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 » face pain near eye

 - UBBFriend: Email this page to someone!    
Author Topic: face pain near eye
hereigoagain
Member
Member # 17663

Icon 1 posted      Profile for hereigoagain   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Has anyone had an extremely tender area between the eye and hairline in the temple area? My hair hurts it - this is bizarre!

I have had significant lazy eye in the same eye but no pain. Have had significant pain within the other eye but that's a deep throbbing kind that I'm learning to live with.

I've been on various antibiotics for close to four months now for chronic lyme.

Thanks for all your help - this site has helped me so much through this. God Bless....

--------------------
-01/11 IGeneX Test:IgM 30+,31IND,34++,39IND,41+,45++,58++
IgG 18+,31+++,34+,41++
- 07/10 RMSF+
- 05/09 CDC positive WB IgM 39 & 41, IgG 41
- 07/08 EBV+
- 11/07 CMV & Parvo +
- 11/01 CDC positive WB IgM 39&41m IgG18

Posts: 64 | From NJ | Registered: Oct 2008  |  IP: Logged | Report this post to a Moderator
Alv
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
check for EHRLICHIA that loves the eye ..but so does BART ..YES DEFINITLY ....THE MAIN symtoms...
IP: Logged | Report this post to a Moderator
wantabe
LymeNet Contributor
Member # 14703

Icon 1 posted      Profile for wantabe     Send New Private Message       Edit/Delete Post   Reply With Quote 
One of my 1st and continuing symptoms.
Does the roof of your mouth hurt too?
Positive test for ehrlichia and bart dx w/ symptoms

wishing you health

--------------------
Lyme+ dx Dec.07
Currently: Levaquin,Cefdinir,Plaquinil,Fluconazole
Nystatin,B12 meth, nortriptyline
Ambien,Clonazepam,many supplements
Dairy, sugar, gluten free diet
infrared sauna and exercise

Posts: 235 | From Iowa | Registered: Feb 2008  |  IP: Logged | Report this post to a Moderator
Alv
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
mine did and was horible...and I had even to remove the tooth as is got so infected the one just below the right eye..that is where the bells palsy took place later
IP: Logged | Report this post to a Moderator
psano2
LymeNet Contributor
Member # 11711

Icon 1 posted      Profile for psano2     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, me too. I think I've connected it to a herx sometimes. This week I started some antibiotic eye drops and in 24-48 hours, my eye/cheekbone just under the outside corner of the eye was very tender to the touch and painful.

This has happened to me a number of times. I really think it's a manifestation of a massive die off of Bb in the area, but that's just my opinion. I think it reflects a huge concentration of Bb in that area.

I also get droopy eyelids.

Posts: 975 | From California | Registered: Apr 2007  |  IP: Logged | Report this post to a Moderator
Dekrator48
Frequent Contributor (5K+ posts)
Member # 18239

Icon 1 posted      Profile for Dekrator48     Send New Private Message       Edit/Delete Post   Reply With Quote 
Wondering if temporal arteritis is a possibility, or maybe it just mimics it, like other conditions.

Here's a link to an article. Scroll down to etiology.

http://www.aafp.org/afp/20000815/789.html

--------------------
The fibromyalgia I've had for 32 years was an undiagnosed Lyme symptom.

"For I know the plans I have for you", declares the Lord, "plans to prosper you and not to harm you, plans to give you hope and a future". -Jeremiah 29:11

Posts: 6076 | From Pennsylvania, USA | Registered: Nov 2008  |  IP: Logged | Report this post to a Moderator
James Marschner
LymeNet Contributor
Member # 13073

Icon 1 posted      Profile for James Marschner     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes.

I was getting cluster headaches. They were EXTREME pain behind one eye.

It would cause extreme watering of the eye as well.

AlV already mentioned bartonella. I have Bart and am convinced that it was causing this specific type of migraine.

breathing pure O2 snuffs 'em out before they can fully get started...within minutes.

Otherwise, the pain is SO bad, nothing even touches it. No narcotic pain reliever anyway.

Posts: 269 | From Valencia, CA | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
hereigoagain
Member
Member # 17663

Icon 1 posted      Profile for hereigoagain   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks to all of you for your responses. I tested negative for Bartonella, Erlichia and Babesia - just lyme came back postitive.

I think this may be herx too but who really knows at this point.


The roof of my mouth does not hurt at this point, that's about all that doesn't though!

Hope everyone finds some relief soon, feel better and thanks again.

--------------------
-01/11 IGeneX Test:IgM 30+,31IND,34++,39IND,41+,45++,58++
IgG 18+,31+++,34+,41++
- 07/10 RMSF+
- 05/09 CDC positive WB IgM 39 & 41, IgG 41
- 07/08 EBV+
- 11/07 CMV & Parvo +
- 11/01 CDC positive WB IgM 39&41m IgG18

Posts: 64 | From NJ | Registered: Oct 2008  |  IP: Logged | Report this post to a Moderator
lymeinhell
Frequent Contributor (1K+ posts)
Member # 4622

Icon 1 posted      Profile for lymeinhell     Send New Private Message       Edit/Delete Post   Reply With Quote 
My guess would be it's referred pain from someplace on your skull. Muscle spazms are quite common, usually from Magnesium depletion.

My 'hair hurt' for close to a year. The top of my skull literally felt like someone had bashed it in with a hammer. I couldn't brush my hair, dry it, or quite often wash it.

My LLMD was the only one to figure it out - I had muscle spazms on the back of my skull and shoulders. They literally were like lumps.

Poke around with a knuckle and see if you can find any. I had no idea they were there. If I pressed REALLY hard on one of them, the spazm would hurt but top of skull no longer did. Which is what referred pain is.

If you can, look up 'Trigger Point Injections' or Prolotherapy. Trigger point injections are shots of lidocaine (numbing) injected directly into the spazm. Blissfully numbs the area for a bit, the injection helps bust up the spazm and restore blood flow to the area.

Oh and btw - I wouldn't believe the results of a coinfection test if my life depended on it (and it did). They're worthless.

--------------------
Julie
_ _ ___ _ _
lymeinhell

Blessed are those who expect nothing, for they shall not be disappointed.

Posts: 2258 | From a better place than I was 11 yrs ago | Registered: Sep 2003  |  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.