Connect with others who understand.

  • Learn from expert-reviewed resources
  • Real advice from people who’ve been there
  • People who understand what you’re going through
Sign Up Log In
Powered By
Real members of MyMyelomaTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

The other day, I was told I am somewhat of a hypochondriac. Having the symptoms of MM and the treatment is absolutely not imaginary. Is the diarrhea or constipation caused by the treatment imaginary? Is the MRI showing degradation and pain in the spine caused by MM imaginary? Is the nerve damage that causes symptoms like numbness or tingling in hands and feet (peripheral neuropathy) imaginary? Is the extreme tiredness that does not improve with rest imaginary? Is the unintentional loss of weight… read more

August 26, 2025
 · 
Reactions

Answer Summary

Members rallied around a question about being called a hypochondriac while living with multiple myeloma, with the overwhelming response being... Read more

Members rallied around a question about being called a hypochondriac while living with multiple myeloma, with the overwhelming response being that MM symptoms are very real and the comment reflects ignorance about the disease. Several members shared that they have stopped explaining their illness to others, choosing instead to say 'I'm fine' to protect their energy, while others suggested educating the person or simply showing them the door. A recurring theme was finding comfort and validation in this community, since many felt that only fellow MM patients truly understand what living with this disease looks and feels like.

A MyMyelomaTeam Member

some people just don't stop to think outside themselves.....till it happens to them.And that was RUDE of them!

September 6, 2025 (edited)
A MyMyelomaTeam Member

Gaslighting! I would say something snappy, like "Oh, you seem to know a lot about hypochondria! When were you diagnosed?", then I'd walk away. Unless it was my boss, that is! 😆
What matters is what you know. If someone made hurtful comments like that, we would never speak again - regardless of what the relationship is. Align yourself with compassionate people - you deserve that at the very least.

January 9
A MyMyelomaTeam Member

Robert, people are so narcissistic and self centered now. Don't waste another minute of your time and energy on this person. They probably don't even know what multiple myeloma is. They won't take the time to find out. I am very careful who I talk to about my health now. I hope you feel safe here. Big hugs your way 🤗

August 26, 2025
A MyMyelomaTeam Member

Tell them - They should hope they never get to know anything about MM

August 26, 2025
A MyMyelomaTeam Member

Robert, my caregiver and I were discussing this just the other day. We came up with this quick response: "Multiple Myeloma doesn't often show on the outside. You do NOT want me to go into detail!" Hypochondria is a very cruel word. Those people who use it don't remotely get our illness, nor how awful it is to tell someone that. It's an insult and they should realize that. By the way, I have all the same symptoms you do, and absolutely not, they are not imagined. And they are very debilitating and limiting. Trust yourself, and try not to be hurt by the ignorance of others. Easier said than done, I know.

September 21, 2025

Related Questions

View All
A MyMyelomaTeam Member asked a question 💭
Hudsonville, MI

Continue with Facebook
Continue with Google
By joining, you accept our Terms of Use, and acknowledge our collection, sharing, and use of your data in accordance with our Health Data and Privacy policies.
Already a member? Log In