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What advice would you give to new caregivers?
As I’m sure we can all agree, SMA impacts not just ourselves but also those around us. This is especially true for caregivers. No matter how long the journey has been, there’s so much learning and adapting that goes into this role.
To all the caregivers here, what resources have been most helpful to you? Looking back, what do you wish you had known from the very beginning that could have made things a little easier?
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