"𝔼𝕡𝕚𝕕𝕖𝕣𝕞𝕠𝕝𝕪𝕤𝕚𝕤 𝔹𝕦𝕝𝕝𝕠𝕤𝕒 𝕚𝕤 𝕔𝕒𝕝𝕝𝕖𝕕 '𝕥𝕙𝕖 𝕨𝕠𝕣𝕤𝕥 𝕕𝕚𝕤𝕖𝕒𝕤𝕖 𝕪𝕠𝕦'𝕧𝕖 𝕟𝕖𝕧𝕖𝕣 𝕙𝕖𝕒𝕣𝕕 𝕠𝕗." 𝕀𝕥 𝕚𝕤 𝕣𝕒𝕣𝕖, 𝕚𝕥 𝕚𝕤 𝕕𝕖𝕧𝕒𝕤𝕥𝕒𝕥𝕚𝕟𝕘, 𝕒𝕟𝕕 𝕚𝕥 𝕚𝕤 𝕕𝕖𝕒𝕕𝕝𝕪. 𝕊𝕠𝕡𝕙𝕚𝕒 𝕟𝕖𝕖𝕕𝕖𝕕 𝕒 𝕔𝕦𝕣𝕖 𝕥𝕙𝕒𝕥 𝕕𝕚𝕕𝕟'𝕥 𝕔𝕠𝕞𝕖 𝕢𝕦𝕚𝕔𝕜𝕝𝕪 𝕖𝕟𝕠𝕦𝕘𝕙 - 𝕨𝕖 𝕔𝕠𝕟𝕥𝕚𝕟𝕦𝕖 𝕗𝕚𝕘𝕙𝕥𝕚𝕟𝕘 𝕖𝕒𝕔𝕙 𝕕𝕒𝕪 𝕚𝕟 𝕙𝕖𝕣 𝕞𝕖𝕞𝕠𝕣𝕪"
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Sophia Grace was loving, sweet, courageous and radiant. She was an inspiration to all who knew her, and continues to inspire us all to be better people, and to fight for a cure for Epidermolysis Bullosa, a rare and debilitating genetic disorder. Sophia deserved to live a life free from pain and suffering; we know her hope would be to see a cure for EB, so that no other child suffers.
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