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Slane - update

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Hi Everyone!

It's been so long since I've been out here, thought I'd reintroduce

myself to the group.

I'm the proud Mom to 7 year old triplets, , , and

. is my RSS boy. is profoundly deaf in both

ears and uses the aid of a Cochlear Implant to hear. He has

congenital scoliosis and a single right kidney. He's has numerous

surgeries - g-tube, undescended teste, 2 Cochlear Implants, 2 Spinal

fusions, fundoplication, numerous ear tubes, etc., etc. He really

doesn't have much hearing with his Cochlear Implant, so relies on

Sign Language as his primary language. He's on prevacid for reflux,

Peptamen Jr. for overnight feeds, periatin, and Nutropin (we just

started this last Fall). So, as you can see, he does keep us

hopping. We live in Connecticut and see Dr. Harbision about every 3

months. is doing well - we don't have any more surgeries on

our plate at the moment. Our big decision at the moment is to

decide where to place him for school for next year. He's been

attending a school for the deaf, but this year we decided to partly

mainstream him in our local school 2 days a week. He's a

Kindergarten, so we felt this was the year to do that. Next year,

we really need to pick 1 school for 1st grade. It's tought because

there are pros and cons to both environments. Other than that, he's

right on schedule for attending 1st grade in the Fall. His siblings

are currently 1st graders.

Well, glad to be back on-line. If I can be of help to anyone, just

let me know. I do have a new email of cwslane@....

Take care.

Cheryl Slane

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