More about me...About SherryBerryposted on Nov 30, 2007
I am trying to live with the fact that my 17 year old son has a rare disease known as Wegeners Granulomatosis and there is no cure. This disease was caught in some of the last stages, therefore he is catagorized as terminal.. So, I can feel everyones pain who is having a trying time as well.. Maybe this site will help keep our minds off of things for a bit, thats what I am hoping for.. If there is anything I could do for anyone I would, I can offer you a friend or just someone to talk to..
If there are any doctors or medical proffesionals on the site, I would be so grateful if you could tell me more about this disease.. Thanks ^ top
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