In 2014, when I was about 12, I began taking ALPROLIX®, and I’ve been taking it ever since. Since starting ALPROLIX, I have not had any spontaneous bleeds. I am grateful I have the protection from bleeds I need, and I really appreciate that I only have to infuse once a week. I go to my hemophilia treatment center (HTC) every 6 months, and my doctor and I agree that ALPROLIX continues to work for me. Please remember this is my experience, and others’ experiences may differ.
Before high school, I didn’t tell many people about my hemophilia. It’s not that I was hiding my hemophilia—I just didn’t feel like it was necessary for others to know about it. Of course, my teachers already knew in case something happened. And if I was playing rough with my friends and they got close to hurting me, I'd say, "Hey, I’ve got a condition. I need you to chill." I wasn’t ashamed of my hemophilia, but at that age, I didn’t want to risk people treating me differently. Over the years, I’ve become more open about it.
When I was 17, I began infusing on my own and really took ownership of my hemophilia management. I am grateful I only infuse once a week because I have more time to focus on what I love, like spending time with my family, working out, watching anime, playing video games, and trying new sports. My hope is that you will be encouraged to speak up for yourself and work with your doctor to find a treatment plan that works for you and your lifestyle.
This is a personal account of an ALPROLIX Peer, reflecting the real-life experiences of a person diagnosed with hemophilia B who has been prescribed ALPROLIX. However, individual experiences may vary. Patient stories are not necessarily representative of what another person using ALPROLIX may experience. ALPROLIX Peers have been compensated for sharing their stories. For medical advice, please consult your own healthcare provider.