We are finally collecting data for our first attention study! If you would be interested in participating, please sign up on our website (https://t.co/7fFJvOzevx) and share :)
#MECFS#ME#CFS#Leicester#research
Let’s give @AAltafUoL a follow and learn more about the study that she is conducting in the UK on The impact of ME/CFS on visual sensory processing and selective attention. More info at the link @MEResearchUK: https://t.co/5fJfa4MVf8 #MECFS#PwME#VisualProcessing#CNS
@ka_ashy @CBMEgroup@s4me_info Hi. If corrected then yes! However for those that are housebound/experience severe symptoms I am designing something else rather than lab sessions. If you would like to know more please email me at [email protected] :)
Hi all and thank you to those that have already registered interest! I am amending my ethics (details can be found here: https://t.co/TPntkQNbM6 via @s4me_info. This means I will need more time before responding with further information. Thank you for your patience :)
New Leicester (UK) #MEcfs & #PostCovid study that is recruiting
Investigating the impact of ME/CFS & #LongCOVID on visual perception & sustained attention using Pupil Frequency Tagging & EEG
https://t.co/WnwJkUQ0H3
@MEResearchUK-funded
Not a biopsychosocial study
#CFS#PwME
Dr Doug Barrett and Anosha Altaf from the University of Leicester are looking for participants for their ME Research UK-funded study on visual sensory processing and selective attention in ME/CFS. To find out more, please visit the study website: https://t.co/Axi8V8wPF9
2/
This study [in Leicester, UK] is currently recruiting individuals with ME/CFS or #LongCOVID, over the age of 18, with normal or corrected-to-normal vision and no known neurological disorders such as epilepsy.
#MEcfs#CFS#PwME
Open - RECRUITING: Investigating the impact of ME/CFS and Long COVID on visual perception and sustained attention using Pupil Frequency Tagging and EEG
https://t.co/TPntkQMDWy via @s4me_info
New Leicester (UK) #MEcfs & #PostCovid study that is recruiting
Investigating the impact of ME/CFS & #LongCOVID on visual perception & sustained attention using Pupil Frequency Tagging & EEG
https://t.co/WnwJkUQ0H3
@MEResearchUK-funded
Not a biopsychosocial study
#CFS#PwME
@SmileForME_xx Almost finished designing the first task of #PhD study investigating the impact of #MECFS on visual perception and attention!! Excited to get into recruitment stage soon for #pwME
Hello @actionforme! I am a #PhD student looking to recruit #pwME for my studies! Please could I have an email or number to share information and talk opportunities? #MECFS
@karenphysiocouk As someone currently completing a #PhD on the effects of PEM and fatigue on cognition for those suffering with #MECFS#pwME, I'd love to hear what people would be more interested in understanding and learning from their personal experiences please!
Recruiting soon! 🚨
A study exploring attentional control in ME and CFS individuals and the effects of fatigue on cognition. Please get in touch for more information or visit my website. I'd love to hear personal experiences to shape future studies!
#pwME#MECFS#research
Recruiting soon! 🚨
A study exploring attentional control in ME and CFS individuals and the effects of fatigue on cognition. Please get in touch for more information or visit my website. I'd love to hear personal experiences to shape future studies!
#pwME#MECFS#research
@karenphysiocouk I'm a PhD student funded by ME Research UK that will be beginning recruitment in the Midlands area soon!! If anyone would like some more information please visit my website and get in touch... I'd appreciate it immensely :)
https://t.co/7fFJvOzevx
If you reside in the Midlands UK, have ME/CFS and are willing to share your personal experiences and everyday struggles, please get in touch! Check out our website for information on my project: https://t.co/7fFJvOzevx
#MECFS#pwME
We are currently developing our 1st computer-based measure and anticipate collecting data from the end of March onwards! Please share your personal experiences with #MECFS in order to shape my PhD projects if you are a #pwME.
We have coordinated an open letter with other M.E. orgs in response to the recent Dragons Den episode in which a contenstant made unevidenced claims regarding the efficacy of 'acu seeds' as a treatment for #MECFS
You can view the letter here: https://t.co/Usy0zf78Ny