HEALTHY BONE MARROW DONORS: Healthy individuals, ages >=  years and toilet-trained, who have been identified by Boston Children's Hospital (BCH) or Dana Farber Cancer Institute (DFCI) providers as / or / (HLA-A, -B, -C, -DRB, -DQB) matched, bone marrow donors for transplantation will also be eligible to participate in this study; healthy donors may be related or unrelated to the bone marrow recipient
HEALTHY VOLUNTEER BLOOD DONORS
Willingness to sign the healthy volunteer informed consent form
HEALTHY SUBJECT: Not taking regularly prescribed medication such as steroids, hormone therapy or immunosuppressive agents
HEALTHY SUBJECT: Not pregnant or breastfeeding
Patients must be healthy enough to undergo a general anesthetic
Previously received docetaxel or are not healthy enough per clinical judgment or declined to receive it
Generally healthy other than for CTCL, or with other stable diseases/conditions that are adequately controlled
Patients enrolled must, in the Investigator's judgment, be healthy enough to stay on the clinical trial for three months.
PILOT PARTICIPANTS AND HEALTHY CONTROLS ONLY: Women with no history of cancer
PILOT PARTICIPANTS AND HEALTHY CONTROLS ONLY: No history of prior chemotherapy
PILOT PARTICIPANTS AND HEALTHY CONTROLS ONLY: Willing to come to MDACC and HIAE for the assessment session
PILOT PARTICIPANTS AND HEALTHY CONTROLS ONLY: Right handed
PILOT PARTICIPANTS AND HEALTHY CONTROLS ONLY: Diagnosis of a formal thought disorder (e.g. schizophrenia)
PILOT PARTICIPANTS AND HEALTHY CONTROLS ONLY: Mini-Mental State Examination score of  or below
PILOT PARTICIPANTS AND HEALTHY CONTROLS ONLY: Undergoing chemotherapy
PILOT PARTICIPANTS AND HEALTHY CONTROLS ONLY: Any extreme mobility issues (e.g. unable to get in or out of a chair unassisted, extremity issues such as neuropathy that limits physical manipulation of objects)
PILOT PARTICIPANTS AND HEALTHY CONTROLS ONLY: Primary caretaker of a cancer patient
PILOT PARTICIPANTS AND HEALTHY CONTROLS ONLY: Patients who have regularly practiced meditation (greater than once per week) in the year prior to study enrollment
Study participants are expected to be generally healthy and non-symptomatic for cervical disease
Non-pregnant female volunteer
CONTROL (HEALTHY) GROUP: Healthy female without known coronary artery disease
CONTROL (HEALTHY) GROUP: Able to hold breath for  seconds
CONTROL (HEALTHY) GROUP: ECOG performance status -
CONTROL (HEALTHY) GROUP: Able to walk at least  blocks without chest pain, dyspnea, shortness of breath or fainting
CONTROL (HEALTHY) GROUP: No history of cancer
CONTROL (HEALTHY) GROUP: Never received chemotherapy, radiation therapy, immunotherapy, or had breast surgery
CONTROL (HEALTHY) GROUP: If previously measured, known LVEF < %
CONTROL (HEALTHY) GROUP: Symptomatic claustrophobia
CONTROL (HEALTHY) GROUP: Severe pulmonary hypertension
Be periodontally healthy; this is defined as all sites with attachment levels =<  mm and probing depths =<  mm) and caries-free, as evidenced by a DMF (decayed, missing, filled teeth) index of < 
Healthy on the basis of medical history
Healthy, medically well girls and boys
HEALTHY CONTROLS: Women with no suspected gynecological cancer
HEALTHY CONTROLS: No contraindications for MR or PET imaging
HEALTHY CONTROLS: Scheduled to undergo a hysterectomy and/or salpingo-oophorectomy
HEALTHY VOLUNTEER: Be able to comprehend the full nature, purpose and risks of the study
HEALTHY VOLUNTEER: A history of surgical breast augmentation, reduction, or biopsy
HEALTHY VOLUNTEER: Lymphedema or chronic edema
HEALTHY VOLUNTEER: Females who are pregnant or nursing or are actively lactating
HEALTHY VOLUNTEER: Exposure to ultrasound contrast agents (UCAs) in the  month prior to study initiation
HEALTHY VOLUNTEER: Known hypersensitivity to UCAs
HEALTHY VOLUNTEER: Significant axillary, supraclavicular, or other chest wall palpable adenopathy
HEALTHY VOLUNTEER: Use of more than  cigarettes/day
HEALTHY VOLUNTEER: Participation in an investigational drug study within the period starting  month before study drug administration
HEALTHY VOLUNTEER: Subject is mentally or legally incapacitated, has significant emotional problems at the time of prestudy (screening) visit or expected during the conduct of the study or has a history of a clinically significant psychiatric disorder within the last  years; subjects who have had situational depression may be enrolled in the study at the discretion of the investigator
HEALTHY VOLUNTEER: Subject has a history of any illness that, in the opinion of the study investigator, might confound the results of the study or poses an additional risk to the subject by his participation in the study
HEALTHY VOLUNTEER: A history of neoplastic disease, with the exception of non-melanoma skin cancer
HEALTHY VOLUNTEER: Any other condition precluding subject participation as per investigator judgment
Note that patients will need to be sufficiently healthy to undergo audiovisual (AV) biofeedback
INCLUSION CRITERIA - FOR NORMAL HEALTHY FEMALE COHORT: Good health conditions or without significant diseases, according to best medical judgement
INCLUSION CRITERIA - FOR NORMAL HEALTHY FEMALE COHORT: If breastfeeding, must be willing to discard breastmilk for  hours following zolpidem
INCLUSION CRITERIA - FOR NORMAL HEALTHY FEMALE COHORT: Ability to swallow study medication
EXCLUSION CRITERIA - FOR NORMAL HEALTHY FEMALE COHORT: Chronic therapy with any drugs, except oral contraceptives
EXCLUSION CRITERIA - FOR NORMAL HEALTHY FEMALE COHORT: History of hepatic, kidney, lungs, gastrointestinal, epileptic, hematologic or psychiatric disease; hypotension or hypertension, of any etiology, that requires pharmacological treatment; history of myocardial infarction, angina and/or heart failure
EXCLUSION CRITERIA - FOR NORMAL HEALTHY FEMALE COHORT: Hospitalization for any reason up to  weeks before enrollment
EXCLUSION CRITERIA - FOR NORMAL HEALTHY FEMALE COHORT: Any condition, according to investigator's best judgement, that prevents the subject to participate in the trial
EXCLUSION CRITERIA - FOR NORMAL HEALTHY FEMALE COHORT: Pregnancy, labor or miscarriage within  weeks before admission predicted date
HEALTHY VOLUNTEER INCLUSION CRITERIA:
HEALTHY VOLUNTEER EXCLUSION CRITERIA:
Subjects must be otherwise healthy except for the diagnosis of cancer, as per the exclusion criteria listed below.
Subjects must be sufficiently healthy to undergo surgery or an endoscopic procedure.