fbpx

Recently Diagnosed or Relapsed? Stop Looking For a Miracle Cure, and Use Evidence-Based Therapies To Enhance Your Treatment and Prolong Your Remission

Multiple Myeloma an incurable disease, but I have spent the last 25 years in remission using a blend of conventional oncology and evidence-based nutrition, supplementation, and lifestyle therapies from peer-reviewed studies that your oncologist probably hasn't told you about.

Click the orange button to the right to learn more about what you can start doing today.

Can you live a normal life with myeloma? Understanding the best of both conventional and non-conventional multiple myeloma therapies allows you to live “the new normal.”

A diagnosis of any cancer, especially a rare blood cancer such as multiple myeloma, is life-changing. While the prognosis for multiple myeloma is limited at best, I think my experience opens the door for more than the conventional standard-of-care for all MM patients.

I hadn’t even heard of a cancer called multiple myeloma when my oncologist gave me the bad news. I had been living with a pain in my neck for several months leading up to my multiple myeloma diagnosis.

Multiple myeloma symptoms, chemotherapy regimens, a bone marrow transplant — I knew nothing about these things. I had a lot to learn…understanding multiple myeloma means that you can live a new normal.

Average life expectancies are currently 5-7 years with 55% of newly diagnosed MM patients living for five years. However, newly diagnosed MM patients with early stage MM (stage 1) achieve a five-year survival rate of more than 77%.

Currently there is no cure for multiple myeloma. In my experience, combining the best of both conventional and non-conventional therapies can improve your prognosis for multiple myeloma and quality of life.

The likely prognosis for multiple myeloma patients will be remissions and relapses over a period of years. It is possible to experience a first remission of years followed by a series of shorter relapses and remissions.

Experience has taught me that it is essential to learn as much as you can about your multiple myeloma if your goal is to live the best possible quantity of life as well as quality of life. This is your new normal life with multiple myeloma.

Every decision you make in the coming years about you and your cancer will depend on understanding your multiple myeloma. As the saying goes, knowledge is power.

This post — Prognosis for Multiple Myeloma — is the entry to the hundreds of pages of studies and experiences cataloged on PeopleBeatingCancer.

I researched and created the Multiple Myeloma Cancer Coaching Program in order to provide MM patients with an evidence-based, step by step program to learn about their Multiple Myeloma.

I am a long-term Multiple Myeloma Survivor and MM Cancer Coach. I research and write about all things multiple myeloma. PeopleBeatingCancer is dedicated to providing the experience and research needed to manage your multiple myeloma.

I work with newly diagnosed MM patients, MM patients who have relapsed,  online MM groups, and I administer a private MM group called Beating Myeloma.


Multiple Myeloma Symptoms

Have you been living with bone or joint pain for a while now? Have you had a skin rash or nerve pain and not understood why? Or maybe you’ve been mis-diagnosed? Bone, joint, skin, and nerve pain are several of the more common multiple myeloma symptoms. That is to say, these are some of the health problems caused by monoclonal proteins before you are diagnosed with multiple myeloma.


Multiple Myeloma Diagnostic Criteria

Multiple myeloma is notoriously difficult to diagnose. Therefore, many tests examining your blood, urine, and even your bone marrow are used to determine if you have multiple myeloma. If you do, your stage at diagnosis is determined by your diagnostic criteria.

Multiple myeloma diagnostic criteria go by the acronym CRAB:

  • Calcium — A test called a Comprehensive Metabolic Panel will measure calcium in your blood (serum).
  • Renal — This same test will measure how your kidneys (renal) are working.
  • Anemia — A test called Complete Blood Count will measure your red and white blood cells to see if you are living with anemia and are experiencing fatigue.
  • Bone — Imaging studies such as X-rays, MRI, PET scans, or CT scans can look inside your bones to determine if you have lytic lesions (MM) growing in your bones.

In addition, you will probably also undergo a serum protein electrophoresis test (SPEP), an Immunofixation test, a Freelight Chain test, a bone marrow biopsy, a Fluorescence in situ hybridization (FISH) test, and possibly others. As I say, multiple myeloma is difficult to diagnose. Thorough diagnostic testing is your most important first step to managing your MM for the rest of your life.


Multiple Myeloma Staging

Staging your diagnosis of multiple myeloma is the second important step for managing your cancer. Multiple myeloma has only three (3) stages: I, II, and III. According to research, 95% of all newly diagnosed patients are stage 2 or 3. 


Multiple Myeloma Conventional Therapies

When I use the phrase “conventional therapies,” I am talking about those treatments that have been researched and approved by the Food and Drug Administration (FDA). They are surgery, chemotherapy, and radiation.

Your Board-certified Oncologist will prescribe only FDA-approved therapies to treat your multiple myeloma. Whether you are newly diagnosed or have relapsed, you will undergo surgery, chemotherapy, and/or radiation to treat your multiple myeloma.

FDA approved treatments (the standard-of-care for multiple myeloma):

  • Induction Therapy — Induction therapy is designed to reduce the NDMM patient’s multiple myeloma as much as possible in preparation for an autologous stem cell transplant.
  • Autologous Stem Cell Transplant — Killing your old immune system and growing a new immune system using your own stem cells.
  • Maintenance Chemotherapy — Undergoing low-dose chemotherapy in order to remain in remission for as long as possible.

Multiple Myeloma Response Criteria & Response to Treatment

The reason why you are undergoing therapy for your newly diagnosed multiple myeloma is to stabilize your disease. How you respond to treatment is referred to as “response criteria” or  your “response to treatment.”

  • Complete Remission — Minimal Residual Disease (- or +)
  • Very Good Partial Remission (VGPR)
  • Partial Remission (PR)
  • Stable Disease (SD)
  • Progressive Disease (PR)

All newly diagnosed multiple myeloma patients want to get rid of all of their cancer as well as all of the monoclonal proteins (multiple myeloma cells) in their bone marrow. Unfortunately, no one responds 100% to treatment. Even the most complete response possible — MRD (-) — means that there are 4 monoclonal proteins for every one million normal cells.

  • Your formal response criteria measures how you respond to treatment.
  • How you respond to treatment can guide your future treatment decisions.

Multiple Myeloma Side Effects

Most of us know about common short-term side effects of cancer therapies. Think nausea, fatigue, hair loss. Hopefully all are temporary health problems. Though I don’t think oncology does a good job of educating the multiple myeloma patient about long-term side effects of treatment, I think treatment-related side effects must be included in the discussion about your multiple myeloma treatment plan.

  • Short-term side effects include nausea, fatigue, and hair loss
  • Long-term side effects include nerve, heart, brain, and joint damage

Multiple Myeloma Non-Conventional Therapies

All multiple myeloma therapies that I refer to as non-conventional therapies are those treatments that have not been researched and approved by the Food and Drug Administration. This isn’t necessarily a bad thing. The FDA doesn’t approve nutritional supplementation for example.

While there are thousands of studies touting the health benefits of exercise for the multiple myeloma patient, for example, you will never see the FDA approve exercise for treatment.

Since I achieved complete remission from my multiple myeloma in April of 1999, I have researched and written about evidence-based non-conventional therapies such as:

  • Anti-angiogenic nutrition
  • Anti-angiogenic nutritional supplementation
  • Lifestyle therapies
  • Exercise — frequent but moderate
  • Whole-body hyperthermia
  • Mind–body therapy

These are just some of those therapies that I define as evidence-based but non-conventional.

You can learn more about my journey here. If you’d like to get a more personalized approach to managing your cancer, I encourage you to sign up for my multiple myeloma coaching program. If you have any other questions, would like to contribute, or otherwise get involved, you can reach out to us here.

David Emerson

  • MM Survivor
  • MM Cancer Coach
  • Director PeopleBeatingCancer

Articles That Discuss Multiple Myeloma

New Myeloma Staging- R2-ISS, MASS

According to two new myeloma staging systems, multiple myeloma is about RISK. To be more specific, your diagnostic criteria all point to your risk of survival as well as your: Risk of relapse Risk of

Continue reading

PeopleBeatingCancer- 501C3 Non-Profit

The Galen Foundation dba PeopleBeatingCancer is an I.R.S approved 501C3 nonprofit organization providing Pre-Myeloma (SPB, MGUS, SMM) full Myeloma,  general cancer as well as long-term and late stage

Continue reading

Myeloma Chemotherapy Kills

“They found that 14 drug trial reports did not include data on SAE s, 22 presented no data on serious events, and two presented no data on deaths (FAE)“ Don’t expect your oncologist to

Continue reading

Free Light Chains- Myeloma-

Because multiple myeloma is a cancer of the blood, diagnostic tests are used to determine what, if any, blood components are out of the normal range. Free light chains are a component of blood that can

Continue reading

Dexamethasone- Best Time- Myeloma-

My experience as a myeloma patient as well as my research is that the best time to take dexamethasone is in the morning with light food or drink. Probably the most common question I read in online MM groups

Continue reading

Surviving Myeloma- Post-Cancer Fear

Today, there are 16.9 million cancer survivors in the U.S., and 64 percent of them are 65 or older. It is estimated that 75,000 of these are surviving MM. I have been living with myeloma since my diagnosis

Continue reading

Myeloma Patients & Caregivers

Do myeloma patients & caregivers think differently?  According to the study linked below- yes, they do. I’ve been both a cancer patient and a caregiver (for my mom in assisted living). Believe

Continue reading

PET/CT Scans- Myeloma Prognosis

PET/CT scans allow you to see inside your bone marrow. Multiple myeloma is a cancer of the plasma cells. Plasma cells that multiply uncontrollably in a person’s bone marrow. In order to diagnose, stage, treat,

Continue reading

Myeloma Diagnostic Testing

Myeloma diagnostic testing has come along way since my initial diagnosis in early 1994. All aspects of diagnostic testing have improved- blood, urine, imaging genetic testing all forms of testing convey

Continue reading

Myeloma- Evidence-based Medicine

“In medicine, the term “evidence-based” causes more arguments than you might expect…Everyone is a bit right here, and everyone is a bit wrong… It’s the old guard versus the new.

Continue reading

Myeloma – Eight Slices of the Magic Bullet

The ultimate myeloma therapy is quantitative- “Plus, Dr Elwood said, “the effect of a lifestyle is quantitative. That is, the more the better. The more exercise the better. The lower the body mass

Continue reading

Myeloma Treatment, Immuno, Antibiotics

“…currently running more than a dozen different trials of experimental multiple myeloma treatments, from new blood stem cell transplant regimens to targeted drugs. Immunotherapy as a multiple

Continue reading