KarenL

[Isaac Bogoch @BogochIsaac]

FYI, my name & image are being used without my consent to sell various unlicensed diabetes/ hypertension products. I do not endorse these products.

I have reported this to various social media platforms & to the Canadian Anti-Fraud Centre.

Obnoxious example below.

Cheers,

IB

[Greenpeace Aotearoa @GreenpeaceNZ]

Bang on from @GeorgeMonbiot.

And something @chrisluxonmp @ShaneJones_MP etc should take heed of as the rush to start new mining and oil exploration.

[Matthew Todd 🌏🔥 @MrMatthewTodd]

This is what it feels like to be alive as we approach the end of the world as we know it. There is time to avoid the worst but it means every single one of us becoming activists. Leave it to other people and we are toast. Listen to David Attenborough who warned us time and again

[Sabrina Poirier (On Hiatus) 🇨🇦 @Sabrina_Poirier]

Before leaving #Twitter, please consider for a moment that those of us with disabilities use this space to #connect, #educate and #advocate.

We worked hard to connect with you.

And we cannot start from scratch on 2-3 other platforms to chase all of you.

[Lars Sander-Green @LarsSanderGreen]

If you have #MECFS, were vaccinated and you caught Covid three or more months ago, is your health now:
#pwME

[KarenL @kmlauk]

@LisaLaFlamme_ I’m so sad to see this. I’ve so enjoyed your class act on CTV national news.

[Millions Missing Can @MillionMissCan]

@cbcwhitecoat Research funding for 600,000 Canadians with #MyalgicEncephalomyelitis but without adequate health care.

Backstory is laid out in this letter that's collecting cosignatories for support.

Read the Letter:
https://t.co/MViYcNJ3hd

Cosign the Letter:
https://t.co/bDdwtPT9sD

[A Life Suspended by ME @b5field]

By not providing adequately for #pwds, provincial government plans like #ODSP are not only allowing the suffering, they're deliberately INFLICTING it.

I have 2 window air conditioners not being used I'd gladly give away to someone in need. Message me if interested.

[Millions Missing Can @MillionMissCan]

#MEAwareness (18)

We’re calling on you — our Leaders — to begin to take actionable steps to give people with #ME back to their families and their lives.

Collaborate with advocates to:

#ChangeTheFuture4ME

#StillSickYearsLater #MyalgicEncephalomyelitis
#HealthEquity

[Millions Missing Can @MillionMissCan]

#MEAwareness (17)

Funding biomedical research & partnering with the #ME community would restore hope for the future. #PwME need to believe our leaders want to engage meaningfully to find solutions.

#StillSickYearsLater #MyalgicEncephalomyelitis
#HealthEquity 4 #MillionsMissing

[Millions Missing Can @MillionMissCan]

#MEAwareness (16)

We’re dialing 911!

and calling for an immediate substantial investment into #biomedical research for the #PostViral diseases of #ME & #LongCOVID, building on the knowledge base of ME.

#StillSickYearsLater #MyalgicEncephalomyelitis
#HealthEquity

[Millions Missing Can @MillionMissCan]

#MEAwareness (15)

As long as #ME #biomedical research is neglected, Governing Bodies are seen as impeding progress.

Continuing to ignore the dire concerns of #pwME is causing distress to Canadian sufferers.

#StillSickYearsLater #MyalgicEncephalomyelitis
#HealthEquity

[Millions Missing Can @MillionMissCan]

#MEAwareness (14)

After decades of #ME being misrepresented, neglected, ignored & maligned… sadly, many #pwME have given up hope.

Suicide is higher than in the general population.

#StillSickYearsLater #MyalgicEncephalomyelitis
#HealthEquity

https://t.co/FZO5PDpbFv

[Millions Missing Can @MillionMissCan]

#MEAwareness (13)

Patients are not treated with the dignity & respect they need & deserve in medical settings & are crushed under the weight of discrimination & stigma.

#StillSickYearsLater #MyalgicEncephalomyelitis
#HealthEquity 4 #MillionsMissing

https://t.co/1f2J2uSXnX

[Millions Missing Can @MillionMissCan]

#MEAwareness (12)

Appropriate medical care is not widely available & trauma to #pwME caused by the systemic discrimination embedded in our healthcare system towards #ME is common.

#StillSickYearsLater #MyalgicEncephalomyelitis
#HealthEquity

https://t.co/91CuSbjf82

[Millions Missing Can @MillionMissCan]

#MEAwareness (11)

The impact of #ME on quality of life is significant. “Normal” needs to be redefined over and over again — often disrupting the lives of the entire family.

#StillSickYearsLater #MyalgicEncephalomyelitis
#HealthEquity 4 #MillionsMissing

https://t.co/BvJVFH6MfW

[Millions Missing Can @MillionMissCan]

#MEAwareness (10)

Adult children with #SevereME lose their independence. It’s common to see them move back home & for their aging parents to become their caregivers.

#StillSickYearsLater #MyalgicEncephalomyelitis
#HealthEquity 4 #MillionsMissing

https://t.co/OODnflUylS

[Millions Missing Can @MillionMissCan]

#MEAwareness (9)

Failure to research #ME has had catastrophic consequences for people. Economic hardship from being forced to abandon careers irrevocably alters lives.

#StillSickYearsLater #MyalgicEncephalomyelitis
#HealthEquity 4 #MillionsMissing

https://t.co/h6BEQWUkOI

[Millions Missing Can @MillionMissCan]

#MEAwareness (8)

The pain can be excruciating — the suffering relentless. Comorbidities are common. There can be dozens of symptoms with widespread bodily dysfunction.

#StillSickYearsLater #MyalgicEncephalomyelitis
#HealthEquity 4 #MillionsMissing

https://t.co/H2DWYRj3T4

[Millions Missing Can @MillionMissCan]

#MEAwareness (7)

#ME profoundly impairs the ability to function with 75% no longer able to work & 25% so severely ill, they are housebound & even confined to their beds.

#StillSickYearsLater #MyalgicEncephalomyelitis
#HealthEquity 4 #MillionsMissing

https://t.co/atptuz80Uy