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Hep C Discussion Forum -> Post Treatment -> Just an Update
Post Info TOPIC: Just an Update
greenqueen


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RE: Just an Update
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Hi Wayne,

Thanks for taking the time to share your success story smile

Wishing you good health and happiness


Love Steff xx



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Geno 3a. 24 wks tx 20/10/05 - 06/04/06. Achieved SVR.
Kirstin


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Wayne, thanks for sharing your story. I have to say that the going has been real tough for me lately but after reading your post it gave me the strength to keep on keeping on.. Thanks again xxx



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Genotype 3a Started tx 11 May 2011 for 24 weeks. With scarring. VL before tx= 4 million.. UND@4 weeks. UND@12 
Minerva


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Really nice of you to stop by and share your story Wayne!!  Thanks. aww  Very inspiring message and it's always good to hear from people on 'the other side', as it were.

Wish you all the best.

Hugs

Heather xxx



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

When You Are Up To Your Neck In It - Keep Your Chin Up!!

'Knowledge. Is knowing that a tomato is a fruit. Wisdom is not using it in a fruit salad'. My dad. X.
Iris Dragonfly


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wow, since 1999....that does give one hopebiggrin4   See ya round?   Iris



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in the silence of the woods, you will not be alone- Chief Seattle

60 years on planet, Female, diagnosed 1978 as non-a non-b, VL 8mill+, Fibro f-1f-2, Genotype 1a, treatment naïve....UNTIL 7-01-18  !!!! started Harvoni 12 weeks. :)

4 weeks=UND, 8 weeks=UND, 12 weeks=UND (EOT= 09-23-2018)
missycat


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What a kindhearted thing to do posting your storyaww

so happy things worked out for yousmile

kaz

xxx



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Lift the hearts of those around you, share the goal that's in your sight. Keep strong, if i can do it anyone can! tx finished virus free :))))
PJ


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Thanks, Wayne, for sharing your wonderful success with us!!

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Diagnosed in 2006. Probably infected in the late 70s or early 80s. Genotype 1B. Starting TX on 5/5/11 with the SOC and Teleprevir. 
Greg


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Thank you Wayne, 

A great post it gave me a boost just to read it.  As James has said your most welocme if you feel like it to share or just drop by and say hello.

Bless you,
Greg



-- Edited by Greg on Wednesday 6th of July 2011 02:46:00 AM

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The mind is like a parachute it works best when it is open. "The Dalai Lama" My blog: http://greghcv.wordpress.com/
Genotype 1a, started tx 1st Feb 2011, for 48 wks. Week 24 PCR 26/07/11 Non-Responder
New TX start date 12th Sept 2016 Harvoni x24 weeks.  VL 7.4 Mil. Week 4 "Undetected"
James10500


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Nice post Wayne, thanks for the inspiration. Welcome to the forum perhaps you can share more of your wisdom.

James

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Diagnosed 4/13/10; Started Tx 8/13/10; SVR 7/27/11
wslandry


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Hi everyone

I wanted to give some positive feedback for people that have Hep C and were blessed enough to respond to treatment.  Im not sure if this is a new room but it doesnt matter if we are all here to receive love and support.  My PCR and liver alts have been normal after doing combo treatment in 1999 and I feel so blessed that when I was going through the highs and lows of treatment I had Seekers room and Janis when she was with us to get such love and support during those times of wondering if I was going to make it through 3 shots a week with the pills also.  We have come a long way since combo treatment and how so many doctors now are aware of how to treat Hep C.   I want to say to those of you that are on treatment now that there is a light at the end of the tunnel and that most of all dont let yourself give in the feelings of despair during treatment.  

             One thing that helped me a lot when I told my doctor while on treatment that I felt so sad and tired that I prayed I could make it through treatment.   His response was I can give you some meds for that but you have to ask yourself did I feel this way before treatment or is it just the meds making me feel so scared, tired, achey and just out right in a funk.   I know it sounds simple but I just kept telling myself that its the combo treatment and not the real me.  Everyone here thats gone through treatment should be very proud of yourselves knowing that it was no cake walk and you did it.  These days Im doing well and life does get better after treatment.  If you are considering treatment or going to wait because you only have inflammation not scaring of your liver just remember Peg has always had a much better response rate than the old combo treatment.  I have a PCR done once a year now and I have given up drinking almost entirely but now and then Ill have a couple of beers but its never the same as when I didnt know I had Hep C.  Every time I have a beer now I think about if Im damaging my liver.  My liver alts have always been normal since 1999 so I do feel really luck and blessed.  I decided to have a couple of beers while enjoying the fireworks last night and it never feels like it did so what can I say.      

 

Thanks to everyone here and on the other Hep C sites with Delphi for helping me through the biggest and most rewarding thing I have ever gone through.  In closing, Love the people around you more and discard the people that bring drama into your life.  Hep C is a real indicator of what unconditional love is all about.    

 

Respect & Love

Wayne             



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