Multiple Sclerosis (MS) Handout

Incidence Approximately 2.5 per 100,000 people per year
Prevalence Approximately 2.5 per 100,000 people per year
Age of Onset Typically between 20 and 50 years old, though it can occur at any age
AT Required 80-90%
Medical Coding Information
ICD-11:
ICD-10-CM: See content
OMIM:
UMLS:
MeSH:
GARD:

Introduction

Multiple Sclerosis (MS) Handout

Name of Disorder: Multiple Sclerosis

Clinical Information

The following data is from validated clinical sources and patient registries.

Core Characteristics

  • Etiology: Genetic
  • Pathology: Variable
  • Rarity Classification: High
  • Typical Onset: Adulthood
  • Gender Impact: Mostly Women
  • Progressive/Degenerative: Yes
  • Seizure Prevalence: No (<10%)
  • Population Trend: Stable

Pathophysiology

Considered an autoimmune disease but clearly has a hereditary element to it

AAC Considerations

Recommended Access Modalities: Touch

Additional Clinical Notes

Very interesting geographic gradient in the prevalence here, worth looking into. I may be underestimating the % of AAC use, there are many coflicting sources.

Formal Name: Multiple Sclerosis (MS)

Demographic Information:

  • Incidence: Approximately 2.5 per 100,000 people per year
  • Prevalence: Estimated at around 1 in 1,000 people in the United States
  • Gender: More common in women than men, with a ratio of about 3:1
  • Onset Age: Typically between 20 and 50 years old, though it can occur at any age

Coding:

  • ICD-11: 8A40
  • ICD-10-CM: G35
  • OMIM: 126200
  • UMLS: C0026769
  • MeSH: D009103
  • GARD: 7314

Quick Reference

| Quick Facts | Details | |-------------|---------| | Incidence | Approximately 2.5 per 100,000 people per year | | Prevalence | ~1 in 1,000 people (approximately 914,000 in U.S.) | | Gender Distribution | More common in women than men (ratio ~3:1) | | Primary Age of Onset | Typically between 20 and 50 years old | | AT/AAC Requirements | Low to Moderate - Approximately 20-25% will require assistive technology; AAC needs increase with disease progression, particularly in severe cases |

Medical Features and Pathophysiology:

  • Etiology:
Multiple Sclerosis (MS) is an autoimmune disorder characterized by the immune system attacking the myelin sheath, the protective covering of nerve fibers in the central nervous system (CNS). The exact cause of MS is unknown, but it is believed to involve a combination of genetic and environmental factors. Genetic predisposition, viral infections (such as Epstein-Barr virus), and Vitamin D deficiency are among the factors thought to contribute to the risk of developing MS.
  • Pathology:
The hallmark pathological feature of MS is demyelination, the loss or damage of the myelin sheath, which disrupts the normal transmission of nerve impulses. This process leads to the formation of scar tissue (sclerosis) in the CNS, primarily in the brain, spinal cord, and optic nerves. The disease can present in various forms, including relapsing-remitting MS (RRMS), primary progressive MS (PPMS), secondary progressive MS (SPMS), and progressive-relapsing MS (PRMS). The exact mechanisms underlying these different forms are not fully understood, but they involve varying degrees of inflammation, demyelination, and neurodegeneration.
  • Symptoms:
- Motor Symptoms:

- Muscle weakness and spasticity - Coordination and balance problems - Tremors - Gait difficulties - Sensory Symptoms: - Numbness or tingling - Pain - Visual disturbances (optic neuritis, double vision) - Cognitive and Emotional Symptoms: - Memory and concentration difficulties - Depression and anxiety - Fatigue - Autonomic Symptoms: - Bladder and bowel dysfunction - Sexual dysfunction

  • Diagnosis:
Diagnosis of MS involves a combination of clinical evaluation, imaging studies (such as MRI), and laboratory tests. The McDonald criteria are commonly used to diagnose MS, which include evidence of CNS lesions disseminated in time and space. Cerebrospinal fluid (CSF) analysis may show the presence of oligoclonal bands, indicative of an inflammatory process in the CNS. Evoked potentials, which measure the electrical activity of the brain in response to stimuli, can also aid in the diagnosis.

Assistive Suggestions and Requirements:

  • Requirement Percentage for Assistive Technology:
A significant percentage of individuals with MS will benefit from assistive technology, particularly as the disease progresses and symptoms become more disabling.
  • Assistive Technology Suggestions:
- Mobility Aids:

- Canes or Walkers: To assist with balance and prevent falls. - Wheelchairs: For individuals with severe mobility impairments. - Communication Aids: - Voice Amplifiers: To assist with dysarthria (speech difficulties). - Speech Generating Devices (SGDs): For individuals with severe speech difficulties. - Home Modifications: - Grab Bars and Handrails: To enhance safety and prevent falls. - Adjustable Beds: To improve comfort and ease of movement. - Feeding Aids: - Adaptive Utensils: For individuals with tremor or reduced hand dexterity.

  • Access Modalities:
- Switch Access: For individuals with severe motor impairments to control communication devices and computers.

- Voice-Controlled Systems: Beneficial for those who retain good vocal strength. - Touchscreen Devices: Useful for those with adequate hand dexterity.

Care Management and Therapeutic Techniques:

  • Aims:
- To manage symptoms and maintain the highest possible level of independence and quality of life.

- To provide supportive care and address complications through a multidisciplinary approach. - To offer education and support to patients and caregivers.

  • SLP Suggestions:
- Assessment and Intervention:

- Regular speech and swallowing assessments to monitor changes and adjust therapy plans accordingly. - Techniques to improve speech clarity and address dysarthria. - Swallowing techniques to ensure safe swallowing and reduce the risk of aspiration. - Augmentative and Alternative Communication (AAC): - Introduction of AAC devices early in the disease progression to ensure familiarity and ease of use as the disease progresses.

  • Special Educator Suggestions:
- Cognitive Rehabilitation:

- Activities designed to enhance executive function, memory, and attention. - Use of memory aids, such as notebooks or electronic organizers. - Behavioral Strategies: - Structured routines to manage apathy and maintain engagement in activities. - Positive reinforcement to encourage participation and effort in tasks.

  • Occupational Therapist Suggestions:
- Daily Living Skills:

- Training in the use of adaptive equipment for self-care activities (e.g., dressing, grooming). - Techniques to conserve energy and manage fatigue. - Home and Environmental Modifications: - Assessing and modifying the home environment to ensure safety and accessibility. - Recommendations for ergonomic furniture and tools to support independence.

AAC Recommendations

Individuals with MS typically retain literacy and cognitive abilities until late-stage disease. Text-based systems with word prediction accommodate motor difficulties while preserving natural language expression. Symbol-based systems are rarely needed unless significant cognitive decline occurs. AAC should be introduced proactively as dysarthria progresses rather than waiting for complete speech loss.

References

1. Lublin, F. D., & Miller, A. E. (2014). Multiple sclerosis phenotypes: Current and future considerations. Neurology, 83(3), 278-286. 2. Compston, A., & Coles, A. (2008). Multiple sclerosis. The Lancet, 372(9648), 1502-1517. 3. Hauser, S. L., & Goodin, D. S. (2012). Multiple sclerosis and other demyelinating diseases. In D. L. Longo (Ed.), Harrison's Principles of Internal Medicine (18th ed., pp. 3395-3409). McGraw-Hill. 4. (2019). Progressive multiple sclerosis: latest therapeutic developments and future directions. Therapeutic Advances in Neurological Disorders. https://doi.org/10.1177/1756286419878323 5. (2018). Practice guideline recommendations summary: Disease-modifying therapies for adults with multiple sclerosis. Neurology. https://doi.org/10.1212/WNL.0000000000005347 6. (2007). Remyelination In Multiple Sclerosis. International review of neurobiology. https://doi.org/10.1016/S0074-7742(07)79026-8 7. (2005). Exercise therapy for multiple sclerosis. Cochrane Database of Systematic Reviews. https://doi.org/10.1002/14651858.CD003980.pub2 8. (1971). Visually evoked responses in multiple sclerosis. Journal of Neurology Neurosurgery & Psychiatry. https://doi.org/10.1136/jnnp.34.3.275

Epidemiology and Demographics

Etiology and Pathophysiology

What causes Multiple Sclerosis (MS) Handout?

What does Multiple Sclerosis (MS) Handout do to the body?

Clinical Features and Stages

Diagnosis

Diagnostic Criteria

Genetic Testing

Differential Diagnosis

Assistive Technology and AAC Interventions

Communication Devices

Mobility Aids

Access Modalities

Environmental Control Units

Clinical Recommendations

🗣️ For Speech-Language Pathologists

For Occupational Therapists

🚶 For Physical Therapists

📊 For Applied Behavior Analysts

🎓 For Special Educators

👥 For All Staff and Caregivers

Care Management

Medical Management

Positioning and Handling

Feeding and Swallowing

Psychosocial Support

Educational Support

IEP Goal Examples

Accommodations and Modifications

Transition Planning

Support and Resources

🏛️ Foundations and Research

🌐 Online Communities

📚 Educational Resources

💰 Financial Assistance

References

Version: 1.0
Created: 2026-02-14
Last Reviewed: 2026-02-14
Next Review:

Disclaimer: This comprehensive clinical guide is designed for healthcare professionals, educators, and families. For specific medical advice, please consult with qualified healthcare providers.