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Stem cell and bone marrow transplants
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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
21 days 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
1 month ago
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
2 months ago
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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
2 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
13 hours 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
5 days 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
6 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
2 days 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
3 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
2 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
2 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
1 month 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
1 month ago
Just wanted to share my Primary Myelofibrosis journey so far…….
Have seen consultants @Guys & now @Addenbrookes to see if I’m a candidate for
stem
cell
transplant
. All agree and they have started to check the donor registers for possible matches.
Have seen consultants @Guys & now @Addenbrookes to see if I’m a candidate for
stem
cell
transplant
. All agree and they have started to check the donor registers for possible matches.
LFCLove
in
MPN Voice
2 months ago
Post stem cell transplant vaccinations
Hi. I am 11 months post transplant (AML). I am due to have my childhood vaccines next week. Just worried about reactions etc and it not being in the safety of the hospital.
Hi. I am 11 months post transplant (AML). I am due to have my childhood vaccines next week. Just worried about reactions etc and it not being in the safety of the hospital.
Platelets2022
in
Leukaemia CARE
7 months ago
have you had trouble getting approved for stem cell transplant?
He believes I am a perfect candidate for
stem
cell
transplant
. So today I go to the consultation with a
stem
cell
specialist and they tell me that because there is a 10-8% chance of failure at their facility I’m not at high enough risk to need the SCT.
He believes I am a perfect candidate for
stem
cell
transplant
. So today I go to the consultation with a
stem
cell
specialist and they tell me that because there is a 10-8% chance of failure at their facility I’m not at high enough risk to need the SCT.
Plasmapool
in
MPN Voice
4 months ago
Travel and Ibrance
My medical history is complicated by having had a donor
stem
cell
transplant
in 2018 for T cell lymphoma. My immune system was compromised from that but now with Ibrance I'm not sure what to expect in terms of traveling and going out to public places.
My medical history is complicated by having had a donor
stem
cell
transplant
in 2018 for T cell lymphoma. My immune system was compromised from that but now with Ibrance I'm not sure what to expect in terms of traveling and going out to public places.
Artesa
in
SHARE Metastatic Breast Cancer
1 month ago
High BLood Pressure, Kidney failure, cause discovered
Scheduled for a
stem
cell
transplant
end of April, or early May.
Stem
cell
doctor told me my kidney function should return to normal with the transplant. I am writing this in case any one else has failing kidneys with high blood pressure and no clear answer why.
Scheduled for a
stem
cell
transplant
end of April, or early May.
Stem
cell
doctor told me my kidney function should return to normal with the transplant. I am writing this in case any one else has failing kidneys with high blood pressure and no clear answer why.
phebamom
in
High Blood Pressure Support
3 months ago
Stem Cell Transplant update
I am now close to 6 months from my sct. I feel well in myself except for side affects from steroids which I should be off in a week. They make it difficult to sleep, make me hungry and over full of energy . Many of my blood counts are in normal range except for platelets. These keep yo-yoing around
I am now close to 6 months from my sct. I feel well in myself except for side affects from steroids which I should be off in a week. They make it difficult to sleep, make me hungry and over full of energy . Many of my blood counts are in normal range except for platelets. These keep yo-yoing around
Scaredy_cat
in
MPN Voice
9 months ago
My Recovery so far post Stem cell Transplant
Sorry I've been absent for so long, my
stem
cell
transplant
journey has been a difficult one to be honest and only now do I feel able to be able to tell the story so far. Thank you to everyone who kindly messaged me to see how I was and apologies for asking so long to respond.
Sorry I've been absent for so long, my
stem
cell
transplant
journey has been a difficult one to be honest and only now do I feel able to be able to tell the story so far. Thank you to everyone who kindly messaged me to see how I was and apologies for asking so long to respond.
Jm954
Administrator
in
CLL Support
8 months ago
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