Eyes :: Recurrent Corneal Erosion Syndrome
Jul 8, 2011
I had this condition undiagnosed for many years its frequency has increased from once a year to twice a month or so. Eye drops such as chloramphenicol and chloromycetin make it worse. Chloramphenicol ointment Chloromycetin ointment and Simple eye ointment seem to be the only treatment that works. I have to sleep on my back to avoid my eye burying into the pillow if I sleep on my side. To ensure I wake up and have no problem I have to apply a blob of chloromycetin and a line of simple eye ointment into both eyes at bedtime.
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I've just moved to a very dry climate and have spontaneously experienced a corneal erosion. I had a recurrent corneal erosion many years ago. Is it possible that this is the same injury returning or is it more likely that I have scratched my eye without realising it?
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Having been officially diagnosed with Sjogren's syndrome about a year ago, I think back on ALL the diagnoses I have had related to it: "nutcracker esophagus and severe GERD", "esophageal spasms", polyarthritis, fibrotic lymph nodes, fibromyalgia, Prinzmetal angina, benign parotid tumor excision (trabecular adenoma), dry skin, dry mucous membranes, etc. and now know they are all part of the same syndrome, which has been steadily worsening and becoming more malignant (and I am only sixty). There are many other more serious difficulties, but now I'm wondering if I, too, will get non-Hodgkin's lymphoma, since that is what some people progress into. It is NOT that this frightens me at all--but now there is something of which to be aware (and I'm not certain my M.D. knows of this). I also have glaucoma and cataracts--so I really have to protect my eyes (and I have had a vitreous bleed into one of them).
My ophthalmologist (a retinologist) placed upper and lower tear duct plugs in my eyes--which has helped, but I still have to use lubrication. Since I am a writer and use the computer extensively, I find it quite hard on the dry eyes. I am extremely careful to drink lots of water and often mix pure fruit juice with my water to avoid calories (sugar) and to make the water more interesting. This does, however, exacerbate my stress incontinence gained after fracturing my back--for which I stay close to a toilet (but my writing is done at home.)
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I have had dry eyes for about 2 year now (I also had lasik in 2005). Within the last 4 months my have have gotten really dry. I have all 4 tear ducts plugged and I am on Restasis. I also use sclera lenses (more for vision but also helps the dry eye). My eye dr said he thinks I may have Sjogren's even though I have never has a Schirmer's test (I am not sure how accurate that would be since i have had lasik anyway). tested positive for ANA 1:80 titer with homogeneous pattern but negative for RF and SSa and SSb. Should I pursue this further? Dry eyes are the only symptom I have.
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I suddenly was diagnosed with Sjogren's Syndrome 4 months ago. I had dry mouth for a year and my breath started to smelled so I thought it was a bad tooth. I started getting my teeth cleaned every 3 months.
Four months ago my eyes were constantly bloodshot. I am on resistais and I had plugs put in my bottom eyelids. I have tried numerous things. My eyes look horrible and my work keeps commenting on them. I want my eyes to look good so my boss will stop asking me if I got enough rest. I am the sole provider for my family and I don't know what to do to get my eyes to look normal again. Has anyone tried anything that works? This is my first posting about Sjogrens because I don't want to believe I have it but my eyes keep reminding me. My mouth has gotten better since my eyes and stomach have been attacked over the last four months. I am on nexium so my stomach is better but I was on nothing for years. I am only 43 years old so I am confused why this is attacking me now. My mom has MS and Rheumatoid Arthritis so I might have received it from her. She wasn't diagnosed until 55 and she had all of her systems in her 20's.
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I was tested for Sjogren's due to my eyes being so dry. I was negative for SSA and SSB but my ANA was 1:80 w/ the hemo pattern. I have read that anything less that 1:100 on an ANA test you can rule out CTD. The only symptom I have is dry eyes. Every now and then my feet tingle a little but that has been going on for as long as I can remember. I do have antithyroid antibodies and have been diagnosed with Hashimoto Thyroiditis. So with only the ANA being 1:80 and only really symptom dry eyes (mainly the right one). Do you think I should see a Rheumy Dr?
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Has anyone heard that HRT increases SS symptoms? I'm on a HRT in the form of a low dose patch. I've been experiencing dry/irritated eyes and read that HRT can make your eyes dryer in addition to the other risks associated w/SS.
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I'm not entirely sure if this is in the right place, but for a good while now, there's been a bit of a 'dent' in my left arm. I can't take a picture because you can only really notice it when you feel it, but there's a definite dent in muscle or fat or something.
Oddly enough, it's the exact place where I used to rest my arm all the time against my desk, but I wouldn't have assumed it's possible for fat/muscle to erode away.
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Just been for my routine 3 yearly smear and doctor found a cervical erosion. Said its totally nothing to worry about and is sending me for it to be cauterised. Just a bit scared for my smear results now as they've always been normal.
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Was wondering if anyone has ever heard of this or has experience with it?
I am not pregnant or on the pill. I am 45 years old & have been told that low progesterone can cause it....anyone else
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I've been told i have a cervical erosion and have been bleeding non stop for 10 days and lots of watery discharge.. can the erosion do this?
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I was just wondering if anyone had been diagnosed with Cervical Ectropion? After many months of being told my abnormal bleeding was just due to PCOS, I finally saw a GP to did a proper examination on my cervix today. She has said I have Cervical Ectropion and that I need a referral to a gynaecologist to have it cauterised. She did say they will have look and around and check everything else is fine, which worried me slightly that there was something she wasn't telling me. But knowing that she has referred me on a 4-6 week referral and not the 2 week referral reassures me a little.
Anyway, I was just wondering if this common with women who have PCOS, the GP explained it was likely due to my hormones, since it usually happens in pregnancy or women who are on the pill.
Any insight/advice/reassurance appreciated.
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Small but geometric -ish shape. This changes in 1/2 hour or more, the shape gets larger forming a getting larger approximate 'C' shape to the left of center. It is almost like me seeing a crude kaleidoscope . Eventually the thing disappears to the left. The shape seems to be of small triangles squares, anything 'sort of' geometric. I can see past it but still have to see the shape. Whichever eye I close I can still see it; close both I can see it! It has now cleared completely as I have not being looking at the sun or any strong light. Is it 'just one of those things' to be tolerated every now and then. I am 75 and in general good health
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I'm late 5s,have had floaters since my 20s,back then they were small black or clear dots,fast forward,late fifties,now i've had pvds in both eyes,vitreous gel shrinks and pulls away from the back of the eye,now i have these clear to gauzy larger floaters,plus one large clumpy black one and I can't ignore them anymore. PVD is age related. I am just lucky enough to have these awful larger ones that can blur and obstruct vision. How does a person deal with it. Oh yes I also am starting to have dry eyes. Both also can cause hazy vision. Unless you've experienced it,no one else can relate
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The squint(left eye) had been developed at an age of 3 or 4 years I think... A cataract was also developed in it.. It had been ignored by me as I was not able to focus on it while seeing things... Cataract was recently removed(At an age of 18) by a laser treatment... But after the treatment also I had not get my vision back for my left eye (lazy eye).. I'm not able to see with that I now... Can I improve my left eye's vision...? If I can't.. Then how can I correct my eyes appearance... My left eye is little outwards from it's actual direction.
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I have this squint since childhood. My eyes move outward. It happens a lot when I'm tired or try to look quickly at something, It was diagnosed early and I was asked to do a regular exercise with pencil. I had to Keep pencil in front of my nose and look at it and then slowly move the pencil forward and repeat it several times. The later I was given glasses and it improved it a little but then again it got as it was earlier. My vision is 6 by 6. But its just I don't have proper control over the muscles. They seem to be aligned but when I'm tired or move eyes they go outward. I wanted to know how it can be permanently corrected. It just disturbs me and I always feel a stress on my eyes. I have this irritation over eyes too and itching which makes it even worse. How it can be treated or it can be operated? I guess it would be easier with operation and I would go for it but I was asked to do exercise and told that it will stay but will get better, It was 30 degrees.
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I had an exposure around 3 months ago, I got a rapid blood finger-prick test at around six weeks and a little more, and it came back negative. However, starting from this month, I kept having mouth ulcers in my mouth,they are small, I'm getting a new one maybe like a week or so, then it goes away about a week. It's been a month and i have a new mouth ulcer each week after the old one heal.
My question is, how much can I trust my 6 weeks rapid test? I know its not conclusive and I'm getting another test soon, but just really wanna know its accuracy.
Also, is keep having mouth ulcers related to HIV?? is it damaging my immune system and cause such situation?
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I used to have recurrent utis about 5 years ago- trimethoprim used to work as a charm and they disappeared after i had my tonsils out (linked?)
I got a uti 4th of nov- got cephalexin. it got better but i still couldn't have trousers on due to uncomfortability which i assumed meant that the infection was there- 2 weeks later i got test results from gp saying i had a resistant form of e.coli and got new set of antibiotics- as i was on them i took a pregnancy test- which was positive (very happy news). last period date being 3 november.
my symptoms for uti are insane- my clit gets uncomfortably stimulated and i feel like i have to rub it to release the tension but if i do that the same feeling comes back with a vengeance. i have to keep pushing in the toilet and if i stand up there's a horrible sensation over my vaginal area which makes me want to jump out the balcony. so this is a major problem for me unlike the symptoms of "i pee a lot with a burning sensation".
i can't bear this feeling anymore. its been 4 days since i finished the last course of antibiotics, and mornings are horrible followed by symptom free nights. luckily i gave another urine sample on friday (waiting for results). can someone help me? starting to think uti came with the pregnancy.
or maybe i have screwed up genital area that needs to be fixed or something. i got the same symptoms when i was little around 4/5- i used to rub myself back then and remember how bad it used to get - my mum had to sit with me in the toilet to help me get through it. and now i just cry in the toilet for a hour before i force myself up and into bed.
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OK, so the problem started at night...
During sleep, I noticed my right ear became blocked. My hearing from this ear became impaired and there was a feeling of fullness. (If I slept on my left ear, it was like I was deaf!). During the morning however, the problem would disappear.
Anyway, this problem kept recurring night after night. After a bit of google research, I figured it was just excess wax in my ear. I went to a local grocery store and picked up some ear drops, claiming to remove excess wax. ("Debrox"). After administering, the feeling of fullness came back...and has now stuck!!
I read in one article, that gently placing your index finger in the ear and moving it up will create a vacuum that will open up the ear. However, within seconds, this whooping sound occurs in my ear and it closes up again. I repeat the process over and over and the same thing keeps happening.
So should I have put the drops in my ear? Is the problem more serious? I also read it could be Middle ear pressure- how can I hear properly through my ear again?
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I cannot find any doctor to help me. It started in November .. I thought I was having some back pain and went to the DR and found out I had a UTI. I was optimistic I would take the antibiotic and all would be fine. Well after I completed the Cipro the UTI was still there. They switched me to Macrobid and it cleared up. I continued having the pain in my back, hip and near my ischial tuberosity (sit bone). The sit bone felt very tender upon palpation and when i would press on it, it would also then initiate an anal reflex. (I think a sphincter is somewhere around there). I have gone to orthopedic doctors, and I have an appointment today with a Urologist as the UTI has come back twice since then. It all seems interconnected. I also have these shooting pain up and down my labia ... to my hip as well. It is all on my right side as well.
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I have suffered for a few years now with my kidneys, first starting off with when I drank alcohol. A few days later I would get really ill with a kidney infection and given antibiotics. It then became more common to get them without drinking. I would also inbetween this get recurring bladder infections.
I am 19, a female, and have had various tests (ct scan, dye put in my arm through a drip to see any problems clearer and a few ultrasounds) done to check the structure of my kidney is all okay and that there isn't any obstructions ( all seems to be okay, and they didn't think that it would be worth looking with a cystoscope just yet.) However something worth noting is that I always seem to have invisible blood in my urine that is discovered through dipstick tests. And recently my brother has been having the same kidney problems (kidney infection, especially after drinking alcohol).
I am also now on medication called 'Hiprex' it has antiseptic qualities to try and prevent getting UTI's/kidney infections however doesn't seem to be working as I still get them.
Really getting fed up now, as when I get ill with it I get super achy, all of my glands swell up, a dry mouth so constantly thirsty and weeing loads, especially at night, and dull aches in my back.
Once when passing urine I passed out from a pain in my right lower side. But like i said, no kidney stones or any problems structurally.
Has anyone else been going through this too? Any ideas what could be wrong?
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