hi hubby about 8wk post tx and this morning he woke up and can hardly see out of his left eye he can just manage a very blurry outline i just wondered if anybody else as had a similar experince before tx his vision was brilliant so obviously it is quite worring any info will be much appreciated thanx Jules
We were told to see an eye doctor before we Treated, and I know these Tx meds do affect vision. I do know of one person that went blind during their Tx, but it is so extremely rare, there is only a handful of people that this has happened to, world-wide, and it happened during her Tx, not post Tx.
I would go to the Doctor and have it checked out right away, is anything
else on his left side feeling weak? I have seen people who have had strokes with their face muscles not working, on one side~
My eyes seem a little red and sometimes and when I wake up my vision is a little cloudy. But I wear contact lenses so it could be related to that. I got my eyes checked by an opthalmologist while on treatment because I was seeing flashes and artifacts but he said all was normal. Your husband's change sounds pretty serious and I would go to an urgent care center to get it checked out.
It may or may not be treatment related. Regardless, when a person loses vision, it is an emergency. With some vision loss problems, if the person is treated immediately the vision can be saved. If the person is not treated immediately, the vision can be lost. So go now, to the emergency room, and get his eyes examined. They may need to call in an opthamologist and they may need to do surgery to save his sight.
I'm very glad to hear it is improving, but unless it is drastically improved, as in nearly normal, I would still urge him to be seen immediately. You do NOT want to have permanent vision loss that could have been saved if treated immediately. Retinal tears are what comes to mind. I had a period when my own vision was threatened (before tx, not during) and my opthamologist have me very explicit instructions that in the event of any sudden change I needed to be in his office ASAP (within 24 hours) for surgical repair, or risk permanent loss. I was especially warned about seeing what would appear like black bugs running through my vision, as that is apparently what it looks like when there is bleeding inside the eye as the retina starts to detach. There is a short time window in which it can be surgically reattached, but beyond that time is just blindness. I also had a less extreme problem during tx, which was just blurry vision, especially bad for an hour or do after awakening. That was probably mostly due to very dry eyes. Eye drops of the "artificial tears" variety helped significantly. Be sure to avoid any drops that say "gets the red out", as these won't help and might irritate. Vision is really precious – be very careful to protect it!
about two weeks into the study I ha an issue with my left eye, it was diagnosed as vitreous detachment - my study doc conferred with my ophthalmologist and they concurred it wasn't from the study drugs - a mixed blessing because my study doc was going to pull me if the ophthalmologist deemed the study drugs could have caused it.
my left eye is still a little blurred and both are runny much of the time.
without conclusive evidence I think it could be party due to the ribavirin though at this point I am going with the flow.
there are many comments in another thread - starting sofosbuvir GS585
Hi I had some problems after treatment with dry eyes now using Restasis and saw my eye Dr. about month ago he said they doing better hopefully will be off them soon they are so exp. I did see eye Dr. before treatment and 3 months into treatment then at end of treatment.
I understand this is what all the Dr.'s that treat Hip C recommend
Good luck and hopefully it wont be anything serious
You should really take your hubby to have that investigated. Eye stuff is nothing to mess around with. I have had a retinal tear before and it's important you get into a eye doctor. If what happened to your husband - happened to me, I would have gone straight to the emergency room like pooh
firmly stated. This could be something not related to treatment. Having a loss of vision where you are only seeing clearly from one eye and the other sees only blurry outline is something to be concerned about. Hope this all turns out ok...but be safe and have it looked at.
Yes, my husband has experienced many symptons due to interferon and ribavirin therapy and they continue even though he had to stop treatment in January of 2006 due to an allergic reaction to the drug. He was completely blind for one year and since 2007 he now has vision in just the upper half of his eyes. It destroyed the retina and the optic nerve is gray, due to a stroke behind the eyes. Mind you he complained to the doctor in October of 2005 and they sent him to an optomotrist and his hep c doctor told him to continue with the treatment as the eyes would go back to normal after treatment was completed. The treatment caused low vision, joint pain, tremors, lesions on his brain (like MS), memory and short term memory loss, autoimmune disorder, lupus and psoriasis, anxiety etc.
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