followers 5K Following💙Art, Nature, Books, Some Music. Severe ME 32 years. Daughter severe 38 years. Furious about treatment of ME. https://t.co/gEIrl86Wim
7K Followers 3K Following30y/o creative, with complex health issues🤞🏼ME/CFS biomedical research. Passion for the wild, for kindness, and helping all people have a voice. Co-author✨
1.2M Followers 324 FollowingSPD Bundestagsabgeordneter, Vorsitzender Ausschuss Forschung, Technologie und Raumfahrt, Bundesgesundheitsminister a.D., der hier selbst und privat tweetet.
9K Followers 692 Followingphysician-researcher, paediatrician, ME/CFS since 2016. This account is about ME/CFS (may also visit: @kinderverstehen: on child development (German)
2K Followers 2K Following#MyalgicE Patient Advocacy 4 better treatment & cure. UR life/dreams are gone before ur eyes! Federal Advocacy Research Education & Funding #Dysautonomia
1K Followers 555 Following#ME💙F.M.💜I.B.S. Glaucoma💚B12💉Addison Biermer
🇳🇱 NL advocate for biomedical research💰and understanding. Life should't be so hard as it is for some👣
383 Followers 2K FollowingA documentary that seeks to shine a light on and tell the stories of those suffering with myalgic encephalomyelitis and Long COVID.
1K Followers 297 Following26, world champion gymnast turned sick person w/ #MyalgicEncephalomyelitis. The account where I accept it + vent, thank you for listening 😇 #mecfs #pwme
4K Followers 2K Following#MECFS #severeME #MCAS #severeMCAS nichtlängenabhängige #SFN #POTS #Sjögren etc seit Feb 2021 dank #COVID
Darf ich Max Ernst zitieren?
1K Followers 791 FollowingFormer musician mostly housebound with #ME. BA in Music. BA in Theatre. 3/4 of a MA in Theatre, had to stop due to MECFS. I write. Languages. Genealogy.
609 Followers 1K FollowingTrying to live with Myalgic Encephalomyelitis. Campaigner for legal cases against PACE and Researcher into biomedical treatments. #MEcfs #pwMe #MyalgicE
1K Followers 845 FollowingFormer investment manager international private banking. Disabled by M.E. and forced to retire after 15 year career. Tweet latest news relating to #MECFS.
2K Followers 2K FollowingFormer mathematician. Life came to a sudden halt due to #LongCovid/ME. Politics & policy, @longcovidnl.
Tweets in Dutch and English.