International ME/CFS and FM Awareness Day is May 12: The World Will Know
Did you know that May 12 belongs to us? Lots of us are aware of this. We share the buzz on it amongst ourselves. We add blue ribbons to profile pictures. We raise our voices, join our hands, mount the few podiums available to us and tug at the sleeve of the rest of the world.
Discuss the article on the Forums.

Patient Advocate: Translational medicine

Discussion in 'Other Health News and Research' started by shrewsbury, Aug 13, 2010.

  1. shrewsbury

    shrewsbury member

    Translational medicine
    This is a catchy term. It is a bit difficult to understand the full ramifications of what it means. Certainly one of the hallmarks of this term is the non-ego based sharing of information. The Patient Advocate took an interest in a front page article in the NYTimes this morning.

    From what the Patient Advocate can understand, this article lays out, in a parallel field, what the Whittemore Peterson Institute is going to accomplish.
  2. Sasha

    Sasha Fine, thank you

    Fascinating - thanks for posting this, Shrewsbury. Really inspiring.
  3. Hope123

    Hope123 Senior Member

    "Translational Medicine" generally refers more to how research findings can be "translated" into clinical care. The issue at hand is that a fair amount of basic research happens in the labs but little of it actually translates to tests/ treatments that healthcare staff can use. Obviously some of this is limited by the trial-and-error process that is a natural part of science but there are also other factors, such as basic scientists not communicating with healthcare staff and vice versa about what each party needs. A second piece is that even when the research is solid, like in some areas of high blood pressure or diabetes care, there are obstacles in place that prevent it from being implemented -- e.g. insurance, health care systems, money, etc.
  4. muffin

    muffin Senior Member

    Interesting. Data sharing with CFS/ME is a problem. But a greater problem, it seems to me and other ultra smart people, is getting that medical research down into the clinical arena and into the hands of the doctors who must diagnose and treat. Now, how is that to be done?

    Great thoughts HOPE123!!!!!

See more popular forum discussions.

Share This Page