How to Live with Muscular Dystrophy

Muscular dystrophies are a group of more thaninfluence due to Vata deregulations. Existing Panch
20 different genetic neuromuscular disorders,Karma and other supportive treatments aim to
some more debilitating than others. The mostcontrol symptoms, such as muscle spasm, and
common, Duchenne muscular dystrophy (DMD)enable people to have a good quality of life. They
affects 1 in 3500 boys. There is a problem in theinclude gentle Pawan Muktasana series of muscle
chromosome that codes for a protein calledexercises, because inactivity can worsen the
dystrophin which maintains the integrity of thedisease. Pawan Muktasana along with certain other
muscle cell wall. Eventually irreversible destructionAsanas such as Bhujangasana may prevent or
of the muscle cells occurs. In early school years, itdelay scoliosis, or curvature of the spine. The
may just seem that DMD boys are slower andBhastrika Pranayama may support Cardio-
clumsier than their peers. The disease progressesRespiratory system and may improve process of
such that the majority will be wheelchair bound bybeta-oxidation at cellular level. Yogic support of
10-14 years.Bhastrika Pranayama is important to boost the
Muscular dystrophies are inherited. Each disease isrespiratory function. When respiratory function
transmitted by a different genetic trait. DMD isdeteriorates, ventilator support may be needed.
inherited in an X-linked recessive transmission.There is no cure for any form of muscular
That means that females may be carriers but dodystrophy some medicines, ayurvedic remedies
not have any debilitating symptoms. A femaleand therapies can slow the course of the disease.
carrier has a 50% chance of transmitting theHuman trials of gene therapy with the dystrophin
faulty gene onto her children. There is nogene are on the near horizon. For instance,
satisfactory treatment in any system of medicine.scientists are researching ways to insert a
It is a progressive muscle-wasting disease due toworking dystrophin gene into the muscles of boys
a mutation in the dystrophin gene and thewith Duchenne and Becker muscular dystrophies.
consequential protein deficiency in muscle. ItPanch Karma procedures are also found useful in
results in chronic inflammation and severe skeletalthe life term management of muscular dystrophy.
muscle degeneration. How the lack of theAyurvedic researchers are investigating the
sarcolemma protein dystrophin gives rise to thepotential of certain muscle-building Rasayana
final disease status is still not clear.medicines to slow down or reverse the
The genetic disease conditions are diagnosedprogression of muscular dystrophy. Other trials
through genetic testing, a physical exam, a familyare looking into the effects of the dietary
medical history, and some specific tests. Thesesupplements Withania somnifera, Curcuma longa,
might include: A muscle biopsy (the removal andCreatine and glutamine on muscle energy
examination of a small sample of muscle tissue)production and storage.
- DNA (genetic) testingSymptoms of muscular dystrophy often can be
- Electromyography or nerve conduction testsrelieved through exercise, Panch Karma therapy,
(which use electrodes to test muscle and/orrehabilitative devices, and Yogic respiratory care
nerve function)with Bhastrika Pranayama, and surgery.
- Blood enzyme tests (which may reveal muscle- Ayurvedic Panch Karma & Yogic Support
damage)can minimize abnormal or painful positioning of the
For DMD and BMD, muscle biopsy may showjoints and may prevent or delay curvature of the
whether dystrophin protein is missing or abnormal,spine. Respiratory care, deep breathing, and
and DNA Test is used to analyze the condition ofcoughing exercises are often recommended.
the related gene.- In Duchenne muscular dystrophy, corticosteroids
There's no definite cure and, although a great dealmay slow muscle destruction.
can be done to help limit the effects of Muscular- In myotonic muscular dystrophy, phenytoin,
dystrophies. Ayurveda considers this condition asprocainamide or quinine can treat delayed muscle
Mamsa-vata-kshaya related to beeja dosha andrelaxation.
impairments of Mamsagni (muscle enzyme). It- In DMD, BMD and LGMD, the Mamsagni
involves deranged Vata and subsequentRasayana has shown muscular protection.
degeneration of muscles and structures related toGenetic counseling, prenatal diagnosis by chorionic
it. Ayurveda consider this condition due to leakagevillus sampling, and antenatal screening of families
of Mamsagni from muscle tissues. This iswith MDs provides an opportunity to prevent
supposed due to sarcolemma membrane defectthese diseases being passed on to children.
in the muscle fibers. Ayurvedic treatment mightAyurvedic primary intention is on treating or
slow or stop the progression of muscledelaying symptoms, enhancing physical mobility
degeneration. The Til Mash Pinda swedana canand preventing cardiac and respiratory
help to stabilize the membrane defect. Thecomplications.
Mamsagni Rasayana show cellular protective