Confused by ontology & epistemology? A short guide to help you navigate this aspect of research design + a simple framework to demystify the different philosophical positions >> https://t.co/jSRlQOxtv7 by @TomFryer4 #phdchat#phdadvice#phdforum#phdlife#ecrchat#acwri
'Virtual reality education on myalgic encephalomyelitis for medical students and healthcare professionals: a pilot study' Anderson T. et al. BMC Med Educ 24, 1018 (2024). https://t.co/BWnICtXgCV
🚨New study now recruiting on vagus nerve stimulation for people with ME.
We are looking for 40 #pwME who live in NW England (UK) and have never tried vagus nerve stimulation.
All details can be found on our website here
https://t.co/lE5to4m1W0
ME Research UK have been asked by the #ThereForME campaign to share an opportunity for researchers - the ‘£100m challenge’
In this, researchers are invited to share ideas on "How to spend £100m annually for five years to solve ME and Long COVID"
Info: https://t.co/17DNGUv4K7
Thank you to all our followers - and a warm welcome to those who are new to @MEresearchzone.
Here, we aim to share:
- New ME/CFS research
- Relevant funding calls
- Relevant conferences and courses
- Resources for researchers and research students
#MECFS#MEresearch
"Research has a diversity problem. Many groups are underrepresented in research including women, ethnic minorities, people with disabilities and socially disadvantaged populations. " Nature - https://t.co/HTAtn7YzuK
FUNDING OPPERTUNITY from @MEResearchUK
Please share with anyone interested in investigating the causes, consequences and treatment of ME/CFS.
Funding available for biomedical studies worldwide.
Find out more: https://t.co/02zczO570F
One of the best ways to help is to participate in ME/LC Research. Here’s how:
🌍Join the @OpenMedF StudyME Registry https://t.co/U7rbtfVClB
🌍 LC studies recruiting near you https://t.co/dFWiJt5ekD @lcstudiesdotnet
🌍 List of ME studies recruiting https://t.co/gwb6GyTmvT
(Worldwide)
I've just received this update.
They are still looking for more people with ME/CFS, Long Covid, #Fibromyalgia, & healthy controls
Sign up here:
https://t.co/re27UGityi
#MEcfs#CFS#PwME#LongCovid
Thank you so much to everyone who has shared our study opportunities for people with ME/CFS, and health care professionals relating to family planning, pregnancy, and parenting. We have had a great response so far! The surveys will stay open until 31st Aug 2024 #MEresearch#MECFS
The faMEly Study for #HealthcareProfessionals - Please share as widely as possible.
PDF Poster: https://t.co/ULwsGYYkK5
Dr @Emma_Slack1 on behalf of the faMEly study team says:
We have a survey for health care professionals, including midwives, health visitors, obstetricians, and experts in the field of ME/CFS, in the United Kingdom.
Link: https://t.co/0EI3HKMEBJ
#MECFS #MyalgicE #MyalgicEncephalomyelitis #Pregnancy #Childbirth #Research #RamsayResearchFund #MedTwitter
Just a quick post to say thank you so much to everyone who has completed our surveys so far, and for the questions and feedback we have had.
Apologies if I have missed anything! If you have any further questions please contact the research team at: [email protected]
Thank you for sharing @MEAssociation!!
Please consider taking part in our study if you are able - we are looking for people with ME/CFS, and health professionals who provide care around family planning, pregnancy, and raising children. #faMElystudy#mecfs#meresearch
@Chronically2784 @Naomi_D_Harvey@MEAssociation It may be that not all questions are relevant but the questionnaire should direct you. You can also leave us feedback on whether you think we should be asking any other questions, and let us know how we could improve the questionnaire. Hope that helps.
@Chronically2784 @Naomi_D_Harvey@MEAssociation Hi, yes — we are looking to hear from a range of people who are over 18, in the UK, and have a diagnosis of ME/CFS. We hope to identify research priorities going forward - including the impact of not being able to have children/MEtaking that decision away.
The faMEly Study: #MECFS and pregnancy – an exploratory mixed methods pilot study.
PDF Poster: https://t.co/WqNSG9EqNO
Dr @Emma_Slack1 on behalf of the team says:
We would like to invite people who have a diagnosis of ME/CFS, are aged 18 and over, and living in the United Kingdom, to take part in an online questionnaire about their thoughts and experiences relating to family planning, pregnancy, and raising children.
https://t.co/NnMB7uFnqm
#pwME #MECFS #MyalgicE #MyalgicEncephalomyelitis #Pregnancy #Childbirth #Research #RamsayResearchFund
@Naomi_D_Harvey@MEAssociation Hi, yes there is - the questionnaire should direct you to the right section based on your responses. We know how many people are in this situation, and agree that it is hugely important to capture. Thank you for your very important question.
Thank you so much to everyone who has already completed our surveys!
We need more health care professionals:
- GPs
- Midwives
- Health visitors
- ME/CFS specialists
Link for HCPs: https://t.co/0XJWVVmVCa
Please complete if you can - and please share! #mecfs#pwme
Thank you for sharing @MEAssociation!!
Please consider taking part in our study if you are able - we are looking for people with ME/CFS, and health professionals who provide care around family planning, pregnancy, and raising children. #faMElystudy#mecfs#meresearch
Thank you for sharing @MEAssociation!!
Please consider taking part in our study if you are able - we are looking for people with ME/CFS, and health professionals who provide care around family planning, pregnancy, and raising children. #faMElystudy#mecfs#meresearch
The ME Association is pleased that the faMEly study is now starting to recruit participants. If you are able to take part, we would encourage you to do so. The study is fully funded by the MEA #RamsayResearchFund (RRF).
#pwME#MECFS#MyalgicE#MyalgicEncephalomyelitis#Pregnancy #Childbirth #Research #HealthcareProfessionals #Midwives #MedTwitter