The Leukemia & Lymphoma Society Blog

The Leukemia & Lymphoma Society Blog

7 Posts tagged with the myeloma tag

The Leukemia & Lymphoma Society (LLS) is proud to offer telephone education programs for blood cancer patients and their caregivers. These programs, which require free registration, are both informative and interactive for those dealing with specific types of blood cancer or certain treatment topics.

 

Free registration is now available for these upcoming October programs.

 

October 14, 2009 - Treating Uncommon Lymphomas: Dialogue with an Expert on T-Cell, Malt, and Waldenström Macroglobulinemia

October 29, 2009 – Managing Myeloma: An Expert’s Update

 

Check the National Education Programs page often to see what is available, or visit any of the archive pages to listen to past programs, download transcripts or to access highlights from many of the past programs (archive pages can be found in each disease education series section – for example, there is a link to the archived programs on the Myeloma Education Series page).

 

Need assistance? Call the Information Resource Center at (800) 955-4572 and someone will be able to answer your question or steer you in the right direction.

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A report in the news this week suggests that 9/11 responders to the World Trade Center may be at an increased risk for myeloma. The report’s authors caution that their findings are very preliminary, however so far eight responders have been diagnosed with myeloma, four of whom are men who were diagnosed when they were younger than 45 years. Myeloma typically is diagnosed in persons who are aged 50 years or older.

 

While some say that it is possible for these myeloma cases to be linked to these patients’ time at Ground Zero, there is also admission that it could just be a coincidence. "In all fairness, it is unusual for this patient population to have multiple myeloma but it's not unheard of," explains Dr. Denise Pereira, assistant professor of clinical medicine at the University of Miami Miller School of Medicine. "But a lot of the things they were exposed to, such as benzene, have in the past possibly been implicated with an increased incidence in the cancer. It does make theoretical sense."

 

This report appears in the August issue of the Journal of Occupational and Environmental Medicine; to read the full news article visit HealthDay.

 

If you’d like to learn more about myeloma, here are some myeloma resources you can find on The Leukemia & Lymphoma Society (LLS) website.

 


As always, our Information Resource Center specialists are available to take your questions Monday through Friday, 9 a.m. to 6 p.m. EST at (800) 955-4572. You may also contact them online.

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A few weeks ago we shared a post on financial insecurity and blood cancer treatment, sharing with you some helpful links to information and programs provided by The Leukemia & Lymphoma Society (LLS). In this post, we wanted to highlight the personal side of our Co-Pay Assistance Program and share with you a couple of stories about myeloma patients who have benefited from this program.

 

Kalimah Jenkins, a 44-year-old African American from Atlanta, GA, was stunned to find out that her bone pain and fatigue were symptoms of myeloma, a difficult blood cancer. She was equally as shocked when she found out how expensive her treatment would be, and wasn’t sure how she would be able to pay for the drugs she needed. It was in her favor that her doctors knew about LLS’s Co-Pay Assistance Program, which helped her pay for her critical treatment.

 

Cislyn Blackwood, a 60-year-old from Fresno, CA, also a myeloma patient, has also benefited from the Co-Pay Assistance Program. Her treatment was already very expensive, but after being laid off from her job and her COBRA benefits running out, her financial situation became ever more challenging. She received the funds she needed through LLS's Co-Pay Assistance Program and was able to pay for her medication.

 

Both women say that LLS’s program has been a tremendous help, and are grateful that they found out about it; unfortunately, some myeloma patients who can’t afford it wind up going off of life-saving treatment.

 

If you or a loved one has been diagnosed with myeloma, visit www.lls.org/copay or call (877) LLS-COPAY to find out if you or they qualify for assistance. Note that other blood cancer patients may quality for assistance as well.

 

If you are a doctor, visit www.lls.org/copayproviders to find out how you can apply for the Co-Pay Assistance Program on behalf of your patients.

 

Learn more about Kalimah’s and Cislyn’s stories.

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This time of year we all seem to have so much more to do. Why not plan some things just for you? If you have myeloma or know someone who does, check out our new fall program at The Leukemia & Lymphoma Society (LLS). We also have several local events (Chapter Education Programs) about all types of blood cancers going on throughout the year. Included below are some offerings you may want consider in the coming weeks and months.

 

National Education Programs

 

October 15, 2008 - Understanding Myeloma: From Diagnosis Through Treatment. Register now for this telephone education program which will feature Dr. Asher A. Chanan-Khan. Participants will have a chance to ask Dr. Chanan-Khan questions during this hour and a half program.

 

Chapter Education Programs

 

Contact your local chapter about the availability of the following programs in your area:

  • Welcome Back: Facilitating the School Experience for Childhood Cancer Survivors - Note that parents are also welcome at this event.

  • Getting the Best Cancer Care at Age 55 and Older

  • Milestones in Myeloma Therapy: An Overview for Patients and Caregivers

  • The Road to Discovery: Emerging Therapies in Blood Cancers

 

There are also other programs that occur all throughout the year. Find out more about the following on-going programs:

 

  • Family Support Groups - These are regularly scheduled meetings that bring together patients, families and friends.

  • First Connection - Be matched with someone who has been through a similar cancer experience. Volunteers are also welcome to join this program.

  • Chat Sessions - Every Monday and Wednesday NHL patients are welcome to come online and chat about their cancer experience.

 

As always, feel free to share suggestions, ideas or questions with our Information Resource Center staff. Contact us via our Contact Us form or by phone at 1-800-955-4572. Or just visit us at www.LLS.org.

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September is an important month for us at The Leukemia & Lymphoma Society (LLS). It is a special time when our ongoing collaboration with patients, caregivers and medical professionals is highlighted by our campaign for leukemia, lymphoma and myeloma awareness. Please join us in this campaign to educate more people about blood cancer.

 

Here are some quick facts* you can share on your own websites, blogs, social networks or in conversations with friends.

  • Today more than 894,000 people in the United States are living with a type of blood cancer.

  • Today about 75 percent of children with acute leukemia and nearly 80 percent of children and adults with Hodgkin lymphoma are cured.

  • Every ten minutes someone dies from a blood cancer.

  • An estimated 52,910 people will die from a blood cancer this year.

  • Since LLS began in 1949, our organization has invested more than $600 million in research to find cures and better therapies.

  • This year alone, LLS will dedicate $71.4 million to research.

 

Another thing you can do this month is help our Public Policy team work to get September officially recognized as Leukemia, Lymphoma and Myeloma Awareness Month by your state. How does this help? It ensures that there will be more media coverage around the month, which means more people will learn about blood cancers. It also means more people could support the fight to eradicate cancer. Contact your local LLS chapter to learn more about how you can help.

 

Learn more about leukemia, lymphoma and myeloma on the LLS website at www.LLS.org, or contact the Information Resource Center with any blood cancer questions.

 

*Note that these statistics are for leukemia, lymphoma and myeloma only.

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We have many resources in English, but in case you didn’t know we have resources that can be of help to people whose native language might not be English.

 

Free Materials

Available in Spanish (Español) and French (Français)

 

Free materials are available in Spanish (Español) - you can download a PDF or order a printed copy - and French (Français), but you can download a PDF only.  When you are on the www.LLS.org website look in the left-hand column and click on Patient Services, then Free Materials, then you will see Spanish Publications (Publicaciones españolas) and French Publications (Editions françaises).

 

 

Financial Assistance

Available in Spanish (Español)

 

Need financial assistance? Spanish-language speakers (las personas que hablan español) can download our Patient Financial Aid application in Spanish (Solicitud de ayuda económica para pacientes) as a PDF. There is also a handy step-by-step guide in Spanish (Cómo solicitar la inscripción en el programa de ayuda económica para pacientes) to help you fill out the application.

 

 

Free Newsletters

Available in Spanish (Español)

 

Visit the following pages in our National Education Programs section for access to our downloadable Spanish newsletters (boletines españoles) available as PDFs.

 

Can’t find what you need? Let us know here by leaving a comment or by contacting our Information Resource Center by calling (800) 955-4572 or filling out our online form.

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Today we are launching The Leukemia & Lymphoma Society’s first blog! There are a few things that we hope to accomplish with this new communication tool, but most of all we want to make this an informative and interesting destination for you: patients, caregivers, and anyone else affected by any of the blood cancers.

 

A few topics we plan to cover are advocacy, teleconferences, news articles, and more…

 

We’d love to get ideas from you, though. What do YOU want us to write about? (To comment you must first register if you haven’t already – registration is easy and free!)

 

To make sure you are the first to know when we have posted a new blog entry subscribe to our RSS feed. Or you can bookmark this webpage in your browser and visit us often.

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