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Hi my partners daughter was diagnosed with spinal muscular atrophy type 2 and he's finding it hard to come to terms with her having a disability. I have a child myself but feel like I can't comfort him because I don't know what it feels like. Is there anyone on here who has some advice on how you came to terms with things? Or does anyone have a child or children with any sort of muscle problems that could give advice please?

Thank you Smile

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