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        <title>HEPCnet Forums - Welcome Wagon</title>
        <description>If youre new, introduce yourself and ask questions. If youre having problems with registering - post that here also, as this is the only forum that does not require you to register.</description>
        <link>http://hepcnet.net/boards/phorum/list.php?9</link>
        <lastBuildDate>Wed, 08 Sep 2010 19:16:41 -0700</lastBuildDate>
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            <guid>http://hepcnet.net/boards/phorum/read.php?9,3136,3136#msg-3136</guid>
            <title>joint pains and arthritis (4 replies)</title>
            <link>http://hepcnet.net/boards/phorum/read.php?9,3136,3136#msg-3136</link>
            <description><![CDATA[ Hi all I am new here.  I was just reading some of your posts and was shocked to read that joint pain and arthritis is common to hepatitis?  Can anyone confirm that this is true for me?  I just thought I had that too not that they were related.  I thought I knew all about Hep.  that I needed to know.  Guess I better brush up.<br />
Also, looks like a lot of you eat special foods.  Do some foods help with Hep.?<br />
If you have any info. on this I would appreciate it.]]></description>
            <dc:creator>Lynn</dc:creator>
            <category>Welcome Wagon</category>
            <pubDate>Fri, 06 Aug 2010 13:17:18 -0700</pubDate>
        </item>
        <item>
            <guid>http://hepcnet.net/boards/phorum/read.php?9,2868,2868#msg-2868</guid>
            <title>Lady Marilyn... (no replies)</title>
            <link>http://hepcnet.net/boards/phorum/read.php?9,2868,2868#msg-2868</link>
            <description><![CDATA[ I have moved your post to the Open Board where more people will see it.   Were you on the old site under this name or did you have another name back then?   Anyway, welcome back to HepCnet and come on over to the other board and join in.]]></description>
            <dc:creator>Gill</dc:creator>
            <category>Welcome Wagon</category>
            <pubDate>Thu, 15 Jul 2010 16:40:10 -0700</pubDate>
        </item>
        <item>
            <guid>http://hepcnet.net/boards/phorum/read.php?9,2817,2817#msg-2817</guid>
            <title>about to start treatments (1 reply)</title>
            <link>http://hepcnet.net/boards/phorum/read.php?9,2817,2817#msg-2817</link>
            <description><![CDATA[ Hey,<br />
I was diagnosed with hep C genotype 2b about 2 weeks ago after going through a couple different doctors who thought it was just the cholesterol meds I was on. My numbers keep going up and down. First results I was 860/1668, next test 193/290, next test 480/1200 and most recent test 260/450. I am giving blood again this Friday. I am seeing a specialist at UCLA now. He said we will see how my numbers are and then start treatments. He said I contracted this about 3 months ago, leaving epidurals I got in my spine for herniated discs as the most likely place I contracted it. I do have tattoos, but didn't get one in the time frame he provided. I have never shot up any drugs or had a blood transfusion. I suffer from all of the symptoms. Aches and pains, fatigue, fever, itching, orange urine, blurry vision, memory loss, My questions are, is it possible for a doctor to pinpoint the time when you contracted it?, how normal is it for my numbers to go up and down the way mine do? How bad are the side effects of the treatments I am about to start? <br />
Thanks for any info.<br />
Eric Shipley]]></description>
            <dc:creator>onedabred</dc:creator>
            <category>Welcome Wagon</category>
            <pubDate>Tue, 13 Jul 2010 16:57:48 -0700</pubDate>
        </item>
        <item>
            <guid>http://hepcnet.net/boards/phorum/read.php?9,1960,1960#msg-1960</guid>
            <title>I can't figure out some things on this site (1 reply)</title>
            <link>http://hepcnet.net/boards/phorum/read.php?9,1960,1960#msg-1960</link>
            <description><![CDATA[ I can't figure out how to get to my private messages.  I click on them and nothings there. I'm not sure how to look at the posts.....Is it just posts from one person at a time? I'm at a loss when it comes to computers.....lol<br />
xoxox<br />
abby]]></description>
            <dc:creator>abby</dc:creator>
            <category>Welcome Wagon</category>
            <pubDate>Thu, 27 May 2010 01:14:08 -0700</pubDate>
        </item>
        <item>
            <guid>http://hepcnet.net/boards/phorum/read.php?9,1901,1901#msg-1901</guid>
            <title>new here (no replies)</title>
            <link>http://hepcnet.net/boards/phorum/read.php?9,1901,1901#msg-1901</link>
            <description><![CDATA[ Hi Everyone<br />
I am don in ks, and I moderate the HepCWebWarriors group in Yahoo groups. <br />
I am the info research guy, and am building a huge 'public' HCV Links Library for every Heppers research use.<br />
<br />
- [<a href="http://health.dir.groups.yahoo.com/group/HepCWebWarriors/links" rel="nofollow" >health.dir.groups.yahoo.com</a>] -<br />
<br />
[You DO NOT have to be a member to use this resource - it is public, and free.]<br />
<br />
I am 59, 1B, DX 2008, no HCV TX yet, labs good.<br />
I am a mbr of just about every HCV website or group, to show my support for the cause.<br />
I want to tell each one of you that you are in my heart, and you are not alone.<br />
Be well my friends. God bless you all.<br />
<br />
love<br />
don in ks<br />
<a href="mailto:&#108;&#117;&#100;&#105;&#99;&#104;&#114;&#105;&#115;&#116;&#50;&#48;&#48;&#48;&#64;&#121;&#97;&#104;&#111;&#111;&#46;&#99;&#111;&#109;">&#108;&#117;&#100;&#105;&#99;&#104;&#114;&#105;&#115;&#116;&#50;&#48;&#48;&#48;&#64;&#121;&#97;&#104;&#111;&#111;&#46;&#99;&#111;&#109;</a>]]></description>
            <dc:creator>xyloid02</dc:creator>
            <category>Welcome Wagon</category>
            <pubDate>Thu, 20 May 2010 14:30:44 -0700</pubDate>
        </item>
        <item>
            <guid>http://hepcnet.net/boards/phorum/read.php?9,1466,1466#msg-1466</guid>
            <title>How to help and support someone with hep c (3 replies)</title>
            <link>http://hepcnet.net/boards/phorum/read.php?9,1466,1466#msg-1466</link>
            <description><![CDATA[ hey everyone<br />
i myself do not have hep c however recently i had noticed that my boyfriend was showing symptoms of jaundice and because of his past history with drugs despite the fact that he had previously tested negative for hep c i urged him to get tested again.  The tests came back a few days ago and it confirmed that he does in fact have it.  More tests are being done to see exactly where everything falls.  I am trying to be as supportive as I can but despite that hes extremely depressed and feels that he is getting what he deserves for the live he used to live(he has been clean for 4 years).  I was wondering if anyone had any suggestions that could help or even anything that would help him feel more optimistic rather than this is the end.  His doctor didn't help him out very much, basically said you have hep c and sent him out the door leaving him guessing about everything which i imagine doesn't help any with thoughts that are probably running through his head.  Thanks for your time]]></description>
            <dc:creator>Ja Lapeno</dc:creator>
            <category>Welcome Wagon</category>
            <pubDate>Mon, 03 May 2010 18:33:22 -0700</pubDate>
        </item>
        <item>
            <guid>http://hepcnet.net/boards/phorum/read.php?9,1091,1091#msg-1091</guid>
            <title>Looking for local support group (1 reply)</title>
            <link>http://hepcnet.net/boards/phorum/read.php?9,1091,1091#msg-1091</link>
            <description><![CDATA[ Hi, I'm looking for a local support group in the New Orleans area.  Not having any luck at all. Thanks for any help. My email is <a href="mailto:&#115;&#98;&#52;&#48;&#57;&#117;&#115;&#64;&#121;&#97;&#104;&#111;&#111;&#46;&#99;&#111;&#109;">&#115;&#98;&#52;&#48;&#57;&#117;&#115;&#64;&#121;&#97;&#104;&#111;&#111;&#46;&#99;&#111;&#109;</a>.]]></description>
            <dc:creator>Sherri Boles</dc:creator>
            <category>Welcome Wagon</category>
            <pubDate>Thu, 18 Feb 2010 22:10:36 -0700</pubDate>
        </item>
        <item>
            <guid>http://hepcnet.net/boards/phorum/read.php?9,1011,1011#msg-1011</guid>
            <title>Everything I read says there are no symptoms but....... (5 replies)</title>
            <link>http://hepcnet.net/boards/phorum/read.php?9,1011,1011#msg-1011</link>
            <description><![CDATA[ Hi,<br />
<br />
It has been a month since the day I got a call from my doctor's office and the nurse informed me that I had hep C antibodies and she had set me up an appointment with a specialist. I went to see him the next week and he acted like it was no big deal, told me to go get some blood tests and come back in 3 weeks, which is this coming Monday. I checked the CDC web site for symptoms and they say that most people are A-symptomatic but some have flu-like symptoms and some fatigue. I was so fatigued today that I couldn't make myself get ready for work... my nerves are so on edge that I yell at my kids for no reason. I've been trying real hard to just not think about it because I know that will just make any symptoms even more pronounced but it isn't working. Am I the only person who feels really rotten even before starting the treatment? I have read what people say about how they feel during the treatment but nothing about before. Am I turning into a monster or did other people feel like this?<br />
<br />
Thanks for any input..]]></description>
            <dc:creator>feellikeagrump</dc:creator>
            <category>Welcome Wagon</category>
            <pubDate>Mon, 17 May 2010 22:27:11 -0700</pubDate>
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