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Stem Cell Transplant for Multiple Myeloma - search for information
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Somya.P
Community managerGood advisor
Somya.P
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Last activity on 09/09/2026 at 3:15 AM
Joined in 2023
1,018 comments posted | 4 in the Living with multiple myeloma group
33 of their responses were helpful to members
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Hello, @Jessie1564, how are you feeling today?
Thank you for sharing your story with us, and I'm very sorry to hear about your husband's diagnosis. Dealing with a diagnosis like multiple myeloma and considering a stem cell transplant can indeed be overwhelming, and it's incredibly courageous of you to reach out for support. I'll invite a few members of our community to weigh in on this topic and share their experiences:
@glennadunn1226 @Harstev @MaHeck @shellmark @Counselor71 @Lods10.10.2023 @Chloegirl @Samsthetwin @Sleelee68 @EMHart @Paso906 @totopeg @RJOHNIGARN1 @Mikepeele @LadyDJP @Ahallphd2017 @Csuefra @Theobaldsherry @MIMIdwina @VirginiaGlover @Chuckkelly @grandpapaul @Randrericson @sleaw1961 @nicholassallie @Deannaw @LupePhillips @Kelly1982 @Ladybug310 @WayneC @Janice69 @Mam982000 @joeblack445 @kgraumann @JanelleS @Sharonjones1109 @sshina @Nannydeb @Blucky @Wgreen1990 @Desg1928 @MaryLillian @cornerpocket1987yahoo.com @sharoncadwell34 @realtor @Ldscimeme @dadachip @Ynetta @Anneelise @Ozarkpd120 @Donnierae @Olveraangel @MPL54! @Kat1948 @LostSock @Vc4him2000 @Christoina007 @cnapolillo
Have you undergone a stem cell transplant or have any resources you found particularly helpful? Your input could make a significant difference in this person's journey.
Thank you so much and take care,
Somya from the Carenity team 🌼
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Jessie1564
Jessie1564
Last activity on 09/01/2025 at 6:09 PM
Joined in 2023
6 comments posted | 5 in the Living with multiple myeloma group
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Hello Carenity,
I wanted to reach out to share a bit of my personal journey and seek insights from those who may have gone through a similar experience. My husband was diagnosed with multiple myeloma last year, and our healthcare team recently recommended a stem cell transplant as part of his treatment plan. We've been doing our research, attending appointments, and gathering as much information as possible, but as you can imagine, it's a lot to take in.
I wanted to reach out to this community for support, advice, and perhaps some shared experiences regarding the stem cell transplant procedure. Has anyone had it and would be willing to share their experiences? As well as any tips you might have.
I'm particularly interested in understanding the recovery process, managing side effects, and any lifestyle adjustments that were beneficial. If anyone has recommendations for reputable resources or support groups specifically focused on stem cell transplant and multiple myeloma, please feel free to share.
Thanks