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Old 04-17-2015, 03:42 AM #11
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Originally Posted by Billylyne5 View Post
Looked at the link - I don't tick any of those causes unless it's the illness one but can't get a diagnosis for that 😏

Ophthalmologist was great she said her treatment is same with or without diagnosis so at least I have good eye drops now on prescription.
is the eye moisture test still reliable, and a lip biopsy, to check for lymphocyte infiltration? Do you get dry mouth and nasal areas as well?

If you have allergies, that also can cause dry eyes as well.
I had dry eyes initially from using anti-histamines/ anticholingernics. if your a female its more likely you have it, its uncommon in male, maybe thats why the rhueumatologist wasnt sure about your diagnosis.

what other symptoms you have.
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Old 04-17-2015, 06:00 AM #12
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While it is not common in developed countries it is possible that low Vit A may be present. This comes with age, and poor diet and
hypothyroid situations. Thyroid hormone is responsible for converting betacarotene in vegetables to retinol . One cod liver oil cap a day (do not increase the dose) or one Vitamin A acetate 8000IU tablet a day (do not increase dose) may help.

Signs of Vitamin A deficiency are similar to Sjogren's.
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Old 04-17-2015, 06:50 AM #13
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Originally Posted by LMPinkereton View Post
Exactly the same here.

Diagnosed with SFN with skin punch test confirming.
Joint pain a severely dry eyes. Some days I feel like I might collapse if I don't lie down.

I have noticed that when my SFN pain in my feet, legs and arms really flares up my eyes really burn. Then when things subside a little, my eyes stop burn, but are still dry.

I too have been to a rheumatologist and had dozens of blood tests too. Several things are slightly "off" but not bad enough to make a diagnosis for other autoimmune diseases. (I do have Graves) I think I am starting to have more autoimmune problems (like Sjogren's), but nobody seems to want to do anything.

I have been complaining to my eye doctor about my eyes and he says my Graves is in check, just use over the counter eye drops. They do nothing for me.

All I know is whatever it is, it keeps getting worse. Just doesn't seem to be anything anyone wants to do. I have run out of options and places to turn. I've been to several different types of doctors and always end up with no relief.

Yes, maybe someone else will chime in and point us in the right direction???

It is frustrating that they can't figure it out or offer treatment.
I have a questionable sjogrens diagnosis and positive SFN and autonomic issues.
I also get feelings like I will collapse and have to lie down on the floor with my knees up till I can get up again.
All they are offering for treatment is plaquenil (I'm still thinking about it) and things like tricyclics and lyrica.
I have reached out to different neurologists and rheumatologists across the country and they recommend IVIG, but in NY I haven't found a doctor who will try it.
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Old 04-17-2015, 06:53 AM #14
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Originally Posted by Billylyne5 View Post
Rheumy agrees I have symptoms of sjogrens and I asked her re 40% of people being sero negative but she said she would never diagonose without a positive blood test.
I have no reason for the dry eyes not on any drugs etc that cause it.
I am in the UK so the early sjgrens test not available here either.

I was convinced it is sjogrens but at the moment I am getting no joy anywhere
Seeing my neuro on Monday so will se where I get with him.
Did you have the lip biopsy? Maybe you can get a second opinion with a new rheumy?
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Old 04-17-2015, 11:36 AM #15
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Did you have the lip biopsy? Maybe you can get a second opinion with a new rheumy?
I am only 44 so my symptoms should not be age related, thyroid is all ok, I haver been offered a lip biopsy the Rheumy was only interested in bloods as her way of diagonosing or offering treatment, she actually said be glad I only have SFN and not sjogrens lol yet she also said some doctors will diagnose sjogrens on symptoms alone....then why should I trust her ????

No allergies I even tried antihistamines in case but they did nothing.
I had the schimers test and the evaporation test showing that I have both poor quality tears and not enough of them.

I get a dry throat, hoarseness, also developed GERD at same time.
My joints hurt a lot hands wrists feet ankles. My feet are incredibly painful all the time and are tender to touch on balls of feet, top and ankle joints. Hands and fingers swell, knuckles go red.
I have petechiae that came on recently
Fatigue - like I have to just lie down and can't move tiredness
Numb fingers and toes plus numb areas all over the place, burning pain in feet and random patches -like sunburn
Wierd rib/chest pain tender areas /stabbing pain
Randomly get a low grade fever
My DSDNA test came back equivocal at 17 but Rheumy didn't even mention that
My white count is always on the low to just on normal
Negative MRI and nerve conduction studies
Oh had ultra sound on my wrists and that showed synovial thickening but Rheumy said it wasn't inflamation but mechanical what ever that means - she put that in the letter discharging me so I haven't been able to ask her.

I am very frustrated and feel like I am struggling to manage the symptoms and getting no where near a diagnosis or even treatment.
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Old 04-17-2015, 12:43 PM #16
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Originally Posted by Billylyne5 View Post
I am only 44 so my symptoms should not be age related, thyroid is all ok, I haver been offered a lip biopsy the Rheumy was only interested in bloods as her way of diagonosing or offering treatment, she actually said be glad I only have SFN and not sjogrens lol yet she also said some doctors will diagnose sjogrens on symptoms alone....then why should I trust her ????



No allergies I even tried antihistamines in case but they did nothing.

I had the schimers test and the evaporation test showing that I have both poor quality tears and not enough of them.



I get a dry throat, hoarseness, also developed GERD at same time.

My joints hurt a lot hands wrists feet ankles. My feet are incredibly painful all the time and are tender to touch on balls of feet, top and ankle joints. Hands and fingers swell, knuckles go red.

I have petechiae that came on recently

Fatigue - like I have to just lie down and can't move tiredness

Numb fingers and toes plus numb areas all over the place, burning pain in feet and random patches -like sunburn

Wierd rib/chest pain tender areas /stabbing pain

Randomly get a low grade fever

My DSDNA test came back equivocal at 17 but Rheumy didn't even mention that

My white count is always on the low to just on normal

Negative MRI and nerve conduction studies

Oh had ultra sound on my wrists and that showed synovial thickening but Rheumy said it wasn't inflamation but mechanical what ever that means - she put that in the letter discharging me so I haven't been able to ask her.



I am very frustrated and feel like I am struggling to manage the symptoms and getting no where near a diagnosis or even treatment.

Are you drinking enough fluids?

Have you tried moisture drops from the drug store?
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Old 04-17-2015, 02:51 PM #17
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Originally Posted by Billylyne5 View Post
I am only 44 so my symptoms should not be age related, thyroid is all ok, I haver been offered a lip biopsy the Rheumy was only interested in bloods as her way of diagonosing or offering treatment, she actually said be glad I only have SFN and not sjogrens lol yet she also said some doctors will diagnose sjogrens on symptoms alone....then why should I trust her ????

No allergies I even tried antihistamines in case but they did nothing.
I had the schimers test and the evaporation test showing that I have both poor quality tears and not enough of them.

I get a dry throat, hoarseness, also developed GERD at same time.
My joints hurt a lot hands wrists feet ankles. My feet are incredibly painful all the time and are tender to touch on balls of feet, top and ankle joints. Hands and fingers swell, knuckles go red.
I have petechiae that came on recently
Fatigue - like I have to just lie down and can't move tiredness
Numb fingers and toes plus numb areas all over the place, burning pain in feet and random patches -like sunburn
Wierd rib/chest pain tender areas /stabbing pain
Randomly get a low grade fever
My DSDNA test came back equivocal at 17 but Rheumy didn't even mention that
My white count is always on the low to just on normal
Negative MRI and nerve conduction studies
Oh had ultra sound on my wrists and that showed synovial thickening but Rheumy said it wasn't inflamation but mechanical what ever that means - she put that in the letter discharging me so I haven't been able to ask her.

I am very frustrated and feel like I am struggling to manage the symptoms and getting no where near a diagnosis or even treatment.
I really really think you need to go to a new rheumatogist. I wasted my time with 2 of them before I found the one I have who is at least willing to treat for sjogrens. She had me go for the lip biopsy based on the SFN and my high ANA. It came back equivocal/borderline for Sjogrens even though my blood doesnt show it. She said normal people don't walk around with lymphocytes infiltrating their salivary glads, and that indicates Sjogrens...so she is at least willing to treat for it with Plaquenil. I am debating trying it, but its somewhat relieving to know that maybe the treatment would work and that I have options.
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Old 04-17-2015, 03:22 PM #18
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I have eye drops on prescription from the ophthalmologist and I drink 2-3 litres of fluid a day on advice of my nephrologist for my PKD which he assures me is not causing any of my symptoms.

My podiatrist has told me about another test for SFN which looks at your eye and is none invasive I can't remember what it's called I will check later

I think I am going to have to look at a second opinion but being in the UK the refferal a are just done to a hospital team so no idea who you will see and I don't want to have a wasted refferal as once you have had two it's pretty hard to get another
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Old 04-17-2015, 03:24 PM #19
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Originally Posted by Billylyne5 View Post
I have eye drops on prescription from the ophthalmologist and I drink 2-3 litres of fluid a day on advice of my nephrologist for my PKD which he assures me is not causing any of my symptoms.



My podiatrist has told me about another test for SFN which looks at your eye and is none invasive I can't remember what it's called I will check later



I think I am going to have to look at a second opinion but being in the UK the refferal a are just done to a hospital team so no idea who you will see and I don't want to have a wasted refferal as once you have had two it's pretty hard to get another

Cool sounds like not being hydrated isn't the issue. Best of luck finding a cause.
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Old 04-18-2015, 02:35 AM #20
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Quote:
Originally Posted by Billylyne5 View Post
I am only 44 so my symptoms should not be age related, thyroid is all ok, I haver been offered a lip biopsy the Rheumy was only interested in bloods as her way of diagonosing or offering treatment, she actually said be glad I only have SFN and not sjogrens lol yet she also said some doctors will diagnose sjogrens on symptoms alone....then why should I trust her ????

No allergies I even tried antihistamines in case but they did nothing.
I had the schimers test and the evaporation test showing that I have both poor quality tears and not enough of them.

I get a dry throat, hoarseness, also developed GERD at same time.
My joints hurt a lot hands wrists feet ankles. My feet are incredibly painful all the time and are tender to touch on balls of feet, top and ankle joints. Hands and fingers swell, knuckles go red.
I have petechiae that came on recently
Fatigue - like I have to just lie down and can't move tiredness
Numb fingers and toes plus numb areas all over the place, burning pain in feet and random patches -like sunburn
Wierd rib/chest pain tender areas /stabbing pain
Randomly get a low grade fever
My DSDNA test came back equivocal at 17 but Rheumy didn't even mention that
My white count is always on the low to just on normal
Negative MRI and nerve conduction studies
Oh had ultra sound on my wrists and that showed synovial thickening but Rheumy said it wasn't inflamation but mechanical what ever that means - she put that in the letter discharging me so I haven't been able to ask her.

I am very frustrated and feel like I am struggling to manage the symptoms and getting no where near a diagnosis or even treatment.
you definetly need a more tests for sogrens, its not only confirmed by blood tests, lip biopsy, "tear production" is also an indicator, or it can show you dont have sogrens. Its like your current doctor is content on the blood tests, results, and is too lazy to do anything further.

-Antihistamines, can cause dry eyes, nasal, mouth symptoms, especially if your using the stronger anticholingenic ones(benadryl, chlorperamine, or any halogenated forms,doxylamine is also another).
You need tests specific for sogrens.
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