Stories of Hope – William’s Wife


This true story is the first in our series Stories of Hope. These stories, about people who have triumphed over their Dry Eye symptoms, will inspire you and give you hope. In this story, William Cravey tells us about his wife who had suffered with Dry Eye since before 1997 and how she finally was able find relief.


Not A Dry Eye BlogIn 1997, my wife’s Dry Eye symptoms were so bad that she finally had to stop working and go on long term disability. Eventually she qualified for Social Security Disability. Over the years she had suffered miserably and said it felt like “having sand in her eyes 24/7/365.” We tried every treatment we could find and she had to use artificial tears every 5 minutes to get relief.

Eventually she became chronically depressed and sleep was almost impossible. It affected every aspect of our life together, including our relationship. We often cancelled plans because she could never predict how she would be feeling that day. The pain and discomfort was tearing our relationship apart and finally we divorced. But I continued to support her and eventually we remarried.

Searching for Serum Tears

My wife’s ophthalmologist finally prescribed autologous serum tears (eye drops made from her own blood) which reduced her pain significantly. Thankfully, we were able to get them locally, but then our local supply suddenly stopped and I began to search for another source in Florida.

I found two. One was in Tampa, Dr. Steven Maskin, and the other was in Miami. I contacted Dr. Maskin’s office to see if we could obtain the drops from him. We were told that he could help and prescribe serum tears, but that as per Florida laws, he would have to examine her first.

My wife made an appointment and after seeing Dr. Maskin, a treatment plan was established. It basically entailed resurfacing her eye. It sounded scary and we were both a little hesitant at first. I spent many hours researching both the procedure and Dr. Maskin, a truly gifted physician. We chose to go forward and scheduled the first surgery. We were both surprised that it was a little uncomfortable but definitely nothing to fear.

Result Gives Hope

The surgery (conjunctivoplasty with amniotic membrane transplants) to resurface her eyes has been completed. Already the pain from the dry eyes is almost gone, her vision is better, and her depression is lifting. She returned to her original ophthalmologist, who examined her eyes for the first time after the surgery, and who had done some partial resurfacing but never a complete resurface. She was amazed. She said to my wife, “If I weren’t looking at you, I wouldn’t believe it’s the same eyes.”

We are still waiting for my wife’s insurance to approve the meibomian gland probing procedure, but even with the resurfacing procedure alone, the results were beyond our wildest expectations. We expect my wife will have her meibomian glands probed soon and, once completed, I will provide an update on her progress.

We are extremely pleased with the outcome. I just don’t know why these treatments and their effectiveness are not better known. If you have Dry Eye and your current treatments are ineffective, I suggest you get evaluated by another physician that is familiar with these conditions and treatment options.

William Cravey

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8 Tips for Managing Dry Eye and MGD Symptoms


Even if you have an excellent doctor treating you for Dry Eye or meibomian gland dysfunction (MGD), there are lifestyle changes you can make to help improve your symptoms. These range from getting a good night’s sleep to washing your hands before touching your eyes. Some lifestyle changes can be hard to make. But when the discomfort from Dry Eye or MGD takes over your life, even small changes can add up to make a big difference. Remember, you can play a big part in managing Dry Eye and MGD symptoms.

1. Sleep with moisture chamber goggles.Not A Dry Eye Blog

If you have aqueous deficiency, MGD, or sleep with your eyes opened (nocturnal lagophthalmos) moisture chamber goggles can help to prevent your tear film from evaporating. Choose goggles that block out light or clear ones that you can see through. Be sure to wash them every day according to the manufacturer’s directions. If your goggles are uncomfortable, contact the manufacturer. If the pair you have is under warranty you should be able to exchange them for a more comfortable pair.

2. Don’t touch your eyes unless you have just washed your hands.

Introducing bacteria to the eyes only exacerbates symptoms. So wash your hands right before you touch your eyes for any reason, even when you’re just putting in an eye drop. And blot them dry them with a fresh, clean, low-lint paper towel. Keep a roll of paper towels on your bathroom counter or wherever you take care of your eyes most often so they are always within reach when you need them.

3. Avoid foods that cause inflammation.

Some foods are known to cause inflammation such as foods that contain high levels of Omega 6 fatty acids. This includes chicken and turkey. Inflammation is not always a bad thing – it’s how the body fends off disease. But chronic inflammation, which is associated with MGD, is the last thing you want to increase when you’re trying to improve eye comfort. Some experts recommend eliminating dairy, sugar, and wheat. But without actual food sensitivity testing, you might be eliminating some foods unnecessarily while not eliminating foods that cause your inflammation. For more information, see our page on food sensitivity testing.

4. Eliminate allergens.

Allergens cause allergic reactions and inflammation, and inflammation is the enemy of the meibomian gland. See tip #3 above. Eliminating allergens completely can be very difficult. For example, dust is almost impossible to completely eliminate or avoid. And it can be extremely difficult, and even heartbreaking, to eliminate it if the allergen is a beloved pet. But the more you can avoid allergens, the less you will exacerbate any symptoms.

5. Increase Omega 3 consumption.

Adding Omega 3 to your diet helps to offset the inflammatory effects of Omega 6’s. You can either increase the foods that have a beneficial Omega 3 to Omega 6 ratio or take a good Omega 3 supplement. If you choose to take an Omega 3 supplement, be sure it’s tested for contaminants.

6. Stop wearing eye makeup.

If you’re used to wearing eye makeup, stopping can be very hard. It might take some extra courage to go out without any on. But tiny particles of eye makeup can flake and fall into the eyes. Powders can rim the eye lid margin, the site of the opening of the meibomian glands. Makeup brushes, sponges, and mascara tubes harbor bacteria. And we don’t even want to imagine the colonies of demodex mites in there, so on to the next tip.

7. Get a good night’s sleep.

Eye tissue is restored when we sleep. When we don’t get a full eight hours, the cells don’t have time to regenerate and we end up exacerbating any eye discomfort. Eight hours is usually recommended. So put on those moisture chamber goggles and go to bed early.

8. See your doctor. Don’t delay.

Doctors can’t help if they don’t know what’s going on. So if you’re not getting better, or you’re experiencing some new symptom, don’t delay and make an appointment. Some doctors will communicate via text or e-mail once you’ve established a doctor/patient relationship. They may even take your call, especially if you’re experiencing acute symptoms. So if you’re experiencing something new, or something you’re pretty sure shouldn’t be happening, let your doctor know. The sooner the better, and before it gets worse.

Managing Dry Eye and MGD symptoms can be challenging, but remember that every little thing you do can add up to help a lot.

View more tips for coping with Dry Eye and MGD.

How do you manage your symptoms? Send your tips and comments to blogger@notadryeye.org and we’ll share them with our readers in future blog posts.

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Pop, Gritty, and Probe

Not A Dry Eye Blog
Pop, Gritty, and Probe


If you’ve had your meibomian glands probed, you probably remember hearing loud “pops” as the probe pierced through a band of fibrotic tissue (periductal fibrosis) somewhere along the length of the gland. Or it could have felt as if the probe was passing through several bands of fibrotic tissue, producing a gritty sensation and a sound like a short machine gun round.

Of course there was no machine gun. Periductal Fibrosis MGD

The pop was just amplified in your head, the way a tuning fork can seem very  loud when it’s held up to your ear, or the way flossing your teeth can seem very loud, but only to you.

The doctor can also feel the fibrosis with the probe as it meets resistance. And he feels a “pop” or something “gritty” when the probe pierces through.

Pop, Gritty, and Periductal Fibrosis

Given how many of us who have been probed have heard and felt “pop” and “gritty,” it’s puzzling that a recent paper published in Bio Med Central Ophthalmology completely misses this essential aspect of meibomian gland physiology and dysfunction (MGD).

The paper claims that evaporative dry eye is thought to be caused by “ductal hyperkeratinization, plugging and obstruction” but doesn’t discuss the role of periductal fibrosis in MGD, something that hyperkeratinization may cause indirectly through obstruction and meibum stasis (stagnation) with inflammation.

(Keratinization is the production of keratin, a protein, by ductal epithelial cells. In meibomian glands, this happens in the cells lining the ducts and at the opening. Hyperkeratinization refers to an excessive production of keratin by these cells. Too much keratin blocks the normal flow of meibum, leading to obstruction, stagnant meibum, inflammation, and eventually periductal fibrosis).

We’re not disputing the fact that hyperkeratinization occurs in meibomian glands. It does. But missing is what it may cause, or what may develop concurrently, from any cause of inflammation – periductal fibrosis. Missing periductal fibrosis means missing an essential fact of MGD, a fact that can alter greatly diagnosis and, ultimately, treatment.

Because if you don’t accept that there’s fibrotic tissue inside the gland, which can be caused by numerous factors that involve inflammation, you’ll never comprehend why probing is an essential treatment. You’ll believe that all you need to do is clear the stagnant and hyperkeratinized cells with warm compresses and lid massage. And you’ll completely miss the fibrotic tissue that can neither be heated, nor massaged, away.

That fibrotic tissue requires a completely different treatment approach – a tiny probe the width of a hair to pierce it.

Send your comments to blogger@notadryeye.org


Question:
Pop, Gritty, and Probe” is very interesting. Does the probing take care of the problem forever or is it necessary to repeat it and how often? Can the block be prevented or at least its build-up slowed down? If so, is there a self-help approach that the doctor could recommend?
Walter, New York

Answer:
Walter, we posed your question to Dr. Steven Maskin. He said:

Probing establishes that the meibomian gland duct is opened. Repeating the procedure is not always necessary, but this depends entirely on the patient and any other conditions or co-morbidities they may have which creates inflammation leading to periductal fibroses and re-obstruction. Our studies show that about 33% of lids are reprobed at an average of 18 months with 67% reprobed at average greater than 2 years. Any other conditions that may cause inflammation of the meibomian glands should also be treated at the same time, including aqueous tear deficiency, or allergies that may require topical treatments, infections, or infestation by demodex mites. Other considerations include oral medications such as Periostat (doxycycline) that can reduce inflammation, supplementation with Omega 3 fatty acids which may reduce inflammation and improve the quality of the meibum, and systemic treatments for autoimmune conditions that can cause systemic and periglandular inflammation. If it is well tolerated and there are no contraindications, warm compresses that can be done easily at home can help to liquefy the meibum, helping to prevent meibomian gland obstruction.


References

Meibomian gland dysfunction: hyperkeratinization or atrophy?
Jester JV, Parfitt GJ, Brown DJ
BioMed Central Ophthalmology
2015 Dec 17;15 Suppl 1:156. doi: 10.1186/s12886-015-0132-x.
View the full report

Intraductal Meibomian Gland Probing to Restore Gland Functionality for Meibomian Gland Dysfunction (MGD)
Maskin SL
May 2012

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Common Sense, Intuition, and MGD


Dr. Robert Wachter gets our vote.

At TEDMED 2015 he told the audience that professional intuition is under assault.

That’s how we feel when some doctors disparage meibomian gland probing, saying it’s too new or citing a lack of evidence as the reason why they’re against it, even while we’re sitting in front of them with our probed (and now Not A Dry Eye Blogfunctioning) meibomian glands.

When they say it’s too new, we say yes, probing might be relatively new. But just because it’s new, doesn’t mean it doesn’t work. Because the way we see it, newness and effectiveness are not mutually exclusive. Besides, meibomian gland dysfunction (MGD) has been around a long time. There’s nothing new about that disease.

Common Sense, Intuition, and MGD

And, fundamentally, doesn’t it just make sense that if a meibomian gland is blocked (think periductal fibrosis – vascularized bands of tissue around the duct that constrict it) something (dare we say a probe?) would need to pierce through that blockage to open up the gland, the way a balloon angioplasty widens and clears obstructed and constricted veins or arteries? So to us, meibomian gland probing as a treatment is obvious, and intuitively makes sense.

And even if it is relatively new, that doesn’t mean there isn’t any evidence of its effectiveness. Its inventor, Dr. Steven Maskin, has plenty of evidence. Plus other independent studies have been conducted all over the world – Japan, Spain, China, Russia, New York State. A double-blind clinical trial was even completed at Harvard last year, but the results haven’t been published yet. (Let’s hope competing interests aren’t suppressing its publication – which, sadly, sometimes occurs in the medical field).

Because, although there’s a place for evidence-based medicine, there’s also a place for intellect, experience, wisdom, common sense, and intuition – elements of science and medicine at their best.

After all, once upon a time, nothing was “evidence-based.” Not even an aspirin.

Send your comments to blogger@notadryeye.org

Reference

Professional intuition is under assault, Wachter says
M. Frellick
Presented November 20, 2015
Medscape Medical News from TEDMED 2015.
November 24, 2015.
http://www.medscape.com/viewarticle/854925

Is It Getting Worse?

An article we found late last year on Medscape Not A Dry Eye Blogpuzzled us. In it the reporter, Diana Swift, did not conclude that Dry Eye symptoms get worse over time. Instead she concluded that,

Despite the general perception, dry eye disease does not necessarily worsen over time. Most patients report no progression, and some even report improvement, according to a retrospective survey-based study of healthcare professionals having the condition for an average of more than 10 years.

Sounds good, right?

But not if you have the disease and not necessarily if you were one of the authors of the study who concluded that:

A proportion of patients with DED experience worsening over time, tending to report with more severe symptoms earlier in the disease.

So it seems there’s a disconnect. The reporter is looking at the data and saying things don’t get worse, but the authors of the study are saying something else.

And when we looked further into the study, we found this

The most common response of study participants was to report no change since the time of their initial DED diagnosis (Fig 1Fig 1): 32.0% for ocular surface symptoms, 52.3% for vision-related symptoms, and 71.1% for social impact. Some amount of improvement since diagnosis was reported by 44.0% for ocular surface symptoms, 19.0% for vision-related symptoms, and 19.2% for social impact. Some amount of worsening was reported by 24.1% for ocular surface symptoms, 28.7% for vision-related symptoms, and 9.7% for social impact.

So although some people reported getting better, others reported getting worse. Could it be that the reporter was simply ignoring the poor people in the study who were getting worse?

In fact, a different interpretation of the same results suggests that, since the time of diagnosis, very few individuals in the study improved at all. Less than 50% improved in Ocular Surface Symptoms (A) and less than 20-25% improved in vision-related symptoms (B) and social impact (C).

And some people clearly got worse:

For ocular surface symptoms, 27.7% of women versus 20.4% of men reported at least some worsening, whereas 30.9% of women and 26.5% of men reported at least some worsening of vision-related symptoms. More men (11.3%) than women (8.0%) reported worsening of social impact of their DED.

Plus this:

Among participants who reported severe OSDI scores … 31.5% experienced worsening of ocular surface symptoms, versus 16.1% of participants with mild to moderate OSDI scores.

So, yes, some people do get worse. But the reporter’s conclusion seems to largely dismiss the symptoms of these individuals, especially those who had mild or moderate symptoms that got worse.

The majority of men and women with DED recalled little or no change in ocular surface symptoms, vision-related symptoms, or the social impact of DED since diagnosis, and a similar number reported an improvement as reported worsening. These results, supported by review of clinical records, call into question the suggested tendency for DED to progress over time.

Why would the reporter conclude that? It clearly gets worse for some people…and most people don’t get better.

Dry Eye Symptoms Get Worse

So here’s a study about Dry Eye with statements that we largely agree with, but that a reporter seems to misinterpret and understate, causing confusion all around.

Because we truly think the authors of the study are on to something when they say that the results

also point to possible inadequacies of current therapies.

It’s more than possible inadequacies. Most of us can attest to that. And it’s especially true if the therapies are the typical ones (lubricating drops, warm compresses, lid wipes and Restasis), stemming from superficial diagnoses – aqueous tear deficiency, evaporative dry eye or blepharitis – without further examining for specific and underlying cause – like obstructive meibomian gland dysfunction (O-MGD).

The authors of the study go on to say, and we agree with them wholeheartedly:

Given the significance of DED as a public health concern, we hope that increasing knowledge of the disease will result in improvements of its clinical management. We would encourage clinicians to not only investigate potential causes of corneal epitheliopathy but also inquire routinely in a more standardized fashion about symptoms of DED. Simple short questionnaires, such as the Symptom Assessment in Dry Eye questionnaire, have been developed and may be useful for this purpose.

And we truly applaud this:

One of the most consistent correlates of worsening was a record of past severe symptoms. This finding is in line with the idea that patients who present with more severe symptoms early in the course of their disease are the ones who are most likely to experience a worsening, usually despite therapy. Patients with more severe symptoms may be more likely to see their doctor more often or to seek specialist care, and this could lead to a skewed perception of disease progression among clinicians.

And perhaps most importantly this:

The present data also suggest the continued need for more effective treatments for DED. … and these new data show that approximately 30% of such patients experience some level of long-term worsening, regardless of therapy. People who reported spending more than $20 per month on dry eye treatments were more likely to experience worsening, likely because people with worsening symptoms seek relief.

Seeking relief. We all know what that’s like. Because yes, Dry Eye symptoms get worse.

Send your comments to blogger@notadryeye.org

References

Dry Eye Disease does not worsen with time in most patients
D. Swift
Medscape Medical News
December 30, 2015

Severity of symptoms, corneal ulcers, and associated factors among men and women with dry eye disease
L.P. Leinert, L. Tarko, M. Uchino, W.G. Christen, D.A. Schaumberg
Ophthalmology
Published Online: November 21, 2015. DOI: http://dx.doi.org/10.1016/j.ophtha.2015.10.011
View the full report

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Blog Break

If you’re wondering why we haven’t had any new blog posts lately, it’s because we’re modifying its landing page so it will be easier to find topics you might be interested in.

You’ll also be able to subscribe to our blog and know whenever there’s a new blog post.

Please visit us again soon.

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Scleral Lenses – 5 Years Later

Not A Dry Eye BlogWe’re pleased to learn that after five years, PROSE lenses, a type of scleral lens fitted at Boston Foundation for Sight, are still helping about ¾ of the people who have them and who suffer with Dry Eye.

And we’re not surprised at the results of the review in which researchers confirmed that:

73.6% of patients were wearing the devices at five years. Patients with a distorted corneal surface were more likely to continue using the PROSE device than were those with ocular surface disease (84% vs. 64%, p=0.0121).

Ocular surface disease, a term sometimes used in place of Dry Eye, can manifest in many ways. About 80% of the time it is due to meibomian gland dysfunction (MGD). That’s why treating the meibomian glands, with probing or other interventions, is so important in the treatment of Dry Eye. This may also be why some people abandon scleral lenses, because the lenses aren’t treating an underlying condition that can cause extreme discomfort. Wearing the lens can even exacerbate discomfort in these cases.

Microbiome of Contact Lens Wearers Studied

Still 74% is significant. Though some of those patients may have other co-morbidities that still need to be treated e.g. the often missed conjunctivochalasis or SLK. For patients with these co-morbidities, scleral lenses may indeed provide relief from pain and discomfort (as long as they can tolerate something in their eyes) but without addressing the underlying cause of their pain.

Even though some patients are able to resume normal activities after being fitted with scleral lenses, a recent study discovered that the microbiomes of the eyes of contact lens wearers differ from the microbiomes of the eyes of those who don’t wear contact lenses. And an altered microbiome may increase the risk of eye infections in contact lens wearers. So to prevent infections, scleral lens wearers should practice good contact lens hygiene.

References

Changes in the eye microbiota associated with contact lens wearing
Shin H, Price K, Albert L, Dodick J, Park L, Dominguez-Bello MG.
MBio
2016 Mar 22;7(2). pii: e00198-16. doi: 10.1128/mBio.00198-16.
View the full report

Prosthetic replacement of the ocular surface ecosystem: impact at 5 years
J.S. Agranat, N.R. Kitos, D.S. Jacobs
British Journal of Ophthalmology
doi:10.1136/bjophthalmol-2015-307483
View the full report

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More Training for UK Doctors

We came across this story today:

New research reveals an alarming, self-acknowledged gap in family doctors’ skills when it comes to diagnosing and treating patient’s eye conditions.

The Vision of Britain report, commissioned by Optegra Eye Health Care, shows that more than three in 10 GPs (32 per cent) say they feel ‘de-skilled’ in diagnosing eye conditions, reflecting the immense pressures and workload on these doctors.

And 44 per cent of GPs say that they feel less confident in dealing with eye conditions than any other part of the body.

Yet more than a quarter of British adults (26 per cent) turn to their GP, rather than an optician, for help if they have an eye problem.

Two in five GPs (40 per cent) surveyed for Vision of Britain state they need more, or refresher, training on all eye conditions.

Dr. Sarah Jarvis, GP and medical broadcaster, says: “As a doctor, I’m only too aware of how little in-depth training I had in dealing with everyday eye problems like dry eye and short-sight. Yet they affect so many patients. It is vital that GPs on the frontline have ongoing support in diagnosing their patients accurately and confidently so they can be put on the right treatment path.

That’s great. Let’s hope the UK’s general practitioners are open to receiving training that covers the entire spectrum of Dry Eye diagnosis and treatment, from mild to severe and everything in between. And then let’s hope that training is expanded to eye doctors.

Reference

New report reveals UK GPs lack confidence in diagnosing eye conditions
Adapted Media Release
Medical News Today
January 4, 2016
View the full report

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New Year’s Resolution: Right Diagnosis

Value-based care, a new buzzword describing mechanisms to reduce the costs of healthcare, is something many of us are already all too familiar with.Not A Dry Eye Blog

Consider this hypothetical cost-cutting scenario described by a health policy expert:

If a patient says he would like an MRI performed, the physician can refer to the list of recommendations and explain that there is insufficient evidence to suggest an MRI is necessary at this time. The physician may then suggest lower-tech interventions such as physical therapy or over-the-counter pain relievers.

In our opinion, the policy expert has fundamentally missed the point. The patient asking for an MRI isn’t asking for intervention. The patient is asking for a diagnosis. Neither physical therapy nor pain relievers are a diagnosis.

Are doctors really going to be willing to take this “value-based” approach?

Sadly, for many Dry Eye patients, this fundamental first step, the right diagnosis for Dry Eye symptoms, is often skipped.

The Right Diagnosis for Dry Eye Symptoms

We don’t know why exactly but suspect that it may be due to the fact that many (most?) ophthalmologists are following the “preferred practice pattern” guidelines promoted by their accrediting body, the American Academy of Ophthalmology. Unfortunately for these doctors and for us, the guideline is outdated, reducing the likelihood that we’ll be diagnosed properly. And then we’re all given the same standard treatments appropriate perhaps for only mild cases (lubricating drops, warm compresses, lid wipes) and Restasis.
But if we don’t respond to these standard treatments, our symptoms are labeled phantom, psychosomatic, secondary to depression, or neurological in nature.

Instead, doctors should examine each of us thoroughly as individuals, not as populations, and then address each diagnosed co-morbidity with targeted treatments, the way some doctors do.

That would be real value-based care, care based on a specific patient’s needs, starting with a right diagnosis.

Reference

An ethical basis for moving from volume to value
E. L. May
Healthcare Executive
2015 Jan-Feb;31(1):28

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Causes of Dry Eye Pain

One of the reasons we started the Not A Dry Eye Foundation was the frustration we felt when confronted by physicians who dismissed our symptoms as being “something we would learn to live with” or “all in our heads.” Not only were we mystified by their (lack of) diagnosis and conclusions, but we were terrified at the prospect of having to live with unbearable eye pain for the rest of our lives, and this without anyone telling us the causes of Dry Eye pain. Not A Dry Eye Blog

When we eventually learned about the ways the disease can quickly escalate and the way it can alter the tissue, secretions, and functioning of various eye structures, we felt vindicated. We knew all along that nothing that we were experiencing was psychological, neurological, or psychosomatic in nature. It was physical – blocked meibomian glands, inadequate aqueous tears, wrinkled conjunctiva, bacteria, twisted lashes, demodex mites, allergies, and more.

Learn about the causes of Dry Eye pain

And there was a lot that could be done about each of these conditions so we wouldn’t have to learn how to live in extreme, debilitating, and unbearable pain for the rest of our lives. There was probing for obstructed meibomian glands, punctal cautery for aqueous deficiency, surgery for the wrinkled conjunctiva, antibiotics for infections, epilation for misdirected lashes, and any number of medications or other treatments for anything and everything else.

But with all of these possible diseases taking hold in the eyes at the same time, is it no wonder that we felt pain? If a single eye lash can stop us cold, why wouldn’t a host of diseases cause unbearable pain in the most sensitive part of the body?

Dubious Causes of Dry Eye Pain

And so we became frustrated once again when we learned that physicians at a prominent teaching hospital and a VA hospital concluded that “neuropathic ocular pain due to Dry Eye is associated with multiple comorbid chronic pain syndromes.”

To us, this is like saying that when you have a diseased finger and are experiencing pain in that finger, the pain is due to some other chronic pain syndrome, not to the disease in your finger.

What?

We wonder if the authors will next conclude that the treatment should be Lyrica or some other anesthetizing pain medication? Or maybe serum tears? Or scleral lenses?

Maybe.

But we think there’s a much better approach.

It has to do first with correct and comprehensive diagnosis, the most important step in alleviating symptoms, and then targeted therapy for each co-morbidity — the approach taken by our doctor, Dr. Steven Maskin.

And so we conclude by citing a different study by some of the same physicians at the same teaching and VA hospitals who concluded that ocular pain associated with Dry Eye may be due to conjunctivochalasis, and that patients should be screened for the disease.

Now we’re getting somewhere. That’s the spirit. Happy New Year!

References

Neuropathic ocular pain due to dry eye is associated with multiple comorbid chronic pain syndromes
Galor A, Covington D, Levitt AE, McManus KT, Seiden B, Felix ER, Kalangara J, Feuer W, Patin DJ, Martin ER, Sarantopoulos KD, Levitt RC.
The journal of pain : official journal of the American Pain Society
2015 Nov 19. pii: S1526-5900(15)00944-X. doi: 10.1016/j.jpain.2015.10.019. [Epub ahead of print]
View the full report

The impact of conjunctivochalasis on dry eye symptoms and signs
Chhadva P, Alexander A, McClellan AL, McManus KT, Seiden B, Galor A.
Investigative Ophthalmology and Visual Science
2015 May 1;56(5):2867-71. doi: 10.1167/iovs.14-16337.
View the full report

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