Blurry mornings: For the past week or so... - My MSAA Community

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Blurry mornings

erash profile image
erash
β€’32 Replies

For the past week or so, my morning vision has been very blurry.hard to read πŸ™ It improves as the day progresses. I've tried using natural tears before bed and in the morning. No help. Not sure if my sleeping pill is causing this or the ms? The sleeper isn't new. So I'm thinking ms? πŸ‘€Any insights? (Ha ha!)

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erash profile image
erash
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32 Replies
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Morllyn profile image
Morllyn

Mine have been doing the same thing erash ! But that is coming from someone who just got told she didn't have MS, after 40 years of being told she had. Sorry, feeling a bit grumpy. Actually my eyes have been blurry in the morning for 2 to 3 weeks now. Sometimes it goes away rather quickly and others it takes a while. Don't know why or what it is.

erash profile image
erashβ€’ in reply toMorllyn

So sorry Morllyn

I asked the pharmacist and she didn't think it was my sleeping pill. Since you may not have a mess I suspect it's also something on the retinal nerve???

Morllyn profile image
Morllynβ€’ in reply toerash

My eye doctor said, when I told him that I had intermittent blurriness but he kept saying no problem, that it could be the optic nerve behind where he could see.

erash profile image
erashβ€’ in reply toMorllyn

Morllyn my neuro said its MS a and the retinal nerve when I mentioned a yr. or so ago. She recommended an OCT if persisted but there's nothing specific they can do for it...I think Iona60 had the OCT?

Iona60 profile image
Iona60β€’ in reply toerash

erash and Morllyn Yes, I did have the OCT. I believe the first one was to use as a baseline. Seems like I read, or the neuro said, that comparing the OCT from year to year is as good, or a better indicator of disease progression than an MRI.

On another note, being on Gilenya, one of the things I am regularly checked for is macular edema. Opthamologist said that the biggest symptom of this is blurriness.

Fattius profile image
Fattiusβ€’ in reply toerash

They didn't even recommend glasses I had to figure that much out myself

Fattius profile image
Fattiusβ€’ in reply toMorllyn

Have your doc/s checked for PML its not even talked about but scary

erash profile image
erashβ€’ in reply toFattius

That would be scary Fattius

I'm not on any DMT so I don't think I have a significant risk

Morllyn profile image
Morllynβ€’ in reply toFattius

I am not on any DMT's either.

agapepilgrim profile image
agapepilgrimβ€’ in reply toMorllyn

What protocols help you then? Is your MS not professing? Are your symptoms not progressing? So afraid not to be on something. MRI showed lesions are bigger and more brain damage scars onbright side and my symptoms getting worse. It's not old age- my family history is working up in the 80s and living til 99s so I get angry when someone says it's just old age!

erash profile image
erashβ€’ in reply toagapepilgrim

agapepilgrim my protocols are??? trying healthy lifestyle. Hope it's working. MRIs have had no change x diagnosis but my symptoms do progress...

agapepilgrim profile image
agapepilgrimβ€’ in reply toerash

I was very disappointed 7/17 showed more damage to right side of brain, but "in acceptance lieth peace". Another favorite poem.

erash profile image
erashβ€’ in reply toagapepilgrim

agapepilgrim my acceptance waxes and Wayne's along with my symptoms πŸ™ƒ

agapepilgrim profile image
agapepilgrimβ€’ in reply toerash

EXACTLY!! I still scream into my pillow in sorrow and sometimes just stomp my feet (holding onto the cabinet of course) in anger

agapepilgrim profile image
agapepilgrimβ€’ in reply toMorllyn

Probably dry eye inflammation. Try systane ultra or anything for dry eyes. Or, if serious, I had to get plusgs put in my tear ducts to conserve tears. Always something @Morilyn

Fattius profile image
Fattius

Not sure but very well could be the MS. My vision has went double

erash profile image
erashβ€’ in reply toFattius

So sorry Fattius

😞

Nom_De_Plume profile image
Nom_De_Plumeβ€’ in reply toFattius

@fattius and others, it must be maddeningly to have double-vision. Is there anything that can be done to help with that?

Fattius profile image
Fattiusβ€’ in reply toNom_De_Plume

Apparently not at least in my situation anyway. Vision problems are very common with people with MS

Nom_De_Plume profile image
Nom_De_Plumeβ€’ in reply toFattius

Fattius

I'm sorry to hear that. It must be difficult. 😞

jennie62 profile image
jennie62

erash

My vision is blurry from time to time. Sorry I never remember to write down when, but I do know it coincides with trying to read books whether in book form or on a kindle.

@Fattius

My vision has gone double a few times. The first time my former country doc blamed Type 2 diabetes, but later apologized when I was diagnosed with MS and told me I don't have diabetes. So must be a part of MS...I think? LOL???

Fattius profile image
Fattiusβ€’ in reply tojennie62

And that right there is the problem. These doctors feel like everybody owes them something when they spend a third of their life and school like we are supposed to owe them some kind of pittance I have met harder working people and fast food then these entitled evil so-called Christians I love how they are religious but play God with people's lives and health

Iona60 profile image
Iona60

erash What I used to think was blurry vision for me, is really double vision. The neruo opthamologist said that some of this is coming from dry eyes and my corneas are getting scratched. I've started using "dry eye relief" drops many times a day.

erash profile image
erashβ€’ in reply toIona60

Iona60 did it mostly bother u in themornings? I've had this before and tried more frequent wetting drops but it didn't make a difference...more transient and not as bad then. Can't hurt to increase the frequency of the drops though.

Iona60 profile image
Iona60β€’ in reply toerash

erash Always in the mornings, but also frequently during the day. I've tried to keep off the overhead fans as this may be contributing to the eye dryness.

BigMar7 profile image
BigMar7

Has your eye doctor seen any cataracts in your eyes? I have a cataract in each eye and my vision is blurry. I was told to wait till it was really bad before I had surgery.

erash profile image
erashβ€’ in reply toBigMar7

BigMar7 had eye exam in November, no cataracts or dry eyes. All was well. I saw a neuro ophthalmologist yrs ago when this first started and told no problems, no ON, just get bifocals...that didn't help.

Less blurry this morn?

greaterexp profile image
greaterexp

erash , I can't help with suggestions, but will applaud your development as a grand punster.

bxrmom profile image
bxrmom

My vision was first blurry before my diagnosis, which ultimately sending me to a ophthalmologist which tried to tell me it was my antidepressant at the time (that I had been on for YEARS).. At night when I'm over tired my vision will sometimes get blurry. After I get a good night rest, then it is better in the morning.

Jessie

agapepilgrim profile image
agapepilgrim

@erash morning blurriness a common everyday thing with me nowadays. Having to blow the screen text up very large (even with glasses on( Ophthalmologist days not MS but very dry eyes. I am on Xiidra (allergic to the other brand),but mornings are still terrible. I must use Systane ultra drops every 4 hours also. It is very frustrating, but eye doc said mornings are worse because we don't blink while we sleep, thus cleans creating of the tear film. It helps to also put warm wet cloth on eyes and hold for awhile. Sometimes blurrineas goes away. Hope this helps, but do try the drops for dry eyes. Neurologist said if it was ON causes I would also have pain. But what do they know?? Lol. The extremely dry eye (forget the disease bane-lol, diesnmy matter it us what it is. Restaurant is what I am allergic to; thankful they invented the Xiidra and more thankful my oinsurance approved and read financial aid to help with co-pay. But HELP with the nausea!

faustkatrina profile image
faustkatrina

i sometimes have blurry vision in the mornings and the afternoons when i am having a little flare up and am when i am fatigued more than usual. For me its part of the MS. I did see a neuroopthomologist and told me there is a certain way to do the MRI to see the nerves. Not sure if this is true or not because i never had this particular MRI. My vision at this time when I saw him cleared up because of going on steroids. The blurriness still comes back intermittently with fatigue like all of my other usual symptoms which occur first thing in the morning until my body wakes up and by the afternoon when I fatigue again and certain things come and go and others are more constant.

Hope this helps.

By the way, what does OTC stand for?

erash profile image
erashβ€’ in reply tofaustkatrina

faustkatrina

OTC over the counter

My blurring is slightly better with consistent use of tear drops but I'm still not convinced it's only dry eyes

Thanks for the info

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