a parent’s worst…nightmare

…or at least one of them…a child with a debilitating disease like…cystic fibrosis.

I’ve been trying to catch up with visiting other blog sites. After all, many so generously take time to visit hugmamma’s mind, body, and soul. You know what they say…”what goes around, comes around.” And I sure as heck like it when folks come around.

Once-in-a-while one post catches my attention, forcing me to pause and take a deep breath. Victoria’s “A summer of CF” did just that. 

How much is a parent able to give as a caretaker, especially for one’s own child, without succumbing to depression? I don’t know, not having been there myself. I can only think to offer up prayers for someone in Victoria’s position, and ask that you do the same…after you read what she shares at http://thevoicefromthebackseat.wordpress.com/2013/08/26/%f0%9f%94a-summer-of-cf/ 

…i’m sure you’ll be moved to say a prayer for this family…and be very grateful for the blessings in your own life…

Victoria, Australia - Great Ocean Road

………hugmamma.

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hugs for sharing some brief thoughts...and keeping them positive

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