1. Patients launch $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
    Check out the website, Facebook and Twitter. Join in donate and spread the word!
Phoenix Rising Adds Two New Board Members
Mark Berry introduces the new President of Phoenix Rising, Dr. Gary Solomon, and welcomes Professor Jonathan Edwards to the Phoenix Rising Board of Directors.
Discuss the article on the Forums.

Dr. Chia as clinician?

Discussion in 'ME/CFS Doctors' started by urbantravels, Apr 9, 2011.

  1. urbantravels

    urbantravels disjecta membra

    Los Angeles, CA
    I've been looking and I don't see any topic about Dr. Chia as a clinician. Has anyone here actually been to him for general CFS care?

    My impression has been that he is all about the enteroviruses and might not have a well-rounded clinical approach (i.e. looking at and treating various symptoms; knowing what to do about OI; which pain meds are best; giving good advice on other meds like immune modulators; etc.) But I really don't know for sure. Does anyone here have first hand experience with his treatment approach?

    In my ideal world, I'd go to see Nancy Klimas (and I might do that after all) but...she's in Miami and Dr. Chia is here in the LA area. So I thought I'd double check on Chia before writing him off.
  2. Timaca

    Timaca Senior Member

    I see Dr. Chia. I like him. I do have Coxsackie B3 and B4 infections. Oxymatrine has helped me. Since you live in the area, I would certainly give him a try. Heck I travel from out of state to see him, so I must like him. :)

    Best, Timaca

See more popular forum discussions.

Share This Page