Enrolling: Bateman-Horne Center Biomarker Study

Who: Lucinda BatemanBateman-Horne
What: Participants will:

  • Receive a comprehensive clinical evaluation
  • Answer questionnaires
  • Provide blood samples
  • Commit to a yearly visit to Bateman-Horne in Salt Lake City, Utah (3-5 years, e.g.)

Information will be shared with multiple research groups searching for biomarkers for FM and ME/CFS.

How to participate: Click here to start the research eligibility form. (If this does not work, click on the link under ‘additional information’).
 
When: Ongoing
 
Where:  Salt Lake City, Utah, USA
 
Additional information:  Click here to see all of Bateman-Horne’s recruiting studies.
Facebook
Twitter
WhatsApp
Email

1 thought on “Enrolling: Bateman-Horne Center Biomarker Study”

  1. Susan Richardson-James

    Good afternoon
    I would love to be able to contribute to research (apart from financially as I am unfit to work at this time).
    Would you know of anywhere in the UK that are running trials at the moment.
    My case is quite complex and may be of interest to researchers.
    Many thanks
    Susan

Comments are closed.

Latest News

a multi-water colored image with the words, Severe ME Artists Project 2024 in white font outlined in black. the meaction action logo in the bottom right hand corner.

Severe ME Artists Project 2024

Quick Overview: Submit one piece of artwork – image, writing, or video Label your artwork with your name as you want it to appear, an underscore, and the number of years with severe ME Example: Lastname_FirstName_14 FirstNameOnly_ No copyrighted material If you are submitting a video, it must be under two minutes. Submission due by

Read More »
Light blue square with rainbows in the top left and bottom right corner. In the middle are the words, -Pride is Valid- No Matter How One Celebrates or Experiences It. #MEAction Board Member, Jennifer England, shares her views on Pride. The #MEAction logo in the top right corner.

Pride Is Valid No Matter How One Celebrates or Experiences It

In honor of Pride Month, #MEAction is sharing a heartfelt message from our board member, Jennifer England, about what Pride means to her and her wife who lives with severe ME. My wife and I have both been queer our whole lives, but in the 70s that was the quiet part you didn’t say out

Read More »

Questions to Ask Prospective MPs About ME/CFS

In the next few weeks, candidates will be knocking on doors seeking votes for the upcoming UK Election. It’s important that candidates from all parties are made aware of the challenges facing people with ME and Long Covid. It can be a little daunting to be unprepared so here are some questions you might want

Read More »
Scroll to Top