Posterior Blepharitis - Bright Red Lid Margins, Bloodshot Eyes
Apr 6, 2015
I believe I have posterior bleph since it affects my Meibomian glands and I've had it for around 5/6 years, although I wasn't aware I had the condition until I saw a fantastic independent optician who also has it (note: don't both with any of the 'fast-food' opticians e.g. Specsavers - they haven't got a clue!).
Until recently, I never really had much of a struggle with it - it was generally more of an irritant, but recently it's become worse despite me upping the usual maintenance. My current routine involves the warming bag + cleaning with Blephaclean pads. There used to be an excellent product called Lid Care but they seem to have disappeared now unfortunately. Other than that, I take Omega-3 supps.
My symptoms lately are the usual e.g. soreness, grittiness, bright red lid margins, bloodshot eyes etc. However, recently I'm struggling a bit as I keep developing badly blocked glands that become a little inflamed and uncomfortable - is this quite common with the condition because I've never really had that? If so, does anyone have any alternative methods to counteract it?
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Earlier this year, I noticed I was blinking a lot more than usual but it wasn't having any negative impact. In the summer I noticed the blinking getting worse and then I went to the optician who said I had moderate dry eye disease. She recommended lubricating drops. Nothing was improving and I went to another optician who said I had Blepharitis. He recommended a warm eye pad and regular cleaning of my lids. This hasn't improved things either. I went to my GP who confirmed the blep and put me on a 4 week course of Doxycycline. I've been on them 3 weeks and guess what, no improvement! It's affecting me quite negatively, have to wear my glasses all the time (previous wearer of lenses for 14 years with no problems). I'm not wearing eye makeup either in case it exacerbates my symptoms. I hate not being able to look groomed, sorry if that's shallow! I'm interested to read that it could be a candida overgrowth, I have suffered fungal infections before. I eat quite well, but suspect there might be a little to much sugar (alcohol etc). My eyelids looks a little red and slightly swollen, my eyes constantly look tired and a little bloodshot, this is worse during the week when I am working at a screen. Any advice at all? I am trying to eat more Omega 3 in my diet as well because I've read this might help. I suspect if it is candida that the antibiotic will be making me worse!
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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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Interested in hearing people's symptoms and experiences with this. I had pvd of the left eye and sure enough 6 months later, right eye. Having problems dealing with it. When both eyes are affected, hard not to think of it 24/7. Would like to hear others stories.
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Due to running excessively in the military, I believe my leg and feet injuries are related to Posterior Shin Splints and Posterior Tibial Tendonitis.
I am a female, 5'7, 160 lbs, and in the military.
I run approximately 15 to 20 miles a week.
I have high arches, and run flat footed.
I have hereditary varicose veins that have gradually become worse over time.
**5½ YEARS AGO** I dropped a three year weight class due to constant painful sores in both inner calves. The pain went away within a couple of weeks.
**2½ YEARS AGO** I received a second metatarsal hairline fracture on my left foot, due to an over excessive rucking competition (nearly 50 miles in two days, with zero training beforehand) I was volun-told to compete in a few days prior to the event. It healed within three months respectively, and the doctor had orthotics made for my feet. The orthotics worked great for walking, but instantly made my feet hurt while running. The problem continued to persist.
**2 YEARS AGO** I deployed overseas with my hairline fracture injury 99% healed. For most of the deployment, I did not experience any major problems. Towards the end, the unit conducted organized physical training, which included long runs. I started experiencing severe inflammation in my shins, inner calves, and swelling in my feet. The issue continued back home.
**1 YEAR AGO** I went to physical therapy when I came back from from deployment, and received deep tissue therapy for my shin pain. The deep tissue therapy helped my shins recover after each run, and the bumps on my shins started to disappear after each session (once a week). After my physical therapy sessions were completely over, I only had sensitive and tender shins after working out.
**½ YEAR AGO** When my unit increased the amount of running per week, I noticed the pains/sores were coming back in my inner calves. My shins remained tender, but the main focus was the pain in my inner calves. I went to the doctor for this issue, and they gave me a no running profile for a month. That was fine and dandy, until I came off profile and the situation became much worse than before. I played the “catch up” game to get back to how I used to be before I was on profile. In order to do this to my superiors standards, I had to to do this much faster and harder to achieve the results they were looking for. In doing this, the pains came back sooner, hurt more often, and did not require a hard physical workout to feel randomly throughout the day.
**PRESENT** Fast forward to present day, and now we run nearly every day of the week. Granted, most of the runs are now short runs, but now my pains are making any running absolutely miserable. I now have sharp pains starting from my inner calves, shooting up my legs, reaching the bottom of my knees. My inner calves are extremely sore and tender to the touch, even when I'm not running. I noticed just recently that I now have lumps/bumps on the bottom of both feet, in between the arch and heel (which I believe is called the Post Tibial Tendon). None of these issues are clearing up, unless I do absolutely nothing at all. But, once I start to exercise again, the pains and problems come back with full force. The bumps on my feet are not going away at all, I have had them for a few months and they continue to grow larger. So here are my questions:
1. Do you think I have Posterior Shin Splints and Posterior Tibial Tendonitis?
2. If not, what condition(s) do you think I have?
3. Do you believe these possible conditions can be fixed on my own, or should I see a doctor again?
4. I really cannot afford to stop working out, is there any low impact workouts that can keep me in shape if this turns into a medical issue?
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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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I've read on several postings about sufferers deciding to give up caffeine in an attempt to aid blepharitis. I was just wondering if anyone had any information about the link between caffeine and blepharitis and whether anyone has given it up and seen their symptoms improve? Do doctors recommend this.
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I've have vitiligo for years and always had dry skin with occasional eczema spots on my body. I also have pityriasis rosea on my side for years which finally cleared with antifungals.
Last summer I started to get blepharitis under my eyes but I thought it was just a one-off or due to a couple stressful events in my life.
The blepharitis did start a few weeks after I started visiting a dog at a pet store in short 20 min intervals a couple times a week until finally purchasing her. I never noticed I had any allergic reaction to the dog when I'm in her presence. No sneezing, runny nose, watery eyes, itchy skin, etc.
I later purchased the pup and my blepharitis continued to get much worse and it eventually spread to other parts of my face and my entire body started getting more eczema spots. It then became very widespread.
I am able to control the symptoms with steroids and Elidel but I'm trying to get to the root of it.
I realize it may sound like it's definitely the dog, and it certainly may be, but I don't notice that when I'm interacting with the dog that I'm itchy or anything.
Before I consider giving the dog to family, I want to understand if it's possible it's something else.
If you do believe it's my pup, are there any options besides ridding myself of my dog -- (I already bathe her, vacuum, etc).
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I've got another flare up on the way and it's dragging me down psychologically. I'm suffering from depression now because of it. I feel sad all the time and want to cry. I have to be honest and say that I'm having thoughts that not being alive would make things easier.
The only thing that ever works for me is antibiotic tablets but I've been told I can't be on them for the rest of my life. The last doctor I saw didn't care and prescribed me drops that never work for me.
My partner says I need to see a Dr about my depression but as there's no cure for my blepharitis I don't see the point? No matter how much counselling I could have it wouldn't change anything. I fear that I'm going to be constantly depressed.
I can't go on like this anymore. This illness is destroying me and its beat me
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Ok so today I woke up and right away went outside which was very bright. I came back into my room and started to see flashes, but then went away in 3 seconds. Is this normal? I've been dealing with blepharitis for a few months now and have been seen by a few doctors including a really good one in Mexico and said everything looked good.
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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 was diagnosed with ocular rosacea and rosacea type 1 last week and have just started antibiotics. I've never had either before. I have no idea how long it's going to take to improve but I wondered if someone who is further along the track could tell me. Does the ocular difficulty come in bursts and go, or is it persistent until it goes. Also, if it goes do you wear eye makeup (girls?)or are those days over for me?
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Does anyone have any suggestions for anti-inflammatory drops, creams, oils or ointments of any type that has helped with your MGD/blepharitis? I do all the hygiene stuff which keeps the crusts absent and eyelashes from falling out which is amazing to a certain point.
My problem is constant inflammation of varying degrees to my eyelids (or to be more precise the Meibomian glands). when they are at their worst inflamed there is literally no oil getting through to my eye which is really irritating and my eyelids become reddened around the lashes which creates a really annoying self-image paranoia + the inability to converse with anyone without being distracted by blinking a million times and feeling like I would like to close my eyes altogether or rip them out lol. I have tried drops but the lubrication effect seems to wear off after 10 minutes and I just don’t have the patients to be doing it that often.
The only thing that has seemed to work well for me so far is a tiny amount of castor oil applied to the lids at night (takes a few days to adjust to it). I have not tried steroids yet or antibiotics with anti-inflammatory properties but right now I am using chloramphenicol drops which are hopefully doing something + bead type warm compresses regularly which are helping but only slightly.
I saw an American youtube video recently about a doctor prescribing androgen gel to patients with MGD/Blepharitis and after researching why I realised that it’s because it reduces inflammation in the body, for the MGD/Blepharitis type that I am sure I have it seems to work well for patients that have tried it. That said there is plenty other things on the market that would have the same effect on the eyelids but more localised and less side effects are preferred, I don’t like the idea of roid-rage, shrinking nether regions and pancreatic cancer etc. It seems like too much of a trade-off in my situation.
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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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In from my evening shift at work, and I have got to say that I spend the time before I had to go in, scrubbing my eye lash margins with a wet cotton ball and baby shampoo (the old standard) both top and bottom, then after rinsing it off, I proceeded to wipe the rest of my face with some full strength tea tree oil on a cotton ball, and let it sit for a while before I took a shower. Scrubbing the margins (insides where the oil glands are) really was a bit uncomfortable (it didn't hurt though) and it did produce some of that lovely old whitish stuff, but I cannot believe how much better my eyes felt all night long (and they look better too) after doing this. Now I am going to hit this full force and keep doing this every single morning and every single night and see what happens. (I fell by the wayside on the Wet Ones, b/c they dried out my skin in the eye area too much, sadly). But I did mention in a previous post that my skin under my eyes felt like it was "pulling" and it was VERY crinkled looking and pulling upward. After doing this, it seemed to lessen that feeling (and it looks better too). I am hoping and praying that with dedication and persistence in encouraging my m glands to produce oils again, this could be something to get excited about. I sure hope so, but wanted to share. Has anyone else had success in doing this persistently? What inspired me to really get to it was watching the video today on the BlephEx procedure. I can't afford to get that done so I thought to myself, well I can certainly deeply clean and stimulate those glands on my own at home (especially after I saw all the gunk that the lady in the vid had come out of those areas). I saw some of the same thing with my own eyes after doing this and it is giving me some hope so I thought I would share.
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I am a 42 year old male that has been battling Blepharitis for over 7 years. It started with severe insomnia and stress in my life. I thought once I fixed my life and my insomnia my eyes would get better. Well guess what? I was wrong. I have tried everything from Wet Ones, baby shampoo, antibiotics, steam, oils, every eye drop you can imagine even dandruff shampoo. Nothing works, nothing. I just want to rip my eyes out. This pain is so bad that I would cut off a toe or finger if it would make the pain go away. These doctors just look at it and say oh it looks really inflamed try some natural drops or baby shampoo. That’s like telling a cancer patient to take some aspirin and see how it goes. If they only knew the pain I was in each day they would find a cure for this. I refuse to accept that I am going to live the rest of my life like this. Every hour I am awake I am in constant pain. I have now keep ice cubes with me and rub them on my eyelids whenever I can. That is the only thing that sooths them. Please God find a cure for this I can’t go on much longer with this constant pain.
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Does anyone have either of these or know of someone who does and was able to go into labor naturally, were able to deliver vaginally? Or did it just end in an induction and C-section? If you did deliver vaginally were you able to get pregnant again without big complications? I have this and my doctor wants to induce because I am due tomorrow and I still haven't even softened, but I have a large chance even without inducing that I will have to have a C-section no matter. Every female on my mom's side has it and all had to have C-sections, except my mom who had my brother naturally and should not of and had to be artificially inseminated(sp) with my sister and I because she was not able to get pregnant on her own after.
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Around 5 months ago out of nowhere, I started having immense headaches which at first I mistakened as just migraines or cluster headaches. I'm not sure how but I managed to endure the severe pain for 8 whole days by staying in bed (This was during exam break so I had no school). I've never suffered such a gratuitous amount of pain in my life! I could barely make it to the bathroom or even sit up to eat (I was 94.5 lbs after not eating for so long!!). After those 8 days I finally accepted the fact that it was not the typical migraine and was rushed to the emergency room. After going through numerous examinations with multiple doctors and specialists, I was diagnosed with posterior scleritis. It was really puzzling to hear that I had such a rare form of scleritis and at such a peculiar age since scleritis usually occurs at ages of 40-50 years. I was then put on 80mg of prednisone which relieved the pain. It was great at first but the heavy side effects eventually caught up with me. Anyways because of my condition, I was physically unable to show up for one of my exams although I wrote all the others while in such an insane amount of pain. I tried to explain why I wasn't able to attend but ended up getting yelled at and disrespected. I was deeply hurt and frustrated that the educators at my school didn't care for the health and safety of their own students ....
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Is there anyone on the site who has had a Posterior Lumbar Interbody Fusion done.
I'm a little apprehensive about this op but I cannot stand the pain anymore, I'm now having problems peeing. God I can't believe I have to wait 4/5 months for this op and that's on the Urgent List.
Nobody understands when you tell them how much pain you're having, I'm so glad that I found this site as most people can sympathise with me.
Sorry for whining but I don't know how much longer I can cope with this Severe Pain & Numbness in my back and left leg and foot.
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The doctor I saw today said he would do the reconstruction for my ruptured posterior tibial tendon as an out patient. That surprised me. Don't they usually keep you overnight?
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