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 Mon Dec 3, 2018, 03:40 AM
AliceKay1 AliceKay1 is offline
Member
 
Join Date: Sep 2017
Location: Walnut Creek CA USA
Posts: 42
MDS to AML and 1 month to live

My doctor told me last Friday that my MDS has progressed to AML and that I have 4-6 weeks to live. Has anybody else been given such sudden news? Does everyone go so quickly with this news?

I've read about a drug, Venetoclax, approved by the FDA November 2018. Has anybody tried this, yet?
__________________
AliceKay1, 80 years old, dx MDS 2017, being treated with Vidaza
Reply With Quote
  #2  
Old Mon Dec 3, 2018, 09:26 AM
whackerswalsh whackerswalsh is offline
Member
 
Join Date: Nov 2017
Location: Dublin, Republic of Ireland
Posts: 8
Hello Alice,

So sorry to hear your news.
My husband recently passed away MDS to AML, however he continued longer than the prognosis.

The only consolation I can give you and certainly from my part on hindsight is to pursue any clinical trials or drugs, push your consultants for any possibilities outside of the "box".

I wish you well in your endeavours and my best wishes.

Barbara
__________________
Barbara wife of Patrick age 60, Diagnosed SAA Jan 2016, 2 Treatments of ATG partial response, continuing with Cyclosporine.
Reply With Quote
  #3  
Old Mon Dec 3, 2018, 07:00 PM
DanL DanL is offline
Member
 
Join Date: Dec 2010
Location: Denver, CO
Posts: 590
I am sorry for the shocking news. That is a pretty sudden and short prognosis, but it is just a prognosis and is based on what the doctor has experienced in most cases.

Looking up Venetoclax, it looks like it has been used in two ways, both in combination therapy for AML:

Venetoclax + Vidaza or Decitabine
Venetoclax + low dose ARA-C

The first combination had response rates up to 73% and the second up to 62%. I think that it would be worth checking to see if your doctor or another may be willing to look it up and see if you fit the criteria for treatment.

https://www.onclive.com/web-exclusiv...x-combo-in-aml

dan
__________________
MDS RCMD w/grade 2-3 fibrosis. Allo-MUD Feb 26, 2014. Relapsed August 2014. Free and clear of MDS since November 2014 after treatment with Vidaza and Rituxan. Experiencing autoimmune attack on CNS thought to be GVHD, some gut, skin and ocular cGVHD. Neuropathy over 80% of body.
Reply With Quote
  #4  
Old Tue Dec 4, 2018, 01:52 AM
AliceKay1 AliceKay1 is offline
Member
 
Join Date: Sep 2017
Location: Walnut Creek CA USA
Posts: 42
Thank you,i Danl

Thank you, Dani. That was really super of you to look into venetoclax for me. I'll definitely follow up on that. Thank you.
__________________
AliceKay1, 80 years old, dx MDS 2017, being treated with Vidaza
Reply With Quote
  #5  
Old Tue Dec 4, 2018, 01:56 AM
AliceKay1 AliceKay1 is offline
Member
 
Join Date: Sep 2017
Location: Walnut Creek CA USA
Posts: 42
Thank you, Barbara

Thank you for your kind words, Barbara. I'm sorry about your husband. I lost my Thayer 3 years ago.
__________________
AliceKay1, 80 years old, dx MDS 2017, being treated with Vidaza
Reply With Quote
  #6  
Old Tue Dec 4, 2018, 10:22 AM
Sally C Sally C is offline
Member
 
Join Date: Dec 2010
Location: Chesterfield, Va.
Posts: 470
Dear AliceKay,
I can't imagine how stunning it must be to get this news. Doctors can only go on what they think - but thankfully it's not in their hands. Keep the Faith as they are quite often wrong. Take care of yourself and believe in Miracles during this Christmas season. I wish you God's Peace.
All the best,
Sally

Last edited by Sally C : Tue Dec 4, 2018 at 11:10 AM.
Reply With Quote
  #7  
Old Wed Dec 5, 2018, 01:20 PM
AliceKay1 AliceKay1 is offline
Member
 
Join Date: Sep 2017
Location: Walnut Creek CA USA
Posts: 42
Thank you, Sally

Sally, how nice of you. Thank you so much for your kind words.
Yesterday I started on oxygen, and what a difference a day makes!. I can breathe again without gasping. Merry Christmas to you and yours.
__________________
AliceKay1, 80 years old, dx MDS 2017, being treated with Vidaza
Reply With Quote
  #8  
Old Thu Dec 6, 2018, 11:16 AM
David M David M is offline
Member
 
Join Date: Sep 2009
Location: Fayetteville, TN
Posts: 92
Prayers for you!

AliceKay1,

I'm sure that was a shocking thing to hear from your doctor!

I want you to know that I am praying for you! I pray for your healing, and I pray God's comfort and peace will be upon you during this time.

David M
__________________
David M, reds/whites/plats slowly declining since 2000; hypo-cellular bone marrow; diagnosed Mild AA; low counts, but stable since 2009; watch and wait -- no treatments required to this point.
Reply With Quote
  #9  
Old Fri Dec 7, 2018, 01:28 AM
AliceKay1 AliceKay1 is offline
Member
 
Join Date: Sep 2017
Location: Walnut Creek CA USA
Posts: 42
Thank you, David

Thank you, David. And I'll be thinking of you!. Goodness, to have all those blood numbers just slowly decreasing over the years and no treatment. I'll look up some of those terms you used.

I get a bone marrow biopsy tomorrow to confirm or deny that it's AML. Wish me luck!
__________________
AliceKay1, 80 years old, dx MDS 2017, being treated with Vidaza
Reply With Quote
  #10  
Old Fri Dec 7, 2018, 12:16 PM
Hopeful Hopeful is offline
Member
 
Join Date: Jan 2009
Location: California, USA
Posts: 769
You are in my thoughts and prayers, AliceKay1. I hope you have a good appointment!

Wishing you peace and comfort.
__________________
58 yo female, dx 9/08, AA/hypo-MDS, subclinical PNH, ATG/CsA 12/08, partial response. small trisomy 6 clone, low-dose cyclosporine dependent
Reply With Quote
  #11  
Old Mon Dec 31, 2018, 11:14 AM
Marimari Marimari is offline
Member
 
Join Date: Jun 2017
Posts: 3
Praying for you

Dear Alice Kay,

I just wanted you to know I am praying for you. My own Mother has gone through this journey. Diagnosed with MDS in 2017 and now AML. She is currently on Venatoclax, having combined it with Dacogen (5 days). She is on her 12thday of 21 days for the Venatoclax.
You are not alone, and I pray for your encouragement and comfort as you experience this tremendous trial. Thank you for reaching out to build community, even in your suffering. Sending you love, strength, peace and joy and thinking of you strongly!
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

Similar Threads
Thread Thread Starter Forum Replies Last Post
MDS - VA assigns diagnostic code 7725 Tommy Daniels MDS 4 Sun Jan 22, 2017 04:51 PM
Husband has MDS; transformed once to AML GoingOcean MDS 19 Thu Jan 23, 2014 07:22 PM
FIL's MDS turned to AML ltw Tell Your Story 5 Fri Aug 24, 2012 01:55 PM
Genetic Mutations In MDS Persist After Progression To AML Sally C MDS 0 Tue Apr 10, 2012 03:34 PM


All times are GMT -4. The time now is 01:17 AM.


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