Re: hemochromatosis

[Guest guest]

You may be a candidate for bloodletting (I'm not kidding, they still do this) or

CCVSI. LDN didn't give me symptomatic relief and it made my legs stiff at the

dosage that I was taking (4.5 mg). You might try a different dose before you

give it up.

>

> 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

[Guest guest]

i take 2000 mg/day of IP6 that i purchased at vitacost. it was inexpensive and

i'm told that ms people have excess iron deposits in the brain. IP6 doesn't

remove bodily iron that is attached to hemoglobin only iron that is in areas

where it doesn't belong..

hemochromatosis

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

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[Guest guest]

Hi Tina,

This site may be of help:

http://tinyurl.com/how-to-obtain-ldn

All the best,

Dudley Delany

http://profiles.yahoo.com/dudley_delany