What Disease Does M'kenna Have, M'kenna is a young girl who has been diagnosed with a rare genetic disorder called spinal muscular, General, what-disease-does-mkenna-have, JPOSE
M'kenna is a young girl who has been diagnosed with a rare genetic disorder called spinal muscular atrophy (SMA). This disease affects the motor neurons in the spinal cord, which are responsible for controlling muscle movement. As a result, patients with SMA experience muscle weakness and wasting, which can lead to difficulty with basic activities such as sitting, standing, and walking.
SMA is a genetic disease, which means it is caused by mutations in specific genes. In M'kenna's case, she has a mutation in the SMN1 gene, which is responsible for producing a protein that is essential for the survival of motor neurons. Without this protein, the motor neurons in the spinal cord degenerate, leading to muscle weakness and wasting.
There are four different types of SMA, which vary in severity depending on the age of onset and the extent of muscle weakness. M'kenna has been diagnosed with type 2 SMA, which typically presents in early childhood. Patients with type 2 SMA are able to sit independently, but may require assistance with standing and walking.
There is currently no cure for SMA, but there are treatments available to manage the symptoms of the disease. M'kenna receives regular physical therapy, which helps to improve her muscle strength and flexibility. She also takes medication to help support the function of her motor neurons.
Despite the challenges of living with SMA, M'kenna is a bright and positive young girl who loves to play with her friends and family. Her parents are committed to providing her with the best possible care and support, and are active in raising awareness about SMA and advocating for research into new treatments and a cure for the disease.
Overall, SMA is a rare but devastating disease that affects many families around the world. While there is still much to be learned about the causes and treatments of SMA, there is hope that with continued research and advocacy, we can find a cure and improve the lives of patients like M'kenna.