Guest guest Posted September 16, 2010 Report Share Posted September 16, 2010 Well I've finally been diagnosed as having hemochromatosis. I''m waiting to see the blood specialist. I know this can make my ms worse. I just need to do some research. I have done research in the past for other family members who have this condition, it runs in my family. I just need to see how it affects my ms. I've been checked for this for years but they never used the correct blood test. They always checked my ferritin levels. Apparently what's more important is the saturation. I've researched and IP6 comes up. Has anyone heard of this or tried it? Also I know this has been posted before, but I am now stuck with needing a doctor to prescribe ldn for me. The doctor who has been prescribing it for me doesn't feel it's doing it's job, because I've had 2 relapses. Does anyone have into? I used to before my computer crashed. thanks for any help. Tina </HTML> Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.