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Read conversations, start a discussion, and connect with others about blood cancer.

Blood Cancer from a Patient and Family Perspective

Blood cancer affects more than just the person diagnosed. From the patient’s side, the experience often begins with confusion, repeated tests, and...

Drs

What not to do to your patients.dont do not give your diagnosis to your patient over the phone. My first dr did...

Did you experience fatigue after receiving CAR T-Cell Therapy?

"My strength slowly returned at what felt like a snail’s pace. I remember still being so fatigued at my thirty-day appointment and...

Uncertain of diagnosis

I'm 43 and I've experienced intermittent double vision, extreme muscle weakness (to the point I'm now in a wheelchair) and sensory changes...

Managing Holiday Stress

How do you usually manage holiday stress with cancer?...

What tips do you have for managing stress over the holiday season?

The holidays can be a stressful time, especially when managing life with blood cancer. Share any helpful tips for managing holiday stress...

Featured

Living with Multiple Myeloma

Welcome to our Multiple Myeloma Community Forum – a Safe Haven for Sharing, Learning, and Connecting. Whether you're a patient, caregiver, or...

What unexpected side effects have you experienced?

Blood cancer and treatment can lead to unexpected side effects. What side effects surprised you?...

Depressed

I have CLL and feeling pretty good most of the time. I take Brukinsa daily. Seems like at Christmas time I have...

What blood cancer symptom/side effect would you say is the worst?

Bone pain, fatigue, neuropathy, brain fog, other? Share with us and tell us what helps you manage them....

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