Connect with others who understand.

Sign up Log in
Resources
About MyMyelomaTeam
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.

You Definitely Have A Place In The Recovery Process Here πŸ™ πŸ™Œ πŸ’ͺ ❀️

A MyMyelomaTeam Member asked a question πŸ’­
Dallas, TX

I was diagnosed in Dec of 2023
Very same symptoms pretty much but no broken bones. I was very sick just like you though and it took me down rather rapidly,,,in a short 3 month period,, anemic, double pneumonia ,,and a long hospital stay,,,it was finally at an eye appointment that the optometrist asked me if I had MM..I had no clue what he was asking,,,so he put it to my primary care provider that he has seen it in several of his patients before..so the pet scan confirmed it,,,along with a… read more

August 3, 2024
β€’
View reactions
Member Spotlight: No Expiration Date Read Article...
A MyMyelomaTeam Member

Thank you. Working together and supporting each other, with help from God and the medical profession, we are going to beat MM!

August 3, 2024 (edited)
A MyMyelomaTeam Member

To all of the Team members I Thank you for all of the information that you let us know about and i want you to know that i never cease asking the Lord to Heal ,Give Peace and wisdom to everyone that have this disease and send a cure to your people.

August 3, 2024
A MyMyelomaTeam Member

I am very happy that I found "MY" to help live with MM and the treatments and the Q&A of things we experiences along the way. I've typed it before and I am again ; I think this journey would have been a lot rougher without all of you!! πŸŒΉπŸ’› ✊

August 3, 2024 (edited)
A MyMyelomaTeam Member

Amen πŸ™ πŸ™ πŸ™ best advice for all in this Myeloma fight,,,love it πŸ‘

August 3, 2024
A MyMyelomaTeam Member

Amen!!!
I prayed I would find a site like this to be able to share my feelings with others who can really understand where you are coming from. Because people who don’t have mm they do not have a clue!

August 6, 2024

Related content

View All

I Also Cannot Pee Without Catheterising.

A MyMyelomaTeam Member asked a question πŸ’­

I Am Approaching Time For My Stem Cell Transplant…would Love To Hear How That Went From Anyone Who Has Had One.

A MyMyelomaTeam Member asked a question πŸ’­
Banks, AL

Has Anyone Used Infra Red Sauna Treatment For Their Multiple Myaloma?

A MyMyelomaTeam Member asked a question πŸ’­
New York, NY
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 Policy and Privacy policies.Your privacy is our priority Lock Icon
Already a Member? Log in