(ALS) Amyotrophic lateral sclerosis, sometimes named as Lou Gehrig’s disease, is a deadly neurological condition that advances rapidly and affects the whole body. It has an effect on motor nerve cells in the brain and spinal cord, causing muscle action to become restricted. To be more specific, the ailment is characterized as the gradual degradation of voluntary muscles as a result of a lack of nutritional intake. In actuality, the illness has no effect on the patient’s emotional or mental well-being; yet, a person may feel severe depression or changes in cognitive abilities that impair memory or conduct, among other things. It has not been proved to have any influence on the sensory neurons that control a person’s capacity to touch, smell, taste, or hear, for example, in any manner or at all.
Neurons are brain cells that may be found throughout the body, including the brain, spinal cord, and lower brainstem. The messenger cells, which are found in the spinal cord, are responsible for connecting the brain to the rest of the body. They are responsible for transmitting information from the brain to various organs, including voluntary muscles. Neurons communicate with one another through the transmission of these signals.
Because of genetic abnormalities or environmental factors that alter the information flow, erroneous information is processed to the voluntary portions of muscles, resulting in severe and gradual degeneration of the muscles. The body’s voluntary muscles weaken, waste away, and twitch if they are not properly processed.
THE HELP OF STEM CELLS
Because of their potential to divide indefinitely and differentiate into a variety of cell types, stem cells are the mother cells responsible for the development of a complete human body from a tiny two-celled embryo. A new approach has made it possible to collect stem cells from the human body, concentrate them in a clean environment, and then transplant them into the body. As a result, stem cell treatment comprises sending concentrated cells to the damaged area, where they can colonize and change the characteristics of local stem cells, as well as re-establish functions that have been lost as a result of disease or injury.
GIOSTAR ALS TREATMENT
The method of collecting the highest number of viable stem cells from either autologous or allogeneic sources to treat ALS patients has been perfected by our team. We are a licensed private enterprise with a state-of-the-art laboratory dedicated to identifying, processing, and enhancing viable stem cells for re-infusion in patients with a variety of diseases. Generally, these cells are delivered using one of the following methods:
- Intrathecal Administration: In this technique, the cells are injected into the CSF via the spinal canal’s subarachnoid areas.
- Intravenous Administration: In this approach, cells are pumped into veins to increase blood volume in the CNS, ensuring maximal cell delivery.
It is possible to inject these stem cells back into the body, where they can form into missing neurons or other damaged supporting cells, allowing the body to operate more freely. We are currently seeing improvements in the symptoms and functional capacity of ALS patients as a result of our standardized, broad-based, and complete treatment strategy.
ALS Treatment Protocol 