• B2B Books on the go

    Check out the book in our B2B series, which cover a wide range of topics that speak to the hemophilia B community. Read them online, download them to your device, or print and take them anywhere.

    Not an actual patient.
  • B2B videos

    Watch patients and caregivers discuss important topics about hemophilia B and share personal stories in the B2B video series, featuring members of the B2B Consumer Advisory Board.

    Not an actual patient.
  • Patient and caregiver stories

    Read firsthand patient and parent stories from members of the hemophilia B community.

    Not an actual patient.
  • B2B PODCAST: B’s IN A POD

    Listen to podcasts featuring patients, caregivers, and friends in the hemophilia B community discussing a variety of current topics.

    Not an actual patient.

EXPLORE B2B

Where Patients and Caregivers Share Their personal experiences

Newest B2B Book

Hemophilia B: Her Voice, Her Life

Historically, hemophilia was believed to affect only males. Because awareness regarding manifestations of hemophilia in women is increasing, there is an opportunity to hear their voices as they share their stories. This book provides support and encouragement to women with hemophilia B on their paths to empowerment.

READ NOW »

B2B Books

Check out the ten books in our B2B series, which cover a wide range of topics that speak to the hemophilia B community.

VIEW ALL B2B BOOKS »

B2B Podcast: B’s in a Pod

Listen to podcasts featuring patients, caregivers, and friends in the hemophilia B community discussing a range of important issues and relevant topics.

LISTEN TO PODCASTS »

B2B Videos

Watch patients and caregivers discuss important topics about hemophilia B.

WATCH VIDEOS »

B2B Stories

Read stories about patients, families, and caregivers who have been featured in the B2B book series.

READ NOW »
  • “I try to foster healthy self-esteem by trying new things with the confidence of a survivor and the wisdom of a mature bleeder. Chronic illness is a blessing when its management is just part of life.”

    Paul B.
    Patient
  • “I think it is so important to make the chronic illness a nondefining part of life. My daughter has hemophilia B, but that certainly isn’t the most important thing I want people to know about her. We’ve worked hard to make sure we keep hemophilia B in a place of balance in our lives.”
    Becky V.
    Caregiver
  • “I strongly encourage other caregivers to get involved. This gives you the tools and strength to better advocate for your care. It also provides that all-important support system.”

    Nina D.
    Caregiver
  • “I go to my hematologist with the direct intent of discussing my treatment plan and product, not empty minded, waiting for instruction.”
    Felix G.
    Patient
  • “Walking is particularly difficult, so I limp in private and swagger in public.”
    Paul B.
    Patient