Lyme and Vision

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Neurogurl
Regular Member


Date Joined Dec 2006
Total Posts : 373
   Posted 5/8/2011 7:39 PM (GMT -7)   
Hi - For those of you that have received a definite diagnosis of Lymes can you please share with me your visual problems?  I have yet to find a diagnosis and one of my very first complaints was my vision -- I would like to compare my visual disturbances to those who suffer with Lymes.  Thanks!!!!

Cheezhead
Veteran Member


Date Joined May 2007
Total Posts : 510
   Posted 5/8/2011 9:26 PM (GMT -7)   
Hi Neurogurl,
I am so sorry you are not feeling well!! I hope you find the answers you are looking for, unfortunately for most of us dealing with Lyme disease there is very few definite s. What you consider a definite diagnosis, I assume you mean a positive blood test. Do you realize the CDC considers Lyme disease a clinical diagnosis? As do most of the doctors that treat chronic Lyme disease. Many of us have a clinical DX, and show several titers on an ELISA, or Western Blot, but not enough to have a positive or "definite" blood test.

I vividly remember my tick exposure, I removed an engorged tick from my backside. I had the classic bull's eye rash and nearly all the Lyme symptoms on the list, although joint pain was minimal. I had the floaters, sparkling, & blurry vision. Along with many cognitive issues..headaches, vertigo, floating sensation, ect. After all this my Lyme test still came back negative. Before my exposure I never had a need to see a doctor. Now I just hope one day the testing for vector borne disease will become accurate enough to help the many undiagnosed, and untreated.

To better understand this disease and those suffering with it, may I suggest you see Under Our Skin. If you have a Netflix account you can rent it there. I wish you the best and hope you find good health soon.

MysteryLyme
Regular Member


Date Joined Feb 2011
Total Posts : 137
   Posted 5/8/2011 10:09 PM (GMT -7)   
My visual problems began as sensitivity to light... which got worse and worse. Eventually it looked like lights had halos around them or streaks coming out of them. Then things just started getting blurry.

I was diagnosed and treated soon after my visual symptoms began and they went away pretty quickly. I still have some sensitivity to lights but mainly just fluorescent lights. Going to a store with lots of fluorescent lights actually seems to trigger my brain fog and anxiety. Slowly getting better though.

-MysteryLyme

springsjean
Forum Moderator


Date Joined Mar 2009
Total Posts : 2057
   Posted 5/9/2011 4:36 PM (GMT -7)   
My vision is one of my most frustrating issues. It is just one eye and the same side I have what the doctor thinks is trigeminal neuralgia - one side of my face by that eye burns like sunburn. The eye gets very red and irritated suddenly with stress or rage. I have managed to keep that at a minimum these days but its still very kinda blurry or hazy around the edges. It's as if it has a drop of water in it and I cannot blink it clear. Its not that bad, just annoying, especially using the computer or reading. I just worry cause I don't want it to get worse. i failed all the visual field tests but neuro-opth couldn't find anything wrong other than small blood vessels in that eye. I never had a problem with it until all the other lyme symptoms reared their ugly head. Drops do seem to soothe it.
Lyme, HME, HGE, bartonella. 4 years undiagnosed despite 10 drs.
Current meds: roxythyroxine, bactrim, doryx, amanatadine, neurontin, xanax, cymbalta Prior meds: amox, minocycline, tetracy, doxy. IV refused by ins. Supplements: potassium, boluke, alpha lipoic acid, AG immune, magnesium, milk thistle, garlic, grapefruit seed extract, resistant microbes, coq10, fish oil, baby aspirin

Dagger
Veteran Member


Date Joined Apr 2008
Total Posts : 1522
   Posted 5/9/2011 5:58 PM (GMT -7)   
I had problems focusing, sometimes it seemed to take forever for my eyes to focus. I was sensitive to bright light and fluorescent lights too.

I had an eye exam and the doc was very interested in what I was telling her. She did the exam, then talked to me a bit, then did the exam again. My prescription had changed! She had me wait in the waiting area while she took care of another patient then she did the whole thing again. My prescription had changed again. She said there was enough of a difference that she didn't want to change my current prescription because she didn't know which test was correct.

I was diagnosed and started treatment shortly after this visit. My eyes started focusing better shortly after I started taking antibiotics but it took a lot longer for the light sensitivity to go away. I still can't stand fluorescents.

Razzle
Veteran Member


Date Joined Aug 2007
Total Posts : 4151
   Posted 5/9/2011 10:16 PM (GMT -7)   
One early visual issue I had, even as a child, was that I often would fail to see something that is right in front of me. This is especially noticeable if the object or my own body (or both) is in motion. So I sometimes will walk into things, almost have been run over by cars when crossing streets, etc., all because my brain somehow does not see the object. This issue is so intermittant and there are no warning signs - it happens out of the blue and then I can go for weeks and months before the next occurrance. My eyesight was 20/20 or better as a child when this was first observed, and usually I pass all the eye tests with no difficulty. None of the eye doctors I've ever been to have been able to find anything abnormal other than dry eye, and more recently, astigmatism. I also have been slowly becoming more and more nearsighted, and starting in 2002, I began to have an extreme sensitivity to bright light (especially sunlight). Is this all due to Lyme? I don't know. I know the failing to see objects (most likely a visual processing issue), dry eye, light sensitivity, and the astigmatism can be caused by Lyme, but not sure about the nearsightedness.
-Razzle

Chronic Lyme, Bart., Gluten & Sulfite Sensitivity, Many Food/Inhalant/Medication/Chemical Allergies & Intolerances, Asthma, Gut dysmotility & non-specific inflammation, Lupus, Osteoporosis, etc.; G-Tube
Meds: Cipro, LDN, Claritin, Singulair, Domperidone, nutritional supplements, homeopathy, probiotics, etc.

jr991
Regular Member


Date Joined Feb 2011
Total Posts : 186
   Posted 7/11/2011 10:41 AM (GMT -7)   
Is there anyone else that can weigh in on this thread. like Neurogurl, I experience a vast array of visual symptoms such as sudden on set of floaters, increased after images, and something similar to visual snow where on certain backgrounds it almost looks like it's raining. These are very, very rare visual symptoms to have which makes me believe possibly this is more neurological as opposed to Lymes disease.

Would appreciate it!

Thanks

Bobbie333
New Member


Date Joined Jun 2011
Total Posts : 10
   Posted 7/11/2011 7:24 PM (GMT -7)   
I have just recently been diagnosed and can relate to the vision issues. I have not had the problem of light sensitivity that many seem to experience but do have the black floaters. My vision has been deteriorating quite a bit over the last couple of years, but I am waiting until I have been on the antibiotics for a while to see if it is an age thing or actually the Lyme.

jr991
Regular Member


Date Joined Feb 2011
Total Posts : 186
   Posted 7/11/2011 7:27 PM (GMT -7)   
Hi Bobbie, do you have any transparent or cell-like floaters?

Lyme14
Regular Member


Date Joined Jun 2011
Total Posts : 381
   Posted 7/12/2011 1:35 AM (GMT -7)   
 
Hi Neurogurl,
 
I have depth perception issues--I was having serious issues driving for a while as a result.  Burbur from NutraMedix helped with that a bit.  I still have some issues with it, but it's better than it was.  I also am sensitive to light.  I have some floaters, and I tend to occassionally see things that aren't there and miss things that are there.  I don't see halos around lights as much as I did before.  I also don't see things as clearly as I used to.
 
Neurotoxins put pressure on the optic nerve, causing deficits in visual contrast.  This is true of all neurotoxin mediated illnesses.
 
Have they tested you for bartonella?  I only ask because you have mentioned (in the past) a lot of neurological symptoms.
 
 
I'm a music teacher, and not a doctor. Anything I post is based on my own experience and lay opinion.
Lyme, Babesiosis, Mycoplasma (Asthma), Fibromyalgia (Soft Tissue Injury), Costochondritis,
CFS (Mitochondrial Dysfunction), IBS (Candida & Leaky Gut), Hashimoto's Thyroiditis, Adrenal Fatigue,
ITP (Low Platelets), TMJ, Plantar Fasciitis, Schamberg Purpura, Tinnitis, Allergies, MCS

Bobbie333
New Member


Date Joined Jun 2011
Total Posts : 10
   Posted 7/12/2011 8:45 AM (GMT -7)   
Hi JR991
As I am new to this I am not sure what transparent or cell-like floaters are. My LLMD called them black floaters as they are black spots that come and go every now and then.
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