Has anyone else took vosevi and did it work,feeling anxious, things keep going through my head to why didn’t epclusa work, did my husband do something wrong??? Has anyone else had to have medicine twice?
Sorry to be depressive, I really wanted to come back and let you all know good news but wasn’t to be 😢
Hi. Sorry to hear this but I've read up on vosevi as I may be offered this if not clear in January as I had very low count after 3 month test. Have to wait for the full 12 months from treatment. I took maviret but some genotype 3 is hardest to treat with these new drugs so no he did nothing wrong. Vosevi has excellent track record. hope is stronger than fear so that's where my head is xx
Hi they haven’t said we have to wait 12 months, my husband will go back in two weeks (within six months of treatment) to start vosevi,how come you have to wait so long?
January is when they are taking my bloods testing the viral load & scan. Everything here has been painfully slow. I guess your husband has started vosevi, I hope you both are doing ok. Pleased to hear they are so good & quick at treatment where you are. Keep me posted, thoughts are with you both. x
Hi yes he has started his tablets, we do feel scared as we feel this is our last hope at the moment, really hope they work for him, I have to keep busy as it gets me down when I think about it, all the best for your tests, did you finish undetected after your meds?I pray 🙏🏼 for all to get cured, and receive treatment, all the best x
Thankyou x
