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Rare Patient Voice

Helping Patients with Rare Diseases Voice Their Opinions

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    • Market Access: A Patient Perspective
    • The Impact of Rare Diseases on Patients and Caregivers
    • The Role of Patient Advocacy Groups
    • Zebras Do Exist: The Diagnostic Odyssey of Rare Disease Patients
    • Patient Insights on Telehealth: A Case Study
    • Hearing is Believing: Reducing Barriers to Amplify the Patient Voice

Helping patients and caregivers share their voices

Amazing Patients and Caregivers

February 3, 2014 Wes Michael

One of the greatest thing about working at Rare Patient Voice is getting the opportunity to meet so many amazing people. Let me tell you about two.

Kathryn Ames (I’ll mention her by name as she has given me permission) is a terrific mom. She struggled when her son Nicholas, who has severe Hemophilia A, wanted to crawl like any other toddler. She created a line of padded pants, and other clothes, and called them Bruz Wear. What a great way to help others while she was coming up with an ingenious solution to the problem she saw! I encourage you to go to her website: www.bruzwear.com.

Another of our members told me that regular rules and regs generally don’t apply to her. She lives in the New York City area. One New Year’s Eve, she decided she wanted to see the famous ball drop. She got in line, worked her way to the front, and security staff told her she couldn’t go further. But somehow she did, her kids saw her on TV right up front next to the celebrity hosts! If having children with hemophilia couldn’t stop her, she wouldn’t let fierce NY security stop her, either!

Filed Under: Community, Hemophilia, Patient

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