Esther Crawley

It depends on whether the light bulb wants to change.

 

Apparently her new study isn't too far from her last. Coxsackie B has been linked to appendicitis and ME! https://www.ncbi.nlm.nih.gov/m/pubmed/4964128/

Maybe she's coming at it through the back door?

 

So to speak

 

I had thought this was s replication study but there are differences to the previous research from Finland.
Only taking follow up to 6 months looks like it may be maximising outcomes ( again)

 

Esther Crawley's new role as Director of Child and Adolescent Health!! aagghh

http://www.bristol.ac.uk/ccah/news/2018/leadership-change.html

 

Just saw it posted by someone in IiME Research Facebook group and they replied..

"The establishment looks after its own as we have seen and no matter what crass, untruthful or hideously self-serving propaganda some people (and organisations) come out with they still continue to retain positions of influence.

Something to remember for those who are repeatedly giving second-chances to organisations and individuals who have let them down, and continue to let down all people with ME."

They added these links:

http://www.investinme.org/IIMER-Statement-1611-02.shtml



http://www.investinme.org/IIME-Newslet-1706-02.shtml



http://www.investinme.org/IIMER-Statement-1709-01.shtml



http://www.investinme.org/IIME-Newslet-1612-01.shtml

 

Their twitter account is https://twitter.com/BristolCCAH

It looks like they've been supporting Crawley's quackery for a while, and it's pretty well in line with most of their other projects.

 

Poor kids!

 

My husband went to Bristol and it was originally on the list of universities for my daughter. Maybe she'll still even apply, knock their socks off and be offered a place. Then I'll send them a letter explaining exactly why she will not be accepting it, listing all the times they let her and other children with ME down by turning a blind eye to bad science. I'll look forward to that day.

 

If she's exiting the CFS field, then surely this is a good thing?

 

She won't leave the field, she is going to her new role to grow the brand. She will use this job to do the governments bidding on declaring more children 'mentally ill', I dont think she has even left the CMRC, she's just got Edwards and the functional crowd on the inside, its all just a big game.

 

Well Bristol CCAH are advertising a vacancy on Twitter for FITNET so ....

 

Wait which Edwards?

 

The one doing the £600,000 functional neurological symtoms study for the CMRC to dump us in the BDD category.

 

someone (#PACEtrial) has been trying to inform Bristol Uni students about Crawleys shenanigans.
Anyone care to sign up and PM them with the latest news about her?

https://www.thestudentroom.co.uk/showthread.php?t=4913512

 

Anyone looked at her CFS clinics site recently?
Evidence Based Treatment
We believe that all clinical care should have an evidence base. We therefore only offer treatment that has been recommended by NICE. Professor Crawley leads a research team based at the University of Bristol which conducts research in to the causes and treatment of CFS/ME. This means that all the treatment offered by the clinical team is based on the most up-to-date research results.

Our service featured in mainstream media
Esther Crawley explains why we do paediatric trials in CFS/ME:
Professor Crawley's TEDx talk, (November 2017)


http://www.ruh.nhs.uk/patients/services/clinical_depts/paediatric_cfs_me/index.asp

 

That's weird, because the Lightning Process certainly isn't recommended by NICE!