Hello people! This is now day 10 and my side effects of maviret are mild. I make sure I rest when my body tells me. I drink plenty of herbal teas and light snacks and am doing well. I hope you all are in good spirits and living your lifesπ I have just done a survey online by this website (healthunlocked) I gave my email at end and they said I would receive a Β£10 amazon voucher, I'm still waiting for it, survey was regarding hep c.
Day 10 of maviret.: Hello people! This is... - Hepatitis C Trust
Day 10 of maviret.
Hi cara good to see you plodding along, I done the survey they other day and did get an email off amazon but canβt work out how to claim it so good luck with thatπx
Email the website and ask them. I would think it would be a code they give you. If I suss it out il let you knowπ
Thereβs no code as such just a blank email saying amount Β£10.00,if you work it out let me know I get my wild bird seed off amazon so the goldfinches will be happy π
Hiπ I took the survey & got the voucher. its a code in the email amazon sent. I just went to my Amazon account and added it via the gift card, redeem voucher box. Yeah I have hep c but I also have Β£10 ππ
Hi,itβs a win,win πI got an email but thereβs no code ,I think I got burned ah well if you and cara get yours thatβs good,
I looked at Amazon and the ways you can make a payment and there is a box you can use for codes. I'm gony email and askπ
Good luck and let us updated
Yey glad you're doing so well. I took the survey and got the Β£10. Bonus ππ πππ
Just got my Β£10.00, haha the email wouldnβt scroll up yesterday so I could see the code,I feel like Iβm a winner in life now ille do more of them surveys bring them on I say π€
Yes, I thought about it but next few I saw I didn't get that feeling. maybe a lottery ticket ππ cold up here. Sawed up an old 4Γ4 8 ft post. took a few sessions but worth it ππͺπͺππ
Well done you I admire your spirit, do the people know theyβve got a fence post missing,I know why you go for moonlight walks now,hope it keeps you warm tonight x
Have you heard from tootsie? Hope she is ok ,sheβs up by you isnβt she?
Oh I don't know. I have no idea where she's located. Cathy comes up closest to me. put my inspector gadget hat on. Maybe like the others, they feel so good so early on. At least I got close . Yeah lovely toasty warm thank you xx
I think she is up by cara,her genome is1 and the meds are heavier than ours do hope she is ok the last I heard she was putting empty tablet boxes in the recycling and was off to get some photos of roe π¦
Yeah Iβm sure sheβll let us see the photos soon,I do like her sense if humour at times,have you had the all clear phone call yet from your liver support nurse and did she say why she went a.w.o.l.over xmas?
She called yesterday, not all clear. Detectable but very low. Maybe others "clear " can be low viral load? we did think it may be as I was 650 when most of you guys are non detectable. So its plan b, keep it down, work it out. Still feel better than I did. Never seen any results. Hardly any contact. feel bit low obviously, don't want to rain on anyone's parade so if I go quiet you'll know why ππππ
So did she offer to sort some more mavirets out for you?obviosly could do with a couple more weeks for the stragglers to focker off
Feeling better is good. I can understand why you feel a bit low. Thankyou for sharing that many may not have and it means alot to me. I don't think anything is 100% and as you said you might quash it. Onwards n onwardsπππ
I don't want to rain on anyone's parade but no one knows the long term effects of this drug! I took tablets for acne years ago and the long term effects were published! The anti depressants I took for years can have long term affects. I don't think any of us will get 100 like we were like before the hep c but progress is progress isn't it?
Thank you honey. yeah I wouldn't have posted it. Al asked. I can't ever give up as it's life, not perfect but whose is at almost 58? πput my plan b in action, if it gets worse I will ask for treatment again, obviously for longer! So glad you're clear early means you're on the mend big time, all my love ππ
I havnt had any blood tests yet to determine my viral load and I'm not getting hopes up! No one has contacted me yet, when do they do it?
You get tested wk 2. Wk 4 wk 8. Most on here report clear wk 2 or 4.and YOU WILL BE ONE OF THEM π I agree with your other reply as regards long term effects Etc. But for most it works and they are perfectly healthy and live a full and long life πππ
Yeh but these drugs are new. So be It, I'm on it now n that's that my quality of life was poor anywayπππ
That's exactly how I felt and even now I would have done the same as I had no choice. I had nearly every symptom and suffering hep c can bring. Its done, I am still here π put it behind me and hope for the best. I asked the nurse at my 1st appt what about patients 12 months on etc no answers. Scary stuff but there's a million chemicals people ingest on a daily basis and I don't so I reckon it's a balance and we'll be fine ππ