Charcot Marie Tooth Disease - CMT Disease - Hereditary Neuropathy

THE FOUNDATION TO SUPPORT THOSE LIVING WITH CMT (CHARCOT-MARIE-TOOTH)
HNF

Bernadette

An Upcoming Documentary about Living with CMT

View Trailer !

 

 

 

 

Arlene has Plans... Big Plans!

Read all about Arlene in  Arlene on the Scene... available in September

Pre-Order your copy now !

 

 

 

 

MEMBER LOGIN

button_become_member
Hereditary Neuropathy Foundation, Inc.
1751 2nd Avenue, Suite 103, NY NY 10128
NY Tel: 212-722-8396
Toll Free: 877-463-1287
info@hnf-cure.org
Register with iGive and shop at brand name online stores through the iGive Mall. A portion of each purchase is donated to your favorite cause.
logo_igive

Linda here: Do we need to make changes and how to know when?

Issue date:  Tue, 10/07/2008 Author Name:  Linda Crabtree One of the toughest things for us to do when we have a progressive syndrome like CMT is to adapt to change.  How do we know when to make changes and what is the deciding factor?  When do we need to change? Full text available to Members Onl...


Please Become a Member to view the full article.


Links  |  Site Map  |  SEO by Sound Strategies