Without a Ribbon
  • About
    • Events
    • Get In Touch
  • Rare Cancer Resources
  • Shop
  • How You Can Help
  • Meet Warriors
  • News
  • Login
  • Register

Select Page

HELP

LEARN

EVENTS

Waldenstrom Macroglobulinemia

Become part of our growing rare cancer community.
Join our Facebook support group

Join Now

Posted by fatima.shakeel@opmc.co | Jan 28, 2026

What is a Waldenstrom Macroglobulinemia?

Waldenstrom Macroglobulinemia is a rare type of blood cancer. It develops from certain white blood cells called B-lymphocytes, which normally help the body fight infections.

In this condition, these cells grow in an abnormal way and produce large amounts of an abnormal protein called IgM. Because of this protein, the blood becomes thicker than normal, which leads to many of the symptoms of the disease.

Incidence

Waldenstrom Macroglobulinemia usually affects older adults, most commonly people over the age of 60. It grows slowly, and many people live with it for years. Waldenström macroglobulinemia is considered a type of non-Hodgkin lymphoma, but it also shares features with blood disorders like multiple myeloma.

Symptoms

The symptoms develop gradually and may be mild at first. Many people feel extreme tiredness and weakness, mainly due to anemia, which means a low number of red blood cells. Some people notice frequent infections, as the immune system does not work properly.

Because the blood becomes thick, symptoms like headache, dizziness, blurred vision, nosebleeds, or confusion may occur. Tingling or numbness in the hands and feet can also happen due to nerve involvement. Some individuals may develop swollen lymph nodes, enlarged liver or spleen, or unexplained weight loss and night sweats.

Diagnosis

Diagnosis is made through blood tests, which show high levels of IgM protein and anemia. A bone marrow test confirms the presence of abnormal cells. Imaging tests may be done to check lymph nodes or organs.

Treatment

Treatment depends on how severe the symptoms are. If the disease is mild and not causing problems, careful monitoring may be enough. When treatment is needed, medicines are used to reduce abnormal cells and control IgM levels. Targeted therapies and chemotherapy are commonly used. In some cases, a procedure called plasmapheresis is done to quickly remove excess IgM protein from the blood and reduce thickness.

Prognosis

The prognosis is generally good, especially because the disease grows slowly. Many patients live for many years with proper treatment and regular follow-up.


You can help us with your donation:

Without a Ribbon is a charity that works hard to aid those who suffer from rare cancers. You can help our cause in a variety of ways:

Donations — Without a Ribbon is grateful when we receive every donation. Giving to Without a Ribbon helps us to provide ongoing support, organise the annual gathering and subsidise the costs of our Warriors attending these conferences.
Sponsorship — If you wish to sponsor our charity, please contact us using this form.
Volunteering — We are always looking for volunteers to help with different aspects of running our charity. So, if you are looking for volunteer work, please feel free to contact us.

Share:

PreviousOur New Resource Page for Diffuse Sclerosing Variant of Papillary Thyroid Carcinoma
NextOur New Resource Page for Waldenstrom Macroglobulinemia

If you need any help or advice just

Get In Touch

© Without a Ribbon 2019. All rights reserved.Powered by WEB 105 Creative

Stay up to date.

Sign up to our newsletter