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PNHdisease · To list is for people with Paroxysmal Nocturnal Hemoglobinuria (PNH), or friends and family members of those who have this rare
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Re: Digest Number 1650   Message List  
Reply | Forward Message #16875 of 17533 |


PNHdisease@yahoogroups.com wrote:


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There is 1 message in this issue.

Topics in this digest:

1. New member here
From:


________________________________________________________________________
________________________________________________________________________

Message: 1
Date: Sun, 10 Oct 2004 01:27:49 -0700
From:
Subject: New member here

Hope to get to know you all. I will try to contribute to the discussion with my thoughts, knowledge, and opinions.


________________________________________________________________________
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Hello,

 

Welcome to the group.  I'm Susan in Chicago.  I was dxed with PNH in 1998.  How long have you had PNH? Do you live in the US?  We have members from all over the world!!

We have moved to our new website www.pnhdisease.org.  It has more features and medical info files.  There is a Forum where everyone can raise or respond to a topic. 

 

Susan



Diag "98 Mild AA Prob since 1975
Low dose Pred., Coumadin, iron, folic acid, Fosomax, preventive
Prilosec. 3 RBC Transfusions, no other treatments

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Sat Oct 16, 2004 8:16 pm

suztree
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PNHdisease@yahoogroups.com wrote: There is 1 message in this issue. Topics in this digest: 1. New member here From: ...
susan todd
suztree
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Oct 16, 2004
8:16 pm
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