Nal
Frequent Contributor (1K+ posts)
Member # 6801
posted
Gosh Im tired of having these stupid flare ups! Ill go months and feel fine and then pooff!!! Right now its my eyes-again.
I get pain in both eyes and a little bit of blurred vision. My eye dr is very familiar with lyme and he tells me convergence disorder. Still, don't know a whole lot about it so i just don't know if i fit into it.
Im tired of the eye pain. Anyone else suffering with this lately? Im only on reglan and nexium. I do natural energy treatments which help a lot with they Lyme. I did have a detox this week and it seemed to flare it in the eyes-why??????
Nancy
-------------------- Life is 10% what happens to you, 90% how you respond to it!
-Chuck Swindoll Posts: 1594 | From Colorado | Registered: Jan 2005
| IP: Logged |
Nal
Frequent Contributor (1K+ posts)
Member # 6801
posted
I did call my eye dr and i go back to see him again in Sept. This just sucks!
-------------------- Life is 10% what happens to you, 90% how you respond to it!
-Chuck Swindoll Posts: 1594 | From Colorado | Registered: Jan 2005
| IP: Logged |
I was looking to see if I could find anything similar to my eye convergence problems.
I have been diagnosed with lyme/babesia was having a hard time reading. Blurry, double, words move around page, bad eye pain, things appear closer to me, or the wrong size. It also looks like everything is "pixely" or grainy like an old tv screen.
Was sent to physical therapist specializing in balance problems associated with the ear, but she said my bouncing vision sounded like a visual processing problem.
I was referred to a doc who does vision therapy with people who have had some type of brain injury. My eyes are healthy, but he has diagnosed me with visual midline shift syndrome.
My brain thinks the center of my body is lined up with my left eye. This causes depth perception problems, balance issues, headaches. I wore temporary prism glasses on three occasions which would correct the problem temporarily. I now have permanent prism glasses which only help sometimes. At the time I had been diagnosed with post lyme syndrome, and this eye doc said something was still attacking my nervous system and I should seek treatment for the lyme......
I was also diagnosed with post trauma vision syndrome. This makes everything look like its moving. I did visual evoked potentials test and my brain is telling my eyes to look out to the side constantly. This causes headaches and extreme eye pain and makes things look slightly distorted. This is the source of my eye convergence problems.
I have been wearing my prism glasses for several months and have been doing home eye convergence exercises for over a year and Im having no improvements. I wonder if I should get another opinion.
Does anyone else have vmss or ptvs or eye convergence problems?
-------------------- -Love and Gratitude Posts: 69 | From another planet far far away | Registered: Oct 2008
| IP: Logged |
I have a question, is your eye pain in just one or both eyes? I think I have something similiar, never new there was a name for it. For me I feel it is like both my eyes see fine independently but when my brain puts the two pictures together it just isn't quite right. I also have horrible depth preception which the bumper of my car can attest to (I seem to park a little to close parking lot dividers).
Tracy
Posts: 41 | From Singapore | Registered: Jan 2008
| IP: Logged |
Yes, my eyes see fine independantly as well. What is wrong is that my eyes don't aim in correctly which has to do with fine motor skills. This can throw off depth perception as well.
The pain is in both eyes, its like the nerves or muscles surrounding them, and sometimes both eyeballs hurt as if theres alot of pressure in them.
-------------------- -Love and Gratitude Posts: 69 | From another planet far far away | Registered: Oct 2008
| IP: Logged |
Nal
Frequent Contributor (1K+ posts)
Member # 6801
posted
Hi you two. Yep, you are TOTALLY describing what I have with my eyes!! My dr says convergence disorder can be seen in Lyme patients. They treat it with adding prisms to your glasses. It does help. Do either one of you also get pin prick type sensations at times in your eyes? I will get that when I am extra tired.
-------------------- Life is 10% what happens to you, 90% how you respond to it!
-Chuck Swindoll Posts: 1594 | From Colorado | Registered: Jan 2005
| IP: Logged |
posted
Lyme likes the eyes. I've read that there are ketes in the eye. They affect the nerves(also from the brain) and muscles.
I drink mangosteen juice (for me, the Ultra version; there are lots of kinds out there) and it stops all my eye symptoms. It's an anti-inflammatory, antioxidant juice. If you try it, go slow and drink a lot of water also.
Posts: 13116 | From San Francisco | Registered: May 2006
| IP: Logged |
posted
For hubby eye pain seems to be more related to babesia and bartonella -- just wanted you to be aware that it is not always Lyme that is the main problem.
Also, the reglan could cause blurry vision and maybe difficulty focusing -- the eyes are effected by cholinergic/anticholinergic meds. Might want to discuss this with your pharmacist.
Bea Seibert
Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004
| IP: Logged |
Nal
Frequent Contributor (1K+ posts)
Member # 6801
posted
I had to stop taking Reglan. My eye problems were only getting worse while I was on it. Now they are doing better. Still having issues, but they are much better.
-------------------- Life is 10% what happens to you, 90% how you respond to it!
-Chuck Swindoll Posts: 1594 | From Colorado | Registered: Jan 2005
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/