Medication for MS

Some people with MS choose to take medication to get their symptoms under control. This is not in conflict with the OMS Recovery Program. We advocate doing whatever it takes to lead a better, healthier life with MS.

Many medications are used to treat MS, but none of them can claim to cure the disease.

Evidence shows that a healthy lifestyle, including stopping smoking, regular exercise and a nutritious diet can slow the progression and manage MS symptoms, so combining lifestyle changes with medication provides a holistic approach.

How can MS medication help?

MS medications generally reduce the rate of relapses – some only modestly. Those that are most effective at reducing disease activity come with a more significant side effect profile and the need for close monitoring for complications.

Some MS medications are known as disease modifying drugs (DMDs) or disease modifying therapy (DMT). Both terms mean a drug that can in some way alter the course of a disease, either by reducing relapses and in turn aiming to reduce disability progression.

For some of the earlier MS medications (B-interferons and Copaxone), it has been difficult to establish their effect on progression of the disease to disability, although some of the newer drugs do seem to slow the disease course.

See our Research News section for the latest studies. 

We offer some advice and guidance on what to think about when making medication choices. Many people feel anything that may help is worth trying, as long as the side effects aren’t too severe.

Take a look at our short illustrated video:

MS medications: Everything you need to know

The following medications are commonly used to treat multiple sclerosis (or have in the past, some have been discontinued). 

Follow the links below for more information about these medications, which types of MS they treat, their side effects, action, background and relevant studies. 

MS medication side effects

If you read through the accompanying information for any medication you will always see possible side effects listed. However, with MS medications, the side effects can range from mild to severe.  As some MS medications can potentially cause harm, your MS team will monitor your health closely with regular blood tests and MRI scans. 

Some possible side effects, depending on the medication, include: 

  • Hair loss and nausea 

  • A change to your heart rate  

  • Flu-like symptoms   

  • Brain infection

  • Chest pain

MS without medication

If you choose to treat your MS without medication, make sure that you have regular check-ups with your doctor, as things can change and you might want to start medication in the future. As well as the MS medicines, there are also medications such as steroids which can relieve symptoms of a new relapse. 

There is little doubt that there are numerous ways in which you can optimise your health and stay well without medication, such as:

✔  Benefitting from a healthy diet

✔  Using physical therapy — such as occupational therapy

✔  Reducing stress — including daily meditation 

 Increasing your exposure to sunlight and vitamin D

An easy way to combine all these — with the added benefit of a support network — is through the OMS recovery program.

Monthly infusions for MS

Infusion therapies can be used to treat MS relapses that don’t respond to corticosteroids.  Intravenous immunoglobulin (IVIG) via a drip helps to boost your immune system and plasmapheresis filters your blood to remove damaging antibodies after which the ‘clean’ blood is put back into your body through a blood transfusion. 

The following Disease modifying drugs are also given intravenously: 

Ocrelizumab (Ocrevus) — you receive this drug in two doses separated by two weeks at first, then you have infusions every six months. It is the first drug to be approved for primary progressive MS (PPMS) and targets damage-causing B lymphocytes.

Alemtuzumab (Lemtrada) — given once a day for five days, then you receive it again over three days, 12 months later. The drug reduces your white blood cells to reduce damage to nerve cells and inflammation (specifically reducing the number of T and B lymphocytes).

Mitoxantrone hydrochloride — you receive this drug once every three months and a lifetime maximum dose is reached within two or three years. This drug is an immunosuppressant and stops your immune system’s reaction to MS attacks. It is also a chemotherapy drug. Due to the potentially very serious side effects it is usually reserved for those with severe MS or in certain cases of  secondary progressive MS (SPMS).

Natalizumab (Tysabri) — you receive this drug once a month. It stops immune cells from entering your spinal cord and brain and causing damage. 

As with all medication there are possible side effects for each drug including reactions like nausea or fatigue. The side effects also include health issues as a direct result of the infusion process itself including skin reactions, chills, and bruising and bleeding at the injection site. There are also serious side effects which implicate potentially life-threatening instances of organ failure and cancer, depending on the drug being received. Like with any medicine, it is administered to help you, but it is vital that you know and understand all the risks involved.

Medication