Sleepover and Muscular Dystrophy
During my childhood, I had many sleepovers. I was still physically abled and didn’t require any care. Nowadays, I need a wealth of care when I stay somewhere that is not my own home.
If you have a child with MD that affects their physical abilities, or they require care, how do you approach sleepovers? What do you discuss with the parents? Do you send a caregiver with your child?
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