Scan QR
Muscular Dystrophy Stem Cell Therapy
This person has been suffering from muscular dystrophy for 12 years. After undergoing stem cell therapy for three months, he is now able to walk 5 kilometers without getting tired. Earlier, he could only walk for one kilometer. He now has confidence in walking; earlier, he used to fall down while walking. He can now go up and down the stairs without any support, which was previously impossible. His energy levels have improved significantly since the therapy.
His CP kinase levels were 2000 before the therapy. After the therapy for 2 years, CP Kinase levels have reduced to 500.
Cell Cure India offers the best muscular dystrophy stem ce...
Scan QR
Muscular Dystrophy Stem Cell Therapy
This person has been suffering from muscular dystrophy for 12 years. After undergoing stem cell therapy for three months, he is now able to walk 5 kilometers without getting tired. Earlier, he could only walk for one kilometer. He now has confidence in walking; earlier, he used to fall down while walking. He can now go up and down the stairs without any support, which was previously impossible. His energy levels have improved significantly since the therapy.
His CP kinase levels were 2000 before the therapy. After the therapy for 2 years, CP Kinase levels have reduced to 500.
Cell Cure India offers the best muscular dystrophy stem cell treatment therapy in India. Limb Girdle Muscular Dystrophy, Becker’s Muscular Dystrophy, Duchenne Muscular Dystrophy, and Facioscapulohumeral Muscular Dystrophy (FSHD) can be treated with Muscular Dystrophy Stem Cell Treatment Therapy in India.
Muscular Dystrophy Stem Cell Treatment/Therapy in India
Dystrophy refers to a group of global diseases that are inherited, and the main characteristic is muscle weakening. In some of these diseases, the heart and other organs may also be affected. Muscular dystrophy has one of nine types, i.e., myotonic, Duchenne, Becker, limb girdle, congenital, oculopharyngeal, Emery-Dreifuss, and distal.
The muscles in this disease become weaker, and the inherited genetic defect makes the body unable to produce new protein, which is necessary for muscle growth and strength. As the years go by, the children diagnosed with this disease will become incapable of sitting and carrying things. The disease is a progressive one and can eventually affect the heart and lungs. The signs may vary depending on the extent of the degeneration.
Loading
