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 » Worried about loss of vision in one eye

 - UBBFriend: Email this page to someone!    
Author Topic: Worried about loss of vision in one eye
jarjar
LymeNet Contributor
Member # 8847

Icon 1 posted      Profile for jarjar     Send New Private Message       Edit/Delete Post   Reply With Quote 
Any help from you guys that have overcome vision problems or send me PM of Opthamologist that have helped you regain fading vision.

So far only one eye is causing problems and presume its bart. Interested in hearing of any abx drops that can go to the heart of the matter also. Any helpful tips would be appreciated.

Posts: 805 | From Utopia | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
Greatcod
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
I don't have an answer, but I know a woman who
went blind in one eye after her second tick bite. She went up to Boston, to the Mass Eye and Ear Infirmary, was told that the Lyme bacteria had attacked her optic nerve, and was treated.
I honestly don't know the outcome of the treatment, I lost touch with her, but you should know that Lyme can attack the optic nerve, and that you proably need to see an opthamologist who has some understanding of what Lyme can do.
I don't know who her doctor at Mass Eye and Ear was. Sorry that I can't be more helpful.

IP: Logged | Report this post to a Moderator
chamade
LymeNet Contributor
Member # 11472

Icon 1 posted      Profile for chamade     Send New Private Message       Edit/Delete Post   Reply With Quote 
Did you have a brain MRI done?

Doxycycline worked after only 10 days for my eye stuff, but that was slight double vision and eye pains.

--------------------
Why me? Well, why not me???

Posts: 411 | From San Francisco, CA | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
tailz
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
I'm bummed out - I had to stop my minocyline due to a black tongue. Now what???

I haven't been able to wear my contacts for almost a year due to severe eye pain.

IP: Logged | Report this post to a Moderator
pineapple
LymeNet Contributor
Member # 11904

Icon 1 posted      Profile for pineapple     Send New Private Message       Edit/Delete Post   Reply With Quote 
Some vision issues can be related to lyme nerve inflammation and can be temporary. Is your vision issue something that comes and goes or is it progressively getting worse over time? Have they ruled out macular degeneration, cataracts, etc?

I have had numerous eye issues due to lyme including seeing floaters, foggy vision, sensitivity to light, seeing shadows, blood shot eyes, bouncing eyes, and the snowing effect. All have improved over time with treatment. When I have a lyme flare my vision will worsen, but it goes back to normal when I feel better again.

Are you currently taking antibiotics jarjar?

Posts: 339 | From nowhere | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
pineapple
LymeNet Contributor
Member # 11904

Icon 1 posted      Profile for pineapple     Send New Private Message       Edit/Delete Post   Reply With Quote 
PM sent with the name of a neuro-opthomologist
Posts: 339 | From nowhere | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
susan2health
LymeNet Contributor
Member # 10446

Icon 1 posted      Profile for susan2health     Send New Private Message       Edit/Delete Post   Reply With Quote 
The herbologist Stephen Buhner says that the herb stephania can help the eyes recover from Lyme.

His book was very helpful to me.

I have a Lymie friend who went to a retina specialist who injected her eye with cortisone for the retinal inflammation.

The injection caused a catarac.

She had the catarac removed by surgery.

The surgery left scars that interphered with her vision, so they did surgery again.

I don't know if her vision is any better now than before.

I'm very cautious about traditional treatments for eye problems related to Lyme.

I hope you can find a LL eye doctor.

Posts: 233 | From United States | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
Reese
Junior Member
Member # 12842

Icon 1 posted      Profile for Reese     Send New Private Message       Edit/Delete Post   Reply With Quote 
I had recently suffered an attack of Optic Neuritis. For some reason, the doctors are not sure of, the optic nerve becomes inflamed, thus causing damage to the outer sheathing of the nerve, therefor affecting vision.

This started by having pain in just one eye (it is typical of ON to affect just one eye). The pain was mainly caused by sudden and extreme eye movement such as glancing to your side or changing lanes in a car, whathaveya.

The best description I can come up with is that the vision in the affected eye is like looking through wax paper.

I started out going to a optometrist thinking that my eyes were just out of whack (and thus aching). .. nope prescription hasnt changed. Then went to an opthamologist (the first time) he found nothing. The second time the vision was wiped out. He then referred me to a retinal specialist who injected dye and photographed my eye extensively. He didnt find anything. He then referred me to an nuero-opthalmologist who then scheduled a MRI of my brain to rule out multiple sclerosis. It came back clean - final diagnosis = Optic Neuritis. No treatment. Had they caught it during the initial attack, they could have administered steroids, which only seems to slightly advance vision correction.

90% of those who have ON, having MS or not, recover "most" vision over the course of 2-6 months. Its been over two months for me and my vision is slightly better. Each person recovers a little differently.

As with Lyme, MS affects mostly women. Of the women who have an attack of ON, some 70% go on to develop MS - of men its some 30%. You may eventually be lead down the path of having an MRI taken of your head if you do indeed have ON.

Reese

Posts: 1 | From USA | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
iceskater
LymeNet Contributor
Member # 8655

Icon 1 posted      Profile for iceskater     Send New Private Message       Edit/Delete Post   Reply With Quote 
PM sent to you with name of neuro opthamologist, who is lyme literate.
Posts: 719 | From Delaware | Registered: Jan 2006  |  IP: Logged | Report this post to a Moderator
Cass A
Frequent Contributor (1K+ posts)
Member # 11134

Icon 1 posted      Profile for Cass A     Send New Private Message       Edit/Delete Post   Reply With Quote 
Bunher recommends stephania root tincture, and topical stephania root eyewash, for Lyme eye problems. One person on lymenet recommends Devils Claw for eyesight problems from Lyme.

Hope you get this sorted out very, very fast!!

Best to you,

Cass A

Posts: 1245 | From Thousand Oaks, CA | Registered: Feb 2007  |  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.