I've been reading lately and am trying to come to terms with naming some of the feelings I have. Grief is hard. As soon as you think you've turned a corner, it smacks you in the face.

Having a family member with special needs and the issues associated with them affect every person in the family. This blog gives a view from each perspective and a window into how we cope as a family in the midst of all the situations presented to us.
4 comments:
Thinking of you Lori. What are you reading?
Grief, I don't think, ever really goes away. It just changes from an open wound to a scar, an everlasting reminder that life changed when we weren't ready.
Love you, L!
Amy's right - although grief can get tucked away, it doesn't ever really go away. It never stops being unpredictable, either.
Our third baby, Jeffrey, was diagnosed with a genetic neuromuscular disease at 2 months; he earned his wings at 5-1/2 months. That was in 1997, and the 'moments' are still readily available. However, most days are really good and have been for many years.
I wrote a book about our brief time with Jeffrey (http://thejeffreyjourney.com) and was a contributing author in From a Lullaby to Goodbye (http://lullabytogoodbye.com), a collection of stories from parents who lost their babies and young children for others families in the same situation.
It helps tremendously to know others DO understand!
Helen/'Lucy'
I'm glad you are seeing some weight lift. Have you considered getting some counseling? It won't make the hurt go away, but might help?
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