Sudden inability to focus, dizziness, double vision: Is it a stroke?
Hi, I have a severe herpes zoster viral infection in my eyes that is getting much better with steroid eye drops and oral anti-viral. I have extreme dizziness when I stand up and never thought to ask the eye dr about it. Now I've done research and found that ocular cranial nerve palsies can produce this kind of thing. When I try to watch TV I get double vision but closing one eye makes it go away. Has anyone had something similar?
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No infection. It is usually vascular , seeing a cardiologist right now . running a lot of test. Narrowing of the arteries in the neck possibly. They could see the plaque running thru a small vein in my eye in photos. Luckily it started going down before it reached my brain. Not out of the woods yet since this just happened in April. Took forever to get referrals .
Just the symptoms I mentioned. But I already had myopic degenerative disease in this eye so vision wasn’t that great and the eye wasn’t that strong. Now I have very limited vision because of this stroke. But when this happened the morning as I was on my phone I had a dreadful feeling come over my body before I lost total vision in the eye. It was dark for several days. Over the past two months there is light but very grainy vision. Drs. Say I am lucky because people usually lose all their vision permanently.
Wow. I recently had a carotid ultrasound and I only had minor narrowing but now that I think about it, it was probably 3-4 years ago when I got diagnosed with Ortho static hypotension I fully believe this is related to a infectious cause because it all began then. How are you now? Feeling I mean in this context?
That must have been very scary. I’ve never heard of that from cervical pathology. My second neurological event was from brachial plexitis and I couldn’t lift my arm high. Doing my hair was not possible I have a medical background and have always done well on medical terminology and look up papers often. Im also a moderator on a FB page for dogs with Cushing’s disease. I very much appreciate your concern and advice. I’ll post an update later on Monday. Thank you again
I believe I know what you’re saying about having symptoms but nothing definitely showing on blood or other tests. I have been there so many times and it can be crushing. I remember crying after an appointment like that but can’t even remember what was wrong Most of those kind of appointments were related to muscle symptoms and doctors wanted to label me with fibromyalgia even though it was only my upper trunk. Like you I had to wait for the diagnosis to be made on nerve stimulation tests and cervical MRI. I very much appreciate your nice post
When you were diagnosed with this did they have you do all the heart tests? Sounds vascular to me . You need to get that checked out again if you haven’t. Narrowing of the arteries doesn’t go away and it makes the blood or plaque get stuck.
As for myself coping with more loss of vision in my eye and worried about this happening again,I haven’t had a single dizzy spell or loss of balance since this happened 2 months ago and hoping they find out what caused this, I thank god this did not head up to my brain. Will keep updating this until they find out where the plaque came from and what can be done to control this.
And your post also. Please keep me updated,
Hey, yes! I have been having like every Neuro symptom… My eye doc says she can’t really see any concern, but I did get my first eyeglasses prescription ever December of 2021. And my vision is getting worse, but my eye doc still doesn’t see a cause. She has offered to refer me to Neuro-Ophthomalogy, which I will follow up on. I currently have very high viral loads of EBV, JCV, and my herpes varicella zoster viral load is high-normal. I recently had a staph infection too on my legs. I am not on immunosuppressants, no diabetes… I am being worked up for CADASIL and MS. I see a Neurovascular doc Tuesday. My brain MRI is messy and progressively so. I can’t talk sometimes. I forget where I am. I get dizzy. I fall. I have gone to the ER. Lots of docs this year… Lots ruled-out and I’m currently being worked up for MS, CADASIL, and microangiopathy-long road… Waiting on results from my second LP this month. Not sure we’re headed down the same path, but any info helps! The brain and immune system are tricky!!! 🤗 I too am doing what I can in the meantime, Pilates (I have no energy or muscles left, I’ve lost 80lbs and counting this year), acupuncture, cupping, massage, Psych NP, counselor, Registered Dietician-I realize my privilege here thanks to my husband’s health insurance, I just had to resign from my job as a nurse of 14 years at Children’s Hospital Colorado 😓 Just 10 minute walks around the block (with my donated new friend Walker 😜) really gives me a mental boost. And just being open, receptive, staying true to me, and giving back. I’m not going to lose Me just because of this crap 🤗🤣 Look forward to following you through your journey!
I do see a Cardiologist too. Abnormal ECG, tricuspid and mitral valve regurgitation, but not concerning for now-annual monitoring is all. I am a 39 year old born female sex. My brother had his first stroke at 44, my dad died at 53 from cardiac arrest (had congestive heart failure)-and his dad and grandpa died even younger than he of cardiac arrest. Lots of dementia and stroke and blood pressure stuff on mama’s side. Keep in mind, there are a lot of details I haven’t mentioned, so make sure and dig deep when researching! 🤗 Happy to answer any questions too of course!
Wow! I'm terribly sorry you are going through SO MUCH! And with a family history like yours, it must make it even more scary. My neurologist suggested I go to Mayo again and I'm seriously thinking about it but will likely wait until another shoe drops. I no longer believe I had a herpes infection. Whatever the virus was could have triggered ocular herpes because I have had that before and it kept going from one eye to the other while on Valtrex. I went to a special eye clinic with the University of California and even they couldn't figure it out. By the time they did a biopsy, I tested negative for all the common eye viruses. The rash I developed on my legs showed red spots that have now turned brown. Typically, especially on my face, I noticed there's a pattern where you see a group of 3 tiny flesh colored bumps with many having a black center. Not pimples and a lot smaller than those too. Now some on. my chin got infected and those leave a large gaping hole/pore. In my mouth I had ulcers everywhere including the back of my throat. They didn't hurt at all, actually nothing hurt. But I got 7 gum line cavities with significant holes. I had had my teeth just cleaned about 3 months ago. Every single break in my skin now gets inflammed/infected for which I'm using Mupirocin. Several months ago I had a sore in my nose caused by MRSA and that started up again. I also got a staph infection on a previous cut just like you. I'm seeing my immunologist on Monday because this has just been way too much. Even though my IgG is low it is not 2 times below normal and is considered as hypogammaglobulinemia However I also have subclass deficiency 1 & 2, low IgM and T cell issues. Probably killer cell deficiency as well and likely the basis for herpes in eyes. I would love to follow your journey as well. The dizziness has become better and what I'm still seeing is likely just my normal orthostatic hypotension