Restoring of the DNA of the Bride

Muscular dystrophy

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Muscular dystrophy

Condition:

Muscular dystrophy

Definition:

Muscular dystrophy is a group of diseases that cause progressive weakness and loss of muscle mass. In muscular dystrophy, abnormal genes (mutations) interfere with the production of proteins needed to form healthy muscle.

There are many kinds of muscular dystrophy. Symptoms of the most common variety begin in childhood, mostly in boys. Other types don’t surface until adulthood.

Symptom:

The main sign of muscular dystrophy is progressive muscle weakness. Specific signs and symptoms begin at different ages and in different muscle groups, depending on the type of muscular dystrophy.

Duchenne-type muscular dystrophy

This is the most common form. Although girls can be carriers and mildly affected, it’s much more common in boys.

Signs and symptoms, which typically appear in early childhood, might include:

  • Frequent falls
  • Difficulty rising from a lying or sitting position
  • Trouble running and jumping
  • Waddling gait
  • Walking on the toes
  • Large calf muscles
  • Muscle pain and stiffness
  • Learning disabilities
  • Delayed growth
  • Becker muscular dystrophy
  • Signs and symptoms are similar to those of Duchenne muscular dystrophy but tend to be milder and progress more slowly. Symptoms generally begin in the teens but might not occur until the mid-20s or later.

Other types of muscular dystrophy
Some types of muscular dystrophy are defined by a specific feature or by where in the body symptoms begin. Examples include:

Myotonic. This is characterized by an inability to relax muscles following contractions. Facial and neck muscles are usually the first to be affected. People with this form typically have long, thin faces; drooping eyelids; and swanlike necks.
Facioscapulohumeral (FSHD). Muscle weakness typically begins in the face, hip, and shoulders. The shoulder blades might stick out like wings when the arms are raised. Onset usually occurs in the teenage years but can begin in childhood or as late as age 50.

Congenital. This type affects boys and girls and is apparent at birth or before age 2. Some forms progress slowly and cause only mild disability, while others progress rapidly and cause severe impairment.

Limb-girdle. Hip and shoulder muscles are usually affected first. People with this type of muscular dystrophy might have difficulty lifting the front part of the foot and so might trip frequently. Onset usually begins in childhood or the teenage years.

Description:

Protocol:

Muscular dystrophy

Topically apply 20-30 drops of the Spinal Therapy over the spine in the evening before bed.

Drink 1 capsule of the DNA Protector once a day after a meal or a small snack.

Diffuse (see below) at night while sleeping, 5 drops each: Brain Blend and Cedarwood 5ml 10ml.

In addition

Supplement with Collagen 350g 450g 700g and Bone Broth 350g 450g and follow a nutritious meal plan.

Diffuse 2-3 drops of each oil; maximum 10-12 drops in total, at a time, unless otherwise advised.

NOTE: Always use an ultrasonic diffuser infinity rose vase (with a diffusing duration of at least 8 hours), to diffuse pure essential oils. Do not use a humidifier, air purifier, or a candle, as they only smell good and have no further effect. An electric, ultrasonic, diffuser dispenses essential oils into the air through vibrations of a plate which causes ultrasonic waves, creating microscopic particles of oils that disperse into the air. It, therefore, breaks open the essential oil volatile molecules, to have a medicinal effect in that it can penetrate through the blood-brain barrier. It is always good to use a diffuser at night while you are sleeping.

 

 

 

 

Precautions & Side Effects:

Recommended Products:

Complimentory Products:

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