Health and Wellness

CIDP

Chronic Inflamatory Demyelinating PolyneuropathyBy Daniel Schwartz

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Length2h 47m

About this audiobook

CIDP: Chronic Inflammatory Demyelinating Polyneuropathy — A Complete Guide by Daniel Schwartz is a comprehensive, accessible 2026 guide to one of the most underdiagnosed autoimmune nerve diseases. CIDP occurs when the immune system mistakenly attacks the myelin sheath surrounding peripheral nerves, causing progressive weakness, numbness, pain, and loss of balance that unfolds over months to years — distinguishing it from the acute, self-limited Guillain-Barré Syndrome it closely resembles. Schwartz walks readers through the full arc of the disease. Written for patients, families, nursing and medical students, and curious non-specialists alike, the book pairs clear plain-language explanations with comparison tables, a full glossary, and practical appendices — symptom diaries, medication logs, and a guide to reading nerve conduction reports — empowering readers to understand their diagnosis and participate meaningfully in their own care.

Healing Psychological Mystery Survival Exploration Futuristic

Audiobook details

GenreHealth and Wellness

Length2 hrs 47 mins

Narrated byListen with 1,000+ voices

FormateBook with Audio

Publish dateApr 13, 2026

LanguageEnglish

1Introduction

2Foreword: A Note to Readers

3Chapter 1: What Is CIDP?

41.1 The Big Picture

51.2 Peripheral Nerves: What Are They?

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61.3 The Word &quot;Demyelinating&quot; — What It Means

71.4 Chronic vs. Acute: How CIDP Differs from GBS

81.5 Why CIDP Is Often Underdiagnosed

9Chapter 2: A History of CIDP

102.1 Early Observations of Peripheral Nerve Disease

112.2 Guillain, Barré, and Strohl (1916)

122.3 The 1950s and 1960s: A Chronic Form Emerges

132.4 Peter Dyck and the Formal Definition (1975)

142.5 The 1980s–1990s: New Treatments and Confirmation

152.6 The 2000s–2010s: Subtypes and Biological Targets

162.7 The 2020s: Targeted Therapies and Personalized Medicine

17Chapter 3: Epidemiology — Who Gets CIDP?

183.1 How Common Is CIDP?

193.2 Age and Sex Distribution

203.3 Geographic and Ethnic Distribution

213.4 Risk Factors and Associated Conditions

223.5 Economic and Social Burden

23Chapter 4: Pathology — What Happens Inside the Nerve?

244.1 The Immune Attack: An Overview

254.2 The Blood-Nerve Barrier

264.3 The Node of Ranvier: Architecture and Vulnerability

274.4 Demyelination, Remyelination, and Onion Bulbs

284.5 What the Nerve Biopsy Shows

294.6 Key Antibody Targets: A New Era of Understanding

304.7 Recognized Clinical Subtypes of CIDP

31Chapter 5: Symptoms — What Does CIDP Feel Like?

325.1 The Typical Presentation

335.2 Motor Symptoms — Weakness and Movement Problems

345.3 Sensory Symptoms — Abnormal Feelings

355.4 Balance and Gait Problems

365.5 Less Common Symptoms

375.6 Clinical Courses Over Time

385.7 Impact on Daily Life and Quality of Life

39Chapter 6: Diagnosis — How Is CIDP Identified?

406.1 Why Diagnosis Is Challenging

416.2 Clinical History and Neurological Examination

426.3 Nerve Conduction Studies (NCS) and Electromyography (EMG)

436.4 Cerebrospinal Fluid (CSF) Analysis

446.5 MRI of the Spine and Peripheral Nerves

456.6 Blood Tests

466.7 Nerve Biopsy

476.8 Diagnostic Certainty Levels and the Treatment Trial: 6.8.1 How Many Nerves Must Be Abnormal? The 2021 NCS Demyelination Criteria

48Chapter 7: Treatment — Managing and Treating CIDP

497.1 The Goals and Philosophy of CIDP Treatment

507.2 First-Line Treatments

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CIDP

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