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Hep C Discussion Forum -> New Members Area -> hello, 8yrs. post transplant
Post Info TOPIC: hello, 8yrs. post transplant
Cinnamon Girl


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RE: hello, 8yrs. post transplant
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Hello Manosdelumbre, Paul,

Just wanted to mention that this is an old thread from 2009, in case you hadn`t realised.

I`ve been reading your posts and I wish you all the best of luck!  We`ll post any new information as it becomes available on post transplant treatment with the new DAA treatments. 

Welcome to the forum! 

~ Jill



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Jill 

(71 yo, lives in UK)

Was Gen 3a, 

24wks Peg Ifn/Riba, Sep 2010 - Mch 2011

UND @ Wk.4, UND @ EOT, 

SVR Nov 2011 --> Still UND @ EOT + 4 yrs.

 

 
Manosdelumbre


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Hello 8 yrs. Transplant , Manosdelumbre here 9 yrs. Transplant .... Have reinfected Liver RNA PCR recently found  2357004 copies virus load.... Will probably go to UCSF for consultation , then Liver Biopsy to exactly what condition my Liver is in after 9 yrs. then hope to get on New drugs Sovaldi or Harvoni . I have Geno type 1A.... Any advice ????? 



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From the Desk of Paul Soto
Vectorwoman


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Welcome aboard and {{{HUGS}}}'

I hope everything goes well for you.handshake.gif

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medusa


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Hello Doris, Sounds like you have been through a lot . I can't imagine what it is like to go through a liver transplant . I don't think they are offered to Hep C patients in France for the reason that the new liver will become infected . You sound like a survivor. Wishing you well,  Annie xxxxx

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Minerva


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Hi Doris and a very warm welcome to the forum!! aww I have moved your post here so that people can see it and welcome you.  Congrats on your successful transplant and i hope all is going ok. 

Have you ever undergone treatment?  Or has it been suggested?
Good to have you with us.

Hugs
Heather
xxx

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Finished TX 2005. Geno 3. Achieved SVR - Heather.

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dying2live


Newbie

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I have written a little about my journey on my bio....I live on the coast of South Carolina, USA.....living one day at a time.....lets talk

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Doris Alvis
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