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The UAB Multiple Sclerosis Clinic provides specialized treatment for MS and other immune-based disorders of the central nervous system, including, but not limited to the following:

  • Multiple Sclerosis
    Multiple Sclerosis (MS) is an autoimmune, inflammatory condition of the central nervous system. Relapsing MS (formerly known as Relapsing Remitting MS) is the most common form and constitutes approximately 85-90% of all cases of MS at the time of diagnosis. Another form of MS is called Progressive MS (PMS). Patients with PMS have slowly worsening courses that do not have typical relapse events. PMS can develop years after RMS is diagnosed or can develop from the start (Primary Progressive MS). Much of the nervous system damage that occurs in MS is due to demyelination (stripping of insulation off of nerve cells), but there is also direct nerve cell death as well.

    Relapsing MS: RMS is by far the most common form of MS. It typically presents in early to middle adulthood, with most patients diagnosed between the ages of 20 and 40. The diagnosis is typically made after a patient has suffered from two separate attacks that have caused symptoms consistent with demyelinating events occurring in the central nervous system. These symptoms may be weakness, numbness, imbalance, vision loss or double vision, or difficulty speaking or swallowing. Many patients experience an initial event that is termed Clinically Isolated Syndrome (CIS) and later go on to develop RMS. When patients present with a history, symptoms and physical exam concerning for RMS, we order tests such as bloodwork, Magnetic Resonance Imaging (MRI), Evoked Potentials or a Lumbar Puncture. Once we are confident in the diagnosis of RMS, we usually recommend some form of Disease Modifying Therapy (DMT). The typical course of RMS is one of relapses that consist of new symptoms that develop over a period of hours or days that often persist for up to a few weeks but then significantly improve. There may be periods of remission, or no disease activity, that persist for months or years at a time.

    Progressive MS: Previously, progressive forms of MS were divided into Secondary Progressive – arising from prior Relapsing MS – and Primary Progressive – progressive disease from the start. However, it seems that the disease process of progressive disease is very similar in both forms, so the MS community has recently revised our diagnoses into simply Progressive MS. PMS is characterized by progressive decline in function of the nervous system and the progressive accumulation of disability. It tends to affect older patients more than younger patients. There may be periods of relapse events occurring in this disease, but the primary disease activity is that of slow progression. The rate of progression can vary from very slow with stable periods to very rapid accumulation of disability. Currently, we have limited treatment options to help with PMS, but this is an area within MS that is currently undergoing much research – including trials at UAB. Despite inadequate treatments for disease modification, we can help significantly with symptomatic management to help our patients achieve a much higher quality of life.
  • Neuromyelitis Optica
    Neuromyelitis Optica (NMO) is an inflammatory condition of the central nervous system with a well established disease process. In this condition, an antibody is produced by the immune system that cross-reacts with a water channel in the brain and this results in inflammation and damage to the nervous system. This disease usually causes vision loss, weakness and numbness in extremities and difficulty walking or upper extremity impairment. Between 10-20 percent of patients who have an initial event or relapse in this condition will not go on to develop another episode. Relapses typically respond to treatment with steroids or plasma exchange – a process similar to dialysis. However, unlike RMS, patients with NMO tend to have less complete recovery from relapses. For patients at high risk for developing additional relapses, we recommend initiating ongoing treatment even with a single attack.
  • Transverse Myelitis
    Transverse Myelitis (TM) is a descriptive term that refers to damage sustained to the spinal cord by inflammation and can have many different causes. Other non-inflammatory conditions can also mimic TM, including stroke, infection, metabolic disturbances or degenerative conditions. Symptoms usually consist of numbness or weakness in the arms or legs that appear rather suddenly, and patients often experience bladder and bowel dysfunction. The prognosis of TM depends on the cause of the spinal cord damage sustained.
  • Optic Neuritis
    Optic Neuritis (ON) is inflammatory damage that occurs in the nerve that carries visual information from the back of your eye to your brain. This is typically characterized by pain with eye movement in one or both eyes that is accompanied by reduced color vision and impaired visual acuity – or blurriness – in the same eye. The pain may precede the vision changes or they may occur simultaneously or the vision loss may occur without pain at all. This event is often caused by inflammation in the nerve but can also be due to reduced blood flow to the nerve.
  • Acute Disseminated Encephalomyelitis
    Acute Disseminated Encephalomyelitis (ADEM) results from acute inflammation that occurs in the brain and causes diffuse dysfunction. It most commonly affects children, but can affect adults as well, particularly younger adults. Patients who suffer from this condition typically become very sleepy and immediately fall asleep after you stop speaking with them. They may have weakness or numbness in some of their extremities or vision loss. Occasionally, ADEM can also affect the spinal cord and cause transverse myelitis. Acutely, patients with ADEM usually require admission to the hospital and various treatments. Both younger and older patients with ADEM usually have improvement following this event but younger patients tend to improve more than older patients. This event does not typically recur.
  • Clinically Isolated Syndrome
    Clinically Isolated Syndrome (CIS) is an event that is suggestive of damage due to demyelination but has occurred without other evidence of prior or ongoing damage to the nervous system. This may herald further damage or may remain an isolated event. When this occurs, we attempt to gather data to determine if the patient is at high risk of having another event. These data determine how we approach further testing and help us decide if ongoing treatment is necessary.
  • Central Nervous System Vasculitis
    CNS Vasculitis (also known as CNS Angitis) refers to inflammation in and around blood vessels that can lead to disruption of blood flow in the CNS. It can arise from a systemic illness affecting the entire body or can arise in isolation, when it is called Primary CNS Vasculitis. It can present with ischemic (reduced blood flow) strokes or with hemorrhagic (bleeding) strokes or with a multitude of other symptoms such as difficulty thinking, headaches, personality changes, etc. There are multiple effective treatments to address this condition.
  • Neurologic Complications of Systemic Illness
    Many inflammatory or autoimmune diseases such as lupus, sarcoidosis, and Sjogren’s disease can affect the CNS through various mechanisms. It is important to recognize neurologic complications of these diseases early and to treat them quickly. Close monitoring by a neurologist for the development of new or worsening symptoms is important in these diseases as prevention of nervous system injury is much more effective than reparative strategies.
  • Neuro-Infectious Disease
    There are several chronic infectious processes that can affect the CNS and result in significant impairment. Lyme disease, Human T-cell Lymphotropic Virus (HTLV), Cryptococcus, Herpes Simplex Virus (HSV), Tuberculosis and various other infections can have prolonged courses that can cause many different neurologic symptoms.
  • Neuro HIV
    HIV can have significant effects on the CNS. These can manifest from different aspects related to the disease, including direct effects from the infection, opportunistic infections that arise from being immunocompromised, or side effects from the medications used to treat HIV. Patients can develop numbness, weakness, difficulty thinking, seizures or many other symptoms that are due to nervous system involvement in this disease.
  • CNS Demyelinating Disease/Leukodystrophies
    Leukodystophies are a group of disorders that involve inadequate production of the myelin around nerves in the central nervous system. They typically begin in childhood, but there are less common forms that begin in adulthood. We follow patients in our center who were diagnosed in childhood and those who were newly diagnosed in adulthood. Although there is no treatment to reverse the effects of this illness, we are able to reduce the burden of many of the symptoms that patients experience.
  • CNS White Matter Disease/Leukoencephalopathies
    CADASIL/CARASIL (Cerebral Autosomal Dominant/Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopthy) can lead to stroke-like events and changes on MRI in the white matter of the brain. These illnesses are sometimes confused with demyelinating disease but these are actually diseases of the blood vessels in the nervous system. We treat many patients with this diagnosis in our center.

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