{"id":9,"date":"2019-10-05T15:11:26","date_gmt":"2019-10-05T14:11:26","guid":{"rendered":"https:\/\/the7.io\/wedding\/?page_id=2"},"modified":"2025-01-15T23:55:34","modified_gmt":"2025-01-15T23:55:34","slug":"home","status":"publish","type":"page","link":"https:\/\/adamlea.eu\/index.php\/pl\/home\/","title":{"rendered":"Home"},"content":{"rendered":"

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Story of<\/h1><\/div>
Adam & Lea vs Sanfilippo<\/div><\/div>
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two kids one fatal disease and our struggle to help them<\/span><\/h2>\n

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News<\/h2><\/div>
Check how we are doing. More on our efforts to support research and raise awareness you can find on website of our organisations: Fundacja Sanfilippo<\/a> and Sanfilippo Initiative<\/a>.<\/div><\/div>[vc_row_inner][vc_column_inner][vc_raw_html]JTVCbXktaW5zdGFncmFtLWZlZWQlMjAlMjB1c2VyX2lkJTNEJTIyODk1MjM1Mzg5MTQ2NzM0NCUyMiUyMHNraW5faWQlM0QlMjI3MjklMjIlMjBmZWVkc19wZXJfcGFnZSUzRCUyMjEyJTIyJTIwY2FwdGlvbl93b3JkcyUzRCUyMjI1JTIyJTIwY2FjaGVfdW5pdCUzRCUyMjElMjIlMjBjYWNoZV9kdXJhdGlvbiUzRCUyMmhvdXJzJTIyJTIwbG9hZF9tb3JlJTNEJTIyMCUyMiUyMCUyMGxpbmtzX25ld190YWIlM0QlMjIxJTIyJTIwJTIwc2hvd19zdG9yaWVzJTNEJTIyMCUyMiUyMCU1RA==[\/vc_raw_html][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row full_width=”stretch_row” equal_height=”yes” content_placement=”middle” css=”.vc_custom_1570460426457{padding-top: 80px !important;padding-bottom: 30px !important;background-color: #f5eff0 !important;}” el_id=”about”][vc_column css_animation=”fadeInLeft” offset=”vc_col-lg-offset-0 vc_col-lg-6 vc_col-md-offset-0 vc_col-md-6 vc_col-sm-offset-0 vc_col-xs-12″ css=”.vc_custom_1570469536499{padding-bottom: 70px !important;}”]
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Our story<\/h2><\/div>
This story is about us: \u00a0Adam and Lea, siblings connected in struggle for life against MPSIII also known as Sanfilippo disease.<\/div><\/div>[vc_column_text]My name is Adam and my younger annoying sister is Lea. It is no so long ago that we entered the world and we\u2019ve already had the first serious flop\u2026 Sanfilippo. What can we say \u2013 each of us had a 25% of having this defect, because of mutations of one damn gen. And guess what \u2013 both of us have it. Well, what can we do\u2026 our parents made their research and it turned out that there is hope for us! But this topic is tackled in other sections of this website. Here you will find a little bit of information about us. Although we have this crap disorder, we are very cool and adorable kids.[\/vc_column_text][\/vc_column][vc_column css_animation=”fadeInRight” width=”2\/3″ css=”.vc_custom_1570469545591{padding-bottom: 50px !important;background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}” offset=”vc_col-lg-offset-0 vc_col-lg-6 vc_col-md-offset-0 vc_col-md-6 vc_col-sm-offset-2 vc_col-xs-offset-2 vc_col-xs-8″]