Salym Liufau’s journey to an ALS diagnosis started in early 2022 when she found she couldn’t stand after squatting to lift her child. Over the following weeks, sensory loss and weakness spread to her left foot until it became paralyzed.
Despite negative initial blood tests suggesting a minor vitamin issue, worsening symptoms led Salym to seek hospitalization. Neurological assessments at Houston Methodist Hospital showed absence of reflexes in her leg, signaling a serious nerve disorder.
After a year of mounting symptoms and daily challenges caring for four young children, Salym received a diagnosis of amyotrophic lateral sclerosis (ALS). This progressive neurodegenerative disease affects motor neurons and leads to muscle function loss.
ALS is often fatal within three to five years, and treatment focuses on symptom management and quality of life. Upon diagnosis, Salym shared the emotional weight of the moment, expressing tears and sorrow for the impact on her family.
A GoFundMe campaign started by relatives is now helping fund life-supporting therapies, assistive technologies, physical and speech therapy, and home modifications to accommodate her growing needs.
