Sally's Safe and Connected Travel
Welcome to Sally’s Safe and Connected Travel — a channel for travelers with chronic illness who want to explore the world without crashing their nervous system.
Hi I’m Sally: a travel advisor, psycho...
So I launched a new YouTube channel this week! youtube.com/@sallyssafea... On it I will be sharing 1) hotel reviews from a chronic illness perspective 2) travel tips for chronic illness 3) my personal experience living and working in Japan (where I’m heading next month for the summer and fall)
22.05.2025 14:28 — 👍 3 🔁 0 💬 0 📌 0
Chaotic good writer and scientist with severe, bed bound MECFS. Writing wholesome stories, science stuff, and funny anecdotes from bed. Lover of memes.
jesshoneybadger.substack.com
currently: sick / haunted in Western Mass, host of No End In Sight - a podcast about life with chronic illness, creator of #NEISVoid | previously: Stories We Don’t Tell in Toronto | she / her
Long Covid, MECFS, ADHD, etc.
Patient-led research is my jam.
A bit obsessed with GIP.
ME/CFS | Long COVID | IACC
Disability Justice
Living with ME, EDS, POTS, MCAS, vascular compressions, spinal comorbidities & more
Ambulatory wheelchair user
Cozy gamer, lazy gardener, hopeful baker
So did the divine right of kings. Long covid class of March 2020, the kind with ME. Would like one more tattoo, minimum. She/her.
Lawyer, advocate, writer, public health
Immunocompromised, chronically ill, disabled
Then: SSI, SNAP, Medicaid
Now: data & policy, disability, healthcare
🔗 matthewcort.land
🔗 It's A Hellscape 📰 patreon.com/mattbc
🏳️🌈 nonbinary
Ella/she/her. I write, I read, I draw plants. Chronically ill en la Ciudad de México. #ME #MECFS #POTS #LongCovid
🥄 in a country where acknowledging activism is dangerous
🏳️🌈 Pronouns: she/they
#livingwithableism #resist
🦠😷♿️#LongCovid disabled | 📢Chicané activist | 🏠LAX | ⚖️health justice | ✊🏽✊🏾✊🏿racial justice
alt text profile pic: tan skinned person in a tan KN95 mask and suit, dark wavy hair with short bangs
Once a lawyer, then a travel writer. Now disabled, writing about curiosity & health.
Travel writing & celiac translation cards: legalnomads.com
Best things I read each month: jodiettenberg.substack.com
MCAS, meditation, & health: jodiettenberg.com
#CommunityEngagement Expert. Life sidelined by #MECFS #MCAS #POTS #Fibro #Gastroparesis +
#MECFS & #LongCovid #ResearchPartner & #Advocate • Chair of #MedicalEducation Group • #PwME #Disability
(Unceded) #Canada
https://linktr.ee/sabrinapoiriercanada
PD Dr. (religion, empirical education research)
mother of Mila who suffers from very severe ME/CFS (Bell 0)
https://milaandmecfs.files.wordpress.com/2022/05/mila-spiegel.pdf
Vienna, Austria
#CleanAir
Founder - Renegade Research
#MECFS #LongCovid
Parisienne Buffalonian linguist spoonie mom. http://bcopley.com "The line separating good and evil passes...right through every human heart." -Solzhenitsyn
#MECFS #MILLIONSMISSING #MEAwareness
#PEM #POTS #MCAS
#PostCovid #LongCovid
#TeamWissenschaft #GdB
https://www.mecfs.de/was-ist-me-cfs/
ME/CFS patient advocate, Open Medicine Foundation science correspondent. Bedbound. Former: exercise physiology, biochemist in training, athlete-Powerlifter, PT, Gym Manager. Jazz grad/Musician. F1/Boxing.
Long (long) time person with ME/CFS/FM, Translator ME/CFS/ fibromyalgia/long COVID/POTS, etc. research and advocate. Creator of Health Rising and Phoenix Rising. Roaming the western US since 2012
Usually a lurker, Chronically Online for #LongCovid and other #IACC | Australia
