Join the National PR Campaign for ME: Power to the Patient (P2tP)
Have you had enough of all the neglect and abuse of ME/CFS patients? Gabby Klein says now is the time for a National PR Campaign for ME/CFS to impress a change. Join the Patient Revolution to restore power to ME patients ...
Discuss the article on the Forums.

Need help with mold tests in Canada

Discussion in 'General ME/CFS Discussion' started by impossible, Feb 17, 2014.

  1. impossible

    impossible

    Messages:
    23
    Likes:
    21
    Hi :)

    Im helping out a friend who lives a couple hours from Winnepeg (Brandon). She moved into a moldy house, you know the rest. She moved out and immediately improved alot but is still suffering some pretty dramatic symptoms.


    Yeast overgrowth is now a problem when not kept in check and we strongly suspect viral activity too, possibly even lyme, who knows.


    We have been wanting to check C3a/C4a and haplotype but are unsure of how to go about it, I have no advice for her in this regard as I am not from Canada.


    She has a pretty open minded doctor who actually even prescribed her cholastyramine to try based on info she gave him, so we have a "normal" doc that is willing to help.


    She would also be willing to see someone else if that is required or would help. Are there even any docs that follow Shoemaker in that area? Any words of wisdom on how to proceed and get these tests?


    Thanks a bunch. She should be on here shortly, I think shes waiting for her screenname
     
  2. Approximately_me

    Approximately_me

    Messages:
    20
    Likes:
    2
    Hi there. Impossible posted this on my behalf. (Thanks!)

    If anyone has any info on how I might get these tests done from Canada or if there might be any knowledgeable Lyme doctors in Manitoba, please let me know!

    Thanks guys!
     

See more popular forum discussions.

Share This Page