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Re: Tubes in ears???---Mosense

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Pulling at the ears is likely infection. The only sign we saw was

that in my NT child and every time we followed up...infection.

Mosense on this board knows the good stuff. It is a drink, knocks

them out, used for short procedures like this and MRI. Mo, can you

help us out here?

Have a lengthy conversation with the anesthesiolost. They want you

to. They do not want to unknowingly harm your kid so help them help

you. Do not be bashful.

Please look at Dr. 's posts on the " off " pain response. There

are labs that may clue you in more on this.

Best Wishes. NACD really gets this huh.

>

> Thanks to everyoe for your posts. It may make sense what Sherry

said, Eva does have sensory issues...she is not walking at almost

three...some days her balance seems worse than others...and she DOES

pull at het ears a lot and also itch her nose constantly (don't know

what that means), but she's never had an ear infection that I've

known about. But you have a good point, maybe she has had a lot, but

the pain just never registered the way it would for a neurotypical

child. Another thing that is strange...she loves to lean back in the

tib with her ears under the water....I tried this one time and

thought it was such an uncomfortable feeling in my ears...this is one

of the reasons why she loves her baths so much. And Lizzy, we don't

have any casein in her diet.. and also, what would be the alternative

to nitrous oxide if we would do the surgery? Thanks so much.

> :-) tara

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> Never miss a thing. Make your homepage.

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