Complex Health Australia

Grassroots #CSX collective
#ComplexHealth #ChronicHealth #MedicalNeglect #Trauma #MedicalGaslighting #Inaccessibility [email protected]

[Proton @ProtonPrivacy]

The 8th edition of the Proton Lifetime Charity Fundraiser is here!

🎟️ Enter the raffle for a chance to win 1 of 10 Lifetime plans

💜 Help us support 10 community-nominated organizations

🎁 NEW: We’re giving away an additional Lifetime plan through a social contest.

⬇️1/6

[Complex Health Australia @ComplexHealthAu]

@lilslimer69 @DafoeWhitney Ever try the pure powder? Try it during the day @DafoeWhitney? Followers of @DorissLoh research often titrated to 1000’s mgs spread across a day during the day. Read right back through her fb posts. Melatonin also potentiates. It is also utilised to potentiate supplementation.

[Complex Health Australia @ComplexHealthAu]

@practiceyrPE It wasn’t only the meditation that you focus on here. The study listed lifestyle change and support. Social. Nutrition..

[Complex Health Australia @ComplexHealthAu]

@ThePOTSPostman See pioneer Sharon Meglathery MD’s RCCX Theory Please credit her https://t.co/tivdTboAVN

[Complex Health Australia @ComplexHealthAu]

@leaferi @NeuroSjogrens See @RCCXTheory_MD

[Sophie Scott @sophiescott2]

@ThePOTSPostman Some great research from Dr Vidia Raj shows POTS patients have lower anxiety levels than the general population once somatic symptoms of POTS are excluded like rapid heart rate.

[ThePOTSPostman @ThePOTSPostman]

"Prior to being diagnosed with POTS, 69% of POTS patients are diagnosed with anxiety or told that their symptoms are "all in their head."

PLEASE listen to patients when they tell you something is wrong and that it is not anxiety!

We know our bodies better than anyone.

[Complex Health Australia @ComplexHealthAu]

@MinorHeretic @drseanmullen @SafetyInfoCan And, prophylactic HDM & AA, c/o @DorissLoh research.

[Complex Health Australia @ComplexHealthAu]

@themathendo Come on, your communication isn’t particularly non violent and welcoming of any movement on these issues and collectivisation.

[The BMJ @bmj_latest]

"I felt I had wasted years of my life trying to convince health professionals of my physical symptoms."

Sarah Clark shares what it is like to experience a misdiagnosis and how health professionals can support someone who has been misdiagnosed
https://t.co/80OAk5mAeV

[Sidor 🏴󠁧󠁢󠁳󠁣󠁴󠁿🇦🇺 Did @SidorDid]

@themathendo Regular Uk police officer don't carry firearms nor tasers. They carry batons, incapacitant sprays, handcuffs & leg restraints. Special forces carry tasers & firearms & are called in as needed.

Regular Scottish Police talk down &/or disarm knife/broken bottle or glass wielders.

[Julian Buchanan, PhD @julianbuchanan]

More prohibition failure.

We don't need more monitoring or data on 'drug' use

We need to end this futile game of cat and mouse we call prohibition.

It's so costly, so damaging and so harmful to so many. https://t.co/pgLKBgrSY5

[The Political Context Machine @pcet2022]

Closing the Gap??

The Closing the Gap report is based on a national strategy to reduce Indigenous disadvantage.

Albo will be tabling the new Closing the Gap report in parliament this week.

And its a shocker.

If you are a Labor person talking about Closing the Gap this week, please remember "we" are part of the gap.

Here's why.

For the past two years we have implemented Scott Morrison's abusive Welfare Policy.

We have been directing Centrelink to deny access to food and medicine to Indigenous people via the barbaric Mutual Obligation policy.

Over 9,000 times every single week on average, we deny access to food and medicine to Indigenous people.

Every week.

For two years.

Including right through the Voice Referendum debate.

Including those weeks where we criticised the Cookers for being racists.

Including during the actual week of the Voice Referendum itself!

9,000 times every single week on our watch, we have denied access to food and medicine to Indigenous people.

And here's the kicker.

Albo will be tabling the new Closing the Gap report in parliament this week.

And guess what we will all be doing this week?

Denying access to food and medicine to Indigenous people over 9,000 times again!

We are the gap.

If you would prefer not to put your name to this barbaric abuse again this week, message

Bill Shorten @billshortenmp

and

Tony Burke @Tony_Burke

Tell them to pause the Mutual Obligation rules immediately, until a new policy is put in place.

#auspol

[Complex Health Australia @ComplexHealthAu]

@YDASvic @carlyfindlay @dana_advocacy Does anyone know of advocacy for polyvictimsied people nationally?

[Complex Health Australia @ComplexHealthAu]

@gemcarey This is / was potential for any ‘RCCXer’ @RCCXTheory_MD circa / post 2009.

We’ve tried to connect / collab. locally but violence of selective social hierarchy is clear where privilege gatekeeps. It’s an absurd sabotage. But, ‘ok’, only when certain mob allow go ahead.. /s

[Sally can't wander right now @WanderingSally]

Science indicates candidate treatments - they're not accessible.

Existing diagnostic tools are often insufficient.

GPs/Specialists lack knowledge or can't (won't) prescribe off-label.

Long wait times.

Too many Drs still think 'its all in your head'.

#LongCovidAwarenessDay

[Sally can't wander right now @WanderingSally]

Most #LongCovid research or treatment is about helping you cope or address deconditioning.

Would you treat a broken leg with exercise or CBT. Why #LongCovid?

Let's build on #MECFS knowledge and target leading hypotheses

#LongCovidAwarenessDay
https://t.co/UauMA0sCdW

[Sally can't wander right now @WanderingSally]

#LongCovid is a serious debilitating illness affecting >65 million. ~1 in 10 C19 infections. >200 symptoms.

Post-viral illness is not new.

#ME/CFS has been ignored and medically mistreated for decades. If we paid attention then, we'd know what to do now.
#LongCovidAwarenessDay

[ME/CFS Priority Setting Partnership @PSPforMECFS]

The Top Ten+ #MECFS Research Priorities are now published in a peer-reviewed journal!

This marks another important step in our work, and we hope to see this article well cited in future research funding applications.

#pwme @LindAlliance @actionforme

https://t.co/qEfKveg6pU

[Fran Haddock @franhaddock_]

He is at risk of death if he is not moved somewhere safe soon. His family are denying him a feeding tube. #MillionsMissing #MyalgicEncephalomyelitis #MECFS #pwME #VerySevereME