New Posts New Posts RSS Feed - Nystagmus
  FAQ FAQ  Forum Search   Events   Register Register  Login Login


Forum LockedNystagmus

 Post Reply Post Reply
Author
Sezza26 View Drop Down
Newbie
Newbie


Joined: 15 May 2010
Points: 6
Post Options Post Options   Thanks (0) Thanks(0)   Quote Sezza26 Quote  Post ReplyReply Direct Link To This Post Topic: Nystagmus
    Posted: 22 February 2012 at 9:58am
Hi just trying to find other parents that have a baby/child with Nystagmus. My baby is 4 1/2 months old.
Back to Top
Sponsored Links


Back to Top
kalias1 View Drop Down
Newbie
Newbie


Joined: 10 September 2011
Points: 9
Post Options Post Options   Thanks (0) Thanks(0)   Quote kalias1 Quote  Post ReplyReply Direct Link To This Post Posted: 03 May 2012 at 2:35pm
Hi Sezza26, Just came across your post doing a google search.

My girl is nearly 16months, she was diagnosed with Nystagmus quite early too, just before 3 months I think. We've since got the diagnosis of ocular albinisim as the cause of the nystagmus. Although are yet to find the cause of the ocular albinisim!!

I'm keen to share info and experiences.
Back to Top
Sezza26 View Drop Down
Newbie
Newbie


Joined: 15 May 2010
Points: 6
Post Options Post Options   Thanks (0) Thanks(0)   Quote Sezza26 Quote  Post ReplyReply Direct Link To This Post Posted: 06 May 2012 at 9:23pm
Hi ya,

Thanks for your reply. It seems that my girl has only got Nystagmus and there is no cause for it. She is doing well and finally has rolled in the last week she is now 7months tomorrow. What is your girls vision like? what have been your challenges so far?
Back to Top
kalias1 View Drop Down
Newbie
Newbie


Joined: 10 September 2011
Points: 9
Post Options Post Options   Thanks (0) Thanks(0)   Quote kalias1 Quote  Post ReplyReply Direct Link To This Post Posted: 07 May 2012 at 2:04pm
Hi, have they done the electro diagnostic testing at the greenlane eye clinic? (Assuming you're in auckland of course!) It was the results of that testing that confirmed ocular albinism for us.

When the nystagmus first appeared, her eye's moved very widely from side to side, but even within the first few months that improved, and now she can hold them still when looking at something up close, and they're just a bit wobbly - quick movements side to side but that don't go so far to either side; when looking at something at moderate distance. Although if she sort of 'zones off' her eyes just drift side to side slowly but wider across IYKWIM. Does your girl have horizontal nystagmus too?

Have you heard of BLENNZ?

http://blennzonlineforfamilies.edublogs.org/blennz-blind-and-low-vision-education-network-nz/

We got referred to them from our opthamologist as I was worried about what to do to help best develop her vision. I guess it might depend on where you live, but here in Auckland they came to the house to do an assessment. They can help right from birth if your daughter meets their criteria.
It was good to see how they check vision, and just talk and get ideas from them.

Not sure how much you know about Nystagmus. My understanding is that the movement makes things more blurry/less clear. And that the more the eyes are moving, the less well they can see.

Early on I found I didn't get any response from my daughter if I was too far away from her face, and she'd get upset if I left her alone on the floor in the lounge for example. As she's got older her vision has improved, and she can see well enough to make out my facial expressions from a good few metres away I think.

She's got some other medical problems, some not fully diagnosed so we've faced quite a few challenges. Including mildly delayed gross motor skills. I don't remember when she rolled over, but she was late to crawl and at nearly 16 months isn't quite standing by herself. But I don't think any of that is to do with the nystagms.

My girl is quite light sensitive. Again she seems to have improved as she's got older, but still won't look up at the sky (to look at a plane for example) unless it's really overcast or she's not facing the sun. When she was younger she calmed down and feed better in a dim room.

Haha that's turned into an essay! Ask away if you have more questions. I'd like to hear about what you've been through so far if you'll share. (Can PM or email if prefer)
Back to Top
EleanorT View Drop Down
Newbie
Newbie


Joined: 17 July 2012
Points: 1
Post Options Post Options   Thanks (0) Thanks(0)   Quote EleanorT Quote  Post ReplyReply Direct Link To This Post Posted: 17 July 2012 at 2:00pm
Hi, I was just googling and came across this, I am not sure if you will get notified that I have commented though.

I have a 5 year old with Nystagmus and he is borderline Ocular Albino as well. He was picked up by plunket at about 3 months. It didnt seem to make too much difference until he was about 4, though he did trip up more than other kids and his behaviour can be a little interesting, probably out of frustration.

When he was 4 and a half it started having more effect. He was turning his head to look through his stable spot and started getting a sore neck and headaches. Just after he turned 5 we had his eyes operated on through his opthamologist to get the stable spot moved to straight ahead. I think this has worked, however he still need regular physio to sort out the neck pain, I am not sure whether this is residual for before the op or not.

He can more or less do anything other kids can do, he has to wear sunglasses outside all the time or he gets headaches, but he is good about this. He has very little spatial awreness, if he is looking forward to where he is going he will trip over strangers in front of him, but he is still little enough that people dont find this strange. He plays sport, but I am not sure this will be his forte - finding balls when you see in snapshots is difficult! Its finding the right active things for him will take sometime I think. He hasn't really worked out what he can do easily and whats harder for him yet. From what I have read of others it will come with time, for example most find riding a bike hard.

I was googling because although he is keeping up at school currently, as the books get longer, tracking is starting to become a problem. I am about to start working with the school to seek additional help, so I wanted to see what was available.   

Sorry - this is also an essay. Happy to chat though :)
Back to Top
kalias1 View Drop Down
Newbie
Newbie


Joined: 10 September 2011
Points: 9
Post Options Post Options   Thanks (0) Thanks(0)   Quote kalias1 Quote  Post ReplyReply Direct Link To This Post Posted: 18 July 2012 at 8:03pm
Hi EleanorT,

It's nice to hear from someone else with a child with nystagmus.

Do my comments above sound similar to your boy when he was younger? I'm interested about him wearing sunglasses - when did you learn/realise he was getting headaches being outside?

How was he when he was learning to walk? apparently they can have trouble with depth perception, have you noticed that at all? I'm guessing that could mean troubles with steps and stairs?

I've got an adult friend with nystagmus and she now snowboards!

You say it started to affect him more when he was about 4&1/2; was there any change in the movement of his eyes - did they look worse/move more? Or was it just when he found and started using the null point/stable spot?

Have you dealt with Blennz previously? They might be able to provide assistance. Also have a look on the ministry of education website; there's info on there about additional resources - although hopefully his school will be aware of them too.
Back to Top
Laurz_20 View Drop Down
Senior Member
Senior Member
Avatar

Joined: 01 January 1900
Location: Christchurch
Points: 347
Post Options Post Options   Thanks (0) Thanks(0)   Quote Laurz_20 Quote  Post ReplyReply Direct Link To This Post Posted: 14 February 2013 at 11:34pm
I come on this site all the time and have missed this completely. My daughter was diagnosed with congenital nystagmus at 1 year we noticed because in every photo we had of her she was always looking at the camera with a head tilt. It took us a long time to get seen by a specialist because the optometrist we were referred to couldn't see the problem. We have now been under an opthomologist for the last 2.5 years and DD has been put on the waiting list for an operation to move her null point.
DD trips a lot and seems to be clumsier than her peers. It's really interesting reading about other people's experiences as I have never met anyone else with this condition. DD also has congenital hypothyroism which we have been told is completely unrelated. EleanorT I would love to hear how your son is doing? And whether u think the operation was worth it?
Back to Top
 Post Reply Post Reply

Forum Jump Forum Permissions View Drop Down

Forum Software by Web Wiz Forums® version 12.05
Copyright ©2001-2022 Web Wiz Ltd.

This page was generated in 0.797 seconds.