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ActiveVoices™ Participation Agreement

By clicking on this box, you should acknowledge and agree that your participation in the ActiveVoices program is completely voluntary. You understand that the role of your Mentor is to provide you with information about his or her own personal experiences living with MS and MS therapies. Your Mentor is an MS patient—not a physician or nurse with medical expertise. Therefore, your Mentor is trained not to provide you with, and you should not rely upon your Mentor for, medical treatment advice. You should understand that your MS and treatment experiences may differ from your Mentor's experiences and that any questions you have about possible side effects, risks or potential benefits of treatment, adverse events, or your MS disease course should be directed to your own health care provider. You also understand that your Mentor is a volunteer and Biogen Idec does not compensate your Mentor for providing you with the mentoring services. Your Mentor does not speak on behalf of or represent Biogen Idec. Your mentor is limited in what he or she can say about Biogen Idec's products by rules from the Food and Drug Administration to information that is consistent with the applicable product's approved label. You may stop participating in the ActiveVoices Mentor program at any time. If you have any concerns or questions about what your Mentor says to you, your relationship with your Mentor, or the ActiveVoices program in general, please feel free to contact MS ActiveSource at 1-800-456-2255.

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Peer Mentor Profile

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Nicolle B., Diagnosed with MS in 2003, Female, 35-44, Other

How did you first find out about your relapsing MS?

I found out I had MS after having some numbness in my left hand and arm. I had blood work, a spinal tap and an MRI done. Based on the results of the MRI, I was diagnosed with MS. I was 26 years old.

What emotions did you experience when first diagnosed with relapsing MS?

I was devastated and in deep denial. I did not want to believe that I had this disease. I researched all my options.

How has your outlook changed today regarding your relapsing MS?

I appreciate what my body can do on any given day. I know that from day to day my body's ability to do things varies. I accept myself and take care of myself better now than I ever did before. I respect myself. I know when to slow down and take it easy. I have MS. MS does not have me.

What would you say to someone who has found out they have relapsing MS?

There is hope. You are not alone.

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