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What resources have helped you advocate for yourself or your child with MG?
Advocacy often requires tools — not just courage. Whether it’s symptom trackers, communication guides, school accommodation templates, or clinical trial resources, the right tools can make a huge difference.
I’ve found that having something tangible — a list, a guide, a script — helps me communicate more clearly and feel less alone in the process.
What resources have helped you advocate for yourself or your child?
Are there tools you wish existed but haven’t been able to find?
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