{"id":1431,"date":"2015-08-27T17:34:27","date_gmt":"2015-08-27T17:34:27","guid":{"rendered":"http:\/\/blog.silviaskingdom.com\/?p=1431"},"modified":"2017-01-20T07:31:25","modified_gmt":"2017-01-20T15:31:25","slug":"nickys-life-part-9","status":"publish","type":"post","link":"https:\/\/blog.silviaskingdom.com\/?p=1431","title":{"rendered":"Nicky’s Life Part 9"},"content":{"rendered":"

This is part 9 of an infinite series of photos I am posting on the Facebook page<\/a> I have for the book I wrote about my journey raising my son\u00a0with RDEB (Recessive Dystrophic Epidermolysis Bullosa) called Butterfly Child<\/a>.<\/strong>\u00a0I am\u00a0posting a few images from Nicky’s life\u00a0and commenting on either what was going on at the time or explaining things about the picture per se.<\/p>\n

This “picture commentary” will serve as a companion for anyone that is kind enough to purchase and read my book as my appreciation and thanks.<\/p>\n

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November\u00a02000 – This photo was taken a week before his 4th birthday. This was right after a bandage change. I took a little break before wrapping his hands, Nicky was still upset from the ordeal, I wanted him to relax a little. I hated inflicting all this pain to my son, as I still do to this day. But what else could I do? Life with EB sucks.<\/p>\n

Here’s the link on where to purchase the book if interested:
\nhttp:\/\/www.butterflychildamothersjourney.com\/?page_id=19<\/a><\/p>\n

Love & Light,<\/p>\n

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\"Vote<\/a><\/p>\n

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