Castleman disease Forum
- 63 members
- 15 discussions
This discussion group is dedicated to patients and families of patients with Castleman disease. Start new discussions and share with others on your experience with living with Castleman disease and its impact on your personal, family, and professional lif
Patients Castleman disease
Living with Castleman disease
What is your Castleman story?
Living with Castleman disease
MCD and lymphoma
Living with Castleman disease
lymphedema after surgery
Living with Castleman disease
Castleman Disease: Feeling uncomfortable lately. Anyone else experiencing that?
Living with Castleman disease
Feeling alone with CD: How do you cope?
Living with Castleman disease
How does it feel being diagnosed with a rare disease?
Living with Castleman disease
Castleman’s disease in the UK: What are your advices?
Living with Castleman disease
What is something you wish others knew about CD?
Living with Castleman disease
Which type of Castleman disease do you have?
Living with Castleman disease
Castleman disease: Would you like to join a patient organisation?
Living with Castleman disease
COVID and Castleman: Have or will you get the COVID vaccine?
Living with Castleman disease
Newly diagnosed: Can you share any advice?
Living with Castleman disease
How can I best support my loved one with CD?
