Home         Forums  

Go Back   Marrowforums > Bone Marrow Failure Diseases > MDS
Register FAQ Search Today's Posts Mark Forums Read

MDS Myelodysplastic syndromes

Reply
 
Thread Tools Search this Thread
  #1  
Old Fri May 31, 2013, 08:40 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
(((survive)))

Hi
i am ali and 27 years old .1 years ago i understand i have MDS 5q del. when i use (((http://www.mds-foundation.org/ipss-r-calculator/)))
result show me 8 years to survive.
what that mean???? 8 years later i am die??? or my MDS go to AML???what happen if i dont use any treatment???
pleas hellping me to know .
i cant speak english well. short abd simply answering.
thank you very much.
Reply With Quote
  #2  
Old Fri May 31, 2013, 09:57 AM
Greg H Greg H is offline
Member
 
Join Date: Sep 2010
Location: North Carolina
Posts: 660
Hi Alawe!

You should ignore life expectancy data. They are based on averages and have little meaning for individuals -- particularly someone as you as yourself.

Are you having no treatment now?

Take care!

Greg
__________________
Greg, 59, dx MDS RCMD Int-1 03/10, 8+ & Dup1(q21q31). NIH Campath 11/2010. Non-responder. Tiny telomeres. TERT mutation. Danazol at NIH 12/11. TX independent 7/12. Pancreatitis 4/15. 15% blasts 4/16. DX RAEB-2. Beginning Vidaza to prep for MUD STC. Check out my blog at www.greghankins.com
Reply With Quote
  #3  
Old Fri May 31, 2013, 10:06 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
Quote:
Originally Posted by Greg H View Post
Hi Alawe!

You should ignore life expectancy data. They are based on averages and have little meaning for individuals -- particularly someone as you as yourself.

Are you having no treatment now?

Take care!

Greg
hi Greg
i know that is averages .no i dont have any treatment now .
but i want to know what is mean???
just tell me
thank you very much geg
Reply With Quote
  #4  
Old Fri May 31, 2013, 10:10 AM
Greg H Greg H is offline
Member
 
Join Date: Sep 2010
Location: North Carolina
Posts: 660
Hi Alawe,

Sorry. The "survival" number is the number of years of life expectancy until death.

The AML/25% number is the number of years it took for one quarter of patients in that category to convert from MDS to AML.

Take Care!

Greg
__________________
Greg, 59, dx MDS RCMD Int-1 03/10, 8+ & Dup1(q21q31). NIH Campath 11/2010. Non-responder. Tiny telomeres. TERT mutation. Danazol at NIH 12/11. TX independent 7/12. Pancreatitis 4/15. 15% blasts 4/16. DX RAEB-2. Beginning Vidaza to prep for MUD STC. Check out my blog at www.greghankins.com
Reply With Quote
  #5  
Old Fri May 31, 2013, 10:16 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
Quote:
Originally Posted by Greg H View Post
Hi Alawe,

Sorry. The "survival" number is the number of years of life expectancy until death.

The AML/25% number is the number of years it took for one quarter of patients in that category to convert from MDS to AML.

Take Care!

Greg
OMG!!
Thank u greg
thank you for your Precision
Reply With Quote
  #6  
Old Wed Jun 5, 2013, 05:56 PM
Lifeguard Lifeguard is offline
Member
 
Join Date: Sep 2011
Location: Australia
Posts: 37
Hi Alawe,

I have Del5q too and have had it for 5 years.

I take Revlimid (Lenalidomide) which works well for our type of MDS.

The survival %s are not so accurate for young people because we do not tend to have other medical issues.

And your young so a Bone Marrow Transplant may be another option for a cure.

Rachael
__________________
Diagnosed MDS Del 5q October 2007, blood transfusions 2010, commenced Revlimid 2010. Transfusion independent.
Reply With Quote
  #7  
Old Thu Jun 6, 2013, 02:16 AM
Lifeguard Lifeguard is offline
Member
 
Join Date: Sep 2011
Location: Australia
Posts: 37
Hi Alawe,

Sorry, Just read your signature, with "boycott No treatment".

It's good that you are treatment free.

I needed transfusions early because my red and white cells dropped too quickly.

Revlimid has allowed me to be active again.

Hope all goes well Alawe.

Rachael
__________________
Diagnosed MDS Del 5q October 2007, blood transfusions 2010, commenced Revlimid 2010. Transfusion independent.
Reply With Quote
  #8  
Old Thu Jun 6, 2013, 06:50 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
Red face

Quote:
Originally Posted by Lifeguard View Post
Hi Alawe,

Sorry, Just read your signature, with "boycott No treatment".

It's good that you are treatment free.

I needed transfusions early because my red and white cells dropped too quickly.

Revlimid has allowed me to be active again.

Hope all goes well Alawe.

Rachael
Hi racheal thank you for reply
yes you know my problem is boycott.if i want to bring revlimid from another country it is very expensive and i can not.any way i just wait .but i hope all and special you get better.and enjoy life.if you do your transfusion tell me i wait for you.Notify me of ok??
thank you.
Reply With Quote
  #9  
Old Sun Jun 9, 2013, 05:57 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
hi
i have question...
is MDS Related with Lymph gland ؟؟؟
my Lymph gland inflated and i have pain???
is that because i have MDS???
Any one have experience ??/
Reply With Quote
  #10  
Old Wed Jun 12, 2013, 08:53 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
Hi
can any one hellp me to know what is the normal rang of pathologis???
any site or Source to show normal rang??
my result:
Erythroblast:53%
Myeloblast:0.5%
promyelocytes:1.5%
myelocytes:11.5%
metamyelocytes:5.5%
bands:6.5%
PMNs:22%
megakaryocytes:0.5%
M/Eratio:0.9
cellularity: 35-40%
is my result fine???
Reply With Quote
  #11  
Old Wed Jun 12, 2013, 07:25 PM
sstewart09 sstewart09 is offline
Member
 
Join Date: Feb 2013
Posts: 65
I'm sorry I don't have a site to give you, but as far as cellularity goes, I was told that it should be 100-your age. If this is true, then your should be 70-75%. Hope this helps a little.
__________________
Samantha, wife of Joe age 34; diagnosed vsaa 2012; MUD BMT February 2013
Reply With Quote
  #12  
Old Thu Jun 13, 2013, 05:56 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
hi thank you .
i need mor info can any one hellp.my dr don't tell me any thing.i need to know.
Reply With Quote
  #13  
Old Thu Jun 13, 2013, 08:03 AM
Bambam Bambam is offline
Member
 
Join Date: Oct 2012
Location: Vancouver, BC, Canada
Posts: 59
Quote:
Originally Posted by alawe View Post
hi thank you .
i need mor info can any one hellp.my dr don't tell me any thing.i need to know.
Aka we, have you tried asking questions of your doctor? Is he a hematologist? If he won't give you information, is there a chance you could see a different hematologist? Hope you can get the answers you need for reassurance.
__________________
DX MDS RA Low Risk August 2012. DX Changed to MDS RAEB1. Progressed to AML July 2013. Participated in clinical chemo trial CPX351 and relapsed four months later in March 2014. Maintenance chemo -VIDAZA (AZA) stopped after 4 rounds. Awaiting full report from BMB.
Reply With Quote
  #14  
Old Thu Jun 13, 2013, 09:22 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
Quote:
Originally Posted by Bambam View Post
Aka we, have you tried asking questions of your doctor? Is he a hematologist? If he won't give you information, is there a chance you could see a different hematologist? Hope you can get the answers you need for reassurance.
hi yes i tried a lot of and questions of him.and he just said me "yes " no" come one month later" i tell you and some thing like that....
and he is a good dr
any way thank you.now i am study hard to book and web and article and...
special marrowforums hellp me a lot.i mean study to found my question.
Reply With Quote
  #15  
Old Sat Jun 15, 2013, 05:24 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
Question

hi
i am sorry for my ridicule question .the truth is i can't speak english well.
thanks to google translate.
any way i have question again.
now i am ok and dont have any problem with my MDS.
now i dont use any drug or blood transfusions.
my dr tell me now i dont need i am ok.
my question:
what is Symptoms MDS ?
i mean what happen for me ?
Dizziness
Nausea
Unconscious?
what doing MDS to die down people??
sorry again and thank to all.
Reply With Quote
  #16  
Old Sat Jun 15, 2013, 05:46 AM
Birgitta-A Birgitta-A is offline
Member
 
Join Date: Oct 2007
Location: Stockholm, Sweden
Posts: 1,918
MDS

Hi alawe,
You know the symptoms of MDS are caused by low counts - that is low hemoglobin, low white blood cells or low platelets. In the bone marrow they find misshaped young blood cells.

If the hemoglobin is low we feel tired, breathless etcetera

If the white blood cells are low we can get infections.

If the platelets are low we can get bleedings.

The most common death cause in MDS is heart problems - remember that MDS patients hardly ever are as young as you but perhaps 50 years older.

The second death cause is leukemia - when they look at the bone marrow they find more than 20% blast cells - immature blood cells.

Then some patients get infections like pneumonia, that is difficult to treat.

Another death cause is bleedings due to the low platelets.

It is common that MDS patients with good counts don't need any treatment.

Kind regards
Birgitta-A
Reply With Quote
  #17  
Old Sat Jun 15, 2013, 10:36 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
Quote:
Originally Posted by Birgitta-A View Post
Hi alawe,
You know the symptoms of MDS are caused by low counts - that is low hemoglobin, low white blood cells or low platelets. In the bone marrow they find misshaped young blood cells.

If the hemoglobin is low we feel tired, breathless etcetera

If the white blood cells are low we can get infections.

If the platelets are low we can get bleedings.

The most common death cause in MDS is heart problems - remember that MDS patients hardly ever are as young as you but perhaps 50 years older.

The second death cause is leukemia - when they look at the bone marrow they find more than 20% blast cells - immature blood cells.

Then some patients get infections like pneumonia, that is difficult to treat.

Another death cause is bleedings due to the low platelets.

It is common that MDS patients with good counts don't need any treatment.

Kind regards
Birgitta-A
thank you thank you thank you....
that help me good.
i ask a lot .you know in iran not any sit or weblog or article for MDS in persian . now i get information about MDS from marrowforums and translate to persian . and i make a weblog to hellping patient
that is my weblog
http://myelodysplastic.blogfa.com/
Reply With Quote
  #18  
Old Sat Jun 15, 2013, 03:25 PM
Birgitta-A Birgitta-A is offline
Member
 
Join Date: Oct 2007
Location: Stockholm, Sweden
Posts: 1,918
MDS

Hi alawe,
Very interesting! Of cause I can't read a single word but I saw that you have a link to Marrowforums.
Kind regards
Birgitta-A
Reply With Quote
  #19  
Old Wed Jun 19, 2013, 05:05 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
hi again
yesterday i gone to my dr...he is crazy .now my wbc very low . ANC 600. he tell me next month i give you thalomid . I have MDS 5q del.
is thalomid good for me??
every month he forget i am 5qdel.i remember him.
pleas any one
is thalomid good for me??
Reply With Quote
  #20  
Old Wed Jun 19, 2013, 06:03 AM
Bambam Bambam is offline
Member
 
Join Date: Oct 2012
Location: Vancouver, BC, Canada
Posts: 59
Exclamation

Quote:
Originally Posted by alawe View Post
hi again
yesterday i gone to my dr...he is crazy .now my wbc very low . ANC 600. he tell me next month i give you thalomid . I have MDS 5q del.
is thalomid good for me??
every month he forget i am 5qdel.i remember him.
pleas any one
is thalomid good for me??
Hello Alawe, I wonder if you can request a second opinion. It is really important that you have confidence in and trust your hematologist. I assume your doctor is a Hematologist and not a family doctor? If you think your doctr is crazy and he has to be reminded about your diagnosis, it's time you ask yourself if he is the right doctor for you. I have a wonderful hematologist who listens carefully and asks lots of questions. You deserve this too. Good luck ... Let me know what you think of this idea ...
__________________
DX MDS RA Low Risk August 2012. DX Changed to MDS RAEB1. Progressed to AML July 2013. Participated in clinical chemo trial CPX351 and relapsed four months later in March 2014. Maintenance chemo -VIDAZA (AZA) stopped after 4 rounds. Awaiting full report from BMB.
Reply With Quote
  #21  
Old Wed Jun 19, 2013, 06:59 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
Quote:
Originally Posted by Bambam View Post
Hello Alawe, I wonder if you can request a second opinion. It is really important that you have confidence in and trust your hematologist. I assume your doctor is a Hematologist and not a family doctor? If you think your doctr is crazy and he has to be reminded about your diagnosis, it's time you ask yourself if he is the right doctor for you. I have a wonderful hematologist who listens carefully and asks lots of questions. You deserve this too. Good luck ... Let me know what you think of this idea ...
hi Bambam and thank you for reply
i visit my dr every month and first i trust him . tow month ago when i ask him about revlimid he told me not good for you . it is for 5q del.i wonder and told him i am 5q dell , then he remember . again , yesterday i told him i have 5< blast and he forget that again . i cant change my dr it is hard to me . i just need to dr listen to my talk good and answering my question . like your dr Bambam .
what your idea???
Reply With Quote
  #22  
Old Wed Jun 19, 2013, 04:04 PM
Birgitta-A Birgitta-A is offline
Member
 
Join Date: Oct 2007
Location: Stockholm, Sweden
Posts: 1,918
Revlimid

Hi alawe,
Revlimid is the best drug for patients with the 5q del.
http://www.ncbi.nlm.nih.gov/pubmed/23432724

I have understood that it will be very expensive for you. I have never read anything about Thalidomide and the 5q del - I don't think it will work as well as Revlimid.
Kind regards
Birgitta-A
Reply With Quote
  #23  
Old Wed Jun 19, 2013, 05:48 PM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
Quote:
Originally Posted by Birgitta-A View Post
Hi alawe,
Revlimid is the best drug for patients with the 5q del.
http://www.ncbi.nlm.nih.gov/pubmed/23432724

I have understood that it will be very expensive for you. I have never read anything about Thalidomide and the 5q del - I don't think it will work as well as Revlimid.
Kind regards
Birgitta-A
hi Birgitta-A
thanks for link . i wish if i can get revlimid i believe the revlimid good for me .
like you i don't think the thalomid is good for me. i don't know what i have to doing i confused.
pleas any one have info about thalomid.
is it good for me???
Reply With Quote
  #24  
Old Tue Aug 6, 2013, 03:23 PM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
hi evry one

hi
right now i am not feeling good. i have many Mouth ulcers...i have pain and my dr tell me i have get revlimid.but the same problems...bycot..
now my ANC 410
and my neutrophil 14%
Reply With Quote
  #25  
Old Wed Aug 7, 2013, 06:22 AM
Birgitta-A Birgitta-A is offline
Member
 
Join Date: Oct 2007
Location: Stockholm, Sweden
Posts: 1,918
Revlimid

Hi Alawe,
It is strange that you are offered Thalidomide but not Revlimid when you live in a country like Iran with good doctors. As other members have written you should try to find another hematologist. Here is a doctor in your city: http://rct.ajums.ac.ir/_rct/document...CV%202012).pdf

The company who makes Revlimid (Celgene) can have a program for compassionate prescriptions for patients who can't afford Revlimid.

Mouth ulcers is not a positive sign - they probably depend on the low ANC. Perhaps you could get Neupogeninjections for the low White Blood Cells.
Kind regards
Birgitta-A
Reply With Quote
Reply


Thread Tools Search this Thread
Search this Thread:

Advanced Search

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

vB code is On
Smilies are On
[IMG] code is On
HTML code is Off
Forum Jump


All times are GMT -4. The time now is 12:11 PM.


Powered by vBulletin® Version 3.6.7
Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.
Forum sites may contain non-authoritative and unverified information.
Medical decisions should be made in consultation with qualified medical professionals.
Site contents exclusive of member posts Copyright © 2006-2020 Marrowforums.org