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Ayurvedic Treatment of Fabry Disease
Fabry Disease Treatment in Medical Astrology
Fabry disease, also known as
Anderson-Fabry disease, is a rare genetic disorder that affects multiple organs, including the
kidneys, heart, and skin. It falls under the category of
lysosomal storage diseases. Ayurvedic treatment of Fabry disease involves the use of specific
herbs and natural remedies to help manage the condition.It is a chronic disease that may worsen if not treated earlier. Since it affects multiple organs, it becomes crucial to understand the symptoms, and only with early intervention can the disease be controlled. Early detection plays a very important role in improving the quality of life. Modern medicines also offer treatments that include enzyme replacement or additional therapy. Ayurveda strengthens internal healing, and
astrology services provide insight into underlying energetic causes.
Overview of Fabry Disease
This disease results from a
genetic mutation that interferes with the function of an enzyme, leading to the accumulation of
biomolecules called sphingolipids. These substances build up in the
walls of blood vessels and other organs, causing significant health complications.
Fabry disease is inherited in an X-linked manner. Males are often affected with the disease, because they are the ones who carry only X Chromosomes. Females rarely suffer from this disease, except for mild symptoms. However, a female can be affected due to her genetics. The disease damages the tissues, increases inflammation, reduces blood flow, and eventually creates a dysfunction of the organs.
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Diagnosis of Fabry Disease
Fabry disease can be diagnosed using a
blood test that measures the activity of the affected enzyme called
alpha-galactosidase. However, in females,
genetic testing is also recommended. Timely intervention slows down the degeneration and helps reduce the damage to several organs. Newborn screening programs are also done to identify cases where
Fabry disease is genetic. Also, before planning future pregnancies, it is essential to get genetic counselling done.
Treatment Approaches for Fabry Disease:
- The treatment varies depending on the affected organs.
- The underlying cause can be addressed by replacing the missing enzyme.
Enzyme replacement therapy (ERT) reduces the accumulation of sphingolipids in the body. Additional or supportive care, like pain management therapy, heart monitoring, kidney monitoring, and lifestyle recommendations are provided. These are conventional treatment approaches. Despite these therapies, the patients continue to be affected by Fabry. At that time, Ayurveda and
Medical Astrology helped to provide holistic support.
What is the Underlying Principle of Fabry Disease?
Principles of Fabry Disease
Fabry disease is an
X-linked lysosomal disorder that leads to excessive deposition of
neutral glycosphingolipids in various organs, including the
vascular endothelium, epithelial cells, and smooth muscle cells. It is a
rare and inherited disease that can have
life-threatening consequences.The functioning of the cells and tissues is imbalanced due to the accumulation of sphingolipids. Gradually, it leads to structural damage, chronic inflammation, and impaired circulation. If the disease is not controlled, it could lead to strokes of the brain and heart, or severe neurological problems.
Organs Affected :
Affected Organs
- Heart
- Lungs
- Kidneys
- Skin
- Stomach
- Brain
Not all cases of Fabry do not experience similar organ failures. In some instances, when the kidney is involved, protein loss begins in the urine, which eventually leads to failure of the kidney. Cardiac issues arise when the heart muscles get thick, and there is an imbalance in heart rhythms. Neurologically, there could be dizziness, headaches, and strokes. Skin also gets affected a lot, and this is one of the first symptoms of the disease.
Who is Affected by Fabry Disease?
Fabry disease affects
both males and females across all ethnic groups. However,
men are usually more severely affected than
women. The symptoms of this disease are not uncommon. Many known diseases carry similar symptoms. However, this becomes more essential for healthcare professionals as well as patients to be aware of the disease to diagnose and treat it correctly.
Types of Fabry Disease
- Type 1 Fabry Disease (Classic FD) – Begins in childhood and is less common.
- Type 2 Fabry Disease – Develops later in life and is more common. Type 1 happens during childhood or early adolescence. The symptoms faced could be pain, skin rashes, or reduced sweating. Organ damage happens rapidly, and if it isn’t treated, it could lead to major health concerns. Type 2 happens during adult life. The symptoms are mild, but the heart and kidney is affected the most.
Other Names for Fabry Disease:
- Galactosidase Alpha Gene Deficiency
- Enzyme Alpha-Galactosidase A Deficiency
- Angiokeratoma Corporis Diffusum
- Ceramide Trihexosidase Deficiency
Understanding these terms is necessary for the patients while consulting specialists.
Symptoms of Fabry Disease
Common Symptoms:
- Burning sensation in hands and feet
- Tingling pain in limbs
- Skin rash
- Dizziness and general fatigue
- Damage to blood vessels in the eyes
- Reduced sweat production
- Intense body pain
- Cramps, gas, and diarrhea
- Stomach problems
- Heart enlargement and irregular heartbeat
- Thickening of the heart muscle and heart failure. Patients will experience burning or stabbing sensations, and these sensations are triggered by stress, weather changes, physical exertion, or even fever. Digestive symptoms happen daily, whereas heart and kidney symptoms will appear after significant damage has happened.
Other Symptoms:
Other Associated Symptoms
- Fever
- Hearing loss (Medical Astrology)
- Lung disease
- Ringing in the ears (tinnitus)
- Inability to perform strenuous exercise. Depression and mental health issues also rise because of the patient’s inability to endure the pain. There could be major psychological factors affecting the patient’s mental health. Therapy and counselling are needed a lot during this period.
What Population is Affected by Fabry Disease?
Fabry disease is relatively rare, but its prevalence has been studied:
Population Affected by Fabry Disease
Ayurvedic Treatment of Fabry Disease
Fabry disease is a
genetic disorder, but it can be
managed through Ayurveda. Ayurveda, an
ancient healing system, focuses on treating diseases using
herbal remedies derived from nature. As per Ayurveda, Fabry disease is not an isolated condition. There are deep imbalances in the doshas, tissues, that lead to Fabry disease. These grow over time and are very deeply entrenched in the body. Ayurvedic treatments treat the underlying causes, and not just the symptoms.
Ayurvedic Approach:
- Uses herbs, tree bark, and roots for treatment.
- Ayurveda identifies RASAYAN in the human body, similar to Ayurvedic herbs.
- Ayurvedic herbs have the potential to heal defective genes, reducing the intensity of the disease."RASAYAN aims to improve cellular health by providing it with nourishment. There are herbs in Ayurveda that support cellular repair, slow down degeneration, and enhance the vitality."
Medical Astrology Consultation for Fabry Disease
If you are struggling with
Fabry disease or any other difficult-to-treat disorder, you can consult our
Medical Astrologer, Prashant Kapoor, for guidance. Medical Astrology examines the planets that indicate chronic illness, organ damage, and long-term health challenges. Birth chart of individuals are considered, and the placement of the planets is analysed to adjust imbalances. Once these placements are identified, certain remedies are provided. These remedies include: Gemstones, Lifestyle changes, Mantras, Yantras, Donation, etc.
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A combined approach of modern medicine with Medical Astrology will provide a holistic path for individuals looking to treat Fabry.
