claderbine.........is this our pill????

New Topic Post Reply Printable Version
[ << Previous Thread | Next Thread >> ]

Gretchen1
Forum Moderator


Date Joined Jan 2007
Total Posts : 3521
   Posted 1/24/2009 6:09 PM (GMT -6)   
Hey everyone........this just in.  Merck Serono has just released the results of its study of a pill.  It looks great!!!  It may be approved later this year!!  I am asking my doc about it when I have my check in Feb. 
 
It is stating nearly 60% efficacy!!!!  Woooo hooooo!!!
 
 
 
Gretchen       co-moderator MS board       diagnosed with MS July 2006
 
I have no lesions on my soul and so I will live with no limits.


rhondab
Veteran Member


Date Joined Mar 2006
Total Posts : 2146
   Posted 1/24/2009 7:56 PM (GMT -6)   
Holy crap!!! Is this for real??? Gosh i am excited!!! Let us know what u'r doc says g!!!
rhonda
Co-Moderator, MS Forum
 
*~*Sometimes the Lord calms the storm. Sometimes He lets the storm rage and calms His child.*~*
 
Things that make u go hummmm......
*I wonder how much deeper the ocean would be without sponges.*
*One day without sunshine is like...um..well...night?*


bohuck2
Regular Member


Date Joined Dec 2008
Total Posts : 196
   Posted 1/25/2009 12:26 PM (GMT -6)   
Rhonda (I meant to say Gretchen geesh must have R on my small brain),
Does it work on PPMS or just RRMS? Either way, it is very good news. Thanks a bunch! I will go on the site you gave and check it out.


 
 
 
 
                                        Chuck the old man :>)
                                   AMWTP Training Instructor
                                          Idaho Falls, Idaho
                                  Diagnosed with PPMS May, 2006
                                   but still working at the present.         
                Tried just about everything there is for MS, including Tysabri
                               Waiting to start Cytoxin Treatments soon.

Post Edited (bohuck2) : 1/26/2009 6:17:34 AM (GMT-7)


mystery reader
Regular Member


Date Joined Jun 2007
Total Posts : 257
   Posted 1/25/2009 1:38 PM (GMT -6)   
I have not heard of this one.  I definitely will ask my neuro if he knows anything about it next month at my appointment.  I have my doubts that he will have any information.  G, make sure you let us know what your neuro says.
Barb/mystery reader
Diagnosed April 2007
Started betaseron --  May 2007 -- experienced allergic reactions after 2 weeks
Started copaxone -- June 2007 -- stopped after 4 1/2 months;experienced  severe 5 IPIR's
Started tysabri -- December 2007
Stopped tysabri -- April 2008 (developed antibodies/severe reactions)


theshultzgang
Regular Member


Date Joined Jan 2009
Total Posts : 38
   Posted 1/25/2009 3:04 PM (GMT -6)   
How exciting! I really feel like a cure will be found soon. I can't wait to hear what your doctor says too!
Envision health and your body will follow!
Diagnosed with RR MS 11/2001
Healing more and more every day
Andrea :)


Sunnycitrus
Regular Member


Date Joined Apr 2007
Total Posts : 334
   Posted 1/28/2009 2:27 PM (GMT -6)   
This one is very exciting! :-)
New Topic Post Reply Printable Version
Forum Information
Currently it is Friday, August 18, 2017 11:42 PM (GMT -6)
There are a total of 2,857,371 posts in 313,501 threads.
View Active Threads


Who's Online
This forum has 155110 registered members. Please welcome our newest member, MMoore.
337 Guest(s), 6 Registered Member(s) are currently online.  Details
Chask, icomputered, ARangel14, Carlito36, RichardNY, 142


Follow HealingWell.com on Facebook  Follow HealingWell.com on Twitter  Follow HealingWell.com on Pinterest
Advertisement
Advertisement

©1996-2017 HealingWell.com LLC  All rights reserved.

Advertise | Privacy Policy & Disclaimer