Home         Forums  

Go Back   Marrowforums > Practical Issues > General Health Issues
Register FAQ Search Today's Posts Mark Forums Read

General Health Issues Diet and appetite, sleep and fatigue, pain management, exercise, etc.

Reply
 
Thread Tools Search this Thread
  #1  
Old Tue Aug 9, 2011, 08:39 AM
Sally C Sally C is offline
Member
 
Join Date: Dec 2010
Location: Chesterfield, Va.
Posts: 470
Jaundice

Good morning all,
I have a question that I hope someone can shed some light on as our doctors don't seem to have an answer and don't seemed to be concerned enough to find out.
My husband Don has MDS (RAMD) - and is currently in the Eltrombopag (Promacta) clinical trial for platelets at NIH. He is tolerating the med very well and his platelets are holding in the 20,000 for the first time since 2009. He is still red cell transfusion dependent. But that's an aside.
He also has some type of colitis/ulcerative colitis but they don't seem to be able to come up with a firm diagnosis as to what exactly he has - even after a colonoscopy. That's an aside as well.
The subject I'm writing about is that he is jaundiced. His face is yellow and parts of the whites of his eyes are yellow. Not terribly but noticeable enough that some of our health care providers have commented about it. The weird thing is that all his liver enzyme tests are normal - bilirubin - everything. He also recently had an abdominal ultrasound which showed a little sludge in his gallbladder and some athersclerosis (small buildup of cholesterol) in his abdominal aorta.
I would appreciate any input if someone has any experience with something like this.
Thanks so much and God Bless,
Sally
Reply With Quote
  #2  
Old Tue Aug 9, 2011, 01:20 PM
Hopeful Hopeful is offline
Member
 
Join Date: Jan 2009
Location: California, USA
Posts: 769
Hi Sally,

Here is something to bring up with your doctors, as I am not an expert and this is pure speculation...When I was red cell transfusion dependent, I also started turning yellow. I just did a quick search on the web for a possible link and found that it could have been caused by a delayed hemolytic reaction to the transfusion itself or by autoimmune hemolytic anemia.
__________________
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
  #3  
Old Tue Aug 9, 2011, 04:08 PM
Marlene Marlene is offline
Member
 
Join Date: Oct 2006
Location: Springfield, VA
Posts: 1,412
How's his iron?
__________________
Marlene, wife to John DX w/SAA April 2002, Stable partial remission; Treated with High Dose Cytoxan, Johns Hopkins, June 2002. Final phlebotomy 11/2016. As of July 2021 HGB 12.0, WBC 4.70/ANC 3.85, Plts 110K.
Reply With Quote
  #4  
Old Wed Aug 10, 2011, 09:00 AM
Sally C Sally C is offline
Member
 
Join Date: Dec 2010
Location: Chesterfield, Va.
Posts: 470
Jaundice

Hi Hopeful and Marlene,
Thank you both for responding to my post.
Hopeful, I will look into autoimmune hemolytic anemia and delayed hemolytic reaction. I know nothing about either of them.
Marlene, I don't know if you're referring to his ferritin (not sure the difference in iron and ferritin). His ferritin is slightly over 1,000. It's been higher so I'm not sure that could be the cause. But I will look into it.
Again thank you both for taking the time to respond. Will let you know if I find out anything.
Take care and God Bless,
Sally
Reply With Quote
  #5  
Old Wed Aug 10, 2011, 10:09 AM
Marlene Marlene is offline
Member
 
Join Date: Oct 2006
Location: Springfield, VA
Posts: 1,412
With a FE at 1000, I doubt that it's a factor. Unless he had an iron problem prior to MDS and transfusions which would mean long term exposure to excess iron. But if the elevated iron/FE is a result of recent transfusions , then it's most likely not the culprit. Hopefully he had a baseline FE done before starting any treatments so you can better assess it. High iron usually takes 10 years to effect organs but it seems to effect the very young and old sooner.
__________________
Marlene, wife to John DX w/SAA April 2002, Stable partial remission; Treated with High Dose Cytoxan, Johns Hopkins, June 2002. Final phlebotomy 11/2016. As of July 2021 HGB 12.0, WBC 4.70/ANC 3.85, Plts 110K.
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 07:17 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