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
  #26  
Old Wed Aug 7, 2013, 05:48 AM
Chirley Chirley is offline
Member
 
Join Date: Oct 2007
Location: Logan City Australia
Posts: 1,100
Hi alawi, sorry you're not feeling well.

I don't understand. Are you refusing Revlimid or is Revlimid not available in Iran?

Regards

Chirley
Reply With Quote
  #27  
Old Wed Aug 7, 2013, 06:31 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
Quote:
Originally Posted by Birgitta-A View Post
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
hi
oh my god i live in ahwaz and i cant find dr like that....i dont know him...how you find it???but i want to call him
is thalomid good for me???
about Celgene i hope they can help me...i want to call him too.
any way thank you very much my freind
Reply With Quote
  #28  
Old Wed Aug 7, 2013, 06:44 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
Quote:
Originally Posted by Chirley View Post
Hi alawi, sorry you're not feeling well.

I don't understand. Are you refusing Revlimid or is Revlimid not available in Iran?

Regards

Chirley
hi thank you for replay
not available in Iran .
Reply With Quote
  #29  
Old Wed Aug 7, 2013, 06:37 PM
Chirley Chirley is offline
Member
 
Join Date: Oct 2007
Location: Logan City Australia
Posts: 1,100
Hi alawe,

I apologise for my ignorance. I just read an article about the lack of medicines in Iran due to sanctions imposed on your Government and the suffering of innocent people as a result.

It's so sad when civilian populations suffer due to politics.

I hope you can get the Revlimid directly through your doctor and Celgene. I wish you all the best.

Regards

Chirley
Reply With Quote
  #30  
Old Thu Aug 8, 2013, 06:59 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
Quote:
Originally Posted by Chirley View Post
Hi alawe,

I apologise for my ignorance. I just read an article about the lack of medicines in Iran due to sanctions imposed on your Government and the suffering of innocent people as a result.

It's so sad when civilian populations suffer due to politics.

I hope you can get the Revlimid directly through your doctor and Celgene. I wish you all the best.

Regards

Chirley
hi Chirley
and thank you.
yes now it is very hard time and people suffer and even die because no drug available in Iran.
i have question
you and Birgitta-A talking about (Celgene) .
is that company??? and how they can help me??
what i have to do??
thank you
i hope some day no boycott in world for any reason
Regards
Reply With Quote
  #31  
Old Thu Aug 8, 2013, 08:47 AM
Neil Cuadra Neil Cuadra is offline
Owner
 
Join Date: Jul 2006
Location: Los Angeles, California
Posts: 2,553
Biotechnology company Celgene has a Patient Support Program to help people in the U.S. get access to their drugs, including Revlimid. I don't know if they have similar programs in other countries but you can contact them at patientsupport@celgene.com to ask about it.
Reply With Quote
  #32  
Old Thu Aug 8, 2013, 09:20 AM
alawe alawe is offline
Member
 
Join Date: May 2013
Posts: 39
Quote:
Originally Posted by Neil Cuadra View Post
Biotechnology company Celgene has a Patient Support Program to help people in the U.S. get access to their drugs, including Revlimid. I don't know if they have similar programs in other countries but you can contact them at patientsupport@celgene.com to ask about it.
hi neil and thank you
i contact them and i wait now to answering.
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 08:27 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