Forum Replies Created
-
AuthorPosts
-
24 September 2016 at 10:05 pm in reply to: I don’t understand my bloods results, or my viral load…. #23263
just a little update…. went to GP Thursday 22nd, she sent me to get bloods done…
I have appointment Monday 26th with my Liver nurse… results of bloods should be back…. fingers crossed XThat’s great news Fara, am so pleased for you.
I’ve been taking mine after food in the afternoon, the food was the advice of my liver nurse!
What is the recommendation? It seems a good idea to have food before taking medications? Hope I’ve been doing the right thing….day 15 todayI’m doing a little bit of everything…. Walking, swimming, yoga, light weights, and pad work ( boxing training)
I need to do something otherwise my mental health suffers18 September 2016 at 1:01 pm in reply to: I don’t understand my bloods results, or my viral load…. #23105Thank You James Freeman… These are my pre treatment bloods… So I’m happy that 12 weeks treatment will probably be enough
18 September 2016 at 12:13 pm in reply to: I don’t understand my bloods results, or my viral load…. #2310318 September 2016 at 11:58 am in reply to: I don’t understand my bloods results, or my viral load…. #23101The viral load is from before I started treatment.
All these results are from before I started treatment18 September 2016 at 11:55 am in reply to: I don’t understand my bloods results, or my viral load…. #23100Hi Everyone, feeling so emotional with all the replies, so kind that you all care. It’s been such a lonely journey these 5 months since I found out I was positive. I am lucky that I was just a bit concerned about a raised ALT reading , I didn’t know what it meant and just remember my GP saying it was high a couple of years back….. Anyway I did nothing as she wasn’t concerned and I was a bit naive …but it must have been in the back of my mind and a friend had liver cancer…so I went back and said can you see if I’m ok please that reading was high! So had a full liver test, and came back as positive and GT 3a. First fibro scan read 7.5, then I had a reading of 6.4. This is my only treatment. Them results are from before I started treatment. The only treatment I was offered here was interferon and ribaviron. I have a child with extra needs, so I need to be able to look after them, so them 2 drugs didn’t look good! So here I am on my journey and I’m so glad I found fix hep c. The side effects I have so far have been waking a lot in the night, 10 + times, but I can sleep and am not awake … Very vivid dreams.. I’ve had fatigue ( but not every day) and tender chest. Anyway these are all manageable and I’m being kind to myself. I have 1 st appointment with my nurse on 26th. I will be getting results of ultrasound. Also she will be doing my bloods ( I think?) I will be 22 days on medications by then. I’m lucky that I will be getting monitored. They did say “no” but I told them I was going ahead and would take treatment regardless of whether they monitored me or not. I took newspaper articles to my consultant, and asked him should I move to the place they would monitor me? He said he would bring my concerns up at next meeting…” It’s time we revisited this” were his words. I was open and honest, I kept in touch with GP and nurse re me getting medication from fix hep c. Consultant, GP and nurse have agreed to monitor. Thanks again to all who replied, really made me feel less alone to wake up to them …
I have just started treatment 16 days ago, I’m GT 3a
I got 12 weeks supply.
So glad I read this post “thank you for posting”
I have decided to get another 12 weeks so that I can have the best chance of clearing this virus.
I’m still in shock really as I had a raised ALT level 66%
So in April asked for a full liver test.
Did not expect the news I was positive.
Hope to get clear with this treatment
I’m F2
My nurse just emailed and said the ally-3 study shows G3. 12 week treatment non cirrhosis 96% achieved svrAm a little confused now with all the different information.
-
AuthorPosts