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Post Info TOPIC: Treatment day 4


Guru

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RE: Treatment day 4
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Yes!!  That`s excellent, Ron, congrats!!    

Looking forward to celebrating with you after your next results!!  biggrin



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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.

 

 



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biggrinbiggrinbiggrin The tests came back today.. UND again!!!!!biggrinbiggrinbiggrin



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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Tig56 wrote:

Congratulations Ron!! Well done Brother! Best of luck with your next UND and the SVR coming...

Tig


 Thanks Tig, I am so grateful for the people here and the support we get, My hat is off to you!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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Sierrajen wrote:

I am sending all kinds of happy thought to you Ron

 

Hugs Jen


 Jen, Thank you and the best of luck with your treatment. I believe these new drugs are a blessing for us all!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!

Tig


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Congratulations Ron!! Well done Brother! Best of luck with your next UND and the SVR coming...

Tig



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Tig

68yo GT1A - 5 Mil - A2/F3 - (1996) Intron A - Non Responder, (2013) Peg/Riba/Vic SOT:05/23/13 EOT:12/04/13 SVR 9+ years!

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I am sending all kinds of happy thought to you Ron

 

Hugs Jen



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Gen 1a -  treatment naive  HepC since mid 70's

started Harvoni 11-06-2014   for 12 weeks

13,000,000 VL to 50 VL in just 4 weeks- 

Post TX Labs 5/5/15 Undetected! CURED!!

 



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Yesterday was the last day of treatment, went this morning to get blood work done. I will know by next week how it comes back, more likely UND!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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Good going, Ron, great to hear you`re almost home and dry now! 

Sounds like you`ve coped pretty well with the sx and the riba rage issues, and it`s looking very promising for you.  Take it easy for a while once you`ve finished to let yourself recover and regain your energy...and give yourself a big pat on the back for getting through it!

Let us know when you hear your EOT results, and best of luck!  smile

 



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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.

 

 



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Hey Ron

Your coming down the back stretch with full power and a head of steam. The rider Ron of the horse call Sovaldi is UND heading for SVR with no obstacles in view.

Your in with flying colors

matt 



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"And in the end, the love you take is equal to the love you make"

61 year old Geno type A1, F4 Cirrhotic, started 24 weeks on Harvoni 12-17-14 ,EOT-5 week = UND, 8-31-15 =UND , SVR-24 Baby YES! 



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4 days left on this treatment! Just looking back and realized that this post was started on day 4. # months is not very long compared to the people who have had to deal with a whole year and much worse meds than I had to deal with. The 12th is my next blood test and I have hope it will come back UND also. will let everyone know.



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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Tig56 wrote:

Hi Ron,

Joy doesn't describe the feeling you (we) all experience with each report of those three letters, UND! I guarantee you that the feeling you will have when you get the next three letter report confirming SVR, is second to none! You've done very well and your journey through treatment has been both successful for you and happy for all of us to follow! 2 more weeks, may seem like 2 months right now, but it will pass quickly and in no time you will be taking your EOT +12 viral load test to confirm SVR. Take the time between tests to plan your celebration!! Your Hep C free future is just around the bend.... WOOT!!!! Good luck!

Tig


 Tig,

Thank you for the words of encouragement they mean so much to me. The bonds we form when we go through these things with another person can't be put into words. The support and true concern is overwhelming. I also wanted to thank you also!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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Jill,

I have been feeling pretty good all in all. The occasional struggle with insomnia but I can deal with that, just a nap in the afternoon is all. The Riba rage is well under control. One thing the 12 step program i am in has given me the tools to deal with that problem it just took a while to see the triggers that bring it on. It is the stupid little things that bother me not the big ones. Some muscle pain and I am use to that so it is not unusual for me. I have noticed some better feeling on some days, almost like the virus is gone is the only way I can describe it. I want to thank every one of you for being here on this journey for me. My gratitude is endless for what has been given me! 



-- Edited by RonH on Thursday 30th of October 2014 09:34:27 AM

__________________

Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!

Tig


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Hi Ron,

Joy doesn't describe the feeling you (we) all experience with each report of those three letters, UND! I guarantee you that the feeling you will have when you get the next three letter report confirming SVR, is second to none! You've done very well and your journey through treatment has been both successful for you and happy for all of us to follow! 2 more weeks, may seem like 2 months right now, but it will pass quickly and in no time you will be taking your EOT +12 viral load test to confirm SVR. Take the time between tests to plan your celebration!! Your Hep C free future is just around the bend.... WOOT!!!! Good luck!

Tig



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Tig

68yo GT1A - 5 Mil - A2/F3 - (1996) Intron A - Non Responder, (2013) Peg/Riba/Vic SOT:05/23/13 EOT:12/04/13 SVR 9+ years!

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Well done, Ron, you`re on the home stretch now!!  It`s looking very promising for you so far...just keep going, and best of luck!!  smile

How are you feeling now? 



__________________

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.

 

 



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The days to the end of my treatment are winding down now 14 days left! Then another blood test and we will see what goes on from there!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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I have thought about this disease many times after I found out I had it. I was nervous and bummed that I had this but my years in a 12 step program helped me to deal with it. There is many days when I stop and think about what this stuff can do to us all it really scares the h**l out of me, and after seeing and hearing the words UND the gratitude that I have cant even be explained! The emotions are like a roller coaster at times, I hope and pray that this crap doesn't come back. Then there are other times that the emotions of those three little letters UND brings tears of gratitude flowing! I am so happy that so many of you can relate to this and I am so grateful that I found this forum!! Thank all of you for being here for me and all of us!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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Talked to the Dr today, he said all my enzymes and blood work looked great. He is very happy that all is going so well! Next blood work is to be done in 27 days. Then he will see me the next week.



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!

Tig


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Great news Ron!! You're over the hump and I feel good sailing and undetectable days ahead! Congratulations!!!! biggrinbiggrin

Tig



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Tig

68yo GT1A - 5 Mil - A2/F3 - (1996) Intron A - Non Responder, (2013) Peg/Riba/Vic SOT:05/23/13 EOT:12/04/13 SVR 9+ years!

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Excellent news Ron, those words "Undected " are the sweetest words a hepper can hear.

I am so happy for you! Now you can focus on the future and life free of Hep C.

God Bless and prayers that the next words or letters you hear are "SVR"

Duane



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53yr M 1a acq 12/83 cirr pre tx MELD 17  tx nv diag 1/29/12  tx S/O 3/5/14  trans list.

EOT 5/28/14 UND 6/12/14 SVR 8/29/14 MELD 14 dx HCC 9/5/2014 tumor ablation 9/24/14

In the 10K lakes State It's not about us but those around us.



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Great news! Congratulations!



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Diag. with hep c in 1992; A3:F2;  GT 1a; IL28B CT; VL 900k, ALT 150, AST 100 on 8/5/2014; SOT 9/5/2014  S/O ---VL 127 after 6 days; VL detected on day 18 but < 15.; --> UND @ EOT+ 1 year SVR!



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Update....The Dr's office called today and told me my results from my lab's, It came back UNDETECTED!!!!!! That was after 6 weeks into treatment! Such great news to hear, I am so happy!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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Called the Dr's office to see if they would tell me the VL numbers, well the nurse said the Dr. wont give me the #'s over the phone I would have to wait to see him first, Grrrrrr. Oh well guess I have to wait!

 



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!

Tig


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Hey Ron,

Will keep my fingers crossed for the results you want to see on your VL. 6 weeks is often the point we see many of the undetectable results shine through and in all likelihood, so will you! I'm proud of you for learning to control the Riba Rage! That's not easy and we know it! Let us know as soon as you hear your results!! Good luck...

Tig

 



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Tig

68yo GT1A - 5 Mil - A2/F3 - (1996) Intron A - Non Responder, (2013) Peg/Riba/Vic SOT:05/23/13 EOT:12/04/13 SVR 9+ years!

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Well I had my blood tests done on Tuesday this past week. No word from the Dr as of yet on the VL I see him on the 15th. I am hoping for und on the results. It will be 6 weeks on treatment. The pain in the joints are almost gone! Just my normal aches and pains from my work! I am learning not to flip out at stupid **** so I guess the watching my mouth is working!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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Thanks Huey, I try to do that it just gets very cold at times!!

 



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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Good Luck,, Keep your stick on the ice.

 



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  HCV Genotype 3a , now Psot-Tx was on S/riba. First VL was 5.8 mil on 7-5-13 then "und" at 3.8 weeks. 06/13/14 still und. off meds 3 days back on 7/29 Last pill 08/10/14 SVR+4

 



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It is a new day! Met with my Dr.today just for the check up, all is well. I go in 2 weeks for my new VL blood tests. I will post the news here first! I am feeling pretty good just joint pain and the normal aches and pains, so all is well!! Keep your heads up New days are a coming!

 

 



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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It has been awhile since i posted here, most of these days have been good a couple not great. I am learning that as long as I stay busy it helps to keep my mind at peace. My shoulder and hips have been sore quite a bit, at least the riba rage has not been that bad. I am finding that as long as I keep talking to other people and try to avoid negative situations it has been much better. Not saying that is all there is to it just what I am tying to do to help keep a check on things. I am grateful that this forum is here and I can look at what people are saying about their treatments and how that helps me. Thank you all for being here!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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As these days are going on I am seeing more pain in my hips if I sit to long. I took a nice walk to the beach with the wife and the dog today, it was nice, no pressure and no time limit. I also have found out that my filter for saying what I am thinking is not as good as it normally is. The last couple days have been ok, well at least no headache. My wife worry's that the meds will affect me negatively and I can understand her feelings. Some of the things we read are horror stories and freak people out, they did me at least. I found a support group near me that I am going to go to and see if it is still there, any extra help will be nice, never hurts! Everyone have a great day unless you made other plans!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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Thanks  Tig, (In about two-thirds of the affected individuals morning stiffness may be severe, resolving after more than an hour. ) this is me in one sentence, less the resovles in an hour, and I also have it in small joints as well as large (hips, back, shoulders, etc...) I had stiffness and joint and muscle pain for years before even knowing I was infected, it has gotten much worse even just since completing tx ? I'm not sure what to think....I literally can't function at any physical level with out pain meds, I hope for enough liver improvement to be able to address this problem with meds that help instead of mask the problem.....however I am doubtful that any doctor would prescribe a medication that may help at the expense of my liver understandably.

So as they used to say.....I just keep on truckin ! Hopin for good roads ahead.

 

Thanks all.......Livin on a prayer!

Duane



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53yr M 1a acq 12/83 cirr pre tx MELD 17  tx nv diag 1/29/12  tx S/O 3/5/14  trans list.

EOT 5/28/14 UND 6/12/14 SVR 8/29/14 MELD 14 dx HCC 9/5/2014 tumor ablation 9/24/14

In the 10K lakes State It's not about us but those around us.

Tig


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Hi Duane,

I have been having quite a problem with arthritis and have, along with Malcolm, talked about it a lot lately. HCV often manifests itself through athritis. I had some mild problems during the chronic phase of my infection but now that I've achieved SVR, the condition has gotten much worse. The specialists I've seen have concluded that the Interferon I took over two courses of Tx is likely responsible. The two articles I've included describe the incidence of both RA (Rheumatoid Arthritis) and non RA arthritic conditions resulting both from Tx and HCV itself. I'm happy that Tx protocols have advanced and the use of Interferon for HCV will diminish itself.

http://www.ncbi.nlm.nih.gov/pubmed/11580301

http://www.biomedcentral.com/1756-0500/6/437

Tig



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Tig

68yo GT1A - 5 Mil - A2/F3 - (1996) Intron A - Non Responder, (2013) Peg/Riba/Vic SOT:05/23/13 EOT:12/04/13 SVR 9+ years!

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Ready to start day 12! Each day is getting better as I find not to just sit around, that is when I stiffen up. Did a lot of work here yesterday, ran a new sprinkler line for our garden so we wont have to water daily now! No real headaches anymore, not even a dull one, so that is a blessing. I think the more water and ice tea i drink to stay hydrated is good, I just dont over do it. I think this am requires a ride to a meeting I used to go to all the time, just for some extra fellowship and to see some old friends. As many of us know it is not good to drink with any liver disease, I wont preach on this matter, we all know what is good for us! Well every one keep your heads up and keep positive thoughts, and remember "not one of us has it all together, but together we have it all"!! Thank you for being here for me!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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RonH wrote:

Well I am happy to report that I some fog lifted and I am posting again. The squirrels in my head kept me very busy the last 2 days! Still no real bad side effects as of yet. As I keep saying just some joint pain but I am not sure if it meds or just me. I have stayed very active around the house this week and even got a couple estimates done! Work is not real pressing as of right now so I am finding out how the meds are working with my system. I have a lot of running to do today so that will keep me busy for the day! Hell I think we will go out tonight and maybe take a nice walk on the beach near sunset if it isn't raining tonight, just because they call for it doesn't mean it will come! I am getting ready to start day 9 and I do feel fine I just need to keep moving and not sit around. I get very stiff just sitting so movement is my friend! I wish everyone has a great day today unless you have made other plans!


 Ahh...another case of joint pain and stiffness,  I go thru that same thing, if I sit still for 15 min i'm like the tin man with no oil can ! This is where my job gets effected the most....I need to travel a lot and ya can't exactly be getting up and down on a plane, not to mention I'm 6'2" and don't have enough room to even wiggle around. So this is one of my greatest wishes is that this resolves, or at least my liver improves enough to do something if it is arthritis. Keeping moving is the only thing that helps, but man the next morning can be really tough, hot showers help but for some tx's its contrary to the skin problems. I'm not sure who here said something about the virus likes the cells in our joints, but why is it so much more prevalent after or during tx? I take 2 different diuretics once a day and I wonder if that also may play a part in this by dehydrating the joints of the fluid that lubricates them ?

Any of our member experts know what could be probable cause?



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53yr M 1a acq 12/83 cirr pre tx MELD 17  tx nv diag 1/29/12  tx S/O 3/5/14  trans list.

EOT 5/28/14 UND 6/12/14 SVR 8/29/14 MELD 14 dx HCC 9/5/2014 tumor ablation 9/24/14

In the 10K lakes State It's not about us but those around us.



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Four out of Five voices in my head say "Go for it!"



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  HCV Genotype 3a , now Psot-Tx was on S/riba. First VL was 5.8 mil on 7-5-13 then "und" at 3.8 weeks. 06/13/14 still und. off meds 3 days back on 7/29 Last pill 08/10/14 SVR+4

 



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Well I am happy to report that I some fog lifted and I am posting again. The squirrels in my head kept me very busy the last 2 days! Still no real bad side effects as of yet. As I keep saying just some joint pain but I am not sure if it meds or just me. I have stayed very active around the house this week and even got a couple estimates done! Work is not real pressing as of right now so I am finding out how the meds are working with my system. I have a lot of running to do today so that will keep me busy for the day! Hell I think we will go out tonight and maybe take a nice walk on the beach near sunset if it isn't raining tonight, just because they call for it doesn't mean it will come! I am getting ready to start day 9 and I do feel fine I just need to keep moving and not sit around. I get very stiff just sitting so movement is my friend! I wish everyone has a great day today unless you have made other plans!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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Paul B wrote:
RonH wrote:

 I have had a few friends that have been through hell during treatment so that is why I held off for so long. I am so glad that the new meds are out and available for all of us.


 Maybe not "all of us".  The new meds are not here in Australia.  I am doing 48 weeks...


 Paul, I am sorry to hear that the new meds are not over there yet. I hope your treatment goes well!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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RonH wrote:

 I have had a few friends that have been through hell during treatment so that is why I held off for so long. I am so glad that the new meds are out and available for all of us.


 Maybe not "all of us".  The new meds are not here in Australia.  I am doing 48 weeks...



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57 Yr old, Diagnosed 1994 Geno 1a. 1995: Interferon 12 weeks.  1998: Int/Rib 10 weeks.  2014: VL 106,000. Peg Int, Ribavirin, Victrelis 48 weeks (commenced June 2014). UND after Peg/Int lead in week 4. Still UND at week 8, 24, EOT. SVR 12.



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I know your taking it day by day, but soon the fog will set in, don't get upset if you miss a day or two.  For me the fog is lifting and I should be back to work after labour day.



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  HCV Genotype 3a , now Psot-Tx was on S/riba. First VL was 5.8 mil on 7-5-13 then "und" at 3.8 weeks. 06/13/14 still und. off meds 3 days back on 7/29 Last pill 08/10/14 SVR+4

 



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Today was a good day, I keep praying that these days are like this each day. sometimes I worry that I will just snap out on some poor unsuspecting fool that really doesn't deserve it. I got to sleep at 10:30 last night but woke up at 3:45 wide awake, well looks like a nap is in store for later today. I am noticing a little pain in my lower back/pelvic area, is anyone else having these pains? I credit some of my pain to the work and bike wrecks I have had over the years so I am not sure if this is normal or not. On another note, I took my bike into the dealer to get the charging system fixed today and the tech called me in at the end of the job when he was almost done and showed me that he screwed up the powder coating on my primary. He was very apologetic and said they would take care of it. (I have been dealing with this dealership for about 8 years now) I did not find it necessary to yell or rant and rave, just said cool take care of it and i will pick up the bike tomorrow! I am so grateful for this forum and a place to just say how I am feeling and hopefully help another person out. I catch myself bouncing around with my thoughts (my wife says I am like a rabid Squirrel) but that is normal for me! Have a great day today everyone and stay blessed! Thanks for being here!  



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Genotype 2, VL 10,000,000

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RE: Treatment day 5
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As another day passes the side effects are almost nil today, just a little lower back pain but I figure that is from my work. Oh and I do like my 2:30 - 3:00 nap now! I am starting to see where my my trigger points are. Considering that I have been in a 12 step program for the last 21 yrs it has given me a lot of training. Now it is a whole new world and set of rules to live by and triggers to see. I am thankful for this forum to share what i am going through with others that are going through it too. These days I stop and think that as these days go by there were a few of my friends that have had this disease and are not or haven't responded to treatment and of a couple that have past from complications for it. I just want to say that I am praying that all of you here are responding positively to the treatment and will be cured soon. Thank you for being here!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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RE: Treatment day 4
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Huey, a lot of good info in there and as you said I dont agree with it all either. Each person is different on what the side effects are and how the treatment is. Some people it doesn't bother at all, some it screws up. I have had a few friends that have been through hell during treatment so that is why I held off for so long. I am so glad that the new meds are out and available for all of us.



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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This is the best explanation of this that I have seen, I don't agree with everything she says but most of it is right on, your chick should watch it too., vary helpfull

https://www.youtube.com/watch?v=5b7o2fBSI2M

 



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  HCV Genotype 3a , now Psot-Tx was on S/riba. First VL was 5.8 mil on 7-5-13 then "und" at 3.8 weeks. 06/13/14 still und. off meds 3 days back on 7/29 Last pill 08/10/14 SVR+4

 



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Day 5, I did catch myself snapping at my wife today over designing our bathroom and looking at tile, so I am starting to see some of the Riba rage! Also a small headache too. Well I will just have to keep myself in check better as these days go on. We talked after a while and I told her that if I do start to be a jerk just let me know and then walk away so I have to look at myself. I do pride myself for having self control but I see that I have to keep watching closely. Each day is different so time to keep my eyes open better. Still no pain other than I have had for a few years now, That is good! Have a great night everyone and a better day tomorrow!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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Good point, I will do that. Thank you, i never claimed to be the sharpest tack in the box!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!



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Hi Ron
glad to hear it is going well. Rather than a new title every day, maybe consider a master thread and just update it. Will be easy for you to keep track of over the course of treatment.

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57 Yr old, Diagnosed 1994 Geno 1a. 1995: Interferon 12 weeks.  1998: Int/Rib 10 weeks.  2014: VL 106,000. Peg Int, Ribavirin, Victrelis 48 weeks (commenced June 2014). UND after Peg/Int lead in week 4. Still UND at week 8, 24, EOT. SVR 12.



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Well another day has gone by and not a thing but a little nap at 4 today! I nodded out for about 20 minutes and woke up refreshed! All I can say is I hope this is all there is, I will keep a positive attitude about it too!



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Genotype 2, VL 10,000,000

Sovaldi 400milligram 1x daily Ribavirin 400 milligram 2x daily. Started treatment 8-19-14, UND 9-30-14 UND 11-12-14!

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