Скачать или смотреть 6-Year-Old With Muscular Dystrophy: Journey with Stem Cell Therapy

Stem Cell Therapy for muscular dystrophy: https://swissmedica.link/stem-cell-mu...

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A family from Croatia came to Swiss Medica with their 6-year-old daughter diagnosed with muscular dystrophy (type D2A) and later also with Prader–Willi syndrome. Symptoms appeared very early — weak muscles, inability to crawl or flip over, and delays in motor development. At age two she began growth hormone therapy to address problems caused by PWS. Today she still tires quickly, has speech difficulties, and needs constant balance between exercise and rest.

Her parents spent months researching and found Swiss Medica after considering other clinics worldwide. With the support of their doctor in Zagreb, who actively follows new therapies, they decided to try regenerative treatment. The therapy lasted two days, and despite minor discomfort from muscle injections, their daughter managed well. The family highlighted the professionalism of the medical team and now hopes for improvements in motor skills and speech over the coming months.

𝘗𝘭𝘦𝘢𝘴𝘦 𝘯𝘰𝘵𝘦: 𝘛𝘩𝘦 𝘤𝘰𝘯𝘵𝘦𝘯𝘵 𝘱𝘳𝘰𝘷𝘪𝘥𝘦𝘥 𝘪𝘯 𝘵𝘩𝘪𝘴 𝘷𝘪𝘥𝘦𝘰 𝘪𝘴 𝘯𝘰𝘵 𝘪𝘯𝘵𝘦𝘯𝘥𝘦𝘥 𝘢𝘴 𝘮𝘦𝘥𝘪𝘤𝘢𝘭 𝘢𝘥𝘷𝘪𝘤𝘦. 𝘐𝘯𝘥𝘪𝘷𝘪𝘥𝘶𝘢𝘭 𝘵𝘳𝘦𝘢𝘵𝘮𝘦𝘯𝘵 𝘳𝘦𝘴𝘶𝘭𝘵𝘴 𝘮𝘢𝘺 𝘷𝘢𝘳𝘺. 𝘈𝘭𝘸𝘢𝘺𝘴 𝘤𝘰𝘯𝘴𝘶𝘭𝘵 𝘸𝘪𝘵𝘩 𝘢 𝘲𝘶𝘢𝘭𝘪𝘧𝘪𝘦𝘥 𝘩𝘦𝘢𝘭𝘵𝘩𝘤𝘢𝘳𝘦 𝘱𝘳𝘰𝘧𝘦𝘴𝘴𝘪𝘰𝘯𝘢𝘭 𝘳𝘦𝘨𝘢𝘳𝘥𝘪𝘯𝘨 𝘢𝘯𝘺 𝘮𝘦𝘥𝘪𝘤𝘢𝘭 𝘤𝘰𝘯𝘥𝘪𝘵𝘪𝘰𝘯.