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Hi. My son is 14 months and he was unable to swallow when he was

little. We went to a program in Cleveland for electrical stimulation

(Marcy Freed) and a few months of intensive trials at home (also did

cranial sacral therapy), he started some tasting and only recently

(September) did he actually " eat " foods. He only takes puree at this

time just because I think liquids are harder to control.

couldn't coordinate breathing, sucking and swallowing so he never had

a bottle and now we're trying to work on liquids from a cup (a dixie

cup). From both a parent and speech therapist standpoint, give him

whatever you can to get/keep those swallowing muscles working...(once

he has been medically cleared). used to get lollipops, toys

dipped in flavored juice, licorice to try and " chew " ...anything. We

make our own puree food to make it higher in calories and either

extra sweet or extra flavorful. It has worked for us! Also, there

is a product called " thick it " that is a commercial thickener to add

to liquids or we even add it to thinner purees.

Good luck and let me know if I can give you any more info.

Barbara, mom to 14 months (chArGE)

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In a message dated 12/30/01 6:26:59 AM Central Standard Time,

rbwarter@... writes:

> We went to a program in Cleveland for electrical stimulation

> (Marcy Freed) and a few months of intensive trials at home (also did

> cranial sacral therapy), he started some tasting and only recently

> (September) did he actually " eat " foods.

Barbara,

It must be so exciting to see " actually eat foods! " Congrats!!

We have a few questions, whenever you have time to reply-

What is cranial sacral therapy, & it's benefits? Did you do the intensive

trials after you saw Marcy?

We talked to Marcy today, the ES therapy sounds fairly promising for :)

But we need to take the glossopexy down first, sometime this spring.

Jan mom to (14.5 mo). CHARGEr wife to

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