Thanks for the Warm Welcome

[Guest guest]

Thanks for the warm welcome and sharing your stories regarding how you made the

decision to put your child on GH. I realize that I have a lot of research ahead

of me on SGA before I make any decisions for . I liked Ken's anaology

" that his child has a growth disorder and why wouldn't they treat it medically

as they would treat something else. " This is exactly how I felt about my

daughter's ADHD and what a world of difference treatment has made to her and our

family.

I did go to the Magic Foundation website as recommended and found the brochure

regarding the convention this summer. Looking at the agenda, it looks like if

we could swing going it would be a great source of information. We live in the

Denver Metro area so it's just not right next door. I will also call Magic

today and ask for a copy of their Magazine and SGA Pamphlet.

One of the things that I am also doing is....I know someone who will make

contact with 's Birthmother (in Eastern Europe) for me. I am hoping that

I'll be able to get a medical and cultural history that might help us.

Also...maybe give her some peace of mind that the baby she had is happy, healthy

and in a loving family. Contact should happen in late March, I have mixed

feelings about contact but know that this will be benefical to Matt in the

future.

I have posted a couple of photos in the photo section under Matt E.

Thanks again for all your help and I look forward to being a part of this

support group.

Sue, Mama to Matt and Aleena

[Guest guest]

Hi Sue,

I just wanted to tell you that I am an RSS adult that also lives in the Denver

metro area. I grew up in and am currently a senior at CU Boulder.

Welcome to the group!

~Hillary

22, RSS

[Guest guest]

--Hi I am christine , I just wanted to say how cute Matt is and how

much I think he resembles my son S( under brandon5 yrs

old in the photo's ) I think it is amazing! Just wantesd to say Hi

and welcome to the

group.

- In RSS-

Support , envse@a... wrote:

> Thanks for the warm welcome and sharing your stories regarding how

you made the decision to put your child on GH. I realize that I

have a lot of research ahead of me on SGA before I make any

decisions for . I liked Ken's anaology " that his child has a

growth disorder and why wouldn't they treat it medically as they

would treat something else. " This is exactly how I felt about my

daughter's ADHD and what a world of difference treatment has made to

her and our family.

>

> I did go to the Magic Foundation website as recommended and found

the brochure regarding the convention this summer. Looking at the

agenda, it looks like if we could swing going it would be a great

source of information. We live in the Denver Metro area so it's

just not right next door. I will also call Magic today and ask for

a copy of their Magazine and SGA Pamphlet.

>

> One of the things that I am also doing is....I know someone who

will make contact with 's Birthmother (in Eastern Europe) for

me. I am hoping that I'll be able to get a medical and cultural

history that might help us. Also...maybe give her some peace of

mind that the baby she had is happy, healthy and in a loving

family. Contact should happen in late March, I have mixed feelings

about contact but know that this will be benefical to Matt in the

future.

>

> I have posted a couple of photos in the photo section under Matt

E.

>

> Thanks again for all your help and I look forward to being a part

of this support group.

>

> Sue, Mama to Matt and Aleena

[Guest guest]

hi sue!!

what a handsome young man you have!!! i love the fire fighter

photo!!! too cute!!

jodie c.

(nicholas-nonrss 6 1/2, christopher-rss 4 27lbs 6oz 36 1/4 "

periactin 4.5cc, ght genotropin .5, assmentry(left side 1cm), ADHD

and OCD possible, johnathon-20m nonrss)