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What do you wish you knew as a caregiver of someone with MG
Most of what is explained in a medical setting is geared toward the patient. But as a loved one who is now a caregiver for someone with MG, what do you wish the doctors had told you?
Did the medical professionals prepare you for what life would be like as a caregiver?
Knowing what you know now, what advice would you give new caregivers?
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