Anyone been to MASS. FFC??

Discussion in 'Fibromyalgia Main Forum' started by ruby711, Aug 10, 2006.

  1. ruby711

    ruby711 New Member

    Am thinking of just getting tested at the Mass. FFC, and am wondering if anyone has had any experience with them.
    I have yet to be tested for even one virus or bacteria. ruby
  2. pammy52

    pammy52 New Member

    I haven't been to the MA FCC but I am going to the Northampton Wellness Center.
    I found the center thru the Dr. Locator on the website.

    Dr. Elson and Dr Lynch both treat FMS..CFIDS and other chronic illnesses.
    I started in May and see Dr. Lynch.
    So far I am very pleased with him and the center.

    Extensive lab work was done on my first visit and I was given the info for out of pocket tests that they will do as well.
    I was provided with a kit for stool analysis that is then mailed to a lab..

    Dr. Lynch is well versed on Dr. Tietelbaums protocol and because I have been wanting to follow that protocol for the past 3 yrs., I am now doing that with his guidance.

    I feel that he will support his patients in any way they are interested in addressing their illness though.
    He will make many recommendations based on his knowledge and experience but leaves the decision to the patient as to how you want to proceed.

    If you are close enough you might want to call them to find out more info..

    Hopefully you will hear from someone who has been to the FFC.
    One thing I can say is that I have compared the price of supp. available thru the FFC and Northampton Wellness Center and the FFC charges 20-35% more for most.
    I order almost everything at this point from Prohealth.

    Good luck,
    Pammy
  3. ruby711

    ruby711 New Member

    Thanks for info on Northampton wellness ctr. I will check it out.
    ruby