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Cluster Headache Help and Support >> Cluster Headache Specific >> Anyone had visual change in your cluster eye?
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Message started by Pixie-elf on Oct 22nd, 2008 at 12:02am

Title: Anyone had visual change in your cluster eye?
Post by Pixie-elf on Oct 22nd, 2008 at 12:02am
My Mom is contacting my neuro, I've noticed this over the past few weeks and told her a few days ago... Just asking in case maybe someone else has had this happen.

I'm mostly worried it's one of my other neurological conditions acting up, but I figured I'd ask here just in case.

*slinks back off to bed*

Title: Re: Anyone had visual change in your cluster eye?
Post by maalstroom on Oct 22nd, 2008 at 12:21am
What exactly do you mean Pixie? Is your sight blurred, or does it perceives colours different?
Does it percevere, or just some short time after a hit? Does it hurt in the eyeball, or not at all?

Speaking for myself, I never experienced anything like that, so let's wait what others say about it.
It wouldn't hurt however to contact a doctor about it, ya never know if it's something to be carefull off.

Keep us posted, okay?

All the best, Pascal.

Title: Re: Anyone had visual change in your cluster eye?
Post by Pixie-elf on Oct 22nd, 2008 at 12:37am

maalstroom wrote on Oct 22nd, 2008 at 12:21am:
What exactly do you mean Pixie? Is your sight blurred, or does it perceives colours different?
Does it percevere, or just some short time after a hit? Does it hurt in the eyeball, or not at all?

Speaking for myself, I never experienced anything like that, so let's wait what others say about it.
It wouldn't hurt however to contact a doctor about it, ya never know if it's something to be carefull off.

Keep us posted, okay?

All the best, Pascal.


Well, I already have bad vision, astigmatisim, and all of that.

What I mean is, the vision has changed in that eye. As in my glasses prescription is no longer what it should be.

It doesn't feel any different other than normal.  I don't mean it changes after a hit. It's the same at all times. It just looks as if my vision in that eye has declined and I need a stronger prescription for that lens.

I only noticed because I realized I was seeing more clearly(with my glasses) out of my right eye than my left. Left is my cluster eye.  

I'm hoping someone else has experienced this, or it's just a coincidence that the vision in my cluster eye is getting worse...

Title: Re: Anyone had visual change in your cluster eye?
Post by Just Plain Carl on Oct 22nd, 2008 at 12:55am
    I have.  I wear a contact lens in my right eye for reading and nothing in my left eye.  My ch is on the left side.
    My vision is not as clear as it was.
    I did read that this is a side effect of Prednisone, so I just attributed it to that.  Maybe something else going on. I don't know.
                        slinking off to bed myself
                               JPC

Title: Re: Anyone had visual change in your cluster eye?
Post by George_J on Oct 22nd, 2008 at 1:08am
No, haven't noticed any vision changes on my CH side--other than the usual over-forty stuff.

I think it may be unrelated--although Karl mentioned to me this evening that his neuro told him he can often tell which side a clusterhead gets hit on by looking at the patient's retina.  Karl didn't know what his neuro meant by that, and I don't either.  

Best,

George

Title: Re: Anyone had visual change in your cluster eye?
Post by sandie99 on Oct 22nd, 2008 at 5:01am
Well, my left eye is my better eye, and left is also the ch side (although I've had shadows and few hits on the right).

I have noticed, however, that if there is some sort of hurting on one eye, it's always on the left side. But I do know now that there's nothing to worry about, although I did think in the beginning that ch can have some sort of impact on my left eye. I check my eye sight regularly, and it has stayed the same since 2004.

Sanna

Title: Re: Anyone had visual change in your cluster eye?
Post by Indestructible on Oct 22nd, 2008 at 6:40am
Yes I have

About 4 years ago I had the worst CH of my life. Afterwards I noticed 'floaters' in my eye, and they've been there ever since.

JOHN

Title: Re: Anyone had visual change in your cluster eye?
Post by DennisM1045 on Oct 22nd, 2008 at 7:17am
Before I was diagnosed with CH I noticed a difference in the function of my eyes.  My right (cluster side) was significantly more blury than my left.  At that time I was convinced that the attacks had something to do with my eye.  After all, that's where the focus of the pain was.

After seeing my Opthamologist, I went through a battery of examinations at the Scapens Eye Research Institute in Boston.  These are some of the best eye Drs in the world.  Other than a slight enlargement of the opitical nerve in that eye, they found nothing wrong with it.  The enlargement was chalked up to a genetics.  I had reached another dead end...

About a year later I finally got my diagnosis.  

Having said all that, I'd consult with my Neurologist just to be safe.

Good luck...

-Dennis-

Title: Re: Anyone had visual change in your cluster eye?
Post by kcopelin on Oct 22nd, 2008 at 11:50am
Pixie,
I haven't had changes like you mention, but I do get floaters and flashes (NOT aura) on the cluster side.  Saw my eye doc and he didn't find anything significant-he strongly recommended that I mention this to my neuro,  which I did,  which just confused the neuro  :-?
I think there is a connection but I'm not a doctor, nor do I play one on TV.

Hope you're feeling better!
PFDAN y'all
kathy

Title: Re: Anyone had visual change in your cluster eye?
Post by Skyhawk5 on Oct 22nd, 2008 at 1:16pm
My CH eye is not as good as the other. In '05 I developed a blocked tear duct and had surgery to put in drainage tubes. I was in cycle and had an attack while being rolled out of the O.R. I was on 80mgs of prednisone at the time and thought I was safe.

I have thought since then that maybe this was caused due to getting pred in my eyes from handling it.?? Makes me curious as to how many with eye questions have or are using pred?       , Don

Title: Re: Anyone had visual change in your cluster eye?
Post by Jeannie on Oct 22nd, 2008 at 1:20pm
Hi Pixie,
 My right eye is my weaker eye.  I don't wear glasses but my left is dominant for sure.  CH is right side for me.

Jeannie

Title: Re: Anyone had visual change in your cluster eye?
Post by Ray on Oct 22nd, 2008 at 1:27pm
Hello Pixie:

I have right sided CH.  My right eye is weaker and I started to notice halos around bright lights after my CH started.  

Ray

Title: Re: Anyone had visual change in your cluster eye?
Post by BarbaraD on Oct 22nd, 2008 at 4:17pm
I have "blurry" days with my left eye (cluster side) and other days that are clear. Never can tell which it's gonna be till I wake up in the morning. Blurry days usually go with a slight shadow.

This really started more after I had catarac surgery back several years ago..

Hugs BD

Title: Re: Anyone had visual change in your cluster eye?
Post by LeeS on Oct 23rd, 2008 at 11:33am
Interesting that you mention cataract surgery Barb.  This came up elsewhere recently, following this recent research abstract (although I do appreciate the very low base):


Quote:
J Headache Pain. 2008 Aug 21. [Epub ahead of print]

Cataract in chronic cluster headache: two case reports and review of the literature.

Benemei S, Nicoletti P, Geppetti P, Bonciani M.
Unit of Clinical Pharmacology, University of Florence, Florence, Italy

Cluster headache (CH) consists of attacks of severe, unilateral orbital/supraorbital/temporal pain, lasting for 15-180 min, occurring once or more times a day, and associated with ipsilateral conjunctival injection, lacrimation and other symptoms. Cataract is clouding of the lens of the eye causing a progressive and painless loss of vision. We describe the cases of two men (not relative, but with the same last name, which originates from north-eastern Italy) that in young adult age, after years of suffering from chronic CH, developed cataract on the same side of the pain attacks. Patient 1 was diagnosed as having cataract 18 years after the onset of episodic (and subsequently chronic) CH. Patient 2 began suffering from chronic CH at the age of 44 years and after 8 years he developed cataract. This is the first report of cataract in patient suffering of CH and occurring in the eye affected by the pain attack.

-Lee

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