In this article, we will explain what Duchenne Muscular Dystrophy is, its signs and symptoms, and the best homeopathic treatments for Duchenne Muscular Dystrophy.
Duchenne Muscular Dystrophy (DMD) is a rare genetic disorder characterized by progressive muscle weakness, mainly affecting boys. It is caused by a mutation in the gene, which leads to the absence or deficiency of the protein dystrophin. This protein is essential for maintaining muscle cell integrity and strength.
Dystrophin is a crucial protein in our bodies, often likened to "muscle glue" due to its role in holding muscle cells together. Encoded by the largest gene in our genetic makeup, the dystrophin gene consists of 79 exons. This protein is important for maintaining the strength and stability of our muscles. However, in conditions like Duchenne Muscular Dystrophy (DMD), a deficiency or absence of dystrophin occurs, resulting in muscle-related problems. Typically, DMD affects specific exons, especially exon numbers 44 to 53. Without an adequate amount of dystrophin, muscles gradually weaken and deteriorate, leading to significant motor functions.
The absence of dystrophin leads to muscle damage during contractions, triggering an inflammatory response. This inflammation results in the replacement of muscle fibers with fibrous tissue, leading to progressive muscle weakness and dysfunction.
Without proper treatment, DMD can lead to severe mobility issues, respiratory complications, and cardiac problems, significantly impacting the quality of life and lifespan of affected individuals.
GMFM score
The Gross Motor Function Measure (GMFM) is a clinical assessment tool designed to evaluate and measure gross motor function in children with conditions such as cerebral palsy and other developmental disabilities. It assesses a child's ability to perform a range of motor skills and tasks related to mobility and physical function. Typically, the GMFM score is expressed as a percentage, with higher scores indicating better gross motor function.
Following investigations are performed to confirm the intensity and severity of DMD
The conventional approach to DMD includes physical therapy, orthopaedic interventions, respiratory support, and cardiac management. However, these treatments mainly focus on symptom management rather than addressing the underlying cause of the disease. whereas homeopathic treatment for Duchenne Muscular Dystrophy aims to target the root cause, offering a holistic approach to managing the condition.
As DMD is a genetic disorder, preventive measures primarily involve genetic counselling for families with a history of DMD to assess the risk of passing on the condition to future generations.
While there isn't a specific diet to treat DMD, maintaining a balanced diet full of essential nutrients can promote overall health and well-being.
Here are the top 5 homeopathic medicines for Duchenne Muscular Dystrophy to address this genetic disorder
1.Causticum
Useful for muscle weakness and stiffness, especially in the lower limbs.
2. Rhus Toxicodendron
It helps relieve muscle pain and stiffness, particularly after periods of inactivity.
3. Arnica montana
Useful for reducing inflammation and soreness in muscles.
4. Phosphorus
It helps strengthen weak muscles and improve respiratory function.
5. Lachesis
Indicated for cardiac issues and breathing difficulties in DMD patients.
Please note that these are general medical recommendations. For the best homeopathic treatment for genetic conditions, it's always advisable to consult with a best homeopathic doctor
Muscles get Inflamed – PSORA
Increase in cell mass – SYCOTIC
Muscles get destroyed – SYPHILITIC
So it is a SYCO-SYPHILITIC disease
In diagnosing Duchenne Muscular Dystrophy (DMD), the first step is identifying the source of the genetic mutation. We achieve this by analyzing both the child's and mother's genes.
·If the mother's test is normal, it suggests a spontaneous mutation in the child. In these cases, we focus on the child's genetics to pinpoint the origin of the condition. Early detection, as seen with patient HJ, can lead to significant improvement.
·If the mother's test reveals a mutation, indicating she's a carrier, we consider both the child's and mother's medical history. This combined data allows us to create a personalized homeopathic treatment plan, often resulting in remarkable recoveries.
Remember, in genetic cases, the gene mutation cannot be reversed but the effect of the mutation on the body can be minimized if the treatment is started at an early age.
By adopting a holistic approach that addresses the underlying genetic factors and supports overall health, homeopathy offers a promising avenue for the management of Duchenne Muscular Dystrophy.
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