{"id":4140,"date":"2017-10-20T19:32:51","date_gmt":"2017-10-20T19:32:51","guid":{"rendered":"https:\/\/gigisplayhouse.org\/maimi11\/?page_id=4140"},"modified":"2025-01-06T12:30:06","modified_gmt":"2025-01-06T17:30:06","slug":"how-gigis-began","status":"publish","type":"page","link":"https:\/\/gigisplayhouse.org\/chattahoocheevalley\/how-gigis-began\/","title":{"rendered":"How GiGi’s Began"},"content":{"rendered":"\n\n\t
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How GiGi's Began<\/h1>\n

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\"GiGi'sWhen my daughter GiGi was born, I thought my family\u2019s life would change forever. About an hour after she was born, the doctors suspected she had Down syndrome. Panic was welling up inside me but I was afraid for anyone to see it. As soon as my husband and I made eye contact I said, \u201cif anyone can handle this we can.\u201d He agreed and said \u201cCan you imagine what better kids Isabella and Franco are going to be because of her?\u201d\u00a0 I knew we were going to get through this together. Don\u2019t get me wrong \u2013 we were petrified! I can not even begin to tell you the total fear and devastation I felt. Everything they were telling us about Down syndrome was so negative! Suddenly no one had eye contact with me anymore, they kept the door to my room closed and they kept sending in the clergy!\u00a0 If this was happening to us already what was life going to be like for our kids? I was so afraid to bring her home and start this \u201cnew\u201d life. I remember when people first came to visit.\u00a0 There were hugs of sympathy not congratulations. They would tip toe towards the bassinet and seemed afraid to look inside to see what she would look like. Then when they finally mustered up the courage to look they saw this beautiful little baby and they were shocked!\u00a0 They always exclaimed \u201cOh my gosh! She is adorable!\u201d I really don\u2019t know what they were expecting to see but finally people started to realize she was just a baby.<\/p>\n

The Promise<\/h2>\n

\"gigi\"One night as I carried GiGi to bed, I could feel the weight of her low muscle tone. A weight you never knew existed due to her never ending smile and sheer determination. At that moment, I realized how strong she actually was. As I carried her up the stairs, I made a promise to her that I would change the way the world looked at a person with Down syndrome; that I would help people understand that she and all of her friends were so much more than a diagnosis. With the help of people like you and the Playhouses across the world, that promise is being kept \u2013 not just for GiGi but for all our children. <\/i><\/p>\n

Life with GiGi<\/h2>\n

What a gift!\u00a0 Once we got settled and got back into a routine at home I realized that she was more like my other kids than she was different. Some things took her longer but she always got it and she never gave up. She inspired me everyday and I had to find a way to live up to my promise to her. I remember my first support group meeting \u2013 we were in the corner of a sterile room at the hospital.\u00a0 It was a great meeting but I just kept thinking, \u2018why isn\u2019t there a place for us\u2019<\/i>?\u00a0 That is what propelled me to create a place where families could come for resources and networking, where kids and adults with Down syndrome could be the leaders, where we could celebrate our diagnosis. With my husband by my side we went out to recruit board members and raise money. My son Franco, drew the GiGi\u2019s Playhouse logo and in just 5 months we opened the doors to the first Down syndrome awareness center in the country!<\/p>\n

The Playhouse<\/h2>\n

My favorite part of the Playhouse is the self esteem that the kids gain.\u00a0 As one Board member states, \u201cMy son has gained so much self confidence from being at GiGi\u2019s.\u00a0 At the Playhouse, he is the leader \u2013 the other kids follow him!\u00a0 He is beginning to transfer this new found self confidence to his class at school.\u201d\u00a0 There are DOZENS of educational activities and programs designed specifically to work on important skills for each child. Many of the programs are facilitated and developed by therapists and educators. Thus the kids are strengthening their gross and fine motor skills, speech and language development, and social skills \u2013 and having so much fun they don\u2019t even realize it! All of the skills are built in a way that they can be transferred into the classrooms. They learn how to socialize with peers, how to read and write, how to take turns and most of all they are gaining self esteem at the same time!<\/p>\n

The Future<\/h2>\n

I have to say having GiGi was like a true love story. It started out with devastation and fear and ended with a love like I have never known. Without living it I would never have understood that.\u00a0 I am just glad that GiGi\u2019s Playhouse has turned into a place where people can see the other side of Down syndrome. As for GiGi??\u00a0 She is rockin\u2019 that extra chromosome! She is an avid texter, hip hop dancer and over all rock star!!\u00a0 Her brother and sisters worship her! I only wish I would have known how amazing life with her was going to be!!<\/p>\n

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Nancy Gianni, Founder and Chief Belief Officer of GiGi\u2019s Playhouse, Author of #GenerationG, and CNN Hero, with daughters GiGi and Bella Gianni, featured on the Today Show.<\/p>\n<\/div>\n\t<\/div>\n<\/div>\n<\/div>\n<\/div>\n\t<\/div>\n\t\t<\/div>\n\t<\/div>\n<\/div>\n

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