Treatment of spinal muscular atrophy Type I in girls Laura with method Bond ex therapy
Laura is one of the few children in the world that have spinal muscle atrophy Type I and have reached the age of 10 (rarely do children suffering from SMA Type I live beyond the age of 3), when breathing with the help of a respirator (during the day she occasionally breathes on her own) she has no difficulty breathing (it is not necessary to clean the airways during the day or night), nor has she had cardiological difficulties for the last 5 and a half years since the Bondex therapy was applied;
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