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Showing posts from March, 2014
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Hearing the laughter of children in the morning particularly Hawke and Canyon for the past 30 minutes... So grateful!! Not taking good health for granted, praising God while I pray for those fighting children in hospitals (my news feed is full this past week of children fighting hydrocephalus among other issues).
24/7
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Hydrocephalus doesn't take weekends off and neither do we at the PHF! We are here for you 24/7/365! When you need us, just reach out to us via email at jason@hydrocephaluskids.org , or by phone at 810-441-9170 or shoot us a note on Facebook. That's how we do it at the PHF. REAL ACTION~REAL CHANGE. https://m.facebook.com/Michiganphf
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Our children play such a major role in Hawke's life and development (thank You Lord). This video stirs some emotions and is a great reminder of what love looks like. Prayers up for Teddy's progress and family.
This short film captures a young girl's love for her brother, who has cerebral palsy.
http://www.nytimes.com/2014/03/11/opinion/my-brother-teddy.html
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It's not about my son, it's about the children and all people fighting hydrocephalus! Raising awareness, raising money for better treatment and a cure!
Article published in Lapeer County Press. It won't let you access online for 30-days :-/
http://mcp.mihomepaper.com/news/2014-03-16/Front_Page/Beauty_Queen_poised_for_crown.html
Slow motion of Hawke standing on his own and taking two steps!!
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