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What is Bests Disease? Best's Disease, more commonly referred to as Vitelliform Macular Dystrophy or Best Vitelliform Macular Dystrophy (BVMD), is an inherited eye disorder affecting the macula - the central part of retina responsible for providing sharp and detailed vision. The disorder was named for Friedrich Best from Scotland who first identified it during early 20th century research studies. Best's disease is typically passed on in an autosomal dominant fashion, meaning an affected individual has a 50% chance of passing the condition onto their children. The cause lies with mutations to the BEST1 gene which plays an essential role in supporting retinal pigment epithelium (RPE), an outer layer of cells located behind photoreceptor cells in the retina. Best's disease is characterized by yellow deposits called "vitelliform lesions" appearing in the macula, typically of variable size and shape. Over time, this may lead to an overall progressive loss of central vision over time - initially experienced through decreased visual acuity, distortion or difficulty performing tasks that require fine detail or central vision such as reading or recognising faces. As the disease advances, vitelliform lesions may undergo changes such as thinning, breaking apart, and scar tissue formation, leading to further vision loss as well as other complications like choroidal neovascularization (abnormal blood vessel growth) which may result in leakage of fluid or even bleeding within the macula. Best's disease typically affects both eyes, although its severity and rate of progression vary depending on an individual. Furthermore, symptoms can begin in childhood or adolescence for some while other may not notice any visual changes until adulthood. What are the Symptoms of Best’s Disease? Best's disease (vitelliform macular dystrophy) symptoms vary depending on who's affected and primarily targets the macula - the central part of retina responsible for detailed vision. Here are some symptoms associated with Best's disease: Blurred or Distorted Central Vision: Best's disease often manifests itself with decreased central vision. This may appear as blurry or hazy vision, difficulty reading small print, difficulty with recognising faces or fine details, difficulty reading small text etc. Metamorphopsia: Metamorphopsia refers to visual distortion where straight lines may appear wavy or bent, distorting their perception or making objects appear disfigured or misshapen. This symptom may affect object perception as they seem irregularly formed or misshapen. As Best's disease progresses, a central scotoma - or blind spot - may appear in the central visual field. This means there is loss of vision directly ahead of a person making it more difficult to see objects directly ahead of them. Vitelliform Lesions: Best's disease is distinguished by yellow or orange-colored deposits known as vitelliform lesions in the macula, typically round or oval in shape and of variable size. They result from lipofuscin buildup within retinal pigment epithelium cells resulting from their accumulation as waste products. Vision changes: Individuals living with Best's disease may experience fluctuations in their vision. This may involve periods of relatively stable vision followed by sudden shifts or worsening episodes. Noting the unique progression and severity of Best's disease for every individual can be daunting, however. While some may experience gradual vision decline over time, others may see symptoms rapidly worsen. If you or anyone you know are exhibiting any of the above symptoms it is wise to consult an ophthalmologist or retinal specialist for a thorough eye exam and proper diagnosis. What are the causes of Best’s Disease? Best's disease (vitelliform macular dystrophy) is generally caused by mutations to the BEST1 gene. This gene provides instructions for producing bestrophin-1 protein that plays an integral part in maintaining normal functioning of retinal pigment epithelium (RPE), an inner layer that protects photoreceptor cells in the retina. Best's disease is typically passed down autosomally dominant, meaning a mutation in one copy of the BEST1 gene from either parent is sufficient to trigger symptoms. Rarely, Best's can also be passed on recessively through both copies of its DNA being altered, necessitating two mutations to manifest. Individuals affected by Best's disease often possess specific mutations of the BEST1 gene that disrupt its normal function and lead to abnormalities within RPE cells and accumulations of lipofuscin waste products inside them, contributing to characteristic macula lesions known as "vitelliform lesions." These lipofuscin deposits contribute to this condition by creating characteristic "vitelliform lesions." Note that mutations to the BEST1 gene are the primary source of Best's disease; however, their exact mechanisms remain unknown and researchers continue to study this condition in order to gain more insights into its underlying causes and identify possible therapeutic approaches.

What is High Myopia? High myopia, also referred to as severe or pathological myopia, is an uncommonly high degree of nearsightedness (myopia). With high myopia, individuals typically exhibit an eyeball that protrudes too far behind the retina instead of directly on it causing light entering to focus in front of it instead of directly onto it and leading to blurred distance vision while near vision may remain clear. High myopia is defined by refractive errors exceeding -6.00 diopters; however, its severity can differ among individuals, with some experiencing refractive errors of greater than -8.00 or even exceeding -10.00 diopters. It typically appears in children or adolescence and progresses gradually over time. Regular eye examinations for those suffering from high myopia are essential in monitoring any changes to vision and early identification of potential complications. Sanjeevan Netralaya's Advanced Ayurvedic eye care has achieved impressive results in treating High Myopia. Through their patient-centric approach, personalized treatment plans are meticulously tailored to each individual's specific requirements and pain-free experiences are ensured without discomfort or side effects. What are the symptoms of High Myopia? High myopia (or severe myopia) is defined by an unusually high degree of nearsightedness. While its symptoms vary according to each individual, common manifestations include: · Blurred Distance Vision: When objects in the distance appear blurry or out-of-focus, near vision may still remain clear. · Difficulty with Distance Vision: People suffering from high myopia often struggle to see distant objects such as street signs, whiteboards and faces from far away. · Squinting or Eye Strain: Individuals with high myopia often strain their eyes when trying to focus on distant objects clearly, leading them to squint or strain their vision in an attempt to improve their vision. · Eye Fatigue: Prolonged visual tasks such as reading or using the computer may cause eye fatigue and discomfort for individuals with high myopia. · Poor distance vision can cause headaches when engaging in activities that require visual focus, leading to frequent headaches as a result of straining eyes. · Difficulties with Night Vision: High myopia may result in impaired night vision, making it challenging to see clearly in low-light conditions. · Increased Sensitivity to Glare: People suffering from high myopia may be particularly sensitive to bright lights and glare, leading to discomfort and vision difficulties. · Squinting or Holding Objects Close: Individuals with high myopia often unconsciously compensate for their blurred distance vision by unconsciously squinting or holding objects closer to their face in order to see them more clearly. Considerations should be given to the fact that these symptoms could also indicate other eye issues; to receive an accurate diagnosis it is vital to visit an eye care professional for a comprehensive eye examination and diagnosis. Regular check-ups for individuals with high myopia are especially essential in monitoring their eye health and detecting potential complications like retinal detachment or macular degeneration which could result from having such condition. Sanjeevan Netralaya’s Advanced Ayurvedic eye care stands as a highly effective treatment modality for High Myopia. At Sanjeevan Netralaya, each patient receives personalized attention, benefiting from meticulously crafted treatment plans that are uniquely tailored to address their specific needs. These specialized interventions prioritize patient comfort, offering a painless and comfortable experience, completely devoid of any associated discomfort or side effects. What are the causes of High Myopia? The exact causes of high myopia, also known as severe or pathological myopia, are not fully understood. However, several factors have been identified as potential contributors to its development. These causes include: · Genetic Factors: There is a strong genetic component to myopia, including high myopia. Individuals with who have a family history are more likely to develop high myopia. Multiple genes are believed to play a role in determining the development and progression of myopia. · Environmental Factors: Environmental factors, such as prolonged near work activities (such as reading, writing, or using electronic devices) and lack of outdoor activities, have been associated with an increased risk of myopia development, including high myopia. Insufficient exposure to natural light and spending excessive time on close-up tasks may contribute to the elongation of the eyeball. · Structural Abnormalities of the Eye: In individuals with high myopia, the eyeball is often longer than normal, which leads to the focusing of light rays in front of the retina instead of directly on it. Structural abnormalities of the cornea or lens may also contribute to the development of high myopia. · Imbalance in the Growth of Eye Components: The growth and development of the eye involve complex processes that require a delicate balance. In high myopia, there may be an imbalance in the growth of certain eye components, such as the sclera (the white outer layer of the eye), choroid (the vascular layer beneath the retina), and retina, leading to excessive elongation of the eyeball. · Hormonal and Systemic Factors: Some studies suggest that hormonal and systemic factors, such as changes during puberty or hormonal imbalances, may influence the development of high myopia. However, further research is needed to establish a clear link. It's important to note that while these factors are believed to contribute to the development of high myopia, the condition is likely influenced by a combination of genetic and environmental factors. High myopia can also be influenced by individual variations and interactions between these factors. Further research is needed to fully understand the underlying causes of high myopia and its complex interplay with various factors. Sanjeevan's Advanced Ayurvedic eye care is effective in treating High Myopia. Sanjeevan Netralaya treats each patient with a unique treatment plan. The specialised treatments are tailored to the individual and cause no pain, discomfort, or side effects. It is important to have your eyes examined regularly so book your appointment now!

What is Eales Disease? Eales disease is an rare, idiopathic vascular condition primarily affecting the retina that results in inflammation and retinal vessel occlusions, first identified by British ophthalmologist Henry Eales in 1880. Primarily impacting young males from India and Pakistan as well as South Asia regions. Although its exact cause remains unknown, vascular abnormalities and genetic predisposition are thought to play a part. Recognizing symptoms such as blurred vision, floaters and peripheral vision loss is essential for early diagnosis and treatment. Sanjeevan Netralaya's Advanced Ayurvedic eye care, recognized for treating over 600,000 retinal cases successfully and providing personalized treatments tailored specifically to individual patient needs is unrivaled in treating Eales Disease. Each Sanjeevan patient receives tailor-made, noninvasive treatment designed for their own specific requirements which ensure a painfree experience - the key element to prioritizing ocular health! To achieve optimal eye health it is vitally important that regular eye examinations be scheduled without delay - secure your appointment immediately to maximize results! What are the symptoms of Eales Disease? Eales disease symptoms vary between people, usually occurring gradually over time. Here are the more frequently seen indicators of Eales disease: · Blurred Vision: One of the main signs and symptoms of Eales disease is blurriness or reduced visual acuity, with affected individuals often finding difficulty in focusing and perceiving objects as blurry. · Floaters: Floaters are small specks or cobweb-like structures that appear to float across your visual field, often appearing dark or transparent, that interfere with clear vision and may obstruct clear sightlines. As eyes move they tend to shift accordingly causing these floaters to drift across. · Loss of Peripheral Vision: Eales disease may lead to the gradual deterioration of peripheral vision, commonly referred to as tunnel vision. Affected individuals may notice their field of view narrowing drastically and their ability to see objects through side vision diminished significantly. · Visual Field Defects: As disease progresses, certain areas of the visual field may become blank or distorted - this may present itself in form of dark spots or patches within vision. · Vitreous Hemorrhage: Eales disease may lead to bleeding in the vitreous gel that fills the center of your eye, potentially resulting in sudden and significant vision impairment, leading to a dark or shadowy appearance of vision. · Retinal Detachment: At advanced stages, Eales disease increases the risk of retinal detachment, in which the retina detaches from its supporting tissue and detaches completely from visual perception. If left untreated promptly, retinal detachment can lead to permanent vision loss; symptoms include flashes of light or the perception of curtains or veil covering part of visual field or sudden increase in floaters. This condition requires medical intervention immediately as failure to do so could be fatal for permanent vision loss. Note that not everyone affected by Eales disease will experience every symptom listed above, though symptoms can differ in terms of their severity and progression; some may only experience mild issues while others could experience more severe visual impairment. It's essential to seek professional medical advice if any symptoms appear; an eye care professional should provide accurate diagnoses and effective management solutions. With an outstanding track record of treating over 600,000 retinal cases successfully, Sanjeevan's Advanced Ayurvedic Eye Care stands out as an effective therapeutic approach against Eales Disease. Sanjeevan Netralaya provides customized treatments tailored specifically to meet each patient's specific needs; their tailored regimens offer unparalleled patient comfort without pain, discomfort or adverse side effects. Scheduling regular ocular assessments is key in safeguarding visual wellbeing - take preventive steps now by booking an appointment today! What are the causes of Eales Disease? The exact cause Eales disease remains unknown, though it has been classified as an idiopathic disorder. Multiple factors are thought to contribute to its development, including: · Vascular Abnormalities: Eales disease is characterized by abnormal changes to retinal blood vessels. These changes include inflammation, narrowing of vessels (vasculitis), and formation of new fragile blood vessels (neovascularization). It is thought that these vascular abnormalities play a key role in its development; however, its cause remains elusive. · Genetics: No specific gene mutation has yet been linked with Eales disease; however, genetic predisposition may increase susceptibility. Studies indicate certain genetic factors could make certain individuals more prone to Eales. More research needs to be completed in order to establish definitive links. · Environmental Factors: Exposure to toxins or infections has been proposed as potential triggers for Eales disease. Some studies have reported an association between exposure to tuberculosis (TB) as well as other infectious agents and Eales disease; however, any direct relationship must first be explored further before any decisions on prevention are made. Note that these factors are considered potential contributors to Eales disease, but none has been conclusively established as its sole cause. Eales disease likely arises from genetic predisposition, vascular abnormalities and environmental influences acting together. More research needs to be conducted in order to understand its underlying mechanisms and identify specific causes. Sanjeevan's Advanced Ayurvedic eye care has achieved resounding success in the treatment of over 600,000 retinal cases, establishing it as a highly effective remedy for Eales Disease. At Sanjeevan Netralaya, each patient benefits from an exclusive treatment plan, meticulously curated to cater to their individual needs. These specialized interventions boast a remarkable feature - they are entirely painless, comfortable, and devoid of any associated side effects. Maintaining a regular eye examination schedule is of paramount importance in nurturing ocular health. Act now by securing your appointment.

What is Stargardt Disease? Stargardt disease, also referred to as Stargardt macular dystrophy or juvenile macular degeneration, is an inherited disorder affecting the macula - the small central area at the back of each eye that provides sharp, detailed vision in straight lines. Disease typically begins during childhood or adolescence and progresses over time to cause progressive vision loss, including central vision loss, difficulty reading, difficulties recognising faces and loss of color vision. Stargardt disease is caused by mutations to the ABCA4 gene, which provides instructions for producing an ATP-binding cassette transporter A4 protein that transports lipofuscin away from retinal cells - in those suffering from Stargardt disease, lipofuscin accumulates and eventually kills macula cells, leading to vision loss over time. Current treatments of Stargardt disease do not offer a permanent solution, but treatments may help manage symptoms and slow progression such as tinted glasses, vitamin supplements, or low-vision rehabilitation. Stargardt disease is an inherited disorder caused by mutations to genes passed down from parent to child. More specifically, Stargardt disease stems from mutations to ABCA4 gene which provides instructions for making an ATP-binding cassette transporter A4 protein involved with transporting lipofuscin out of retina cells. Sanjeevan's Advanced Ayurvedic eye care is effective in treating Stargardt Disease. Sanjeevan Netralaya treats each patient with a unique treatment plan. The specialised treatments are tailored to the individual and cause no pain, discomfort, or side effects. It is important to have your eyes examined regularly so book your appointment now! What are the causes of Stargardt Disease? Stargardt disease is caused by mutations to the ABCA4 gene that lead to an accumulation of lipofuscin in cells of the macula, ultimately leading to their death and gradual vision loss. Stargardt is passed down autosomally recessively; meaning a person must inherit two copies from each parent in order to develop symptoms; those inheriting only one mutated copy from either parent are known as carriers who do not usually show signs or symptoms but can pass the gene onto future generations. Stargardt disease can be caused by mutations to the ABCA4 gene, with severity and progression depending on which mutation has taken place. Sanjeevan Netralaya's Ayurvedic Advanced Eye Care is an effective treatment for Stargardt Disease. Sanjeevan Netralaya's specialised tailor-made treatments do not cause any pain, discomfort or adverse side effects. It is important to have your eyes examined regularly so book your appointment now! What are the symptoms of Stargardt Disease? Stargardt disease affects central vision, or your ability to see fine details and objects directly in front of you. Symptoms may differ depending on the person suffering, but may include: Blurry or distorted vision when looking directly at objects. Difficulties reading text that appears smudged, distorted, or blurry. Loss of color vision where colors appear washed-out or faded-out. And difficulty recognising faces or familiar objects as soon as they enter your field of vision. Sensitivity to bright light or difficulty adapting to changes in lighting. Visual hallucinations or illusions such as seeing patterns or shapes that do not actually exist. Progressive vision loss over time that could eventually lead to legal blindness. Stargardt disease typically impacts both eyes equally, with symptoms often starting in childhood or adolescence; however, they can sometimes appear later in life. Not everyone experiencing Stargardt experiences all of its symptoms, as its severity and progression varies considerably among individuals. Sanjeevan Netralaya has a customised treatment plan for each patient and treats Stargardt Disease effectively. There is no discomfort, pain or side effect from the treatments. You should have your eyes checked regularly, so make an appointment today!

What is Parafoveal Telangiectasia? Parafoveal telangiectasia, also known as idiopathic juxtafoveal telangiectasia type 2 or Macular Telangiectasia Type 2, is an uncommon eye disease that affects the blood vessels of the macula–the central part responsible for sharp, detailed vision–as a progressive and irreversible condition. Parafoveal Telangiectasia is more common in those over 40 years of age and more prevalent among women than men. Though the exact cause remains unknown, it’s believed to be caused by disruptions to blood flow and oxygen supply to the retina. Parafoveal Telangiectasia may present with blurred vision, difficulty reading faces and face recognition, visual hallucinations or “phantom images,” for some individuals. Parafoveal Telangiectasia is currently incurable, but treatments like intravitreal injections and laser therapy can be used to alleviate symptoms and slow down its progression. To identify any visual changes and determine the most suitable treatment option, patients should receive regular eye exams with their vision monitored to detect any changes and determine the most suitable course of action. What is Parafoveal Telangiectasia Type 2? Parafoveal Telangiectasia Type 2 (also referred to as Macular Telangiectasia Type 2 and Idiopathic Jxtafoveal Telangiectasis Type 2) is a rare condition that affects the blood vessels of the macula, or central part of the retina. This condition is most common among those over 40 and typically diagnosed as part of general aging. Parafoveal Telangiectasia type 2, while its cause remains unknown, is thought to be due to both genetic and environmental factors. It has been linked to mutations in the CA4 gene that regulates blood flow; this has also been associated with parafoveal telangiectasia type 2. Parafoveal Telangiectasia type 2, which may manifest in various ways, usually causes blurry or distorted vision and difficulty reading faces. It may also result in a gradual loss or reduction of central vision. Some individuals may even experience visual hallucinations and “phantom images”. Parafoveal Telangiectasia Type 2 is currently incurable; however, intravitreal injections or photodynamic therapy can be used to treat symptoms and slow down its progression. Patients with parafoveal telangiectasia type 2 should receive regular eye exams to detect any visual changes and determine the most suitable treatment options. What are the Symptoms of Prarafoveal Telangiectasia? Parafoveal Telangiectasia symptoms vary depending on the severity, but typically include: Vision blurred or distorted Difficulty recognizing faces or reading them Gradual loss in central vision with time Color vision abnormalities Sensitivity to bright light or glare Visual hallucinations and “phantom images” Vision hallucinations or ghost images? Blind spots and dark spots in the vision field At the early stages of diabetes, some people do not experience symptoms. However, routine eye exams may detect it early on; symptoms become more evident as time goes on and can interfere with everyday tasks like reading, driving, using a mobile device or computer. Parafoveal Telangiectasia symptoms may be due to other eye conditions as well. To accurately diagnose this condition, an optometrist or ophthalmologist must perform a comprehensive eye exam. What are the Stages of Parafoveal Telangiectasia? Parafoveal Telangiectasia type 2 may be divided into three stages depending on its severity and extent. Stage 1: At this stage, there are no visible changes to the retina. People with parafoveal Telangiectasia type 2 may not feel any symptoms and this condition is typically detected through routine eye exams. Stage 2: At this stage, there may be visible dilation or abnormal branching of the retina’s blood vessels. Leakage of fluids or blood from these blood vessels can lead to swelling and edema around the macula, leading to blurred vision, difficulty reading faces or recognizing them, as well as other visual symptoms. Stage 3: At this stage, retinal changes continue to progress with the appearance of small holes or cavities in the macula. This can result in loss of central vision, difficulty reading or driving, and facial recognition problems. Parafoveal Telangiectasia Type 2 may not progress through all three stages at once; some individuals may experience a slower progression. Regular eye exams and monitoring are essential to detect vision changes and determine the most suitable course of treatment. What are the Causes of Parafoveal Telangiectasia? Research continues to elucidate the cause of parafoveal telangiectasia, suggesting there could be both genetic and environmental elements at work. Genetics: Studies have revealed that Parafoveal Telangiectasia Type 2 is often caused by mutations in the CA4 gene, an enzyme which regulates blood flow to the retina and may lead to abnormal blood vessel formation or function. Environment: Studies have suggested that environmental factors, such as smoking and exposure to chemicals, may also have an impact. Parafoveal Telangiectasia can be caused by various idiopathic conditions. Parafoveal Telangiectasia, though rare, does occur occasionally. People with a family history or other risk factors for the disorder may have an increased likelihood of developing it; however, this is not always the case. To detect vision changes and determine the most suitable treatment plan, those at greater risk should receive regular eye examinations and monitoring to detect them early. What is Idiopathic Parafoveal Telangiectasia? Idiopathic Parafoveal Telangiectasia (IPT) is an unrelated form of Parafoveal Telangiectasia that has no known medical cause. IPT may also be referred to as Parafoveal Telangiectasia Type 1. IPT (irreversible proliferative hyperplasia) is an uncommon disorder that affects the blood vessels of the macula (central part of the retina). It typically affects those over 40 years old and causes blurry or distorted vision as well as difficulty reading faces or recognizing people. Some IPT patients may experience visual hallucinations and “phantom” images in rare cases. Though the exact cause of IPT remains uncertain, researchers believe it to be a result of both genetic and environmental influences. Unlike Parafoveal Telangiectasia Type 2, however, this condition isn’t linked to any particular genetic mutation. Unfortunately, there is currently no cure for IPT. However, treatments like intravitreal injections or photodynamic therapy can help treat symptoms and slow down its progression. It is recommended that those with IPT receive regular eye exams to detect visual changes and determine the most suitable treatment option. What does Perifoveal mean? The area surrounding the fovea, known as perifoveal, provides sharp and detailed vision. Measuring 500-1500 microns across, this central region of the retina contains abundant blood vessels and photoreceptor cells for enhanced vision. Our visual system is highly dependent on the perifoveal region. This region processes fine details, color vision and visual acuity – essential for reading faces, recognizing objects, and performing other visual tasks. Vision loss or distortion can be caused by conditions in the perifoveal region. To detect changes and determine the best course of action, have regular eye exams and monitor your vision closely. What is Parafoveal Area? Parafoveal is a small area in the middle of the retina just outside the fovea, responsible for sharp and detailed vision. At 500-1500 microns wide, this region contains abundant photoreceptor cells as well as blood vessels. Parafoveal is an area that plays a significant role in our visual system, responsible for fine details, color vision and visual acuity. It helps us read faces, recognize faces and perform other visually demanding tasks. Parafoveal Telangiectasia is a condition in which blood vessels in the parafoveal region become affected, leading to abnormal branching and dilation of vessels as well as other retinal changes. This may cause blurry or distorted vision as well as other visual symptoms. To detect changes and determine an appropriate course of action for patients suffering from Parafoveal Telangiectasia, they should have regular eye exams with monitoring their vision.

What is Optic Neuropathy? Optic neuropathy is the term for damage or dysfunction of the optic nerve, which transmits visual information from the eye to the brain. There are various causes of optic neuropathy such as injury, inflammation, infection, exposure to toxins, and underlying medical conditions like multiple sclerosis or diabetes. When the optic nerve is damaged, it can lead to a variety of symptoms depending on its severity and extent. These may include blurred or reduced vision, loss of peripheral vision, difficulty distinguishing colors and in severe cases complete blindness. Treatment for optic neuropathy depends on what caused it and may include medications, surgery or lifestyle changes. It’s important to seek medical help immediately if you experience any changes in your vision or other symptoms that could be related to optic neuropathy. What are the Signs and Symptoms of Optic Neuropathy? Optic neuropathy presents with a range of signs and symptoms depending on the cause and extent of nerve damage to the eye. Common indications include: Vision impairments such as blurry vision or difficulty focusing, loss of visual acuity/ sharpness, reduced peripheral vision (tunnel vision), difficulty distinguishing colors, increased sensitivity to light sources and pain or discomfort around the eyes may all occur. Loss of contrast sensitivity (difficulty distinguishing objects from their backgrounds) Witnessing flashing lights or other visual disturbances Partial or complete vision loss in one or both eyes It’s important to note that some people with optic neuropathy may not experience any symptoms when first diagnosed; the condition can often be detected during a routine eye exam. If you notice any changes to your vision or other symptoms that could be indicative of optic neuropathy, seek medical help promptly. What type of genetic disorder is Leber’s hereditary Optic Neuropathy? Leber’s hereditary optic neuropathy (LHON) is a mitochondrial genetic disorder. Mitochondrial DNA is passed down from the mother, so LHON can be inherited maternally if her mother carries a mutation causing LHON; therefore, her offspring could also be at risk of inheriting this mutation. LHON is caused by mutations in mitochondrial DNA that alter the function of mitochondria in the optic nerve, responsible for transmitting visual information from the eye to the brain. When these mitochondria fail to work properly, vision loss and other symptoms associated with LHON may develop. LHON (Leukodystrophies of the Ocular Nerve) is a relatively uncommon genetic disorder, typically affecting young adults in their 20s and 30s. Unfortunately, there is currently no cure for LHON; however, treatments may help slow its progression and improve visual function for some individuals. Therefore, those living with this condition should receive ongoing care from an experienced healthcare provider like Sanjeevan Netralaya to monitor progress and receive advice as necessary. What Causes Optic Neuropathy? Optic neuropathy can be caused by a number of factors, including: Trauma: Any injury to the head or eye may result in damage to the optic nerve. Inflammation: Optic nerve inflammation can be caused by autoimmune disorders, infections, or other underlying medical issues. Toxins: Exposed to toxic agents such as methanol, ethylene glycol or tobacco smoke can damage the optic nerve. Ischemia: When blood flow to the optic nerve is disrupted, it can result in ischemic optic neuropathy. Infection: Certain infections such as herpes, Lyme disease or syphilis may lead to optic neuropathy. Genetics: Genetic disorders such as Leber’s hereditary optic neuropathy (LHON) can lead to optic neuropathy. Nutritional Deficits: A lack of vitamin B12 or other essential nutrients may cause optic neuropathy. Medications: Some medications, such as some antibiotics, may cause optic neuropathy as a side effect. Medical Conditions: Underlying medical conditions like multiple sclerosis, diabetes, or high blood pressure may increase the likelihood of developing optic neuropathy. It is essential to seek medical help if you experience any vision changes or other symptoms associated with optic neuropathy. Your healthcare provider can accurately diagnose the cause and recommend appropriate treatment. Can Optical Neuropathy be Prevented From getting worse? Optic neuropathy can vary in severity depending on its underlying cause and extent of nerve damage. In some cases, early diagnosis and treatment can help slow or even stop its progression; for instance, if diabetes or high blood pressure is to blame for developing optic neuropathy, managing these conditions effectively could help protect against further nerve damage. In certain cases, such as Leber’s hereditary optic neuropathy (LHON), there may not be a cure available; however, treatments like idebenone – an antioxidant – may help slow its progression and enhance visual function for some individuals . It is essential to seek immediate medical help if you experience any changes in your vision or other symptoms that could be indicative of optic neuropathy. Early diagnosis and treatment will improve outcomes and protect the optic nerve from further damage. How is optic Neuropathy Diagnosed? Diagnosing optic neuropathy usually involves a medical history review, comprehensive eye exam and additional diagnostic tests. At a medical history review, your healthcare provider will inquire about your symptoms, when they began, and any underlying medical conditions or medications that could be contributing to them. A comprehensive eye exam includes several tests to evaluate the function and health of your eyes and optic nerve, such as visual acuity tests, visual field tests, pupil exams and examination of the back of the eye with an ophthalmoscope. Additional diagnostic tests that could be utilized to confirm optic neuropathy include: Optical Coherence Tomography (OCT): This imaging test utilizes light waves to produce detailed pictures of the retina and optic nerve. Visual Evoked Potential (VEP): This test measures the electrical activity in the brain in response to visual stimulation and can help evaluate the function of the optic nerve. Magnetic Resonance Imaging (MRI): This imaging test can help detect any abnormalities or injuries to the optic nerve. Blood Tests: Blood tests can identify any underlying medical conditions that could be causing your symptoms, such as diabetes or autoimmune diseases. The specific diagnostic tests required will depend on the cause and extent of your optic neuropathy. Once a diagnosis has been made, your healthcare provider can suggest appropriate treatments to manage the condition and protect the optic nerve from further harm. What is Optic Neuropathy Vision? Optic neuropathy vision refers to vision changes caused by damage to the optic nerve. The optic nerve transmits visual information from the eye to the brain, so when this nerve is damaged it can lead to various visual symptoms. Optic neuropathy vision symptoms vary depending on the underlying cause and extent of damage to the optic nerve. Common signs that someone may suffer from optic neuropathy vision include: Blurred vision Loss of peripheral vision Decreased color vision Diminished contrast sensitivity Central scotoma (a blind spot in the center of one’s visual field) Visual distortion such as straight lines appearing wavy or distorted Visual hallucinations (in some cases) The severity of these symptoms depends on the extent of damage to the optic nerve. In some cases, symptoms may be mild and develop gradually over time; conversely, other cases may present with more immediate manifestations. If you notice any symptoms that could be related to optic neuropathy vision, it is essential that you seek immediate medical help. Your healthcare provider can determine the source of your symptoms and suggest treatments to manage the condition while protecting the optic nerve from further damage. Is Optic Neuropathy Progressive? Optic neuropathy may progress slowly or rapidly, depending on the underlying cause and extent of damage to the optic nerve. In some cases, mild damage may take place over time while in others it may be more severe and progress more rapidly. The progression of optic neuropathy may differ based on the treatments available and their efficacy. For instance, if the cause is an underlying medical condition like high blood pressure or diabetes, proper management of that condition could potentially slow or even stop progression towards optic neuropathy. It is essential to seek medical help if you experience any vision changes or other symptoms associated with optic neuropathy, as early diagnosis and treatment can help slow or stop its progression. How Common is Optic Neuropathy? The incidence of optic neuropathy varies depending on its underlying cause. Common causes include glaucoma, ischemic optic neuropathy and optic neuritis. Glaucoma is one of the leading causes of optic neuropathy and estimates indicate it affects over 60 million people worldwide. Ischemic optic neuropathy affects between 2-10 per 100,000 individuals annually, while optic neuritis strikes anywhere from 1-5% annually. Leber hereditary optic neuropathy (LHON) is a rare genetic condition that affects approximately one in 30,000 individuals. Generally, LHON occurs in young adults and more often affects men than women. Optic neuropathy is a rare disorder, but it can have an enormous effect on vision and quality of life. If you are noticing changes to your vision or other symptoms associated with optic neuropathy, it is essential that you seek prompt medical care from an experienced healthcare provider. Can You Recover from Optic Neuropathy? Optic neuropathy has an underlying cause and the severity of the damage to the optic nerve. In some cases, recovery may be possible and full vision restored with timely treatment; in others however, irreversible damage has occurred and vision loss is permanent. If the optic neuropathy is due to a treatable condition such as nutritional deficiency or medication toxicity, treating the underlying issue can help improve vision. In certain cases, medications or surgery may be employed to manage symptoms of optic neuropathy and protect the optic nerve from further harm. However, in cases of significant optic nerve damage such as advanced glaucoma or traumatic optic neuropathy, vision loss may be permanent and irreversible. In such cases, management of the condition should focus on preventing further vision loss while improving quality of life through vision rehabilitation and support services. It is critical to seek medical help if you experience any changes in your vision or other symptoms that could be indicative of optic neuropathy. Early diagnosis and treatment can help avoid further damage to the optic nerve and increase the chances for recovery. What are the best Treatments for Traumatic Optic Neuropathy? Sanjeevan Netralaya has ADVANCED AYURVEDIC EYE CARE treatments which are the best for treating Optic Neuropathy. Sanjeevan Netralaya has treated over 6,000,000 patients with a range of retinal issues. Their success rate is 100%. Additionally, all of our treatments are customized to each patient so that there is no discomfort or side effects.

Optic Atrophy occurs when the optic nerve gets damaged due to shrinkage by the degeneration of the retinal ganglion cell axons and stops carrying impulses from your eye to your brain. One of the most common reasons for the Atrophy (deuteriation) occurs due to poor blood flow and is more common in adults. Optic Atrophy causes multiple vision problems, eventually leading to the patient being blind. What are the causes of Optic Atrophy? Impulses are sent to the brain from the eye through the optic nerve which comprises of nerve fibres. Optic Atrophy occurs when these impulses aren’t able to be sent to the brain due to factors and interferences. These factors include: Poor Blood Flow Glaucoma Anterior Ischemic Optic Neuropathy, otherwise known as a stroke in the Optic Nerve Pressure on the Optic Nerve that is caused by a tumour The Optic Nerve may get swollen due to inflammation caused by Multiple Sclerosis A birth defect Family History What are the symptoms of Optic Atrophy and when should I see a doctor? Symptoms of Optic Atrophy may seem mild in the beginning but it is imperative to visit your doctor at the earliest for any kind of vision problem. Symptoms of Optic Atrophy include: Blurry Vision or reduction in the sharpness of vision Problems identifying colour Problems with Side Vision or Peripheral Vision All vision related issues must be dealt with as soon as symptoms start to appear as they may be a part of bigger health problems. How does my doctor diagnose Optic Atrophy? Optic Atrophy is diagnosed by an ophthalmologist using an op ophthalmoscope. The doctor will examine the optic disc, which is at the back of the eye where the optic nerve enters the eye. If the doctor suspects a tumour, you may be asked to get an MRI Scan. Can Optic Atrophy be treated? Although Modern Medicine does not have a cure for Optic Atrophy, the cure depends on that the cause of the problem is. For instance, if the cause of the Optic Atrophy is an inflammation due to MS or a Tumour, vision might return to normal when the inflammation reduces. For patients with Glaucoma, if Glaucoma is caught early, optic Atrophy can be treated to grow slower which is why it is important to visit your doctor as soon as problems in vision arise. The most effective way of treating Optic Atrophy is with ADVANCED AYURVEDIC EYE CARE treatments provided by Sanjeevan Netralaya. Sanjeevan Netralaya has treated over 6 lakh patients suffering from an array of retinal issues with a 100% success rate. Moreover, our treatments are tailer made to every patient making sure they are treated to perfection without causing harmful and uncomfortable side effects.

What is Central Retinal Artery Occlusion Central Retinal Artery Occlusion is a condition where blood flow to the retina is stopped. This is usually caused by a clot (or embolus) that travels to central retinal artery, and gets lodged in the vessel. The blockage cuts off blood flow to all of the retina. Permanent vision loss can be prevented by prompt medical attention for CRAO. The vision loss in the affected eye is often permanent and will cause vision loss. CRAO is similar to BRAO in that it can be caused by trauma, atherosclerosis and hypercoagulable states. It is important that CRAO is less common than BRAO but has a worse prognosis. Sanjeevan Netralaya's Advanced Ayurvedic Eye Care has effectively treated over 6 lakh patients across India and successfully treats Central Retinal Artery Occlusion without causing any harmful side effects or discomfort. Do if you have any symptoms of Branch Retinal Artery Occlusion, do not prolong your treatment. Book your appointment at your closest Sanjeevan Netralaya clinic today. What are the causes of Central Retinal Artery Occlusion Central Retinal Artery Occlusion is caused by a blockage of the central retinal artery. This is the main blood vessel that supplies blood the retina. The causes of CRAO are the same as those of Branch Retinal Artery Occlusion. 1. Atherosclerosis is a buildup of plaque in blood vessels that can lead to blood clots in the retinal blood vessel. 2. Cardiac Emboli is a form of blood clots in the heart that travel to the retinal artery and become stuck and prevent blood flow. 3. Hypercoagulable states are medical conditions that increase the risk of blood clot formation, such as antiphospholipid syndrome and factor V Leiden deficiencies. 4. Giant cell arteritis is an inflammation of blood vessels that can cause blockage of the retinal vessel. 5. Trauma: A clot can form in the retinal vessel if there is an injury to the head or eye. 6. Vasculitis is an inflammation of blood vessels that can lead to narrowing or obstruction of the retinal vessel. 7. Carotid arterial stenosis: A narrowing of the carotid vein can lead to emboli that travel to the retinal bloodstream. It is important to remember that CRAO can be caused by many factors. An ophthalmologist, along with other specialists, will need to examine the patient thoroughly in order to determine the cause of the problem and offer appropriate treatment. Sanjeevan Netralaya's Advanced Ayurvedic Eye Care has effectively treated over 6 lakh patients across India and successfully treats Central Retinal Artery Occlusion without causing any harmful side effects or discomfort. Do if you have any symptoms of Branch Retinal Artery Occlusion, do not prolong your treatment. Book your appointment at your closest Sanjeevan Netralaya clinic today. What are the symptoms of Central Retinal Artery Occlusion The symptoms of Central Retinal Artery Occlusion can vary depending upon the extent and location of the occlusion. However, they are usually: Sudden, unremarkable loss of vision: This is most common symptom in CRAO. It can cause mild to severe vision loss and even complete blindness. Visual field defects: This is the loss of vision in one eye. There is usually no peripheral vision. Blurred vision: Although this is less common in BRAO than it is in BRAO. However, it can still occur when the occlusion has been partial. Color vision may change: Because the retina is not receiving enough blood, the affected area may appear grayish or white. Redness in the eye may be caused by inflammation of blood vessels. Headaches: Occlusion can cause headaches in some people. Systemic symptoms: Other conditions, such as giant cell arthritis, can cause systemic symptoms like fever, malaise and jaw claudication. It is important that you remember that symptoms of CRAO may appear suddenly and can progress quickly. Usually, within minutes. To prevent permanent vision loss, seek immediate medical attention if you have sudden vision loss or any other symptoms of CRAO. Sanjeevan Netralaya's Advanced Ayurvedic Eye Care has effectively treated over 6 lakh patients across India and successfully treats Central Retinal Artery Occlusion without causing any harmful side effects or discomfort. Do if you have any symptoms of Branch Retinal Artery Occlusion, do not prolong your treatment. Book your appointment at your closest Sanjeevan Netralaya clinic today. How is Central Retinal Artery Occlusion diagnosed? Usually, Central Retinal Artery Occlusion is diagnosed by a combination eye exam and imaging tests. The following are some of the most commonly used diagnostic tests to diagnose CRAO: 1. Ophthalmoscopy is an examination of the eye with a special instrument called an "ophthalmoscope". This allows the doctor to view the blood vessels within the retina. 2. Fluorescein angiography is a test that injects a special dye into a vein. Photographs of the retina are taken to identify blockages in blood vessels. 3. Optic coherence tomography: This non-invasive imaging technique uses light waves to produce detailed cross-sectional images. 4. Ultrasonography of your eye: This is a test that uses sound waves and creates images of your eye, including blood vessels. 5. Doppler ultrasound: This is a test that uses sound waves in order to determine the direction and speed of blood flow within the retinal vessels. 6. Magnetic Resonance Angiography, (MRA), or Computed Tomography Angiography(CTA) are imaging tests that show blood vessels in the brain and eyes more clearly. Sometimes, additional tests are required to diagnose the root cause of CRAO. These tests include blood tests to rule out blood clotting disorders and tests to assess the heart and blood vessels. It is important to remember that CRAO can be a serious condition and requires immediate medical attention in order to prevent permanent vision loss. For the best possible outcome, it is important to get a prompt referral to an eye doctor who is experienced in retinal vascular disease. Sanjeevan Netralaya's Advanced Ayurvedic Eye Care has effectively treated over 6 lakh patients across India and successfully treats Central Retinal Artery Occlusion without causing any harmful side effects or discomfort. Do if you have any symptoms of Branch Retinal Artery Occlusion, do not prolong your treatment. Book your appointment at your closest Sanjeevan Netralaya clinic today. What is the treatment for Central Retinal Artery Occlusion Sanjeevan Netralaya's Advanced Ayurvedic Eye Care has effectively treated over 6 lakh patients across India and successfully treats Central Retinal Artery Occlusion without causing any harmful side effects or discomfort. Do if you have any symptoms of Branch Retinal Artery Occlusion, do not prolong your treatment. Book your appointment at your closest Sanjeevan Netralaya clinic today. Can Central Retinal Artery Occlusion be cured Permanent vision loss can result from Central Retinal Artery Occlusion (CRAO). Treatment success depends on the cause, prompt diagnosis, treatment and how severe the damage to the retina. If the occlusion has been caused by a clot, embolus, or other condition that can either be surgically or medically dissolved, prompt treatment can help prevent further damage to blood vessels and restore blood flow, although vision loss may still be present. In most cases, however, vision loss is irreversible. Most patients will experience permanent visual loss. It is important to remember that CRAO can be a serious condition and requires immediate medical attention in order to prevent permanent vision loss. For the best possible outcome, it is important to get a prompt referral to an eye doctor who is experienced in retinal vascular disease. Sanjeevan Netralaya's Advanced Ayurvedic Eye Care has effectively treated over 6 lakh patients across India and successfully treats Central Retinal Artery Occlusion without causing any harmful side effects or discomfort. Do if you have any symptoms of Branch Retinal Artery Occlusion, do not prolong your treatment. Book your appointment at your closest Sanjeevan Netralaya clinic today.

What is Branch Retinal Artery Occlusion Branch retinal artery occlusion is a condition where the blood flow to a branch is blocked. This can cause vision loss or decreased in the affected eye. This can be caused by a clot (or embolus) that travels to a branch of the retinal artery. It blocks blood flow to a part of the retina. BRAO is a serious condition and requires immediate medical attention in order to prevent permanent vision loss. Sanjeevan Netralaya's Advanced Ayurvedic Eye Care has successfully treated more than 6 lakh patients in India and treats Branch Retinal Artery Occlusion without causing side effects and discomfort. If you are experiencing symptoms of Branch Retinal Artery Occlusion please begin your treatment immediately. Book your appointment at your closest Sanjeevan Netralaya clinic today. What are the causes of Branch Retinal Artery Occlusion There are many factors that can cause branch retinal artery occlusions (BRAO). The most common causes are: 1. Atherosclerosis is a buildup of plaque in blood vessels that can lead to blood clots in the retinal blood vessel. 2. Cardiac Emboli is a form of blood clots in the heart that travel to the retinal artery and become stuck and prevent blood flow. 3. Hypercoagulable states are medical conditions that increase the risk of blood clots, such as factor V Leiden Deficit, antiphospholipid syndrome, and others. 4. Giant cell arteritis is an inflammation of blood vessels that can cause blockage of the retinal vessel. 5. Trauma: A clot can form in the retinal vessel artery from injury to the head or eye. 6. Vasculitis is an inflammation of blood vessels that can lead to narrowing or obstruction of the retinal vessel. It is important to remember that BRAO can be caused by many different causes. An ophthalmologist, along with other specialists, will need to examine the patient thoroughly in order to determine the cause of the problem and offer appropriate treatment. Sanjeevan netralaya's Advanced Ayurvedic Ear Care has helped over 6 Lakh patients across India. The treatment successfully treats Branch Retinal Artery Occlusion without any side effects or discomfort. Do not delay your treatment if you experience symptoms of Branch Retinal Artery Occlusion. Book your appointment at your closest Sanjeevan Netralaya clinic today. It is important to remember that BRAO can be a serious condition and requires immediate medical attention in order to prevent permanent vision loss. For the best possible outcome, it is important to get a prompt referral to an eye doctor who is experienced in retinal vascular disease. Sanjeevan Netralaya's Advanced Ayurvedic Eye Care has successfully treated more than 6 lakh patients in India and treats Branch Retinal Artery Occlusion without causing side effects and discomfort. If you are experiencing symptoms of Branch Retinal Artery Occlusion please begin your treatment immediately. Book your appointment at your closest Sanjeevan Netralaya clinic today. Sanjeevan Netralaya’s Advanced Ayurvedic Eye Care Treatment has successfully treated Branch Retinal Artery Occlusion in India. There have been over 6 lakh patients who have received effective retina care from Sanjeevan Netralaya without any side effects. Book your appointment at your closest Sanjeevan Netralaya clinic today. Can Branch Retinal Artery Occlusion be cured? Branch Retinal Artery Occlusion is a serious condition that can cause vision loss and blindness. Treatment success depends on the root cause, severity, promptness, diagnosis, and treatment. Sometimes, vision loss due to BRAO can be reversed if there is a clot, embolus, or a condition that can dissolve with medication or surgically removed. Early treatment is important in these cases to prevent further damage to blood vessels and to restore blood flow to the affected areas, which can potentially improve or restore vision. In cases where there has been permanent damage to blood vessels, vision loss can be irreversible. These cases may require treatment to prevent further damage and preserve vision. Low vision rehabilitation can also be used to help the patient adjust to their visual impairment. It is important to remember that BRAO can be a serious condition and requires immediate medical attention in order to prevent permanent vision loss. For the best possible outcome, it is important to get a prompt referral to an eye doctor who is experienced in retinal vascular disease. Sanjeevan Netralaya's Advanced Ayurvedic Eye Care has successfully treated more than 6 lakh patients in India and treats Branch Retinal Artery Occlusion without causing side effects and discomfort. If you are experiencing symptoms of Branch Retinal Artery Occlusion please begin your treatment immediately. Book your appointment at your closest Sanjeevan Netralaya clinic today. Symptoms of Branch Retinal Artery Occlusion Branch Retinal Artery Occlusion symptoms (BRAO) may vary depending on where and how severe the occlusion is. The most common symptoms are: 1. Sudden, unremarkable loss of vision: This is most common symptom in BRAO. It can be mild to severe. 2. Visual field defects: This is a condition that causes vision loss in a small area of the visual field. It is called scotoma. 3. Blurred vision can be caused by an occlusion of a small branch in the retinal artery. 4. Color vision may change: Because the retina is not receiving enough blood, the affected area may appear grayish or white. 5. Redness in the eye may be caused by inflammation of blood vessels. 6. Headaches: Occlusion can cause headaches in some people. 7. Systemic symptoms: Other conditions, such as giant cell arthritis, can cause systemic symptoms like fever, malaise and jaw claudication. Sanjeevan Netralaya's Advanced Ayurvedic Eye Care has effectively treated over 6 lakh patients across India and successfully treats Branch Retinal Artery Occlusion without causing any harmful side effects or discomfort. Do if you have any symptoms of Branch Retinal Artery Occlusion, do not prolong your treatment. Book your appointment at your closest Sanjeevan Netralaya clinic today.

What is Anterior Ischematic Optic Neuropathy? The Optic Nerve is responsible for taking impulses from the eye to the brain. When there is an interruption in the blood flow in the Optic Nerve due to Inflammation leading to sudden loss in vision, it is known as Anterior Ischematic Optic Neuropathy or AION. The interruption in the blood flow in the Optic Nerve leads to the lack of Oxygen and nutrients which are imperative for the blood vessels to survive and carry information or impulses from the eye to the brain leading to vision loss or even damage to the optic nerve. When the loss of vision is not caused by an inflammation, it is known as Non Arteric Anterior Ischematic Optic Neuropathy What are the symptoms of Anterior Ischematic Optic Neuropathy? Anterior Ischematic Optic Neuropathy can be categorised into: 1. Arteric Anterior Ischematic Optic Neuropathy 2. Non Arteric Anterior Ischematic Optic Neuropathy Arteric Anterior Ischematic Optic Neuropathy When a patient suffers loss of vision because of an inflammation due to giant cell arteries, it is known as Arteric Anterior Ischematic Optic Neuropathy. Giant Cell Arteries, also known as temporal arteritis causes a patient medium as well as large sized artery inflammation. If not treated quickly, Arteric Anterior Ischematic Optic Neuropathy can lead to complete loss of vision and can even be fatal. Arteric Anterior Ischematic Optic Neuropathy affects women more than men mostly over the age of 55. Some of the symptoms of Arteric Anterior Ischematic Optic Neuropathy are: 1. Pain or tingling sensation in the scalp 2. Neck Pain 3. Fever 4. Sudden weight loss 5. Appetite Loss 6. Tiredness and Fatigue 7. General muscle pains or pain in the upper legs/arms 8. Pain while chewing food With Sanjeevan Netralaya’s Advanced Ayurvedic Treatment, the symptoms mentioned above can be managed, without any side effects. Our medication does not cause any discomfort like main stream medicine and helps treat the patient effectively. It should be noted that symptoms pertaining to vision in Arteric Anterior Ischematic Optic Neuropathy are usually painless. Patients might get temporary blurry vision or even vision loss for while before the vision loss gets permanent. It is very important to visit your doctor immediately. Non Arteric Anterior Ischematic Optic Neuropathy Non Arteric Anterior Ischematic Optic Neuropathy is most common for people over the age of 50 and can appear in both men and women. Non Arteric Anterior Ischematic Optic Neuropathy occurs when inflammation is not the cause of blockage in the blood flow of the optic nerve. It can be caused by: 1. Severe drop in blood pressure 2. Increase in pressure in the eye ball 3. Increase in thickness of blood 4. Thinning Arteries 5. Decrease in blood flow in the Optic Nerve There are a number of factors that contribute to Non Arteric Anterior Ischematic Optic Neuropathy: 1. High Blood Pressure (Hypertension) or drop in Blood Pressure 2. Cholesterol 3. Smoking 4. Increased Cholestrol 5. Heart Problems or blocked arteries 6. Sickle Cell Trait 7. Inflammation of a blood vessel Usual drop in blood pressure during sleep paired with other health problems causes sudden loss of vision or blurriness in vision felt when waking up is a main symptom of Non Arteric Anterior Ischematic Optic Neuropathy. Sanjeevan Netraleya tailored treatments are unique as different patients require different specialised care. We treat patients with Non Anterior Ischematic Optic Neuropathy effectively without steroids and without giving them harmful side effects.

What Retinitis Pigmentosa? Retinitis Pigmentosa, also know as RP is a rare eye condition that affects the layer of the eye that is sensitive to light - the Retina. Retinitis Pigmentosa is a genetic disease that is passed on through generations and the type of vision loss varies. Patients suffering from Retinitis Pigmentosa lose eyesight over time but do not become completely blind. What are the causes of Retinitis Pigmentosa? Patients suffering from Retinitis Pigmentosa lose eyesight over time but do not become completely blind. Being a genetic issue, the main cause of RP is generational that happens because of changes in our genetics that end up leading to damage in the control cells in the Retina. What are the symptoms of Retinitis Pigmentosa? The main symptoms of Retinitis Pigmentosa are: - Loss in side vision or peripheral vision - Loss if vision in the night or in the dark - Problems distinguishing colours - Loss of central vision If you are facing any of the above symptoms, it is impetrative to meet your doctor at the earliest. Doctors at Sanjeevan Netralaya understand that every patient is different with different genes and understand the patient history before prescribing effective Ayurvedic Medication that is not only effective but also causes absolutely no side effects. How is Retinitis Pigmentosa Diagnosed? As RP is a genetic disorder, your doctor may do a number of tests to make sure that you are given the right treatment. They include: - OCT or Optical Coherence Tomography, which is a test that takes highly detailed pictures of the retina - Genetic Testing, where a blood sample or a tissue sample might be taken to study your genes to determine the extent of the disease as well as the course of action - Electroretinography is a test that measures the electrical activity and checks the reaction of the Retina to light. - Visual Field Testing helps check your peripheral vision and blind spots. Every case of Retinitis Pigmentosa is different and doctors may want to do multiple tests to make sure they have caught the extent and severity of the disease. Doctors at Sanjeevan Netralaya understand that every patient is different with different genes and understand the patient history before prescribing effective Ayurvedic Medication that is not only effective but also causes absolutely no side effects. Can Ayurveda Cure Retinitis Pigmentosa? Retinitis Pigmentosa is a disease that is generational. The Ayurvedic treatment from Sanjeevan Netralaya is known to be the best for RP and is very effective in reversing the effects of the disease. Our doctors take the time to study and understand every patient before prescribing medication because every case of RP is unique. Sanjeevan Netralaya’s Advanced Ayurvedic Eye Care has helped over 6 lakh patients across India in effectively reversing all retina related problem without the use of injections and heavy medications that cause harmful and painful side effects. What is the best treatment for Retinitis Pigmentosa? Retinitis Pigmentosa is a disease that is generational. The Ayurvedic treatment from Sanjeevan Netralaya is known to be the best for RP and is very effective in reversing the effects of the disease. Our doctors take the time to study and understand every patient before prescribing medication because every case of RP is unique. Sanjeevan Netralaya’s Advanced Ayurvedic Eye Care has helped over 6 lakh patients across India in effectively reversing all retina related problems without the use of injections and heavy medications that cause harmful and painful side effects Can Retinitis be cured by Ayurveda Retinitis Pigmentosa is a disease that is generational. The Ayurvedic treatment from Sanjeevan Netralaya is known to be the best for RP and is very effective in reversing the effects of the disease. Our doctors take the time to study and understand every patient before prescribing medication because every case of RP is unique. Sanjeevan Netralaya’s Advanced Ayurvedic Eye Care has helped over 6 lakh patients across India. What is now treatment for Retinitis Pigmentosa in India? As every case of Retinitis Pigmentosa is different, there is no single line of treatment. Researchers Scientists are still working on what causes RP to detoriate so much. Doctors prescribe Vitamin A which is known to slow down the disease. Other medication may also be prescribed. In certain cases, injections are given under the eye. Surgery is also an option to treat the other effects of RP like Cataract. An artificial retina may also be helpful for some patients. Can Sanjeevan Netralaya Hospital cure Retinitis Pigmentosa? The Advanced Ayurvedic treatment from Sanjeevan Netralaya is known to be the best for RP and is very effective in reversing the effects of the disease. Our doctors take the time to study and understand every patient before prescribing medication because every case of RP is unique. Sanjeevan Netralaya’s Advanced Ayurvedic Eye Care has helped over 6 lakh patients across India. What age does Retinitis Pigmentosa start? Retinitis Pigmentosa can begin at the age of even 10 years old. Some patients may lose complete vision by they are 30, and other may have vision even at the age of 80. RP varies from case to case. How many people with Retinitis Pigmentosa go Blind? Around 30% of the patients suffering from Retinitis Pigmentosa lose majority of their vision and around 12% lose complete vision. The most effective way of treating Retinitis Pigmentosa is with ADVANCED AYURVEDIC EYE CARE treatments provided by Sanjeevan Netralaya. Sanjeevan Netralaya has treated over 6 lakh patients suffering from an array of retinal issues with a 100% success rate. Moreover, our treatments are tailer made to every patient making sure they are treated to perfection without causing harmful and uncomfortable side effects. Can I still drive with Retinitis Pigmentosa? Retinitis Pigmentosa affects your vision. In the initial stages, you may be able to drive but as the disease progresses, it is not advised. The Ayurvedic treatment from Sanjeevan Netralaya is known to be the best for RP and is very effective in reversing the effects of the disease. Our doctors take the time to study and understand every patient before prescribing medication because every case of RP is unique. Sanjeevan Netralaya’s Advanced Ayurvedic Eye Care has helped over 6 lakh patients across India. Is there hope for Retinitis Pigmentosa? With Sanjeevan Netralaya’s Advanced Ayurvedic Treatment, yes there is. The most effective way of treating Retinitis Pigmentosa is with ADVANCED AYURVEDIC EYE CARE treatments provided by Sanjeevan Netralaya. Sanjeevan Netralaya has treated over 6 lakh patients suffering from an array of retinal issues with a 100% success rate. Moreover, our treatments are tailer made to every patient making sure they are treated to perfection without causing harmful and uncomfortable side effects. What Vitamin helps with Retinitis Pigmentosa? Vitamin A is sometimes prescribed as it slows down the effects of RP. What is the future of people suffering from Retinitis Pigmentosa? Around 30% of the patients suffering from Retinitis Pigmentosa lose majority of their vision and around 12% lose complete vision. But there is hope. The most effective way of treating Retinitis Pigmentosa is with ADVANCED AYURVEDIC EYE CARE treatments provided by Sanjeevan Netralaya. Sanjeevan Netralaya has treated over 6 lakh patients suffering from an array of retinal issues with a 100% success rate. Moreover, our treatments are tailer made to every patient making sure they are treated to perfection without causing harmful and uncomfortable side effects. Is there a cure coming soon for Retinitis Pigmentosa? Researchers and Scientists are still working on what causes RP to detoriate so much. The Ayurvedic treatment from Sanjeevan Netralaya is known to be the best for RP and is very effective in reversing the effects of the disease. Our doctors take the time to study and understand every patient before prescribing medication because every case of RP is unique.

What is Branch Retinal Vein Occlusion? Branch retinal vein occlusion (BRVO), is a medical condition where one of the veins that drain blood away from the retina becomes blocked. The blockage can lead to blood accumulation within the vein. This causes swelling, bleeding, and other problems in the affected part of your retina. Brittle Retinal Vein Occlusion can happen in one eye. It may cause a sudden or gradual loss in vision, depending on the severity and location. High blood pressure, diabetes and atherosclerosis are all risk factors for BRVO. After performing a thorough eye exam, an eye doctor can diagnose BRVO. This may include dilation of pupils and specialized imaging tests like fluorescein angiography (OCT), or optical coherence tomography (OCT). Depending on the extent and severity of the retinal damage and blockage, there are many treatment options available for BRVO. One of the most effective treatments for Branch Retinal Vein Obstruction is Sanjeevan Netralaya’s Advanced Ayurvedic Eye Care. Treatments at Sanjeevan Netralaya are tailor made for each patient and case absolutely no side effects. What are the symptoms of Branch Retinal Vein Occlusion? Depending on the severity of the obstruction, the symptoms of branch retinal vein occlusion (BRVO), can vary. Some people will not experience any symptoms while others might experience sudden or gradual vision loss in one or more of their affected eyes. BRVO is characterized by the following symptoms: · Vision blurred or distorted: If there is a blockage in the retinal vessel, the central or peripheral vision can become blurry, distorted, or disappear. · Vision loss: In certain cases, BRVO may cause a gradual or sudden loss of vision in one or more eyes. · Eye pain: People with BRVO can experience mild to severe pain in their eyes, particularly if there is inflammation or high pressure. · Floaters are floating specks and cobwebs that move in your field of view. · Sensitivity towards light: Bright lights can cause discomfort, particularly if inflammation is present in the eye. · Color vision may change: This could be a result of changes in your color perception. For example, you might see colors that are less vibrant or faded. For proper diagnosis and evaluation, it is important that you see an eye doctor if you have any of these symptoms. Early treatment and detection of BRVO can prevent vision loss. Sanjeevan Netralaya's Ayurvedic Eye Treatment is one of the best treatments for Branch Retinal Vein Occlusion. Sanjeevan Netralaya's treatments are custom-made for each patient, with absolutely no side effects. What are the causes of Branch Retinal Vein Occlusion? A blockage in one of the veins that drain blood from the retina can cause branch retinal vein occlusion. Atherosclerosis is the most common cause of BRVO. This is a condition where fat deposits build up on the walls and cause them to narrow down or become blocked. The risk of BRVO can also be increased by other factors, such as: · Age: BRVO occurs more frequently in those over 50. · High blood pressure: Hypertension may cause damage to the blood vessels and increase the chance of BRVO. · Diabetes: People suffering from diabetes are at greater risk of developing retinal blood vessel disease, which could lead to BRVO. · Glaucoma: Because of the high intraocular pressure, which can lead to retinal vessel damage, people with glaucoma are at greater risk for developing BRVO. · Smoking: Cigarette smoking can cause damage to the blood vessels of the eye and increase the chance of BRVO. · Hypercoagulable states: A history of blood clots, blood clotting disorders or elevated blood cholesterol and lipid levels can increase your risk of developing BRVO. · Cardiovascular disease: Hypertension and atherosclerosis are two of the most common causes of BRVO. To reduce the risk of developing BRVO, regular eye examinations are essential. Sanjeevan Netralaya's Advanced Ayurvedic eye Care is the most effective treatment for Branch Retinal Vein Occlusion. Sanjeevan Netralaya’s treatments are tailored for each patient with no side effects. What is the treatment for Branch Retinal Vein Occlusion? Sanjeevan Netralaya's Advance Ayurvedic Eye Care is one of the most effective treatments to treat Branch Retinal Vein Occlusion. Sanjeevan Netralaya offers customized treatments for every patient. There are no side effects or discomfort. These measures may help to reduce the risk of complications. However, it is important that you remember that BRVO can be a serious medical condition and should be evaluated promptly by an eye doctor. Sanjeevan Netralaya Advanced Ayurvedic Eye Care is one of most effective treatments for Branch Retinal Vein Occlusion. Sanjeevan Netralaya’s treatment has no side effects, and each treatment is custom made for each patient.