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 » Treatment for lyme in the eye

 - UBBFriend: Email this page to someone!    
Author Topic: Treatment for lyme in the eye
maps
LymeNet Contributor
Member # 19758

Icon 9 posted      Profile for maps     Send New Private Message       Edit/Delete Post   Reply With Quote 
Have been having trouble with eye inflamation. Now on prednisone, 1 drop each hour plus isopto homatropine three times a day and mexidex before bed.

I was told today that they could find no reason for the inflamation and that I should suspect lyme.

I see my llmd next wednesday but would appreciate hearing from anyone on how this would be treated.

Have to admit I am feeling shocked and a little scared.

Thanks for your help.

regards
maps

--------------------
1999 CFS, 2002 CMV Myco pneumonia
1 year antibiotics on and off
2002 EBV, 2009 Positive Igenex Borellia and Babesia, Brain mri severe white matter disease
Monoclonal Gammopathy. On and off antibiotics since sept. March 9 started iv antibiotics

Posts: 328 | From somewhereelse | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
MorningSong
LymeNet Contributor
Member # 19989

Icon 1 posted      Profile for MorningSong     Send New Private Message       Edit/Delete Post   Reply With Quote 
Maps-

Im sorry to hear what you are going through regarding your eye. I know it is very scary. Im not a doctor, and what I have learned from others on this site is that eye inflammation can have many causes.

Some have stated it is Lyme. Also some medications we take can cause them:

http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1125522

Are you having other symptoms?

Posts: 515 | From In His Loving Care | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
maps
LymeNet Contributor
Member # 19758

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

I don't know what you mean about other symptoms, i am positive for lyme and babs.

The eye specialist knows what I am taking and she is the one who said we have to consider lyme as everything else has been ruled out.

regards

--------------------
1999 CFS, 2002 CMV Myco pneumonia
1 year antibiotics on and off
2002 EBV, 2009 Positive Igenex Borellia and Babesia, Brain mri severe white matter disease
Monoclonal Gammopathy. On and off antibiotics since sept. March 9 started iv antibiotics

Posts: 328 | From somewhereelse | Registered: Apr 2009  |  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 
Hi - All my Lyme eye symptoms disappear by drinking a little mangosteen juice daily. It's an antioxidant, anti-inflammatory juice.

It's sold at health food stores, online, and the strongest is Xango, sold multi-level.

I drink the Ultra brand, with 70 minerals added.

If you try it, just drink a little, with water.

Posts: 13117 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
savebabe
Frequent Contributor (1K+ posts)
Member # 9847

Icon 1 posted      Profile for savebabe     Send New Private Message       Edit/Delete Post   Reply With Quote 
Bart is the co-infection that really hit my eye. I found that levaquin and lyme treatment really helped with my eye inflammation.
Posts: 1603 | From ny | Registered: Aug 2006  |  IP: Logged | Report this post to a Moderator
Pocono Lyme
Frequent Contributor (1K+ posts)
Member # 5939

Icon 1 posted      Profile for Pocono Lyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
I had pretty much the same experience as savebabe.
Levaquin or Cipro cleared my Iritis/ Iridocyclitis. Been on both. First Levaquin when the Iritis was cleared.

I did have a problem with steroid drops though.
The blood vessels ruptured, extreme pain, and an increased intraocular pressure of 47.

I was switched to Xibrom which is a nonsteroidal drop.
They work well without the nasty side effects.

--------------------
2 Corinthians 12:9-11


9 But he said to me, �My grace is sufficient for you, for my power is made perfect in weakness.� Therefore I will boast all the more gladly about my weaknesses, so that Christ�s power may rest on me.

Posts: 1445 | From Poconos, PA | Registered: Jul 2004  |  IP: Logged | Report this post to a Moderator
Lymeorsomething
Frequent Contributor (1K+ posts)
Member # 16359

Icon 1 posted      Profile for Lymeorsomething     Send New Private Message       Edit/Delete Post   Reply With Quote 
Did anyone have floaters as a symptom of inflammation?

--------------------
"Whatever can go wrong will go wrong."

Posts: 2062 | From CT | Registered: Jul 2008  |  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 
Yes, and gone from drinking mangosteen juice.
Posts: 13117 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
maps
LymeNet Contributor
Member # 19758

Icon 1 posted      Profile for maps     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for the input, so it looks like this can be treated by my llmd then.

regards
maps

--------------------
1999 CFS, 2002 CMV Myco pneumonia
1 year antibiotics on and off
2002 EBV, 2009 Positive Igenex Borellia and Babesia, Brain mri severe white matter disease
Monoclonal Gammopathy. On and off antibiotics since sept. March 9 started iv antibiotics

Posts: 328 | From somewhereelse | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
Pinelady
Frequent Contributor (5K+ posts)
Member # 18524

Icon 1 posted      Profile for Pinelady     Send New Private Message       Edit/Delete Post   Reply With Quote 
I did antibiotic drops that burned like fire in the

beginning. So I think it hit it as now it does not.

Eyes are in the top 5 for finding in autopsy of

animals. So If you dont have a virus such as

shingles or herpes I would treat for lyme too.

--------------------
Suspected Lyme 07 Test neg One band migrating in IgG region
unable to identify.Igenex Jan.09IFA titer 1:40 IND
IgM neg pos
31 +++ 34 IND 39 IND 41 IND 83-93 +
DX:Neuroborreliosis

Posts: 5850 | From Kentucky | Registered: Dec 2008  |  IP: Logged | Report this post to a Moderator
klutzo
Frequent Contributor (1K+ posts)
Member # 5701

Icon 1 posted      Profile for klutzo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I had a large floater and pain, plus goo running out of my eye and down my face from my right eye. This turned out to be uveitis from Lyme.

My left eye put out showers of sparks on the left side. This turned out to be a separation of the vitreous humor from the eye wall, due to uveitis from Lyme.

My right eye quickly became dependent upon steroid drops. I could not miss a dose or all hell broke lose again.

I was very upset about having to use steroids with Lyme, so I started researching for other options.

Also, uveitis is the third leading cause of blindness in the USA and the steroids can eventually cause cataracts, macular cysts, and other problems.

I found Benfotiamine and within 3 weeks was off the eye drops and all eye pain was gone. My opthalmologist was so impressed, he asked me to get him a copy of the study I read that gave me the idea to use benfotiamine.

The study is from the University of Texas. They used the benfotiamine for 12 weeks before it equaled the results of the steroid drops, so my inflammation may not have been as bad as some.

Benfotiamine is a lipidized form of Vitamin B1 (Thiamine). I take one 150 mg. capsule daily. It costs $11.77 for a 4 month supply at www.vitacost.com.

If trying it, I would keep it away from any other B complex vitamins you take, so you don't develop an imbalance.

It may not work for you like it did for me, but it's safe, cheap, and worth a try.

klutzo

Posts: 1269 | From Clearwater, Florida, USA | Registered: May 2004  |  IP: Logged | Report this post to a Moderator
maps
LymeNet Contributor
Member # 19758

Icon 1 posted      Profile for maps     Send New Private Message       Edit/Delete Post   Reply With Quote 
Maybe dumb question but does that mean that this inflamation is going to be a long term thing or will the meds I am on make it better.

Another thing, in which way are the steroids bad?

Thanks for all the replies.

regards
maps

--------------------
1999 CFS, 2002 CMV Myco pneumonia
1 year antibiotics on and off
2002 EBV, 2009 Positive Igenex Borellia and Babesia, Brain mri severe white matter disease
Monoclonal Gammopathy. On and off antibiotics since sept. March 9 started iv antibiotics

Posts: 328 | From somewhereelse | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
Lymeorsomething
Frequent Contributor (1K+ posts)
Member # 16359

Icon 1 posted      Profile for Lymeorsomething     Send New Private Message       Edit/Delete Post   Reply With Quote 
Klutzo, thanks for the interesting info. Here is a related abstract....

Lipophilic Vitamin-B1 Analogue Benfotiamine Prevents Endotoxin-Induced Uveitis in Rats
http://tinyurl.com/bff3tp

--------------------
"Whatever can go wrong will go wrong."

Posts: 2062 | From CT | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
Pinelady
Frequent Contributor (5K+ posts)
Member # 18524

Icon 1 posted      Profile for Pinelady     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sometimes steroids can save your site as talked about here not too long ago.

--------------------
Suspected Lyme 07 Test neg One band migrating in IgG region
unable to identify.Igenex Jan.09IFA titer 1:40 IND
IgM neg pos
31 +++ 34 IND 39 IND 41 IND 83-93 +
DX:Neuroborreliosis

Posts: 5850 | From Kentucky | Registered: Dec 2008  |  IP: Logged | Report this post to a Moderator
WildCondor
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
I saw a Lyme literate Eye doc and needed 2 different types of antibiotics for the eye. One was a drop, one was a cream. After treatment, my Lyme of the eye was gone for good.
IP: Logged | Report this post to a Moderator
klutzo
Frequent Contributor (1K+ posts)
Member # 5701

Icon 1 posted      Profile for klutzo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Dear LYMEORSOMETHING,
That link you provided is the one I got my idea from and is the same 15 page study I printed and gave to my eye doctor. Brilliant minds think alike ;-)

- - - - - - - - - - - -

Dear MAPS,
Steroids suppress immunity, so they are never good for people whose immunity is already suppressed, like ours is.

The innate half of our immune system is as suppressed as it is in AIDS patients, which is why some researchers call this "AIDS Minor".

The acquired half of our immunity is running all the time, in an over-reactive mode, hence all the allergies, chemical sensitivities, etc.

Each half handles different things, and they can't both run at the same time. Lyme is a disease that would normally be killed by the innate system, so it cleverly convinces the immune system that it is a bug that should be killed by the acquired system, thus allowing it to grow unimpeded.

Steroid eye drops are not nearly as bad as injections, which are not nearly as bad as orals.

I can testify to this personally,having been stung 9 times by insects I am allergic to in the past 7 years.

Because my reaction to a recent insect sting came back again and my throat started to close again on the second day, I was given a total steroid dose of 300 mgs., which is outrageous. (A normal insect anaphylaxis dose is 120 mgs.)

When using the eye drops, it is recommended to put your finger over your tear duct and squeeze your eye shut for the first two minutes.

The finger will prevent any of the steroids from traveling down your lachrymal duct and going into general circulation (per www.uveitis.org).

I also read that a PICC line should be inserted and backup ABX started 48 hrs. before starting the drops, the drops should not be used more than 14 days, and the ABX s/b continued 48 hrs. after the drops are stopped.

Many of us become dependent upon the steroid drops, and stopping them after 14 days is not possible. The result of stopping for me was an instant loss of vision, and the long term result can be blindness.

A surprise to me in reading about all this was to learn that no part of the immune system can reach many areas in the eye, one reason why Lyme likes to go there.

Also, I am allergic to all of the Lyme effective ABX, so I had no back up to protect me from the Lyme growth that would occur if the drops got into my circulation.

Those are some reasons why I decided to try the benfotiamine.

I am suffering horribly right now from injected and oral steroids that I had to take to save my life after a fire ant sting.

I have had thrush, intestinal yeast, vulvar vestibulitis, and some mild signs of lung yeast for over a month, despite taking every drug and supplement known to man.

I may have to go in the hospital and have dangerous intravenous drugs to stop the yeast overgrowth. A person with a normal immune system does not get this severe reaction to steroids, not even to the amt. I was given.

I was reading on an HIV web site about how to get rid of yeast, where an HIV doctor said that nobody with a CD4 count above 100 will ever get thrush. He said a normal count is 500.

This implies a serious immune deficiency. So, in summary, sometimes steroids are the lesser of two evils, but a vitamin is always preferable to a steroid, IMO, and long term use of vitamins will not cause cataracts or cysts.

Also, for those of you who are female, my eye doctor warned me that eye makeup is strictly off limits when using steroid eye drops. The risk of infection is too high.

klutzo

Posts: 1269 | From Clearwater, Florida, USA | Registered: May 2004  |  IP: Logged | Report this post to a Moderator
maps
LymeNet Contributor
Member # 19758

Icon 1 posted      Profile for maps     Send New Private Message       Edit/Delete Post   Reply With Quote 
Klutzo:

Thank you for taking the time to post this in detail for me, it has answered all my questions very well.

I have stopped taking clarithamicin just to make sure this is not being caused by the antibiotics.

Lymeorsomething: going to print the link you gave me, will be seeing llmd on Wednesday so going to give him the info.

Thanks everyone for your input.

Hoping that it turns out to be caused by the antibiotics.

regards
maps

--------------------
1999 CFS, 2002 CMV Myco pneumonia
1 year antibiotics on and off
2002 EBV, 2009 Positive Igenex Borellia and Babesia, Brain mri severe white matter disease
Monoclonal Gammopathy. On and off antibiotics since sept. March 9 started iv antibiotics

Posts: 328 | From somewhereelse | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
imagine2
LymeNet Contributor
Member # 3136

Icon 1 posted      Profile for imagine2     Send New Private Message       Edit/Delete Post   Reply With Quote 
Wild Condor,
Can you tell me more about the abx you took for the eyes and how long you took it. I had no idea this was a possibility.

I have not been diagnosed with uveitis but eye symptoms have been one of my worst lyme symptoms and have gotten worse since starting amox.

Eyeball sore to touch, difficult to read, stinging,blurred vision. It started when I was driving. Had to blink constantly to focus on the road. Scared me.

I dont know of a lyme literate ophthalmologist but would like to ask my llmd if I can try your abx.

Thanks for your help

Posts: 677 | From Virginia | Registered: Sep 2002  |  IP: Logged | Report this post to a Moderator
WildCondor
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
I'm honestly not sure what they were since it was 10 years ago now. They were common antibiotics though. After treatment all my eye symptoms went away. I took the drops for 2 months and the cream for 4 weeks.

Wish I could remember the names!

IP: Logged | Report this post to a Moderator
CheriAnn
Member
Member # 19673

Icon 1 posted      Profile for CheriAnn     Send New Private Message       Edit/Delete Post   Reply With Quote 
I so wish you could remember what you took WildCondor. My on remaining symptom is a ever so slight blurriness in my right eye and a slight halo at night. This thread has been so helpful. I have wondered if I should even keep considering this a symptom since it is so minor but am hesitant to go of ABX til every "symptom" no matter how minor is gone.
Posts: 27 | From Ohio | Registered: Mar 2009  |  IP: Logged | Report this post to a Moderator
WildCondor
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
I saw a good Lyme literate Opthamologist. I suppose I can call and get my records and let you know what it was. I will try!!
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.