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As a caregiver of someone with MG, what is the “thing” that is hardest for you?
Being a caregiver of someone with a rare disease is HARD, especially if that someone is someone you love like a family member.
What is the hardest part of being a caregiver for someone with MG?
Is there a specific symptom that bothers you the most?
Too many appointments?
Lack of social life?
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