Can You Drink Alcohol If You Have Multiple Sclerosis?

Multiple Sclerosis (MS) is a chronic condition affecting the central nervous system, including the brain, spinal cord, and optic nerves. The immune system attacks myelin, the protective sheath covering nerve fibers, disrupting communication throughout the body. Understanding the impact of lifestyle choices, such as consuming alcohol, is important for managing symptoms. This article explores the current evidence regarding alcohol use in the context of MS.

How Alcohol Affects Common MS Symptoms

Alcohol is a central nervous system depressant that can intensify or mimic symptoms caused by MS-related nerve damage. Even a single drink can affect neurological function, potentially worsening existing issues with balance and coordination. Since MS often causes ataxia, or unsteadiness, consuming alcohol increases the risk of falls and makes gait difficulties more pronounced.

MS-related fatigue can be exacerbated by alcohol’s depressive effect. While alcohol may cause initial drowsiness, it disrupts sleep quality, leading to increased daytime fatigue and physical weakness. Many people with MS also experience cognitive dysfunction, or “cog fog,” involving slower processing speed and memory issues. Alcohol consumption can impair these functions further, making cognitive lapses more severe.

Bladder issues, such as frequency and urgency, are common in MS due to nerve signal disruption. Alcohol acts as a diuretic, increasing urine production and irritating the bladder lining. This diuretic effect significantly worsens existing urinary symptoms, potentially leading to more frequent nighttime awakenings or increased incontinence risk.

Alcohol’s Interaction with MS Medications

The combination of alcohol with MS treatments requires careful consideration, particularly concerning the liver and the central nervous system. Many Disease-Modifying Therapies (DMTs) can affect liver function and require regular monitoring of enzyme levels. Since alcohol is metabolized primarily by the liver, combining it with these medications adds stress to the organ.

This interaction increases the potential for hepatotoxicity, or drug-induced liver injury, reported with various DMTs. The general recommendation is to limit or avoid alcohol use to reduce the cumulative burden on the liver. Patients should discuss their alcohol intake with their neurologist, especially when starting a new DMT that requires liver function monitoring.

In addition to DMTs, alcohol interacts dangerously with many symptom management medications. Drugs prescribed for spasticity, pain, or sleep are often central nervous system depressants, such as muscle relaxants like baclofen. When alcohol is consumed alongside these medications, the sedative effects are compounded, leading to severe drowsiness, confusion, and impaired judgment. This also increases the risk of dangerous side effects, including slowed breathing.

Current Research on Alcohol and Disease Progression

The relationship between alcohol consumption and the long-term course of MS is complex. Heavy or long-term alcohol use is generally detrimental to the nervous system and overall health. This consumption level is associated with increased inflammation and can compromise the immune system, which relates to MS pathology.

Epidemiological studies have explored the impact of light to moderate alcohol intake on disability accumulation. One large, long-term study found that low and moderate alcohol consumption was associated with a reduced risk of disability progression compared to abstaining. This effect was primarily observed in individuals with relapsing-remitting MS (RRMS) and appeared more pronounced in women.

These findings do not suggest that non-drinkers should begin consuming alcohol, as the underlying biological reason is not fully understood. It is hypothesized that low amounts of alcohol might have a modest modulating effect on the immune system. Overall, heavy drinking is discouraged, but current evidence does not strongly link moderate alcohol use to accelerated MS progression or increased relapse rates.