Hi everyone. Am hoping to get some advice. Has anyone had any experience with changes in vision since taking acyclovir as suppresive therapy?
I've been taking it about 8 months now and didn't have any noticable side effects. But recently I've had vision problems... blurred vision and a rash on my eyelids. I got my eyes checked at the opticians and they couldnt find anything , I went to my doctore who referred me to the Eye Hospital and they couldnt really see much either, gave me a steroid cream for my eyelids which cleared the rash up but it came back two weeks later. I used the cream again and it cleared up again. However the blurred vision is still a problem.
I have looked online and see that some people do experience this. The logical thought would be to come off the tablets and see what happens but I can't, I'm in a new relationship and cannot either risk my partner contracting HSV or tell him that I am having these issues as it will scare him right off to think that I'm freaking out over this and that should he contract it from me he may have thses worries too, I'm lucky enough to have found someone who accepts me with the virus.
I don't actually care too much about a bit of blurred vision, my main worry is - what is happening to cause the blurred vision and is it doing any lasting damage? Or would it just cease if / when I end up coming off suppresive therapy.
Any advice or experience would be great!