Please use this forum to meet other people affected by Hairy Cell Leukemia. Have you been diagnosed with HCL or has someone you care about been diagnosed? Feel free to share your information with one another, but please keep in mind that detailed patient information or names should be avoided to protect patient privacy rights regarding HIPAA. (Posts asking or sharing personal health information will be deleted and the poster will be warned. If the violation of this rule continues, the poster will be banned from this forum and their user account will be deleted. Thank you for understanding. If you notice a violation on this message board, please email info@hairycell.org to report it and have it removed. Thank you!)