Defeat Congenital muscular dystrophy

Muscular dystrophy refers to a group of genetic, hereditary muscle diseases that cause progressive muscle weakness. Muscular dystrophy are characterized by progressive skeletal muscle weakness, defects in muscle proteins, and the death of muscle cells and tissue. Nine diseases including Duchenne, Becker, limb girdle, congenital, facio scapulohumeral, myotonic, oculopharyngeal, distal, and Emery-Dreifuss are always classified as muscular dystrophy.



Congenital muscular dystrophy
Age at onset: birth; symptoms include general muscle weakness and possible joint deformities; disease progresses slowly; shortened life span.

Congenital muscular dystrophy includes several disorders with a range of symptoms. Muscle degeneration may be mild or severe. Problems may be restricted to skeletal muscle, or muscle degeneration may be pair with effects on the brain and other organ systems. A number of the forms of the congenital muscular dystrophies are caused by defects in proteins that are thought to have some relationship to the dystrophin-glycoprotein complex and to the connections between muscle cells and their surrounding cellular structure. Some forms of congenital muscular dystrophy show severe brain malformations, such as lissencephaly and hydrocephalus.

Principal symptoms include:
* Progressive Muscular weakness
* Poor Balance
* Frequent Falls
* Walking Difficulty
* Waddling Gait
* Calf Pain
* Limited Range of Movement
* Muscle Contractual
* Respiratory Difficulty
* Drooping Eyelids
* Scoliosis (curvature of the spine)
* Inability to walk

Some types of Muscular Dystrophy can affect the heart, causing cardiomyopathy or arrhythmias.

The prognosis for people with muscular dystrophy varies according to the type and progression of the disorder. Some cases may be mild and progress very slowly over a normal lifespan, while others produce severe muscle weakness, functional disability, and loss of the ability to walk.

There is no known cure for muscular dystrophy. Inactivity (such as bed-rest and even sitting for long periods) can worsen the disease. Physical therapy, Occupational therapy, speech therapy and orthopedic instruments (e.g., wheelchairs, standing frames) may be helpful.


IS THERE A WAY OUT?

To a family with a child with muscular dystrophy, it must seem like the worst disease. To what extent might the remedy enable the sufferer to overcome the existing condition? There is considerable good news.


Dr. Ramesh Bhardwaj, a senior homeopathic consultant, president of homeopathic medical association has proved that there is a way to lead a healthy and normal productive life for muscular dystrophy. Good diet and homeopathic remedy found to be very effective and successful in muscular dystrophy patients.

It is found that, with the start of medicine there is gradual improvement in the patientโ€™s condition with marked improvement in muscle strength, improved sleeping and eating patterns and weight gain within 1-2 months. Early initiation of treatment in the course of this disease can help a lot in reducing future disability and prolonging survival.

Patients unable to lift their heads before treatment were able to do so after treatment and their speech and walking ability improved as well. And with long term medicine patient can lead to normal healthy and productive life.

"HOMOEOPATHIC TREATMENT IS STRONGLY RECOMMENDED"

DR. BHARDWAJ HAS BEEN AWARDED WITH "BEST HOMOEOPATHY FOR TREATING MUSCULAR DYSTROPHY 2014"

contact:-Dr. Ramesh Bhardwaj
Homoeopathic World, Noida, India
contact no:-0-9811127065
email id:- dr.rameshbhardwaj@yahoo.com
website:- www.homoeopathic-world.com