
Through the Internet, you will find hundreds of blogs talking about Trisomy 21 (T21). This is because October is the awareness month for T21 (Down syndrome). I joined to the group of bloggers who are celebrating 31 for 21.
The little extra chromosome in my son has given me extra pride when I talk about him. The extra chromosome has changed my life with extra love, extra care, extra courage, and extra faith. Having a little extra is not bad, I think having a little extra is what make people with T21 the most powerful people in the world. I am not afraid of what the future may grant for my son, after all, I had the opportunity to know and meet terrific people with T21 at 1st Annual Fashion Show organized by the local Down syndrome Association. I was impressed of all the models and their abilities. I consider them as the Pioneers of a new generation of super heroes with T21.
This event was wonderful because I could meet other families and members of the Association. I got involved in the organization of the event, and off course, my son was also a model. This event was very well organized. The atmosphere was very positive and full of love, happiness, cooperation and FUN. I feel that the Down Syndrome Association is like my second family; If my son wouldn't have a little extra I would have missed the opportunity to be member of this great organization.
Thank you to our family and friends for supporting us in this great event. Enjoy the video.
Tommy and Rosa rock! Too cute!
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