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Read conversations, start a discussion, and connect with others about blood cancer.

Diagnosis

My initial diagnosis was MM in 2015. Now it is MM Bone Marrow in 2025 year of my relapse....

How has brain fog impacted you?

Many people living with blood cancer report being significantly impacted by brain fog and cognitive impairment as treatment side effects. These issues...

Handling Anxiety and Cancer

There are no easy fixes when it comes to how to feel with blood cancer. What have been some of your coping...

Daily multiple vitamins

I asked my Oncologist yesterday about adding a daily multiple vitamin to my daily pill regimen. (I had taken them before my...

Dealing with Comparisons

How and have you dealt with anyone comparing your blood cancer with something else...perhaps less life-threatening? I recall explaining multiple myeloma, but...

Am I being ghosted or am I over sensitive

Hi. I was diagnosed with CLL in late January. Told family and some friends (some of whom I've known for 35 years)...

CML

I was diagnosed with CML in 2020. I don't know anyone with it. I have a wonderful oncologist who monitors my symptoms....

Featured

CAR T-Cell Therapy Experiences

Welcome to our forum dedicated to sharing experiences with CAR-T cell therapy. Whether you've undergone treatment or supported a loved one through...

Aml

I didn't know I had a problem until we were on vacation and passed out in the shower. I didn't know that...

What's one piece of advice you would give to someone newly diagnosed with blood cancer?

Share your advice below!...

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