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About Lymphoma
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Support & Survivorship

Last update: 03/16/2010

TOPICS
Alerts / Keeping Safe
| PsychosocialDoctorsFinancial & Insurance | Drugs | Immunization Guide | Treatment Support & Tips  | Patient-to-Patient (right column)

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Late Effects of Cancer Therapy

Alerts and Keeping Safe

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Consumer Guide on Counterfeit Drugs 
how to avoid and report the sale of bad medicines

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Keeping Safe - how to minimize your risk from medical errors

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Health Supplement Alerts 

Psychosocial and Physical Effects

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Dr. Wendy Harpham on Survivorship 
"I began to focus my hope on things 
within my reach ... living fully."

 
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Anxiety and Depression 
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Books that provide guidance
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Caregiver Stress & Caregiver Tips
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Complementary practices
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Exercise & Diet  | Yoga
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Encouragement 
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Fatigue
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Health Care Proxy
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Pain Management 
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Palliative Care / Hospice
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Patient Stories
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Support Groups  | "Buddies" Programs
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Support Organizations & Events
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Survivorship: Dr. Wendy Harpham
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Talking with your child about your cancer

Doctors

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Communicating with your doctor  
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Locating Doctors  & Cancer Centers
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Preparing for doctor visits | Bring List PDF
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Questions for your doctor - checklist 
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Your Medical Rights

Drug resources
 

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Drug Payment Support

Financial, Insurance & Legal support

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Careers and workplace discrimination 
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Financial support
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Drug Payment Support
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Help with drug payment
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Family and Medical Leave Act
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Insurance

What if I have no insurance?
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The Legal Clinic for the Disabled
provides free services to low-income people with physical disabilities in Philadelphia, Bucks, Chester, Delaware and Montgomery Counties, PA
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Managed Care
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Travel help 

Immunization Guide

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Re-immunization after SCT

Treatment Support

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Diary
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Risks and Benefits / Secondary Risks 
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Drug administration:  IV, Catheters, Ports
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Patient Stories
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Treatment Support and Tips
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Diet for Immune suppressed / to control nausea

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Tips
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for Blood Draws and IVs
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for CHOP+R Treatment
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for Rituxan ... a checklist

Patient-to-Patient Support | Patient Stories

Art 
Images and poems created by patients and caregivers that portray the experience of living with lymphoma. 
 

Books 
Patient-recommended books on living with lymphoma and its treatment 

Caregiver Stress
Help with identifying and relieving caregiver stress.

Caregiver Tips

"Buddies" Programs - peer-to-peer support with guidance on 
How to Help a Friend

Doctor-Patient Relationships 
Guidance on how to communicate with your doctor, and how to create a support team to optimize your care. 

Encouragement
Reasons to be optimistic; guidance on the shock of diagnosis

Guidelines at Diagnosis
Checklist to help when you are first diagnosed. 

Life After Cancer Journal  

Patient Stories
Inspirational, patient-to-patient guidance; Memorials

Patient Case Histories & Treatment Summaries  
a good treatment summary  helps doctors serve you better. 

Printable Guides & Tools  
Free printable brochures, checklists, spreadsheet to help patients obtain optimal care. 

Support Groups - This page lists a variety of online support groups. It also allows you to change some subscription settings, such as no-email or daily digest. 

Tips for Coping with CHOP+R treatment

Tips for "Skick"y Situations Blood Draws and IVs: Tips for Minimizing Anxiety and Pain
 

 

Lend a hand to PAL:  Donate Your Used Vehicle or Make an Email-Pledge or Donate by Mail or

Donate online with a credit card.  It's easy, safe and secure: 

The patient-to-patient support section relies on the input of lay persons, primarily. We seek reputable sources of information. As with all material on this site, please consider it a starting point for discussions with your physician.  We welcome input from patients, caregivers and medical professionals.  What follows is an excerpt from the Report of the Leukemia, Lymphoma, and Myeloma Progress Review Group. It fits well, we think, in this section as it speaks to the need for timely information. - Karl Schwartz 
 

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From the Progress Review Group Report:

"The time is ripe to identify and develop strategies for providing information to patients to improve medical decision-making, quality of care during active treatment and follow-up, and quality of life. The need is especially great for patients with hematological malignancies. 

First, the hematological malignancies affect a diverse patient population in terms of age, sex, and race. 

Second, short- and long-term side effects and complications vary by disease. For example, myeloma patients often experience severe bone pain, whereas leukemia and lymphoma patients face secondary cancers and the long-term health consequences of treatments. 

Third, treatments for hematological malignancies are evolving rapidly due to new scientific discoveries and advances. Recent research shows that hematological malignancies are even more diverse than previously thought and that tailoring treatment to the specific disease subtype can ensure that patients receive treatments that are more effective and less toxic than earlier ones. 

Finally, longer life for LLM survivors creates a need for more information about coping with cancer. This is especially true for the many LLM patients who are young and for those who are advised to "watch and wait" rather than pursue aggressive treatment. For all of these reasons, treatment and follow-up care information must be up to date, easily accessible, and tailored to the circumstances of the patient."

 - From the Report of the Leukemia, Lymphoma, and Myeloma Progress Review Group, May 2001 full text

 
Disclaimer:  The information presented on Lymphomation.org is not intended to be a substitute for 
professional medical advice or to replace your relationship with a physician.
For all medical concerns,  you should always consult your doctor. 
Patients Against Lymphoma, Copyright © 2004,  All Rights Reserved.