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Over the years I've noticed that spouses respond to our paralysis by either
being 110% supportive or by checking out. That's tough. When I became paralyzed,
my husband checked out. He lives in the basement and I sometimes don't see him
for days. It took a long time to adjust to a situation I didn't want. Then
there's the absence of touch. With ALS I can feel EVERYTHING, EVERYWHERE... I
just can't move. So sex COULD be great but I lost my partner. Has anyone else
had to deal with this?
Sandy |
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