Jason’s Story<\/p>\n
I first heard about GiGi\u2019s Playhouse from friends who had toddlers with Down syndrome, and I assumed, like many people I’m sure, that it was primarily directed toward and for younger children.<\/p>\n
In a wonderful and appropriate way, our son showed us that is not the case. \u00a0This is our GiGi’s story.<\/p>\n
Our son Jason was born with Downs Syndrome almost 20 years ago. \u00a0In my parent measure of time, he has zoomed from the tow-headed boy who loved dinosaurs and big trucks to a young man who loves music, movies, and sports.<\/p>\n
Throughout his life, we have always worked to be sure that he and everyone else knew that he was a PERSON with Down syndrome – his diagnosis is a part of who he is, but it does not define him. And while we are always aware of how he is different – as we plan academics, athletics, recreation, and life in general – we also focus on the similarities he shares with those around him. (I truly believe it is a process used by all parents for and with all their children, just at a different level with children who have special needs!)<\/p>\n
During his senior year in high school, self-advocacy became a more focused part of his education. \u00a0This included more frequent discussions about Downs Syndrome and use of the term “disability” and how that applied to him in life and his future.\u00a0Even\u00a0with the inclusion of his strengths and the fact that everyone has areas that we need help, even with his involvement in and love for his 6 years of Special Olympics, the reality of his being a part of a “disabled” population was hard for him. He would often tolerate short conversations and then say, “Can we be done?”. \u00a0He had good school experiences and a mix of friends from his special education and regular classes. \u00a0At this age, especially, it was important for him to be like everyone else. \u00a0“Disability” did not fit his idea of that at all. \u00a0He came to a point of quiet, non-participating tolerance on the subject.<\/p>\n
Last year he began attending the Transition Plus Program, where he blends life skills learning with community based work and volunteer experiences. \u00a0About a year ago, an addition appeared on his schedule: a weekly volunteer opportunity at Gigi’s Playhouse doing some cleaning and organization.<\/p>\n
I have to say here that Jason is, age and gender appropriately, not the most generous of communicators about his day. \u00a0One of our family traditions is that everyone has to share something at the dinner table about their day. \u00a0This can still be a time and energy consuming experience for Jason … and the family!<\/p>\n
After his second week at Gigi’s, Jason came in the door hollering, “MOM!” and waving a piece of paper. \u00a0When I asked him what it was, he said, “You know! Friday Friends? It’s for people with Downs Syndrome – just like me!!” \u00a0As I stood there stunned and almost in tears, he started listing all the people he knew with Downs Syndrome. \u00a0It was as if a door had opened and a new journey had started.<\/p>\n
Since then, Friday Friends has been a regular part of our schedule, and, more importantly, Jason’s life. \u00a0He has invited friends to come and continues his efforts to recruit more. \u00a0He loved the winter dance and looks forward to playing Wii and foosball, having pizza and doing karaoke every month. \u00a0Along with those wonderful activities though are the many unexpected and invaluable benefits: \u00a0he has a safe place to practice making friends and to socialize\/hang out with friends – with and without disabilities. We have watched him become more self-confident and willing to try new experiences and independence in other aspects of his life, and seen him be more encouraging and supportive of people around him.<\/p>\n
Jason’s experience with Gigi’s Playhouse has helped him to have a new sense of himself, his world, and his future. \u00a0And while he still doesn’t embrace “disability”, he is more accepting about how it might fit into his life.<\/p>\n
Gigi’s Playhouse TRULY offers foundational learning opportunities for individuals with Downs Syndromes, their families, and the community. \u00a0And so much more!<\/p>\n
We are blessed and grateful!<\/p>\n
-Jason’s Mom, Sarah<\/p>\n","protected":false},"excerpt":{"rendered":"
Jason’s Story I first heard about GiGi\u2019s Playhouse from friends who had toddlers with Down syndrome, and I assumed, like many people I’m sure, that it was primarily directed toward and for younger children. In a wonderful and appropriate way, our son showed us that is not the case. \u00a0This is our GiGi’s story. Our…<\/p>\n","protected":false},"author":21,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-3193","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"_links":{"self":[{"href":"https:\/\/gigisplayhouse.org\/twincities\/wp-json\/wp\/v2\/posts\/3193","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/gigisplayhouse.org\/twincities\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/gigisplayhouse.org\/twincities\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/gigisplayhouse.org\/twincities\/wp-json\/wp\/v2\/users\/21"}],"replies":[{"embeddable":true,"href":"https:\/\/gigisplayhouse.org\/twincities\/wp-json\/wp\/v2\/comments?post=3193"}],"version-history":[{"count":0,"href":"https:\/\/gigisplayhouse.org\/twincities\/wp-json\/wp\/v2\/posts\/3193\/revisions"}],"wp:attachment":[{"href":"https:\/\/gigisplayhouse.org\/twincities\/wp-json\/wp\/v2\/media?parent=3193"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/gigisplayhouse.org\/twincities\/wp-json\/wp\/v2\/categories?post=3193"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/gigisplayhouse.org\/twincities\/wp-json\/wp\/v2\/tags?post=3193"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}