Study at UNB
DOES YOUR SPOUSE/PARTNER HAVE FIBROMYALGIA?
A team of researchers at the University of New Brunswick, led by Dr. Sandra Byers, are conducting research about relationship and sexual well-being of men and women who have a partner with fibromyalgia. We are interested in hearing your first-hand account of how your partner’s fibromyalgia has impacted your relationship and sexual well-being.
If you are a man or woman aged 21 or over who is in a romantic relationship of at least 12 months and your spouse/partner has been diagnosed with fibromyalgia, you can participate in this study. However, we will not be able to include people with certain serious illnesses.
By participating, you will complete a background questionnaire and participate in an audiotaped individual interview. The interview will take approximately 1.5 hours. To compensate you for your time, you will be given a $50 gift card.
Research at University of Oklahoma
If you suffer from chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME)? How have your interactions with medical providers and others in your life affected you? Would you like to share your experiences with others? Please participate in the survey below to add your voice to the body of research on chronic fatigue syndrome/myalgic encephalomyelitis. After completing the survey, please share this link with others who suffer from CFS/ME.
[CO-CURE] NOT, RES, ACT: Invest in ME (Research) Press Release – 1/2 Million Reasons for Progress with ME
UK Charity Invest in ME (nr 114035) today announces that its biomedical research fund for ME has now passed a major landmark.
Together with our fantastic supporters we have initiated major biomedical research into ME projects which will change how ME is researched, treated, perceived and eventually funded.
With the visionary Let’s Do It For ME team, using positive campaigning to achieve progress, we have together enabled progress for the benefit of all people with ME and their families.
Read our full press release at http://www.investinme.org
describing our biomedical research fund which has passed “£1/2 MILLION”– raised over the last four years by ME patients, their families and friends.
Congratulations to all our supporters.
Thank you for all your past and continuing efforts.
“Things Do Not Have To Be The Way They Are – We Can Change Things” – Dr Ian Gibson
Let’s Do Change
Invest in MEUK Registered Charity Nr. 1114035
PO BOX 561
Eastleigh SO50 0GQ
10th International ME Conference 29th May 2015
Biomedical Research Colloquium 5 27-28th May 2015 London, UK
New study on CFS
In myalgic encephalomyelitis/chronic fatigue syndrome, increased autoimmune activity against 5-HT is associated with immuno-inflammatory pathways and bacterial translocation.
Update from our research being conducted by Dr. Paul Grof:
A briefing on the medication Trazadone prepared by Shannon McCloskey, BA, MEd, CCC, Research Coordinator/Counsellor, Mood Disorders Centre of Ottawa.
[CO-CURE] RES, MED: Difficulties with reading: an experimental study
The research program at the University of Leicester into the problems people with ME/CFS have
with their eyes and vision is powering ahead, and ME Research UK has now provided funding for investigations into another aspect – the specific difficulties patients have with reading.
ME Research UK and the Irish ME Trust helped to initiate the program in 2011, and the Leicester team recently obtained additional support from 2 ophthalmic charities to allow work on a range of topics, including distance focusing and depth of vision.
Research with Plymouth University
A comprehensive survey into the symptoms of people with ME/CFS, fibromyalgia and irritable bowel syndrome (IBS)
Breaking Research News
The Clock Was (Is) Ticking: Major Study Suggests ME/CFS is Hit and Run Disorder