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This forum is for questions and support regarding What Causes Lyme Disease, Diagnosing Lyme Disease, Joint Pain issues, Living with Lyme Disease, Nervous System issues, Prevention, Risk Factors, Skin Disorders, Symptoms and Treatments.
Has anyone experienced this?... I have noticed that my viterous floaters have become now white. I still have the translucent ones that you can really see in a well lit room or outside. But i keep thinking I see things. I keep thinking i am seeing fibers/dust particals in the air, but I think they are floaters?
I've heard of that type of floater being a symptom of LD.
I have the floater problem too. Never noticed them before I had Lyme Disease, so I didn't have them. Now that I have them, I try just to ignore it. Along with everything else this punishing disease has to offer.
You may try and research an ophthalmologist familiar with Lyme (if there is such a thing).
Yep. sure have, I recently expressed this and other concerns to a doc and to my...LOL...surprise,he wasn't concerned.I ask myself why do I keep subjecting myself this ridicule...OH, that's why cause I want to get better.Good thing he was so willing to refer me to the LLMD, otherwise i had visions of him swinging from the ceiling by his tie...I'm not really that violent but the thought was fun to entertain.
I have already had a test for Lymes and it came out negative. That is one reason I had never checked out Lymes. My sister does have it, and has been treated for years--but she seems to be doing well now.
Is there another test for Lymes? (if there is another thread or more info, you can just point me to that.....)
I have the floater problem too. Never noticed them before I had Lyme Disease, so I didn't have them. Now that I have them, I try just to ignore it. Along with everything else this punishing disease has to offer.
You may try and research an ophthalmologist familiar with Lyme (if there is such a thing).
Maybe because they don't have Lyme or probably anything else. If THEY ever got Lyme it'd be a year's worth of Doxy nonstop.
More floater fun!
Thanks and I will post a question after I read up some more about this disease....
have a blessed day!!
suanne
I have already had a test for Lymes and it came out negative. That is one reason I had never checked out Lymes. My sister does have it, and has been treated for years--but she seems to be doing well now.
Is there another test for Lymes? (if there is another thread or more info, you can just point me to that.....)
thanks!
suanne
It's more sensitive to native lyme bacteria. Everyone else tests for European lyme.
That's what someone told me at least. Don't know how true it is. Also, have your results read by a LLMD.
Good luck and I hope you get the answers you seek.
Cindy
I would think if your sister has lyme and you live in the same area your chance of having it would be much higher.
I researched and found this site
http://www.eyefloaters.com/
I am not brave enough to try it, but it's very tempting as more and more are amassing in there. Doc says it's broken blood vessels. Sux.