The @bcndp budget has once again failed our community. @Josie_Osborne we urge you to act immediately and prioritize the care this community deserves. Please see our response here - https://t.co/JN9n5RxG8W
Last chance — triple matching ends June 1!
Every dollar still counts triple.
Donate in the name of someone who has supported you & invite them to be part of this community. 💙
Don't let this opportunity pass.
Donate: https://t.co/PyRJU9nUMG
@operamariposa
art: @GraeSalisbury
What a beautiful #BlueSunday2026! So much gratitude for everyone who showed up in whatever way they could. This is what ME/FM solidarity looks like. 📷
If #BlueSunday inspired you, there's still time to turn that love into action
https://t.co/PyRJU9osCe
@OperaMariposa
You don't have to navigate this alone.
Social Prescribing links you with a Community Connector who builds a personalized wellness plan, including access to food programs like the Good Food Box. Available across BC for those 60+.
Learn more: https://t.co/ezEXYnyz2z
Change starts with awareness.
Thank you to Health Minister @Josie_Osborne for standing with the ME/Long COVID community on May 7th, and to every MLA who wore our button and read our cards. Your support means everything.
#MEAwarenessDay#LongCOVID
Halfway through May — have you donated yet? 💙
Every dollar is tripled until June 1.
And Blue Sunday Tea is this Sunday with @OperaMariposa, May 17 at 1pm PT on Zoom.
Register: https://t.co/4ETue5nbwo
Donate: https://t.co/PyRJU9osCe
Your impact matters.
Art: @graesalisbury
Every donation to our May fundraiser is TRIPLED until June 1!
Donate in the name of someone who has supported you & invite them to Blue Sunday Tea with @OperaMariposa on May 17.
Register: https://t.co/4ETue5nbwo
Donate: https://t.co/PyRJU9osCe
Art: @graesalisbury
📢 Young Canadians — Trent University needs you!
Participate in a research study if you:
-In school with ME/CFS or unexplained fatigue
-Left school due to ME/CFS
-In school without fatigue conditions (control group)
Sign up: https://t.co/hklH42YDXp
#MECFS#MEAwarenessMonth
1 in 29 people will experience ME/CFS in their lifetime. That's not a rare disease; that's an underrepresented one.
Share this to help spread the word this May Awareness Month.
Learn what the research really shows: https://t.co/jbk1xxeBWP
Join @OperaMariposa and the ME | FM Society of BC for an online tea party fundraiser on Sunday, May 17 at 1pm PT / 4pm ET on Zoom.
Donate or post your Blue Sunday pics using #MariposaBlueSunday for a chance to win amazing prizes!
🔗 Register now: https://t.co/Nl54mYvu6j
Sharing a meaningful initiative 💙
Opera Mariposa’s Benefit + Awareness Month supports our cause, raising awareness for ME/CFS, Long COVID, and fibromyalgia.
Enjoy online events, art, and accessible ways to get involved.
Learn more: https://t.co/oyylfSOrRt
Join the online National Volunteer Week celebration on April 23, featuring Farah Mohamed and volunteers sharing their stories and impact across Canada.
A chance to get inspired and see how the difference starts with you. Register through the link.
https://t.co/izoVPqxNAc
Many Canadians qualify for support but never claim it because of the overwhelming process.
Barrier-Free Benefits is here to change that. They help access current support programs with free one-on-one guidance.
Book a free appointment.
https://t.co/QB7FChk23P
@InclusionCA
The holidays can be tough when you're managing ME, FM, or Long COVID. We've got you. 💙
Sign up for a extra Support Group with Shannon — Mon, Dec 22, 1pm for anyone needing connection - https://t.co/0n7axjHMMj #MECFS#LongCOVID#Supportgroup
Join @OpenMedF for a webinar: OMF’s Research Portfolio
📅 October 30 | 🕙 1 PM PT
Hear from Linda Tannenbaum, OMF Founder & CEO, and Danielle Meadows, VP of Research Programs, about OMF Global & OMF Canada’s research progress, with live Q&A.
👉 Register: https://t.co/zPiCc8lIHD
🔥Mount Sinai launched a clinical manual for treating Infection Associated Chronic Illnesses #LongCovid#MECFS#Lyme
Patients can download as well.
Great resource made by great people. Loving the transparency as always! @PutrinoLab@microbeminded2@ravenscimaven
As Severe ME Day comes to a close, we light a candle to remember those we have lost. We send our love to all who are grieving. We hold each other in our hearts as we each have a list of names that goes through our minds as we light our candle.
#SevereMEday#UnitedforME
What if your body couldn’t bear light, sound, movement — or even touch?
Today, #SevereMEDay, we ask you to imagine living that way not just for a day… but for years.
For people living with Very Severe ME, this isn’t a metaphor — it’s reality.
🧵