Experiences with

Stem cell and bone marrow transplants

🎉Finally out🎉 Allogeneic Stem Cell Transplant for Myelofibrosis and Myelodysplastic Syndromes: A Contemporary Review https://onlinelibrary.wiley.com/doi/10.1002/ajh.27660 Thank to Nico Gagelmann M.D.

will be needed a stem cell transplant after my third round for Flagida Chemotherapy. Has anyone had similar?

If you or someone you know has had a successful haplo stem cell transplant, I’d love to hear your story—it would mean a lot right now. Thanks for your support!

Might possibly help with stem cell transplants and could even help with regard to myeloma… here’s link. https://www.medscape.com/viewarticle/high-fiber-diet-linked-improved-stem-cell-transplant-gvhd-2024a1000mm2?

I have been seeing a transplant doctor at Dana Farber in Boston for about a year and he feels I’m strong enough now to have one. Now we have to find a donor and I have to start making preparations. We are shooting for April or May.

Stem Cell Treatment in Tokyo, Japan *Total cell dose, treatment session dates will be scheduled for 6-8 weeks after lipoaspiration appointment *Travel, lodging, meal costs are not included Cost Breakdown Our current stem cell banking pricing for lipoaspiration, stem cell banking for 20 years,

My husband had an allogenic stem cell transplant last August 22 to treat high risk “treatment related” MDS that he developed 9.5 years after completing 6 months of FCR chemotherapy for CLL. The transplant process was every bit as challenging and demanding as we were told it might be.

Hello All I have had asthma all my life, but now have a compromised immune system due to Myeloma and a stem cell transplant which I had a while back. Like many of us, I developed a horrible chest infection at the start of December 24, and yes, I’m still getting over it.

I’m now working my way to a stem cell transplant at Moffitt Cancer Center in Tampa, FL. My reason for writing is to find out if anyone else has experienced this and to make others aware that this outcome is possible. I have no idea if my experiences are linked.

Hi all, just an update on the clinical trial that I started in December 2024 after rapid lymph node enlargement post Stem Cell Transplant. (Allogenic) The trial is a combination of Zanubrutinib and BGB-16673 (BTK degrader).

What science does not know is how often it comes back after a stem cell transplant. My entire immune system was wiped out. The stem cell transplant I had was my own stem cells Right now bone biopsy shows no cancer and no MGUS protein cells.

Are there more possibilities then stem cell transplant? Has any one experience with alternatives? CLL poor risk 17P deletion TP53 complex cytogenetic unmutated

in the end I decided not to have the stem cell transplant maybe physically I could have got through it even though would have been hard but mentally I wasn’t in a good place and without that inner resolve it would have been impossible at the time .

Have been through induction but not needing a stem cell transplant yet. Latest scan showed no signs of progression. I've moved to 1 scan every year for PCA (assuming no change in PSA level.) Still having FDG scans every few months for MM.

(In Ireland we dont have access to our results) Had appointment today and I asked for more clarification on the "mild fibrosis" as its been bothering me, as they told me months ago that "it's not a matter of if you will need a stem cell transplant, it's a matter of when".

Hi All An update to what I would have described as a failed Stem Cell Transplant has actually been a part success- I don’t seem to have any sign of CLL but instead I am back to SLL status which is what I was initially diagnosed with 10 years ago.

Hi there was a post last week about stem cell transplant in Japan. I thought I had saved it but obviously not! Does anyone have a link for it please?

He also did a peripheral bone stem cell transplant to help the bone growth.. hopefully it will work . As for the surgery recovery. I am doing remarkably well. Far better than I have expected in a long time . I have never been this good my legs have never been this good.

I’ve been wanting to update my Stem Cell Transplant journey with good news and today I was going to post that, instead I’ve been told that a lot of my lymph nodes are enlarged again.

I had decided prior to this to do a stem cell transplant, but now I’ve decided to reevaluate every 28 days after getting the FC MRD CLL Interpretation and Report. My Aberrant % total, MRD cells has dropped from .39 to .007 in 4 months.