Advanced Distal Muscular Dystrophy Treatment in India
Are You at Risk for Distal Muscle Dystrophy?
If you answered yes to any of the above question, it’s possible that you are at risk for distal muscle dystrophy, a progressive disorder that affects the muscles of the arms, legs, and core.
Early diagnosis is key in effectively managing the disease and preventing its progression. With treatments like Stemcell therapy, physical therapy, and lifestyle modifications, those with distal muscular dystrophy can live a more normal life.
The rapidly advancing field of genetics has made it possible to identify distal muscle dystrophy before the symptoms become too pronounced.
A simple genetic test can be done to check for the presence of certain gene mutations, which are associated with the disorder.
Therapies like stem cell therapy can help improve muscle strength and flexibility, while physical therapy can help prevent contractures.
Check out the story of our patient, Mark whose son was diagnosed with distal muscle dystrophy in his teens with the help of stem cell therapy and physical therapy, his son has made a remarkable recovery.
Mark Peterson was a successful IT Manager living in Lagos, Nigeria. He had a loving family of four and his son was the apple of his eye.
But one day when Mark and his son were chit-chatting his son began to share his symptoms of distal muscular dystrophy – an incurable genetic condition that affects the muscles severely.
This news filled Mark with fear for his son’s future and he wanted to do everything in his power to make sure that he could live as normal a life as possible.
Desperate for answers, Mark did extensive research into potential treatments for muscular dystrophy but nothing seemed promising until one day at work when he mentioned it to one of his colleagues – Mr. Robert who suggested MedicoExperts – a well-known name in the healthcare industry specializing in cutting edge treatment plans and therapies.
Intrigued by this suggestion, Mark decided to look further into MedicoExperts and what they had on offer before reaching out to them with all of his concerns about finding the best possible treatment plan for his son’s condition.
The team collaborated with Mark throughout every stage of the process and ultimately identified that he was experiencing health problems, including immune deficiency, leg weakness, and pain, that were contributing to his declining health.
With the help of stem cell therapy and physical therapy, they were able to craft a personalized treatment plan for Mark’s son. Stem cell therapy was used to regenerate the damaged muscle fibers and physical therapy improved the strength of his muscles.
What is Distal Muscular Dystrophy?
Muscular Dystrophy is a group of genetic diseases that affect the muscles.
Muscular dystrophy is a condition that results in the gradual weakening and reduction of muscle mass due to abnormal genes (mutations) that disrupt the production of necessary muscle-building proteins.
The type and severity of the muscle weakness depend on the specific gene mutation present. There are several treatments available to mitigate the severity of symptoms and slow down the progression of this disorder.
Although the symptoms of distal muscular dystrophy can be debilitating, there is hope.
What are the symptoms of distal muscular dystrophy?
Distal muscular dystrophy (DD) is a rare form of MD that typically affects the hands, feet, and lower legs.
The symptoms of DD can vary depending upon the specific mutation present and may include:
- muscle weakness,
- cramping,
- twitching,
- joint contractures,
- unusual fatigue, and
- difficulty with fine motor skills.
Other symptoms may include:
- foot drop, which is an inability to lift the toes due to weakened calf muscles,
- as well as hammertoes and clawed hands.
As time passes, the symptoms of DD can become more pronounced and lead to further mobility limitations.
What are the causes of distal muscular dystrophy?
Distal muscular dystrophy is caused by a genetic mutation that affects the production of proteins needed for muscle development and maintenance.
This mutation prevents your muscles from receiving the necessary proteins, weakening muscles over time.
The exact cause of the genetic mutation is unknown, but research suggests it’s important to remember that distal muscular dystrophy is not contagious and cannot be passed from person to person.
There may be different names given to some DDs based on their symptoms, but they could be caused by defects in the same gene.
What is the diagnosis of distal muscular dystrophy?
The diagnosis of distal muscular dystrophy can be difficult as the symptoms are variable and can take many years to become apparent.
To diagnose DD, your doctor will look at a combination of family history and genetic testing to determine if certain gene mutations are present.
Your doctor may also use imaging tests like CT scans or MRIs and muscle biopsies to better understand the extent of muscle damage.
Once a diagnosis of distal muscular dystrophy is made, your doctor can begin to talk about treatment and lifestyle modifications that could help you manage the condition.
The diagnostic procedures are comprehensive and include a range of tests to thoroughly evaluate muscle and nerve function. As follows:
- Tests like electromyography (EMG) and nerve conduction velocity can help identify the specific type of DD you have, as well as determine if any further tests are needed.
- Your doctor can also use genetic testing to determine if certain gene mutations are present, as well as to identify potential carriers of the DD gene.
- In addition, they conduct a creatine kinase (CK) test which can detect muscle damage by locating the presence of the enzyme in the blood.
- Finally even muscle biopsy can also be used to examine the muscle tissue and determine the amount of damage that’s been done.
These tests are important in helping to diagnose and treat distal muscular dystrophy. Treatment is important in managing the symptoms of DD, as well as allowing sufferers to remain as independent as possible.
What treatment options exist for distal muscular dystrophy?
Stem cell therapy is a type of regenerative treatment that aims to repair damaged cells in the body by reducing inflammation and regulating the immune system.
For example, injections of muscle-derived stem cells can help regenerate the muscles and improve their functionality. In numerous instances, this impact can significantly enhance the patient’s quality of life and also prolong the progression of the disease. Muscle strength and physical function typically improved over time.
This helps to maintain joint flexibility and mobility, as well as strengthen the muscles.
For example, range of motion and strengthening exercises can help improve mobility, muscle coordination, and balance.
This may help with daily activities such as writing, eating, or dressing.
For example, adaptive equipment can make everyday tasks easier and more efficient.
These can help improve balance, coordination, and ability to perform tasks.
Examples include wheelchairs or walkers.
These help to support and stabilize joints.
Examples include splints or orthotics to help correct foot deformities.
Certain medications may be prescribed to reduce muscle pain, improve sleep or appetite, or enhance mobility.
This includes anti-inflammatory medications, muscle relaxants, pain relievers, and more.
This is an experimental treatment that uses modified genes to correct the genetic mutation that causes distal muscular dystrophy.
For Example, gene therapy involves inserting new genes into a person’s cells to replace or repair damaged ones.
Other therapies may also be considered to help manage symptoms. Examples include massage therapy, acupuncture, and yoga.
It is important to speak with a healthcare professional about the best treatment plan for you and your condition. With the right support, those living with distal muscular dystrophy can manage their symptoms and live an active, independent life.
Due to the different symptoms of each subtype, treatments can vary depending on an individual’s specific needs.
Certain medications may be prescribed to reduce muscle pain, improve sleep or appetite, or enhance mobility.
This includes anti-inflammatory medications, muscle relaxants, pain relievers, and more.
What is the cost of distal muscular dystrophy treatment in India?
The cost of treatment for distal muscular dystrophy in India can vary depending on the type and severity of the condition, as well as the type of treatment chosen.
- Generally, treatments such as physical therapy and occupational therapy may cost between 3,000-10,000 rupees per session $40 – $140 USD.
- Medications, braces, and other assistive devices may cost between 5,000-75,000 rupees ($70-$1,050 USD).
- Stemcell therapy cost ranges from 1,60,000 to 2,00,000 rupees per cycle ($2,000-$2,500 USD).
- Ozone Therapy can cost up to 20,000 rupees ($280 USD). It is important to speak with a healthcare professional and your insurance provider about
However, these costs may vary depending on the individual’s specific needs. Ultimately, the cost of treatment for distal muscular dystrophy in India may be high, but with the right support and resources, those living with the condition can manage their symptoms and live independent life.
Conclusion
Dealing with a long-term condition, especially if it is getting worse, can be difficult. However, there are physical and emotional therapies that can help you cope.
Medicoexperts consider stem cell therapy as a viable treatment option for muscular dystrophy in India. Through a proven and trustworthy process, it has been shown to enhance physical activity and muscle strength in DD patients.
This therapy allows patients to increase their mobility and live a more autonomous life.
We are here to help you every step of the way, so reach out today and get started on your journey toward better health.
Our patients have reported positive outcomes and improved quality of life with a combination of treatment and plans.
We understand the cost associated with distal muscular dystrophy treatment in India can be high, but our team is here to help you find the most affordable and effective treatment options available.
If you have questions about distal muscular dystrophy or need help finding the right support for you, contact us today and speak with one of our knowledgeable and caring specialists.
We are here to provide you with the best possible care. Thank you!
Frequently Asked Questions and patient concerns:
1. What test confirms distal muscular dystrophy?
A genetic test is usually needed to confirm the diagnosis of muscular dystrophy.
This can include a blood test, MRI scan, muscle biopsy, or skin biopsy. Your doctor may also order additional tests such as an electromyogram (EMG) or nerve conduction velocity (NCV).
2. What are 2 interesting facts about muscular dystrophy?
- Muscular dystrophy is an inherited, progressive disease that affects the muscles and can lead to diminishing muscle strength and mobility over time.
- There are several types of muscular dystrophies, each of which has different causes and characteristics. Duchenne Muscular Dystrophy is the most common type of muscular dystrophy.
3. What is the prognosis of muscular dystrophy?
The prognosis of muscular dystrophy depends on the type and severity of the condition.
In some cases, muscular dystrophy can lead to a shortened life expectancy.
However, with advances in treatment and lifestyle changes, many people can live independent lives for a longer period of time.
MedicoExperts offers support and resources to help individuals living with muscular dystrophy in India.
Contact us today to learn more about our services.
4. Which organs can muscular dystrophy affect?
While certain types of MD may show signs during infancy or childhood, others may not be noticeable until middle age or beyond.
The severity and incidence rates differ between the various forms of dystrophies, but each one leads to a gradual breakdown of skeletal muscle, and in some cases, it affects the heart muscle as well.
5. What foods should a muscular dystrophy patient avoid?
People living with muscular dystrophy should avoid foods that contain high levels of saturated fats, trans fat, and cholesterol.
Reducing the intake of processed food and sugary drinks is also recommended.
Eating a healthy and balanced diet with plenty of fruits, vegetables, whole grains, lean protein sources, and low-fat dairy can help manage symptoms of muscular dystrophy.
It is also important to stay hydrated, as dehydration can worsen muscle weakness.
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Author Bio:
Dr. Khushbu Jain is a dedicated professional with a passion for advancing healthcare through cutting-edge treatments. She has a special interest in researching regenerative medicine and advanced treatment for diseases that are difficult to treat with conventional treatment options. Her deep understanding of these progressive treatments allows her to offer patients personalized and effective solutions for a variety of health concerns.
Content Medically Reviewed By MedicoExperts Editorial & Clinically Review Board
