Skin sensations

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New Member

Date Joined Dec 2006
Total Posts : 2
   Posted 12/12/2006 12:14 AM (GMT -7)   
 Hello everyone, I am new to the board but not to Hep C I was diagnosed over three years ago, did the interferon trip for 7 months which only made me sicker. I do have a question, do anyone or do you know of hep c carriers know anything about skin sensations? I have them on my mouth, it feels like when we get novacaine and your mouth feels big and tingly.They come everyday, different times and lasting up to 45 mins, any suggestions will be much welcomed.
Thanks for reading...God bless sad

Regular Member

Date Joined Dec 2005
Total Posts : 446
   Posted 12/13/2006 3:31 AM (GMT -7)   
Sorry showgirl. I can't help with this problem. I have cold sores though. When I was first diagnosed with AIH in May 2004 I had sufferred cold sores on the lips for about two months prior. For the past three months this has returned but lately, since changing my herbs from the chinese doctor, the cold sores have disappeared. I have been taking isatis leaf for the cold sores.
Hope someone else can help you.

New Member

Date Joined Dec 2006
Total Posts : 2
   Posted 12/13/2006 3:08 PM (GMT -7)   
Thanks Marg for responding, I kinda wish mine were sores so I could put meds on, but its just a stupid feeling..lately my legs have been feeling like they are wet, and when I touch them there is no water. I hate this stupid diease..
God Bless
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