Home         Forums  

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

PNH Paroxysmal nocturnal hemoglobinuria

Reply
 
Thread Tools Search this Thread
  #1  
Old Tue Jan 8, 2013, 12:38 AM
Heather8773 Heather8773 is offline
Member
 
Join Date: Jan 2013
Location: Houston, TX
Posts: 254
Pnh labs

So today I picked up my husbands labs

Hgb 5.5 lowest it has been
Plateletts 14 continuing to trend down quickly
Rbc 1.28 gone down
WBC 3.6 only thing that has gone up instead of down this time
Hct 15.0 down

I hope that things start going up
__________________
Heather, wife of Ronald 36; dx PNH 2012; Dx VSAA 2013; eculizumab(Solaris) hATG 2/20/13 cyclosporine 400 mg daily. 37 units RBC and 15 units of platelets. Post BMT -pentam,vorconizole,valtrex, valcyte, actigall, Pepcid , prograf, magnesium.
10/10 MUD 10/10/13
Now no PNH or AA. Mixed Chimerisim
Reply With Quote
  #2  
Old Tue Jan 8, 2013, 02:28 AM
Neil Cuadra Neil Cuadra is offline
Owner
 
Join Date: Jul 2006
Location: Los Angeles, California
Posts: 2,556
Heather,

Ronald's low counts sound very familiar to me because when my wife was first diagnosed with aplastic anemia she had HGB of 4.7, platelets of 14, and WBC of 3.3. That's very close to Ronald's lab results.

Two thing that have changed since my wife's treatment: One is the level of knowledge of the doctors, who learn more about bone marrow failure and its treatment every year. They may not have found a cure for PNH yet but they've made leaps and bounds in understand its biological mechanics. The other changes is the availability of drugs like Soliris that have revolutionized PNH treatment and made such a big difference to so many patients.

I look forward to hearing news of higher counts on your husband's next CBCs.
Reply With Quote
  #3  
Old Tue Jan 8, 2013, 10:40 PM
Heather8773 Heather8773 is offline
Member
 
Join Date: Jan 2013
Location: Houston, TX
Posts: 254
Thank you

It's very comforting to know someone eles has been this low. I was sitting in my car (parked) just staring at the results frozen for awhile. Thinking nooooo! What do/can I do!!! How low is someone humanly able to go!!!

I really appreciate you responding and the second part about advancements being made. At this point I have no idea the game plan. We're just staying w eculizumab and drawing more labs Monday.

I talked to my boss today about taking days off to volunteer w be the match, regional gulf coast blood, and support group meetings and he was so cool and helped me realize i am not the Dr but I can help in some way
__________________
Heather, wife of Ronald 36; dx PNH 2012; Dx VSAA 2013; eculizumab(Solaris) hATG 2/20/13 cyclosporine 400 mg daily. 37 units RBC and 15 units of platelets. Post BMT -pentam,vorconizole,valtrex, valcyte, actigall, Pepcid , prograf, magnesium.
10/10 MUD 10/10/13
Now no PNH or AA. Mixed Chimerisim
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
8th Annual Walk for PNH in New York, September 22, 2013 Marrowforums News and Events 0 Sat Aug 10, 2013 01:16 PM
Possible Cure for PNH Tom Cramer PNH 16 Tue Aug 16, 2011 10:41 PM
PNH Webinar, September 2009 Marrowforums News and Events 0 Mon Sep 14, 2009 05:43 PM
PNH Webinar, May 2009 Marrowforums News and Events 0 Thu Apr 23, 2009 02:16 AM
PNH Webinar, March 2009 Marrowforums News and Events 0 Wed Feb 25, 2009 07:06 PM


All times are GMT -4. The time now is 06:02 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