Jenny Meagher
@jennmeagher.bsky.social
Life stolen by Myalgic Encephalomyelitis.
Waiting to be rescued by science.
Science waiting to be funded by governments #MECFS
Waiting to be rescued by science.
Science waiting to be funded by governments #MECFS
Thank you to @emergeaustralia.bsky.social for organising this important event.
November 2, 2025 at 10:02 PM
Thank you to @emergeaustralia.bsky.social for organising this important event.
Reposted by Jenny Meagher
I speak to Australian ME/CFS researchers who rely on either the austerity ridden UK or US based grants. Since Labor came to power, the NHMRC has allocated a grand total of ZERO in research grants for ME/CFS, a condition that impacts hundreds of thousands of Australians.
October 23, 2025 at 1:24 AM
I speak to Australian ME/CFS researchers who rely on either the austerity ridden UK or US based grants. Since Labor came to power, the NHMRC has allocated a grand total of ZERO in research grants for ME/CFS, a condition that impacts hundreds of thousands of Australians.
For ppl w disabling conditions like #MyalgicEncephalomyelitis #MECFS, the #MRFF underspend is beyond frustrating. Our lives pass us by while we wait for research to find a treatment. Our researchers are ready to go. Funding should be commensurate w prevalence & burden of disease.
Thank you Monique.
Thank you Monique.
September 29, 2025 at 12:48 AM
For ppl w disabling conditions like #MyalgicEncephalomyelitis #MECFS, the #MRFF underspend is beyond frustrating. Our lives pass us by while we wait for research to find a treatment. Our researchers are ready to go. Funding should be commensurate w prevalence & burden of disease.
Thank you Monique.
Thank you Monique.