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20 June 2018 at 7:24 am in reply to: Reduction of itching, keeping a daily log and setting an alarm #28187
Hi. I’m really pleased to read that things are going well. I loved your dog story. They are so intuitive.
Good luck with the rest of your treatment.Coral
Hi John, I can see that you’re about to start treatment and are putting your mind at rest with some questions before you do. This is good because usually somewhere there is someone with the same or similar queries. I’ve said it many times but how lucky are we to have Dr James?
I had the viekira pack and ribavirin for my treatment and I am all cured and living a life without HepC. I don’t think I had ‘Riba rage’ (well I don’t think I did – nobody said anything!). I think that It did make me tired and headachy but nothing that couldn’t be managed and ofcourse it was well worth it.
Jump on in John and good luck.
Coral
Hi Kaju,
I could see that your results look good and I think you have about 2 weeks to go in your treatment. I hope things are still going well. Keep taking those pills until the very last one.
Looking forward to hearing about your next set of results.
Coral
Hi mcmak,
I was pretty hard to treat and relapsed after a significant treatment of Sof/Dac then Sof/Led. My next treatment was the Viekira Pak, Solvadi and Ribavirin. I know we all need different cocktails. Ribavirin gave me a few more side affects than the other medications but nothing that I couldn’t handle. I just felt that I wanted to throw everything I had at the retreatment and it worked for me.
Relapsing just sucks. I really wish you well in sorting out the best approach.
Coral
Thanks fretboard. Yes it does suck. The only positive thing out of that story is the few sentences at the end that indicate that Hep C can be readily treated. It may prompt someone who is sitting anxious and silent with the virus to seek information about the new medications.
Hi lifepivoting,
Congratulations on starting your treatment (and getting them out of US Customs).. You never know if that unwanted expertise might be useful to someone on the forum oneday.
As much as I try I sometimes don’t drink enough water so it was a bit of a battle for me to remember to rehydrate while I was on treatment. The headaches would eventually remind me though. I don’t know an amount but it is a bit more than usual.
Good luck…..looking forward to reading your posts.
Hi mrcleanrt,
Those results are looking really good. Those phone calls can really lift your spirits.
I’m about to spread a mountain of mulch. I don’t like actually doing it but I like the results.
Good luck with the rest of your treatment and results.Coral
Hi Vivcus,
I’m catching up on posts and I’m happy to see that Epclusa has done the job for you. I know what you mean about getting your life back!
Hi Balance,
I know how important those tests are and how anxious they can make us while we are waiting for the results. Everything is crossed for you Balance.
I am beaches but there’s a part of me that will miss Lindsey Buckingham. I’d be happier with both!
Hi Cristine,
Everyone has given you great advice so I’ll just say congratulations on starting your treatment and welcome.
The main thing is to try to take the tablets about the same time every day. I used to take mine in the morning because I was in danger of forgetting to take them later at night. I’d like to blame the brain fog but I think it may just be my memory because the Hep C brain fog has well and truly gone now.
Hi Sharmon,
Sorry to hear about those frustrations in relation to testing. I remember how important those test results were to me when I was under treatment. Hang in there…..
That’s 4 weeks done and dusted Songbird – well done. May the next 4 weeks fly by.
Hi Kaju,
I’m really pleased that you are not having any side affects so far. I love it that you are a formidable patient. Keep on asking those questions! People on this forum become quasi liver specialists and get to know their own pretty intimately.
Good luck with those first results…
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