“Ampyra’s been part of my way of continuing to walk and live my life.” -Lisa

Who Should Take AMPYRA?

Is someone you care about living with multiple sclerosis (MS)?

AMPYRA® (dalfampridine) is indicated as a treatment to improve walking in people with multiple sclerosis (MS). This was demonstrated by an increase in walking speed.

Not everyone responds to AMPYRA. Individual results may vary.

If your loved one could benefit from an improvement in walking related to their MS, you may want to encourage them to talk to their doctor about AMPYRA.

MS affects people's walking in different ways

There are many factors in determining if AMPYRA may be right for your loved one. It's important to understand how MS affects how they walk, and how this might affect their everyday life.

Learning their symptoms, how they start up, how often they occur, and if they're getting better or worse can all play key roles in helping their healthcare team decide if they should try AMPYRA.

It’s also important to know whether they have a history of seizures or have kidney problems or are allergic to dalfampridine (4-aminopyridine), the active ingredient in AMPYRA, since people with these conditions must not take AMPYRA.

Taking a walking self-assessment can help

Your loved one can use this tool to see how MS may be affecting their walking. All they have to do is answer a short list of questions and then discuss the results with their healthcare team.

Before you and your loved one talk to the doctor, you can create your own Talking to Your Doctor Discussion Guide. The Guide is free and can help you start the conversation with your healthcare provider about your loved one's walking.

AMPYRA Conversations

Watch a one-on-one interview with a family living with MS as they talk about signs a caregiver may notice and can help assess when it comes to observing changes in walking.

AMPYRA is indicated as a treatment to improve walking in patients with MS. AMPYRA improved walking in significantly more people with MS than placebo (sugar pill) in two clinical trials (34.8% vs. 8.3% and 42.9% vs. 9.3%). This was demonstrated by an increase in walking speed.

Not everyone responds to AMPYRA. Individual results may vary.

Noticing changes in walking — a caregiver's perspective
Open to see text version
Kristie Salerno Kent:

When you first noticed changes in Joy’s walking, what did you think?

Ben Bryant:

Well, I notice that she slows down, or loses control of her speed altogether. And which, either one of those situations can be dangerous. Especially if we're in a crowd of people, or if there are obstacles in the way.

I remember vividly that I had to ask her, you know, "Let's take a break, let's stop." So that she can go ahead and regain control of her foot speed. Because, you know, it can be a dangerous issue, especially at a mall. And the last thing that I want her to do is to fall and hurt herself.

Kristie Salerno Kent is a paid spokesperson for Acorda Therapeutics®, Inc. Kristie is living with MS and is currently taking AMPYRA. The people interviewed by Kristie for the AMPYRA Conversations video series are real people living with MS and real healthcare professionals who treat people with MS. All participants have been compensated for their time.

AMPYRA® (dalfampridine) is indicated as a treatment to improve walking in patients with multiple sclerosis (MS). This was demonstrated by an increase in walking speed.

IMPORTANT SAFETY INFORMATION

Do not take AMPYRA if you have ever had a seizure, or have certain types of kidney problems, or are allergic to dalfampridine (4-aminopyridine), the active ingredient in AMPYRA.

Take AMPYRA exactly as prescribed by your doctor.

You could have a seizure even if you never had a seizure before. Your chance of having a seizure is higher if you take too much AMPYRA or if your kidneys have a mild decrease of function, which is common after age 50.

Your doctor may do a blood test to check how well your kidneys are working, if that is not known before you start taking AMPYRA.

AMPYRA may cause serious allergic reactions. Stop taking AMPYRA and call your doctor right away or get emergency medical help if you have shortness of breath or trouble breathing, swelling of your throat or tongue, or hives.

AMPYRA should not be taken with other forms of 4-aminopyridine (4-AP, fampridine), since the active ingredient is the same.

The most common adverse events for AMPYRA in MS patients were urinary tract infection, trouble sleeping, dizziness, headache, nausea, weakness, back pain, and problems with balance.

Before taking AMPYRA tell your doctor if you are pregnant or plan to become pregnant. It is not known if AMPYRA will harm your unborn baby.

Tell your doctor if you are breast-feeding or plan to breast-feed. It is not known if AMPYRA passes into your breast milk. You and your doctor should decide if you will take AMPYRA or breast-feed. You should not do both.

Please see the full Prescribing Information and Patient Medication Guide.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.

AMPYRA®, ACORDA THERAPEUTICS® and the stylized ACORDA THERAPEUTICS® logo are registered trademarks of Acorda Therapeutics, Inc. | AMPYRA® is marketed by Acorda Therapeutics, Inc. and manufactured under license from Alkermes Pharma Ireland Limited (APIL), Ireland. | AMPYRACONNECT™ is a trademark of Acorda Therapeutics, Inc. | The stylized path logo and the stylized Acorda logo are trademarks of Acorda Therapeutics, Inc. | © 2013 Acorda Therapeutics, Inc. All rights reserved.

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