If some of you wonder what it's like being a parent with special needs sometimes it's just nice not knowing a diagnosis for what your child might have with the hopes that you don't have that label stamped forever on your precious child. For other parents out there that suffer not knowing a condition that could be life altering literally this can be the most challenging experience of them all. Not only is the test fees a challenge to the pocket, the trauma of the test is challenging and often times heart breaking as no parent ever wants a child to have a series of blood drawn, cat scans, MRI's, sleep disorder studies just to name a few. I have met and LOVE many dear parents out there that are in the trenches loving, supporting, parenting, teaching, explaining and forever hoping that their child's life will be one of peace and that others will love them as much as we/they do. One of my friends has a blog she's writing about her plight of forever waiting, forever testing and forever hoping that the news is good about her dear child whom I love dearly. This child always has a giant warm hug and the most infectious smile that warms my heart each and every time I see them. Please help me support my dear friend in her journey.
http://lifelovelessonstolearn.blogspot.com/2011/12/waiting.html?spref=fb
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