Have you ever considered the social impact MS has on the children of those living with the condition? Our amazing social worker Traci Paxton spoke on this sensitive topic at our recent MS CME and I’ve included a clip of her talk here. These two quotes are both quite poignant:
“Although children must assume sometimes significant responsibilities when a parent has MS, they should never be called upon to manage a parents direct care needs.”
“We must educate our children to understand that they are not responsible for the condition.”
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