ALS Stem Cell Treatment

Stem Cell Treatment for Amyotrophic Lateral Sclerosis

Stem Cell ALS Treatment: Amyotrophic Lateral Sclerosis (ALS) is a rare neurological disorder which is mainly related to nerve cells. Our neurons are responsible for muscle movements, like chewing, talking or breathing, just to name a few. It is a severity disease which means it will be increasing over the course of time. ALS Stem Cell Therapy is available now at our treatment center in Bangkok, Thailand.

Stem Cell ALS Treatment

It is reported that every day, an average of 15 people are newly diagnosed with ALS — more than 5,600 people per year. Most people who develop ALS are between the ages of 40 and 70, although the disease can occur at a younger age. It occurs throughout the world with no racial, ethnic or socioeconomic boundaries.

The causes of ALS are not known, but a study in 1993 showed that the patient’s body produced Cu/Zn superoxide dismutase (SOD1) which was associated with some cases of ALS. The primary cause can be considered as genetics, many scientists in their study have found out that the mutant SOD1 can become toxic. Even environmental factors such as diet, infection agents, and viruses can also be the causes.

At first, symptoms of ALS tend to be overlooked but as time passes they become more severe and progressively turn to atrophy. The early symptoms can be muscle twitches in arms, legs or tongue, muscle cramps, difficulty in chewing or swallowing, stiff and tight muscles. Many people who are affected by ALS have observed that the first sign has been seen in arm or hands; they are unable to do regular chores such as writing, opening a lock with the key, or putting the buttons of their shirts, hence why quite often one cannot say precisely where or when they got the first sign or symptom.

ALS Stem Cell Therapy

There are no single tests that can detect ALS. The physician has to review the medical history and then conduct neurological examinations periodically to check whether the symptoms are getting worse or not. The primary diagnosis is made by observing the signs and symptoms by the physician after running a series of tests. These tests can be electromyography (EMG) wherein the electrical ability of the muscle fibers is checked through special recordings. Then there is Nerves Conduction Study (NCS) and this test is done on the nerves. The doctor may also refer to Magnetic Resonance Test (MRI) including a set of laboratory tests such as urine and blood tests.

MSC´s have plasticity properties and the ability to provide growth factors which modulate the immune system. The transplantation of Mesenchymal Stem Cells (MSCs) leads to the increase in the survival of neurons as these cells are known to produce proteins that are helpful in the growth and survival of new-developing and mature neurons. Moreover, the idea of replacing the dying neurons with new stems cells is now more realistic, feasible and appealing. Patients who have been treated with stem cells have shown improvements in coordination, balance, speech, swallowing and few other areas as well.

Beneficial Actions of Stem Cells for ALS

Ross the endothelial brain barrier
Migrate to sites of injury (chemotaxis)
Communicate with and alter nearby cells (paracrine effect)
Encourage existing cells to self-repair (autocrine effect)
Immune modulation
Transform into neurons and glia
Promote the formation of nerve cell axons (axogenesis)
Release neuroprotective factors
Encourage existing cells to adapt (neuroplasticity)

Results Achieved with Stem Cell Treatment for ALS:

Slowing of disease progression
Improved breathing ability
Improved speech
Improved ability to swallow
Reduced levels of muscle wasting

Mesenchymal Stem Cell Treatment Mode of Action and Therapeutic Benefit for ALS

Mesenchymal stem cell (MSC) treatment has shown promise as a potential therapeutic approach for Amyotrophic Lateral Sclerosis (ALS). While the exact mode of action is still being studied, several mechanisms have been proposed to explain the therapeutic benefits of MSC treatment for ALS. These include:

Anti-inflammatory effects: MSCs have immunomodulatory properties and can suppress inflammation in the central nervous system. In ALS, neuroinflammation contributes to the progression of the disease. MSCs release anti-inflammatory molecules and regulate immune cell responses, thereby reducing inflammation and protecting motor neurons.
Trophic support: MSCs can secrete various growth factors, such as brain-derived neurotrophic factor (BDNF), glial cell-derived neurotrophic factor (GDNF), and vascular endothelial growth factor (VEGF). These factors promote the survival and growth of neurons, enhance neuroprotective mechanisms, and support the survival of motor neurons affected by ALS.
Modulation of oxidative stress: Oxidative stress plays a role in the progression of ALS. MSCs possess antioxidant properties and can reduce the harmful effects of reactive oxygen species (ROS) on motor neurons. They secrete antioxidant enzymes and molecules that counteract oxidative damage, thus protecting neurons from further injury.
Immunomodulation: In ALS, immune dysregulation contributes to the neurodegenerative process. MSCs can modulate the immune response by suppressing harmful immune cells and promoting the activity of regulatory immune cells. This modulation helps create a favorable environment for neuroprotection and repair.
Paracrine effects: MSCs secrete a variety of bioactive factors that exert beneficial effects on neighboring cells. These factors can promote tissue repair, angiogenesis, and the formation of new blood vessels, which may enhance the microenvironment for motor neuron survival.

Therapeutic benefits observed in preclinical and clinical studies of MSC treatment for ALS include:

Slowing disease progression: MSC treatment has shown potential in slowing the progression of ALS, as evidenced by improvements in disease markers and motor function in some patients.
Extended survival: Some studies have reported prolonged survival in ALS patients who received MSC treatment compared to those who did not receive the treatment.
Improved motor function: MSC therapy has been associated with improvements in muscle strength, motor skills, and functional capacity in ALS patients. These improvements can enhance quality of life and prolong independent living.
Reduced neuroinflammation: MSCs’ anti-inflammatory properties can reduce neuroinflammation in ALS patients, potentially slowing disease progression and preserving motor function.

Price and Treatment Duration

Supportive Therapies Included

Take Home Therapy Package