User talk:Bronzeguy

This is a good article; however, I can’t help pointing out that one aspect (the most important of all) has either been omitted or deleted, and without it the article loses much of its impact.

I quote: “Warder realized that she had been provided with proof that much of what she had been told about the disorder was incorrect: women could develop Hemochromatosis, and it was not only a disease of middle-age.”

What is misssing from the statement is the vital fact that she realized that the DISORDER WAS HEREDITARY! This, in fact, was what drove her to start sounding the alarm in the first place, and this is what drives her to this day! Because the genetic factor is now taken for granted, what must be considered is that knowledge of that fact was  not generally the case before she embarked on her crusade... To this day,despite het untiring efforts, many doctors still fail to warn the newly-diagnosed that all first-degreee relatives should be investigated!

It is for this reason that her mantra - and that of every society she has founded - is ‘FIND US ONE PERSON AND WE HAVE HOPE OF SAVING A FAMILY!” I have reason to be grateful that I read that!

There are several links to the Canadian Society in this article and on the Net, that illustrate this.

I long to edit the paragraph but I am afraid of doing something wrong.

Bronzeguy (talk) 06:35, 13 July 2010 (UTC) Bronzeguy (talk) 06:41, 13 July 2010 (UTC)