[vc_row css=”.vc_custom_1582209999872{padding-top: 5.15rem !important;}”][vc_column css=”.vc_custom_1582207915173{padding-bottom: 2.1rem !important;}”][vc_column_text css=”.vc_custom_1584361995916{margin-bottom: 2.5rem !important;}”]<\/p>\n
[\/vc_column_text][vc_row_inner equal_height=”yes” content_placement=”top” gap=”20″][vc_column_inner width=”1\/2″ css=”.vc_custom_1582208381733{padding-bottom: 2.15rem !important;}”][vc_column_text]When the chaos of rare disease arrived in our lives the scariest part was feeling so alone, not knowing who to talk to, where to go, what to ask or what to do. \u00a0I realized I spent hours on the internet looking for\u2026. answers?? help?? what to do?? a guide??<\/p>\n
I spent so many lost hours until I began to\u00a0organize my ideas and came to the clumsy conclusion that I had to help other people in my situation. \u00a0It was my responsibility to find other scared lost families fighting rare diseases and offer my hand, create a community, come together as individuals to create the strength of a community. \u00a0I wanted to give them the answers, support and direction\u2026 I wanted to help those other children like Chloe born into a destiny the meant learning to rewrite it. \u00a0That is how Bubbles and Dreams was born. \u00a0A world full of happy children, bright colors, healthy and sick where their differences brought them together and made them all better.[\/vc_column_text][\/vc_column_inner][vc_column_inner width=”1\/2″][vc_single_image image=”1580″ img_size=”large” alignment=”center”][\/vc_column_inner][\/vc_row_inner][vc_row_inner equal_height=”yes” content_placement=”top” gap=”20″ css=”.vc_custom_1582211804866{padding-top: 2.1rem !important;}”][vc_column_inner width=”1\/2″ css=”.vc_custom_1582208381733{padding-bottom: 2.15rem !important;}”][vc_single_image image=”1581″ img_size=”large” alignment=”center”][\/vc_column_inner][vc_column_inner width=”1\/2″][vc_column_text]BUBBLES AND DREAMS<\/strong>\u00a0is a Non-Profit organisation who\u2019s objective is to benefit children who suffer rare diseases and their families. \u00a0 The majority of rare diseases are severe and handicapping and many are degenerati, this makes time of the essence to fight them and you can never let your guard down if you want maintain the quality of life for the sufferer. \u00a0For more than 7 years we have been developing therapeutic programs focused on helping the children who suffer rare disease.<\/p>\n INSTAGRAM<\/a><\/strong><\/p>\n