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Mahrya was checked two times. One time by the geneticist and the othr

through a research program that we were involved in on mosaic ds. They came

up with the same % at both places. Hope this makes sence. >>

Hiya Luanne,

Thank you so much for taking the time to explain the percentage thing to me!

I understand it a bit more (seems pretty complex), but will probably need to

read it over a few more times, to get the real gist of it! heehee

You mentioned you were involved in an MDS research program! Sounds very

interesting. Did you get lots of helpful information or not? There is so

little information out there on MDS, that I'm beginning to wonder whether it

really exists! I found the name and addy of a woman doctor down in a

university in Virginia (I think), who had compiled a study on MDS! I wrote

to her, requesting this study, but the mail was returned to me (user

unknown). I'm still looking for resources, but have had no luck so far!

I think that's so neat that you're enrolling Mahrya in this program, for

children who have delays! I think it will benefit her very much, as well as

you and your family. I'm still not sure whether I would say anything to

these people, because her delay in speech could be the ONLY set-back she

ever has.....know what I mean? I guess I'll have to wait and see if I am

ever put in this type of situation, to see how I would really handle it!

Bree

New mommy to , born July 17th, 1999

Mommy also to , age 11, , age 9, and ,

9-year-old step-daughter

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