📲 Social Media Snippets for LifeLineBC Campaign
Hashtags:
#SaveBC_CLMF #LifeLineBC #ProtectVirtualCareBC #MEawareness #LongCOVID #Fibromyalgia
Key Handles:
Minister of Health: @JosieOsborne (twitter/X) @josie_osborne (instagram)
Premier’s Office: @DavidEby (twitter/X) @davideby (instagram)
MLA accounts: google your MLA to search for their handles
MSP’s new cap will dismantle BC’s effective virtual care model for Long COVID, ME/CFS & Fibromyalgia.
BC-CLMF’s virtual group visit model saves lives, reduces system pressure, and supports 5,000+ patients.
Thousands of vulnerable patients will lose access unless the government acts to protect this care.
Twitter / X SAMPLES
🆘 BC is about to cut off care for 5,000+ patients with Long COVID, ME/CFS & Fibromyalgia.
MSP’s Sept 1 cap will gut a model that works: virtual groups that save money, reduce ER visits & reach those too sick to travel.
@Josie_Osborne must act now. We need this care to survive.
#SaveBC_CLMF #LifeLineBC #ProtectVirtualCareBC #bcpoli #DEI
⚠️📢 On Sept 1, BC’s most effective virtual clinic for ME/CFS, #LongCOVID & Fibromyalgia faces collapse.
MSP’s cap on virtual group visits will gut care for 5,000+ patients- many too sick to access alternatives.
Urge your MLA: demand a real solution. 👉 [www.lifelinebc.ca]
#SaveBC_CLMF #LifeLineBC #ProtectVirtualCareBC
Thousands of chronically ill British Columbians are about to lose access to care.
On Sept 1, MSP will cap virtual group visits- gutting a virtual model that works for Long COVID, ME/CFS & Fibromyalgia patients.
Virtual group visits cost less, reach more, and reduce ER visits.
So why is BC slashing a model that actually saves money and lives?
@Josie_Osborne: This is policy failure in motion.
#SaveBC_CLMF #HealthJustice #bcpoli #DEI #VirtualCare
I’m not asking for special treatment.
I’m asking BC to protect the only ongoing care that’s ever worked for my complex chronic illnesses.
Sept 1 will gut it.
Please @Josie_Osborne - find a solution.
#LifeLineBC #LongCOVID #MECFS #ChronicIllness #bcpoli
BC’s most invisible patients- homebound, disabled, and post-viral- are being abandoned.
MSP’s cap will cut off care for 5,000+ who cannot access in-person visits.
This is a disability issue. A justice issue.
@Josie_Osborne, act now.
#SaveBC_CLMF #DisabilityJustice #bcpoli #LifeLineBC
If you believe in equity, disability rights, and evidence-based care:
📣 Speak up.
BC is about to gut a successful virtual care model for Long COVID, ME/CFS & Fibromyalgia.
Sept 1 is the deadline.
Protect BC-CLMF.
#ProtectVirtualCareBC #SaveBC_CLMF #LifeLineBC #bcpoli
Facebook / LinkedIn
🚨 Save BC’s Complex Chronic Disease Care Model 🚨
On September 1, BC will cap virtual Group Medical Visits at 20 patients/hour — threatening to collapse the only effective, scalable virtual model supporting 5,000+ people with #LongCOVID, ME/CFS, and Fibromyalgia.
The BC Centre for Long COVID, ME/CFS & Fibromyalgia (BC-CLMF) serves 50 patients per session, saving money, reducing ER visits, and reaching those too sick to attend in-person care.
This model is cost-effective, accessible, and essential for people with disabling chronic illness- and there is no real alternative. Cutting this means cutting off care entirely for many of us.
📧 Tell Health Minister Josie Osborne to act NOW: HLTH.Minister@gov.bc.ca
We’re not asking for more - just to protect what already works.
#SaveBC_CLMF #LifeLineBC #ProtectVirtualCareBC #bcpoli #ChronicIllness #HealthEquity #DEI
🚨 Urgent: BC is about to cut off care for 5,000+ chronically ill patients 🚨
The BC Centre for Long COVID, ME/CFS & Fibromyalgia (BC-CLMF) provides group-based virtual care for patients with disabling chronic illness- reaching 40–60 patients per Zoom session. It’s efficient, accessible, and saves the system money by reducing ER, GP, and specialist demand.
But starting September 1, 2025, MSP will cap group visits at just 20 patients/hour- a change that will dismantle this proven model and leave thousands without care.
This isn’t just bad policy — it’s a healthcare crisis in the making.
📣 Contact your MLA, Minister Osborne, and Premier Eby today.
Tell them: Don’t let this care model collapse. Protect the patients and act now.
📧 HLTH.Minister@gov.bc.ca
#SaveBC_CLMF #ProtectVirtualCareBC #LifeLineBC #bcpoli #ChronicIllness #HealthEquity
Instagram Caption / Story
💔 BC’s Chronic Illness Care Model Is Being Dismantled
Starting Sept 1, MSP will cap virtual group visits at 20 patients/hour- a change that threatens to collapse a care model that works for Long COVID, ME/CFS & Fibromyalgia.
Clinics like the BC Centre for Long COVID, ME/CFS & Fibromyalgia currently serve 40–60 patients per session, delivering real, tangible, irreplaceable care- with patient testimonials to prove it. These visits are lifesaving for people who are housebound, rural, and chronically ill- and they reduce pressure on ERs, GPs, and specialists.
If this model disappears, thousands will be left behind.
📧 Email @Josie_Osborne now: HLTH.Minister@gov.bc.ca
Tell her: Find a real solution. Protect this model. Patients can’t wait.
#SaveBC_CLMF #LifeLineBC #LongCOVID #MECFS #Fibromyalgia #VirtualCare #DEI #HealthEquity #ChronicIllness #bcpoli
Tell your MLA: Minister Osborne must find a solution—before it’s too late.
Pro Tip: Encourage supporters to tag their MLA’s Twitter/X handle and use stories + screenshots of sent emails to amplify momentum.
🎥 Instagram Stories / Reels Script
Slide 1: 🩺 Did you know?
Hundreds of thousands of British Columbians rely on virtual group care as the only thing that’s worked for managing for Long COVID, ME/CFS & Fibromyalgia.
Slide 2 (clip/static):
💻 Group Zoom visits with 40–60 patients
Save lives, reduce wait times, and reach those too sick to travel.
Slide 3:
⚠️ But on Sept 1…
MSP will cap group visits at 20 patients/hour — threatening to collapse the only virtual clinic that works.
Slide 4:
📢 Swipe up to contact your MLA
Tell them: We need this incredible life-saving model funded. Patients can’t afford to be left behind.
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