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Stem cell and bone marrow transplants
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Japan and stem cells treatment
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?
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?
Bluebell2022
in
Cure Parkinson's
3 months ago
Stem cell transplant
cell
transplant
team my conversation was very grim and my chances of coming out of hospital alive are small her words were if she took 100 patients like me down she would be happy come back with 1 I have a 5 per cent chance iam young so that goes in my favour and I have a 12/12 match but iam high risk
cell
transplant
team my conversation was very grim and my chances of coming out of hospital alive are small her words were if she took 100 patients like me down she would be happy come back with 1 I have a 5 per cent chance iam young so that goes in my favour and I have a 12/12 match but iam high risk
Leighcox85
in
MPN Voice
4 months ago
stem cell for et?
Would
stem
cell
transplant
be an option for ET? I cannot take the Hydrea or Anagralide. Thanks for your feed back
Would
stem
cell
transplant
be an option for ET? I cannot take the Hydrea or Anagralide. Thanks for your feed back
Preacherswife
in
MPN Voice
5 months ago
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Stem cell transplant
Hello, Has anyone woth AMN here ever had a
stem
cell
transplant
as a result of a diagnoses involving cerebral involvement? Please tell all! Is it a viable treatment option?
Hello, Has anyone woth AMN here ever had a
stem
cell
transplant
as a result of a diagnoses involving cerebral involvement? Please tell all! Is it a viable treatment option?
A7x1823eb
in
AMN EASIER
6 months ago
Glad to see more and more players are jumping into the stem cell therapy
https://sbiomedics.com/eng/products/ted_a9.php https://parkinsonsnewstoday.com/news/embryonic-
stem
-
cell
-
transplant
-safety-parkinsons-trial/
https://sbiomedics.com/eng/products/ted_a9.php https://parkinsonsnewstoday.com/news/embryonic-
stem
-
cell
-
transplant
-safety-parkinsons-trial/
Farooqji
in
Cure Parkinson's
6 months ago
stem cell transplant survival with MF
This link gives some figures for overall survival with or without a transplant. The headline really is the initial mortality close to the transplant is only worth risking if your MF is quite bad. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7218417/
This link gives some figures for overall survival with or without a transplant. The headline really is the initial mortality close to the transplant is only worth risking if your MF is quite bad. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7218417/
Scaredy_cat
in
MPN Voice
4 months ago
STEM CELL TRANSPLANT FINALLY SCHEDULED (WE HOPE)
He referred us to the Mayo Clinic for
stem
cell
transplant
, as it is the only chance for a cure. The transplant specialist at Mayo agreed with our local oncologist. They put together a plan for David to receive several cycles of a drug called vidaza.
He referred us to the Mayo Clinic for
stem
cell
transplant
, as it is the only chance for a cure. The transplant specialist at Mayo agreed with our local oncologist. They put together a plan for David to receive several cycles of a drug called vidaza.
dwolden
in
CLL Support
2 months ago
11 months Post SCT
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’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.
Billarina
in
CLL Support
1 month ago
On another subject …
Inspired bya post on another site I’d like to ask if anyone has high risk mutations and has NOT had a
stem
cell
transplant
and has NOT progressed to leukaemia?
Inspired bya post on another site I’d like to ask if anyone has high risk mutations and has NOT had a
stem
cell
transplant
and has NOT progressed to leukaemia?
lizzziep
in
MPN Voice
4 months ago
Stem cell transplant (SCT) 15 months on
I'm now 15 months after my SCT and in my my recent review my figures are improving:WBC 4.0 HB 139 Neut 2.3, lymph1.12 and platelets 106 ( highest for a couple of years). I also had my CD4 lymphocytes measured and can now come off Acyclovir and pentamidine. Hooray! I hated those nebulisers. This leaves
I'm now 15 months after my SCT and in my my recent review my figures are improving:WBC 4.0 HB 139 Neut 2.3, lymph1.12 and platelets 106 ( highest for a couple of years). I also had my CD4 lymphocytes measured and can now come off Acyclovir and pentamidine. Hooray! I hated those nebulisers. This leaves
Scaredy_cat
in
MPN Voice
4 months ago
Anyone turn down a stem cell transplant?
I have post ET MF. Currently I'm on Rux and getting monthly cycles of 5 aza. I don't need transfusions. Day to day I feel pretty good and can do most of what I want. The SCT was recommended because of the risk of progression to AML. I'm finding the decision making to get the SCT very difficult. My
I have post ET MF. Currently I'm on Rux and getting monthly cycles of 5 aza. I don't need transfusions. Day to day I feel pretty good and can do most of what I want. The SCT was recommended because of the risk of progression to AML. I'm finding the decision making to get the SCT very difficult. My
LongETinUS
in
MPN Voice
4 months ago
Still on hold for stem cell transplant
The good news is, they have identified a primary and a secondary donor for the
stem
cell
transplant
. They tell us to plan to proceed in 8 weeks. In other news, extensive studies of the bone marrow showed zero CLL. but "only 20% cellularity."
The good news is, they have identified a primary and a secondary donor for the
stem
cell
transplant
. They tell us to plan to proceed in 8 weeks. In other news, extensive studies of the bone marrow showed zero CLL. but "only 20% cellularity."
dwolden
in
CLL Support
5 months ago
Stem Cell transplant register search goes on…
Unfortunately my next appointment with Consultant has been delayed until early April as they are no further advanced in their search for matches on transplant register. The Nuclear medicine tests that I have just had will be added to MyChart which Addenbrookes uses to show appointments, test results
Unfortunately my next appointment with Consultant has been delayed until early April as they are no further advanced in their search for matches on transplant register. The Nuclear medicine tests that I have just had will be added to MyChart which Addenbrookes uses to show appointments, test results
LFCLove
in
MPN Voice
6 months ago
Momelotinib for Myelofibrosis
She has also asked me to consider
stem
cell
transplant
. I wonder if there is anyone on the forum who has been approved for Momelotinib and, if so, how it is working. Any info would be appreciated as it is a difficult time for me right now.
She has also asked me to consider
stem
cell
transplant
. I wonder if there is anyone on the forum who has been approved for Momelotinib and, if so, how it is working. Any info would be appreciated as it is a difficult time for me right now.
Cazbolac
in
MPN Voice
5 months ago
One year stem cell transplant anniversary
This week a year ago I received my donor's stem cells. For those of you not following my posts, it was hard going in the early months but by late June things were looking a lot better both mentally and physically and my hair started its return.. My platelets were one of the slowest things to recover
This week a year ago I received my donor's stem cells. For those of you not following my posts, it was hard going in the early months but by late June things were looking a lot better both mentally and physically and my hair started its return.. My platelets were one of the slowest things to recover
Scaredy_cat
in
MPN Voice
7 months ago
SCT journey update No.3
Hi all, just to give you an update on my journey towards my *Allogenic
Stem
cell
transplant
, my transplant team @ Addenbrookes Hospital are working towards me starting chemotherapy at the end of July with the transplant taking place approx one week later at start of August.
Hi all, just to give you an update on my journey towards my *Allogenic
Stem
cell
transplant
, my transplant team @ Addenbrookes Hospital are working towards me starting chemotherapy at the end of July with the transplant taking place approx one week later at start of August.
LFCLove
in
MPN Voice
2 months ago
SCT journey update No.2
Anyway my Nuclear medicine tests have come through as “normal”, so just have X-ray and lung function tests to do before I see my consultant @Addenbrookes in a couple of weeks time who will confirm the plan of action towards
stem
cell
transplant
.
Anyway my Nuclear medicine tests have come through as “normal”, so just have X-ray and lung function tests to do before I see my consultant @Addenbrookes in a couple of weeks time who will confirm the plan of action towards
stem
cell
transplant
.
LFCLove
in
MPN Voice
5 months ago
ASXL1 mutation 39% Worried about MF turning into leukemia
I have no
stem
cell
transplant
donor. If one day I transfer to leukemia, I will have to rely on chemotherapy, and my quality of life will be poor, ultimately leading to death.
I have no
stem
cell
transplant
donor. If one day I transfer to leukemia, I will have to rely on chemotherapy, and my quality of life will be poor, ultimately leading to death.
merlisa
in
Fight MPN
1 month ago
Start of my stem cell journey 0.3.1 ambulatory care
I have been offered Ambulatory Care (treatment in a specialised day unit) for my
stem
cell
transplant
has anyone else gone through this process?
I have been offered Ambulatory Care (treatment in a specialised day unit) for my
stem
cell
transplant
has anyone else gone through this process?
Grizly
in
MPN Voice
10 months ago
New member - Post ET MF (Australia)
My doctors have recommended that I start thinking about a
stem
cell
transplant
(SCT); however, the best donor they can find is a 9/10 unrelated donor. I'm currently participating in the INCA033989 CAL-R antibody trial but also on Hydrea to try to control my platelets.
My doctors have recommended that I start thinking about a
stem
cell
transplant
(SCT); however, the best donor they can find is a 9/10 unrelated donor. I'm currently participating in the INCA033989 CAL-R antibody trial but also on Hydrea to try to control my platelets.
Hatchie
in
MPN Voice
4 months ago
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