USC ALS Center of Excellence

We offer expert care for amyotrophic lateral sclerosis (ALS) to help slow your disease progression and manage your symptoms.

USC ALS Center of Excellence

We offer expert care for amyotrophic lateral sclerosis (ALS) to help slow your disease progression and manage your symptoms.

Compassionate Care in a Supportive, Family-Oriented Atmosphere

At the USC ALS Center of Excellence, we offer deep expertise in treating people living with amyotrophic lateral sclerosis (ALS), formerly called Lou Gehrig’s disease. By bringing together a dedicated team of health care professionals — including neurologists and other specialists, therapists, nurses, dietitians, social workers and more — we offer personalized care that addresses the diverse needs of you and your caregivers. We strive to create a supportive environment that empowers you and improves your quality of life, with a focus on innovation, accessibility, community trust and advancing treatment options through clinical trials.

As an ALS Association Certified Treatment Centers of Excellence™, we’ve been recognized for our work to provide people living with ALS with compassionate care to enhance the quality of life and support families impacted by ALS.

Our clinic features advanced technology and cutting-edge equipment, which allows us to provide the best possible care and treatment options. This environment fosters an integrated approach to care, ensuring that you receive the most up-to-date treatments available. Being part of an active research team means that you may have access to clinical trials and the latest treatments before they become widely available. Our focus is to slow your disease progression and manage your symptoms so that you can live a better life.

We strive to make you feel heard and involved in decision-making. We have created an environment where you have a voice in your care, helping you navigate treatment options, symptom management and end-of-life planning. ALS impacts families as well, and our clinic regularly provides resources and support for caregivers, such as caregiver training and support groups.

Convenient Care When and Where You Need It

We understand that convenience and accessibility are important. Our clinic offers both virtual and in-person appointments, allowing you to choose the option that works best for you and ensuring continuity of care no matter where you are located.

 

Conditions We Treat

  • Amyotrophic lateral sclerosis (ALS), formerly called Lou Gehrig’s disease
  • Kennedy’s disease (spinobulbar muscular atrophy)
  • Motor neuron diseases (MNDs)
  • Primary lateral sclerosis (PLS)
  • Progressive bulbar palsy (PBP)
  • Progressive muscular atrophy (PMA)

Treatments We Offer

  • Assistive devices: We offer wheelchairs, speech-generating devices, feeding tubes and ventilators as your disease progresses to aid in your mobility, communication and breathing.
  • Feeding tubes/Percutaneous endoscopic gastrostomy (PEG): PEG stands for percutaneous endoscopic gastrostomy, a procedure in which a flexible feeding tube is placed through the abdominal wall and into the stomach. PEG allows nutrition, fluids and/or medications to be put directly into the stomach, bypassing the mouth and esophagus. Feeding tubes can be an important consideration for people with ALS, especially as the disease progresses and swallowing difficulties (dysphagia) become more pronounced. The decision to use a feeding tube typically centers around maintaining nutrition, hydration and overall quality of life. However, it can also bring up emotional, social and practical concerns. Our professionals can help guide you through this process and decide if it is the right option for you.
  • Nutrition guidance: Nutrition plays an important role in managing ALS. As ALS progresses, it can impact your ability to swallow, chew and digest food, which can lead to malnutrition, weight loss and muscle weakness. Our dietitians can help ensure you are getting the proper food and nutrition.
  • Pharmacological treatments: We offer FDA-approved medications such as riluzole, tofersen and edaravone, which aim to slow progression, while others manage symptoms like pain, muscle spasms and sleep issues.
  • Physical therapy: Our physical therapists help you maintain as much independent function as possible, including mobility, strength and flexibility using various techniques like exercise, assistive device recommendations and caregiver training.
  • Respiratory support: If you experience breathing difficulties due to weakened respiratory muscles, our respiratory support options can help make your breathing easier.
  • Speech therapy: Speech therapy can help, and when speech becomes difficult, there are alternative communication methods like communication boards or devices that help you speak using your eyes or facial movements.
  • Tofersen (Qalsody): Tofersen (Qalsody) is a targeted treatment for ALS patients who have the SOD1 gene mutation, which accounts for about 2%-3% of ALS cases. The drug is administered through a spinal injection.

Screening & Diagnostics We Offer

These diagnostic tools help us confirm your diagnosis, understand your disease stage and rule out other conditions, all of which guide your treatment plan.

Clinical Examination

Your doctor will perform a thorough physical and neurological exam to assess your muscle strength, reflexes, coordination and ability to perform basic tasks. This helps us identify any signs of ALS and understand how your body is functioning.

Electromyography (EMG)

This test measures the electrical activity in your muscles. We’ll insert fine needles into your muscles. It helps us see if there’s any abnormal activity that might suggest ALS.

Nerve Conduction Study (NCS)

This test checks how well your nerves can carry electrical signals to your muscles. Small electrodes are placed on your skin to measure how well your nerves are functioning. This test is often done alongside the EMG.

Magnetic Resonance Imaging (MRI)

An MRI uses powerful magnets and radio waves to create detailed images of your brain and spinal cord. While it doesn’t directly show ALS, it helps us rule out other conditions that might cause similar symptoms like tumors or spinal cord problems.

Blood Tests

We’ll take a blood sample to check for other conditions that might be causing your symptoms and also detect biomarkers for ALS.

Genetic Testing

This test looks for genetic mutations to further categorize your ALS type.

Cerebrospinal Fluid (CSF) Analysis (Lumbar Puncture)

In some cases, we may need to do lumbar puncture. This test involves taking a small sample of the fluid around your brain and spinal cord. It helps us rule out other conditions like infections or inflammatory diseases.

Pulmonary Function Tests and Other Respiratory Muscle Function Assessments

These tests measure how well your lungs are working. Since ALS can affect your breathing muscles, it’s important for us to assess your lung function regularly to catch any early breathing issues.

Swallowing Studies (Videofluoroscopy or Fiberoptic Endoscopic Evaluation of Swallowing)

These tests help assess your ability to swallow safely. A videofluoroscopy uses X-rays while you swallow different foods and liquids. The fiberoptic test uses a small camera to look directly at your throat and swallowing muscles.

Muscle Biopsy (Rarely Used)

In rare cases, we might remove a small sample of muscle tissue for examination under a microscope. This helps us look for muscle damage patterns typical of ALS, but this is not commonly needed.

Neuropsychological Tests

These tests help us understand your cognitive abilities, as some people with ALS may experience changes in thinking or behavior. We’ll ask you questions or have you complete some tasks to see how your memory, attention and decision-making are working.

Functional Scales, Such as ALS Functional Rating Scale (ALSFRS)

We use different scales to assess how well you can perform everyday activities, like walking, speaking and swallowing. This helps us track the progression of ALS and how it’s impacting your life. Additional scales are also used to measure quality of life.

Patient Experience

Referral Process

Patients are referred by other neurologists for a second opinion or to confirm a diagnosis of ALS or a related neurodegenerative motor neuron disease. Referrals can also come from other specialties such as ENT, spine surgery, pulmonary or speech therapy.

Initial Assessment

Medical records are reviewed for neuromuscular patients suspected of having ALS or a similar condition. Appointments are scheduled within two weeks to ensure timely care and diagnosis confirmation.

Diagnosis Confirmation

After confirming the ALS or degenerative motor neuron disease diagnosis, the information is shared with you and your family.

Follow-Up Care

After the diagnosis is confirmed, you are scheduled for regular follow-up appointments at the ALS clinic for ongoing care and management.

Your Team

The ALS multidisciplinary clinic is composed of a dedicated team of health care professionals working together to provide comprehensive care. This team includes:

  • An ALS clinic coordinator and nurse navigator who oversee the clinic’s day-to-day operations, ensuring smooth coordination of appointments, services and patient care
  • DME (Durable Medical Equipment) specialists who help ensure patients have the appropriate equipment for mobility and daily activities
  • Gastroenterologists who address gastrointestinal issues
  • Genetic counselors who provide insight into genetic factors relating to ALS
  • Interventional radiologists for procedures that support disease management
  • Mental health professionals who support emotional well-being and coping
  • Neurologists (neuromuscular specialists) who diagnose and manage ALS
  • Neuromuscular nurses who coordinate care and provide patient education
  • Nutritionists/dietitians who provide guidance on maintaining strength and managing nutritional needs
  • Palliative care specialists focused on symptom management and quality of life
  • Physical and occupational therapists who work with patients to maintain mobility, strength and independence
  • Pulmonologists who address respiratory care and breathing issues
  • Research team members who conduct clinical trials and studies to advance treatments for ALS
  • Respiratory therapists who help manage breathing difficulties and provide guidance on respiratory support
  • Social workers who assist with psychosocial support and resource navigation
  • Speech-language pathologists who help manage speech and swallowing challenges

Together, this multidisciplinary team provides holistic care and works to improve the lives of both you and your caregivers.

 

Frequently Asked Questions

What is ALS?

ALS is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord, leading to muscle weakness, loss of motor control and eventually paralysis.

What are the symptoms of ALS?

Early signs can include muscle weakness, difficulty speaking or swallowing, muscle cramps and twitching. As the disease progresses, it affects motor skills and respiratory functions.

What is the cause of ALS?

The exact cause of ALS is still not fully understood, but it is believed to result from a combination of genetic and environmental factors that affect the motor neurons, which are responsible for controlling voluntary muscles.

Can ALS be inherited?

In about 5%-10% of cases, ALS is familial and inherited. Most cases are sporadic, meaning they occur without a family history. In sporadic ALS, the exact cause is unknown, and it is not directly inherited, but there may still be a genetic component involved.

How is ALS diagnosed?

ALS diagnosis is based on clinical examination, medical history and the exclusion of other diseases. Tests like EMG (electromyography), nerve conduction studies and MRI may be used.

What is the difference between ALS and other motor neuron diseases?

ALS is a type of motor neuron disease, but there are other conditions like primary lateral sclerosis (PLS) and progressive muscular atrophy (PMA), each with varying symptoms and progression.

How fast does ALS progress?

ALS progression varies by individual. On average, ALS may lead to severe disability within three five years, but some people live longer with appropriate care. A certain percentage of people with ALS have slower progression and live longer.

Are there clinical trials for ALS?

Yes, we offer clinical trials aimed at finding better treatments for ALS. Patients may be eligible to participate in trials, and it’s important to consult with our doctors about options.

What should caregivers know about caring for someone with ALS?

Caregivers need to understand ALS progression, provide physical assistance, manage communication challenges and offer emotional support.

What are other resources for ALS management and care?

Doctor and nurse taking care of a senior Caucasian woman with a head cover caused by chemotherapy cancer, smiling and sitting in a wheelchair.

Palliative Medicine and Supportive Care

We help you navigate the complexities of serious illness and live well at any stage of treatment.

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Pulmonary, Critical Care and Sleep Medicine

We offer specialized treatment of various pulmonary disorders.

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Speech Therapy

We focus on evaluation and intervention to improve communication skills — speech, voice, language and swallowing difficulties.

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Clinical Nutrition

Our dietitians offer evidence-based clinical nutrition care to help you manage and achieve your health goals.

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World-Class Leadership

Our internationally renowned physicians and clinicians are dedicated to delivering high-quality patient care. We are leaders in cutting-edge treatments, breakthrough research and exceptional outcomes.

Said R. Beydoun, MD

Director, USC ALS Center of Excellence

Leila Darki, MD

Co-Director, USC ALS Center of Excellence

Beyond Clinical Care

Residency

USC/Los Angeles General Medical Center Neurology Residency

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Clinical Trials

Participating in a clinical trial gives you access to new and promising therapies.

Find an open trial

Fellowship

USC/ Los Angeles General Medical Center Clinical Neurophysiology Fellowship

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Donate

Support our efforts to advance and innovate ALS care.

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