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Worried about my eyes
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Lyme Disease
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Cdavislyme
Regular Member
Joined : Dec 2014
Posts : 110
Posted 12/17/2014 1:39 PM (GMT 0)
Hello everyone!
I did look up some llmd's, read the New to Lyme post, and have talked to several members through email (whom I would like to personally thank!)
However, it seems like every second, I am worried about
a new symptom. My eyes have been kinda irritated lately. I thought they were yellow, but everyone says they are not! However, they are bloodshot and watery.
I haven't been tested yet, but pretty sure I have babesia, among other things. I don't know if this is a common symptom, but it is worrying me because today I am noticing extra redness and wateriness.
This could be due to the fact that the infection has disturbed my sleep for a month now. I also am constantly looking up things on my phone (I mean almost all hours of day/night because of the insomnia). I also have been having a lot of anxiety and PANIC modes. I have been in a panic for a month.
If anyone is familiar with this, please let me know. I don't want to overlook something that can be serious!
Fronton
Veteran Member
Joined : Sep 2014
Posts : 521
Posted 12/17/2014 3:46 PM (GMT 0)
I get red eyes from time to time and notice it is usually when I get poor sleep. I am also on my phone a lot and work a desk job. . .
Girlie
Forum Moderator
Joined : May 2014
Posts : 48365
Posted 12/17/2014 5:13 PM (GMT 0)
I get red eyes when I have had less then 7 hours of sleep. I was like this pre-lyme, too.
I think most of us are worried about
new symptoms, especially when we haven't had a confirmed diagnosis.
Hopefully you will be able to see a LLMD soon...or at least have an appointment you can look forward to.
Hang in there!!
IHL
Veteran Member
Joined : Aug 2014
Posts : 2167
Posted 12/17/2014 5:23 PM (GMT 0)
Like the others have said get to an LLMD. or a LLND. I've had major issues with my eyes. I don't think they would've got to the point they are now if I would've found a doctor sooner.
I think Bartonella is notorious for getting in the eyes.
Girlie
Forum Moderator
Joined : May 2014
Posts : 48365
Posted 12/17/2014 5:38 PM (GMT 0)
IHL - did the LL Dr. do something specific for your eyes...or is just treating bart the answer?
livingwithlyme
Regular Member
Joined : Oct 2014
Posts : 29
Posted 12/17/2014 5:41 PM (GMT 0)
I would DEF get your eyes checked. My Lyme began in my eyes 2.5 years ago and I had no clue what was going on until I saw my eye doc. I have that part of my Lyme under control for the most part. but definitely get checked out!
Traveler
Elite Member
Joined : May 2007
Posts : 36573
Posted 12/17/2014 5:48 PM (GMT 0)
For red and watery eyes though, it's likely something like a Benedryl will help. It's a starting point at least.
James_B
Regular Member
Joined : Oct 2014
Posts : 75
Posted 12/17/2014 7:03 PM (GMT 0)
I probably got this as a follow up after Lyme Problems
Heliotrope rash
goo.gl/HGBg6Z
That above rash is linked to this
en.wikipedia.org/wiki/Polymyositis
Post Edited By Moderator (Traveler) : 12/17/2014 12:25:20 PM (GMT-7)
Traveler
Elite Member
Joined : May 2007
Posts : 36573
Posted 12/17/2014 7:06 PM (GMT 0)
Are you sure James? Did you see a LLMD and they determined this? Because it looks like the RMSF rash, and it's likely only a LLMD would think of this and test for it.
Oh, and your first link didn't work. I just used the link for a rash in the second link that you posted.
James_B
Regular Member
Joined : Oct 2014
Posts : 75
Posted 12/17/2014 7:10 PM (GMT 0)
Now the link work :)
Personally I'm more close to Heliotrope rash.
Not diagnosed yet, but my muscle inflammation points to Heliotrope.
Traveler
Elite Member
Joined : May 2007
Posts : 36573
Posted 12/17/2014 7:27 PM (GMT 0)
Thanks, James. I edited only to use a shorter link. Long links like that bother some peoples eyes - makes the hurt and the image jiggles.
So your rash is around your eyes like that? Wow! I'm sorry to hear this! Are you going to be seeing a doc about
this soon?
IHL
Veteran Member
Joined : Aug 2014
Posts : 2167
Posted 12/18/2014 3:02 AM (GMT 0)
Girlie- just treating me. I now have anisocoria which just means my pupils are different sizes. It's worse in less light. He said it could be permanent damage at this point but there's no way to know for sure :(
dmw52
Regular Member
Joined : Jul 2010
Posts : 369
Posted 12/18/2014 12:24 PM (GMT 0)
My eyes are one of my worst symptoms.....very irritated in the morning, little pains at times, lots of floaters. I went to the ophthalmologist, but he said I didn't have anything serious. He did prescribe a steroid eye drop (restasis) but I didn't use it. When I herx or have a flare up of symptoms, my eyes are worse. I have tried many kinds of eye drops and a gel but they are worse when I use them.
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