LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Problems with eyes...Info please.

 - UBBFriend: Email this page to someone!    
Author Topic: Problems with eyes...Info please.
carolann2013
LymeNet Contributor
Member # 39964

Icon 1 posted      Profile for carolann2013     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have stopped my treatment as of this past March. I feel symptoms coming back but all in a different way.

I have had trouble with my eyes. They have been very dry and burning. WEnt to the doctor and he said I had dry eyes and for me to use Systane 3 times a day.

I did this and not much help. This was in March when I went to the eye doctor.

I had a problem yesterday morning...my periphireal vision was not right. Out of my right eye Some of my vision was blocked.

I went to the doctor and the tests said that I had blockage of vision in my upper right quadrant. But the problem did not come from my eyes, it was something going on in my brain.

Today, except for the headaches, my vision is fine. I am scheduled for an MRI this afternoon.

I am going to feel like an idiot if my MRI comes up fine.

Does this sound like a symptom of Lyme and will it be terrible one day and then perfect the next day? Will my MRI come up normal since my vision is good today?

Posts: 213 | From Tennessee | Registered: Jan 2013  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

Icon 1 posted      Profile for Robin123     Send New Private Message       Edit/Delete Post   Reply With Quote 
If you get a test result that shows something, then that can be helpful. But so many times, we don't get any result when we have symptoms. So you don't need to feel bad if your test comes out ok!

If you feel like trying an experiment, as I cannot say what's going on with your eyes, this is something that helps mine - I drink mangosteen juice, an anti-inflammatory juice, to stop my eye symptoms, which have been floaters, light sensitivity, muscle eye pain and blurred vision.

I drink the Mango-Xan version, as it is the most tart. It's in healthfood stores and online.

Posts: 13171 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
carolann2013
LymeNet Contributor
Member # 39964

Icon 1 posted      Profile for carolann2013     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks Robin, but it does make me feel bad.

These tests costs money, which is something I don't have a lot of.

Also, this is what causes people, family, to think you are crazy.

So if we have symptoms, many times those symptoms do not show up in medical tests?

Do these symptoms come one day and gone the next?

It is enough to make a person crazy.

Posts: 213 | From Tennessee | Registered: Jan 2013  |  IP: Logged | Report this post to a Moderator
carolann2013
LymeNet Contributor
Member # 39964

Icon 1 posted      Profile for carolann2013     Send New Private Message       Edit/Delete Post   Reply With Quote 
Just had my MRI.

I asked the person that gave me the MRI how they looked. He said they looked okay to him, but he didn't know what the docs were looking for.

The MRI person said that most of the tests that he gives is usually normal. He has been giving them for awhile.

The doctor will call me tomorrow to get the actual results.

So, I shouldn't be surprised if they come up normal?

My vision hass been good today. The only thing is I still have pressure behind the eyes and a headache, and the headache isn't really a bad one, a lot of pressure.

Posts: 213 | From Tennessee | Registered: Jan 2013  |  IP: Logged | Report this post to a Moderator
Razzle
Frequent Contributor (1K+ posts)
Member # 30398

Icon 1 posted      Profile for Razzle     Send New Private Message       Edit/Delete Post   Reply With Quote 
Some migraine headaches can cause partial vision loss as part of the migraine...it is temporary, only lasting for part of the migraine. I think an MRI in this situation would be normal...

--------------------
-Razzle
Lyme IgM IGeneX Pos. 18+++, 23-25+, 30++, 31+, 34++, 39 IND, 83-93 IND; IgG IGeneX Neg. 30+, 39 IND; Mayo/CDC Pos. IgM 23+, 39+; IgG Mayo/CDC Neg. band 41+; Bart. (clinical dx; Fry Labs neg. for all coinfections), sx >30 yrs.

Posts: 4167 | From WA | Registered: Feb 2011  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

Icon 1 posted      Profile for Robin123     Send New Private Message       Edit/Delete Post   Reply With Quote 
It's the nature of this illness to be erratic, as it does whatever it pretty much pleases, so we need to get used to symptoms changing around and go with the flow - I call it whack-a-mole! And remember that, when we get a new symptom out of the blue in a new body area, that it might be the Lyme acting up.

2nd, it's the nature of this illness for us to go through tests and test normal. It happened to me for example when a neuro-opthalmologist tested my eyes when I was developing blurred vision. My tests all came back normal even tho he had to anesthetize my eyes for me to be able to look at light.

I suggest you read a little more about the spirochetes and how they operate in the body, then YOU can start telling others how it works, and not the other way around! Knowledge is power.

And yes, the money part of it can be hard. That's why I think it's important that you go in with your eyes open to the fact that you may, or may not, get a test result that shows something.

The one test I'm aware of that can show stuff going on in Lyme patients' brains is the SPECT scan, which can show hypoperfusion, areas where bloodflow is not happening fully. Then after treatment, a SPECT scan can show "the lights are on again," so to speak!

Posts: 13171 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
carolann2013
LymeNet Contributor
Member # 39964

Icon 1 posted      Profile for carolann2013     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks Robin

I have a hard time reading and comprehending if it is in the least bit complicated. I read and think I have it and then I realize that I don't understand a thing that I have read.

I have always learned by reading. It just doesnt' work like that for me anymore. But, it isn't impossible, it just may take me longer for it to soak in. May have to read it three or four times.

Posts: 213 | From Tennessee | Registered: Jan 2013  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


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, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.