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Amen Janice, Amen to that! We have caught this early everyone with my boy

who is 3. 5years old. Life is getting better every day and so are the vision

issues. I encourage you all to get you kid's eyes checked!

Colleen

Mother of Charlie 3.5 years

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I am in Illinois and am not sure if it is for all 50 states or not but the

infant- see program is awesome! You can take your baby and get his eyes examined

free of charge.. They found an astigmatism in my 8 month. Eye and now we are

keeping an eye on it to see if it corrects itself or if he will need glasses.

Sent from my BlackBerry® wireless device from U.S. Cellular

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  • 1 year later...

I've had a lot of problems with lights and focusing too....so bad, to the point

of having to cover my eyes sometimes when I talk or hear or when trying to focus

on someones face when talking to them up close. Tunnel vision too, i think is

what it would be called when i go to the store and walk down the aisle...if i

turn my head and look at things in motion, it totally freaks me out and i need

to leave the store. I can't read much anymore, instant narcolepsy and can

last10-15 mins on a computer and i'm done. anyone else with these problems?

ultra sensitive to sound to and certain pitches....phone calls, after about 30

minutes i start slurring my words and falling asleep on the phone. very weird

disease! please tell me if anybody else has heard of anything like this or am i

going totally crazy?

>

> Vision issues are very common with neuro lyme. My LLMD has described

> numerous strange vision problems with his lyme patients and there is a

> considerable scientific literature linking vision problems to lyme.

>

> One effect can occur when the spirochete in the brain affects the optic

> nerve which then ceases to respond effectively to changes in light and

> ceases to focus as it did before. Also, on occasion, optic neuritis.

>

> I have had vision symptoms since the beginning of my lyme saga....my vision

> has always improved when on antibiotics.... This has been one of most

> difficult symptoms for me as I live in a large city and simply don't feel

> safe crossing streets and so forth with vision which is erratic. Nor can I

> drive. Fortunately I can see the computer screen fine....

>

> What a dreadful disease.

>

>

>

>

>

>

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Nope. Not crazy. Any neurologist will tell you that it's weird if Lyme *doesn't*

create vision and hearing problems.

I've had severe light sensitivity, which has become markedly better with

treatment. (I used to spend days hiding under my covers from the minimal light

in a dark room.) But the worst thing was the auditory processing problem, which

I didn't really understand until my son was diagnosed with one. Turns out

central auditory processing problems run in my family -- my dad and brother both

had them, too -- but Lyme exacerbates them. (So does menopause, which of course

comes even harder for us.)

This is why I am not a phone person. My fortieth birthday gift to myself was

permission to turn off my answering machine. I tried to buy a phone without an

answering machine, and couldn't find one. So when you call my house, and you get

a message that says (politely): Don't leave a message, because I won't listen to

it. Most of the time, I won't pick up, either. A lot of people are deeply

offended by this -- " I couldn't reach you!! " -- but I'm very explicit that the

best way to reach me is e-mail, always. I'll usually respond within an hour or

two. (And if you don't have my e-mail, odds are good you're not someone I wanted

to talk to anyway.)

When I instituted this policy, I didn't even know why I was doing it. I was just

trying to set some boundaries around my life, and stop energy leaks. A single

phone call could interrupt a much-needed nap, force me to sprint across the

house when I could barely stand, or destroy the mental focus on a project that

had taken hours or even days to summon up. Often, I just couldn't be polite (or

even coherent) on command like that. It was intrusive, a violation of my private

space. I had to give it up.

So now, even though I'm feeling better, I don't answer the phone unless I'm

feeling very, very good (and I like what I see on Caller ID). It's just too hard

to listen and process the conversation if I'm getting it in just one ear.

Two-earphone headsets work much better (a good thing, since I attended most of

my grad school classes online via Skype or Blackboard). My hearing's fine, but

the piece of my brain that prioritizes incoming sound doesn't work like it once

did. The result is like listening to a cheap tape recorder: everything in the

room comes in at the same priority, and I have to work very hard to pick out the

thing I want to pay attention to.

Language processing is just HARD when you've got this glitch. Besides making

phone conversations hell, it also makes it exhausting to be in crowds for very

long. And listening to anything for very long just makes you tired. CAPD was the

root cause of my son's dyslexia, as it is for many dyslexics. It has a lot of

causes -- genetics, hormone changes, brain trauma, infection -- and Lyme is

right in there as one of the big ones.

This has gotten some better with treatment, and I'm looking forward to more

gains.

Sara

On Feb 27, 2010, at 4:41 57PM, robin c wrote:

>

> I've had a lot of problems with lights and focusing too....so bad, to the

point of having to cover my eyes sometimes when I talk or hear or when trying to

focus on someones face when talking to them up close. Tunnel vision too, i

think is what it would be called when i go to the store and walk down the

aisle...if i turn my head and look at things in motion, it totally freaks me out

and i need to leave the store. I can't read much anymore, instant narcolepsy

and can last10-15 mins on a computer and i'm done. anyone else with these

problems? ultra sensitive to sound to and certain pitches....phone calls, after

about 30 minutes i start slurring my words and falling asleep on the phone.

very weird disease! please tell me if anybody else has heard of anything like

this or am i going totally crazy?

>

>>

>> Vision issues are very common with neuro lyme. My LLMD has described

>> numerous strange vision problems with his lyme patients and there is a

>> considerable scientific literature linking vision problems to lyme.

>>

>> One effect can occur when the spirochete in the brain affects the optic

>> nerve which then ceases to respond effectively to changes in light and

>> ceases to focus as it did before. Also, on occasion, optic neuritis.

>>

>> I have had vision symptoms since the beginning of my lyme saga....my vision

>> has always improved when on antibiotics.... This has been one of most

>> difficult symptoms for me as I live in a large city and simply don't feel

>> safe crossing streets and so forth with vision which is erratic. Nor can I

>> drive. Fortunately I can see the computer screen fine....

>>

>> What a dreadful disease.

>>

>>

>>

>>

>>

>>

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