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Where can I read about patient stories and experiences?
Are clinical trials and investigations being carried out? What stages are they in and how can I stay up to date?
Are there any medicines or therapies to cure or alleviate the disease?
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Where can I make specific medical consultations? Are there reference doctors for LAMA2-CMD?
What LAMA2-CMD patient associations are there?
How rare is LAMA2-CMD?
What’s the difference between the several names used for the same muscle disease?
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