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 Sat Mar 8, 2014, 08:14 PM
ussoccer004 ussoccer004 is offline
Member
 
Join Date: Feb 2014
Location: Orlando, FL
Posts: 21
PNH Specialist Florida

Does anyone know if there is a PNH specialist in Florida at all? I know we have M.D. Anderson Cancer Center that is now the University of Central Florida Cancer Center.

I began my Soliris last week and starting to feel amazing, less headaches, shortness of breath getting better. All symptoms of PNH are starting to slowly subside. I have a large clone size and had a blood clot in my head recently which scared my hematologist in starting Soliris ASAP. To my amazement she seems to think that one day I will be able to come off soliris and this is what scares me because I thought this was a life long disease lol?
Reply With Quote
  #2  
Old Sat Mar 8, 2014, 08:23 PM
Kathy S Kathy S is offline
Member
 
Join Date: Nov 2013
Location: Leesburg, Fl
Posts: 72
Have you checked with Moffit Center in Tampa?
__________________
Kathy,wife of 69 year old male with DX June 2013 with MDS= RAEB 2refractory with Extra Blast Very High Risk WBC 1.9-RBC 2.29-HGB 8.1-PLT 32-, as of Aug 2013:. BMB 12/4/13= WBC 5.57/RBC 4.86/HGB 15.5/HCT 42.8/RDW 49.6/PLT 188. 3% blast.BMB 4/11/14 WBC1.6,PLT12,RBC2.6,HGB9.2
Reply With Quote
  #3  
Old Sat Mar 8, 2014, 11:49 PM
Neil Cuadra Neil Cuadra is offline
Owner
 
Join Date: Jul 2006
Location: Los Angeles, California
Posts: 2,556
I think Dr. Chieh-Lin Fu is a PNH specialist in Weston, Florida.
Reply With Quote
  #4  
Old Fri Nov 28, 2014, 11:45 PM
Susan Susan is offline
Member
 
Join Date: Sep 2003
Location: Chicago, Il
Posts: 101
FL PNH Spec

Keep in mind there are only 7 or 8 true PNH experts here in the states. These specialists will have seen over 100 PNH patients, (many of them have seem 300+ patients), be both PNH researchers and clinicians and be up to date on the latest research. This usually means being a member of the International PNH Interest Group. PNH is so rare you want to see someone who has as much experience as possible.

The closest one to Florida is Dr Carlos De Castro at Duke. He took over Wendell Rosse's PNH clinic. He is ok. Dr Monica Bessler at Univ of Penn is excellent. On the east coast there is also Dr David Araten at New York University. He is a sweetheart and is quite popular. I see both Araten and Bessler, Bessler more often just because I'm not that fond of NYC.
__________________
AA/PNH Dx 1998, Warfarin, Soliris
Reply With Quote
  #5  
Old Tue Dec 2, 2014, 11:52 AM
mharrell mharrell is offline
Member
 
Join Date: Dec 2008
Posts: 11
We're in NE FL. We took our son to see Dr. De Castro at Duke. I liked him.
Reply With Quote
  #6  
Old Tue Dec 2, 2014, 05:14 PM
GoodDay5150 GoodDay5150 is offline
Member
 
Join Date: Sep 2014
Location: Centennial, CO
Posts: 150
I had a STC for PNH in 2011. I was referred to a specialist by my HMO that I had at the time. I, like most ppl had never heard of PNH until my diagnosis. You can probably check the NORD website and maybe Alexion for specialist info. I have also been told that many experts are going to be affiliated w/ med school med centers, but my clinic is not; their prim. focus are cancers of the blood. Good luck in your treatment.
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
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 01:15 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