Saturday, July 16, 2011

I had decided

I had decided to write for her. For my little 2 months girl, Aseman, who is a sweet, adorable and so much lovely girl by lots of beautiful smile and also by an abnormality she has in her chromosomes. My little angle has Down syndrome, she is translocation 21;21 and it made her lots of difficulties such as heart problem. She has Complete AVSD and should be go on the surgery in October. But it’s not all.  
I had decided to write for her because she should know our feeling; she should know that we look her as a serendipitous. But it’s not all.  
I had decided to write for her and I did  it in Farsi (my native language) but after all I think to do it in English because I want Aseman be a member of DS cyberspace society which is very supportive and  friendly . In fact during the agonizing days we passed, the inspiring and honest and appreciable mom’s blog of DS children encourage me and my husband to insist and be brave, so, in spite of my little knowledge in English, I start it and I wish my virtual friend help me to insist and do my best.
I want to write about my girl and also about condition of these angles in Iran (which is very poor) and last but not least, I also what to write about steps we take to make a charity for these people in Iran. Help me to continue. And it’s not all…


 
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