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.

Anyone Care To Share Their Experience With Stem Cell Transplant? I Hear It Is Horrible.

A MyMyelomaTeam Member asked a question 💭
Poplar Grove, IL

I have stage 3 Multiple Myeloma

February 9
View reactions
A MyMyelomaTeam Member

I was very nervous to have the stem cell transplant. But I did it anyway. I’m only a little over 100 days out. Almost complete remission and in maintenance. I decided that I needed to do everything possible to fight this

February 16
A MyMyelomaTeam Member

Stem cell transplant was not that bad, just follow what they tell you to do, yes your tired, stomach diarrhea n weakness but it’s all worth it

February 10
A MyMyelomaTeam Member

My husband told me the knee replacement surgery was much harder than the stem cell transplant. The nurses involved with sct were always one step ahead with nausea meds, etc. He walked laps on his ward every day and ate even when it tasted blah.

February 9
A MyMyelomaTeam Member

Different patient in MM transplant will never get the same experience. I just go through the transplant 3 months ago. I got the pain so terrible, body cold, headache, sore throat n mouth , leg pain fm knee to toe 3/4 pain level no appetite, loss weight the hair all gone maybe l not go for another transplant

February 9
A MyMyelomaTeam Member

No. It is not horrible. My doctor told me every possible reaction and I only had half of them. He said you will be real sick on days 5, 6, and 7 so I was prepared. Day 6 I did not walk the halls (they want you walking every day) and just laid in bed. They constantly check your blood levels and restore whatever is needed. All food tastes gross, even your favorite so be ready to drink Ensure. I told doc it was like traveling through a wormhole. You fall in helpless, bottom out and then see the light at the end of the tunnel. By day 14 you go home; weak but alive. Your WBC will go to zero during that day 5, 6 and 7. My ASCT ended June 3, 2023.

February 9

Related content

View All

How Many Days Did You Spend Harvesting Cells?

A MyMyelomaTeam Member asked a question 💭
Framingham, MA

Caregivers During ASCT

A MyMyelomaTeam Member asked a question 💭
Danville, PA

Can Anyone Share Their Experience With Stem Cell Transplant And The High Dose Chemo Leading Up To It?

A MyMyelomaTeam Member asked a question 💭
Mundelein, IL
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