Trisomy 21 Online Community
   
     

ABOUT FORUMS


www.trisomy21online.com

All rights reserved on
the design & content of
this site 2003-07.
Pictures, personal stories
and experiences on this
site are the property of
the owner and may not
be copied or reproduced
without written permission.
 
Site hosted by
Fortune City.
Forums hosted by
Network 54.

Site designed and
maintained by
Katrina.


 
 
We are a group of friends who have come together because we share the common bond of caring for someone who has Trisomy 21. We are here to share therapy tips, medical issues, laughs, accomplishments and yes, even frustrations. We embrace what Trisomy 21 has brought into our lives. We feel that it has taught us to appreciate the true meaning of life. We count our children as blessings! We will fiercely protect them and fight for their lives to be valued just as all other peoples' are. We share our pictures, our stories and our hearts here not only to provide friendship and support for each other, but also in the hopes that others will open their minds and their hearts to our unique children and, in turn, make a better world for everyone.
 


  << Previous Topic | Next Topic >>Return to Index  

new parent

February 2 2007 at 9:59 PM
  (Login burch11906)

 
Hi my name is janice and i have a daughter with down syndrome she just turned a year old i was reading the message boards about the birth to 3 program and believe it or not i've been with the since my daughter was 3months old and they have yet to place me in a support group they say theres just none around me my husband i sometimes feel very alone with everything because no one else we know has had a child with down syndrome and when i seen your message boards and everyone asking and answering questions i wish i would have found this site a year ago its been hard and its been amazing just know one else knows exactly what were going though i would love to talk to parents and get advice and be informed on what to do next because my daughters pediatricain has never cared for a child with ds and sometimes i feel like if i don't read up and check things out myself i could miss something or i have missed something and we don't know about it i really need help i live in a very small town so its really limited to what is provided to me. Please ask me anything or give me advice. i want to talk to the experts the parents..thank you

 
 Respond to this message   
AuthorReply

(Login sheenazzy)

Janice

February 7 2007, 5:09 PM 

hi Janice..welcome ...same thing would have happened to me if i didnt start searching and found this place and a few others.my sons dr didnt seem to care either.
Good for you being proactive!How is your daughter doing? what is her name?
looking forward to getting to know you...take care!


Sheena
Mom to Connor- Aug 3,2006 and 5 other children
connorandtessa.blogspot.com
Photobucket - Video and Image Hosting
Photobucket - Video and Image Hosting

 
 Respond to this message   

(Login burch11906)

my daughter

February 7 2007, 9:25 PM 

hi i just went to a support group last night for the first time that i found by myself over the internet it was a hour drive but worth it it was so nice to talk to other parents and see that were not alone my daughter's name is Mallory i'd like to put a pic up but i have yet to figure out how to she is so amazing and i love her more than anything she makes a new face or does something silly everyday i'm so lucky to have her

 
 Respond to this message   
Current Topic - new parent
  << Previous Topic | Next Topic >>Return to Index  
 Copyright © 1999-2009 Network54. All rights reserved.   Terms of Use   Privacy Statement