# Participants needed for CMT study

**URL:** <https://forum.livingwithpolyneuropathy.org/t/participants-needed-for-cmt-study/1391>\
**Category:** General CMT Discussion\
**Created:** [April 12, 2013, 4:52am UTC](https://forum.livingwithpolyneuropathy.org/t/participants-needed-for-cmt-study/1391 "2013-04-12T04:52:49Z")\
**Posts on this page:** 2\
**Page:** 1

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**Author:** ![Melinda\_L](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithpolyneuropathy.org/melinda_l/32/1269_2.png) [@Melinda\_L](https://forum.livingwithpolyneuropathy.org/u/Melinda_L)\
**Post date:** [April 12, 2013, 4:52am UTC](https://forum.livingwithpolyneuropathy.org/t/participants-needed-for-cmt-study/1391/1 "2013-04-12T04:52:49Z")

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[Participants needed for CMT study](http://www.cmtausa.org/index.php?option=com_content&view=article&id=664%3Aparticipants-needed-for-cmt-research-study&catid=7%3Anewsflash&Itemid=61)

The Inherited Neuropathies Consortium (INC) of the Rare Diseases Clinical Research Network (RDCRN) is conducting a research study looking at what symptoms and day-to-day issues are specifically important to adults with Charcot Marie Tooth (CMT) neuropathy. This study will help doctors and researchers develop a scale that will be able to measure CMT more accurately than the general ones currently available.

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**Author:** ![SImone\_B](https://sea1.discourse-cdn.com/flex019/user_avatar/forum.livingwithpolyneuropathy.org/simone_b/32/1359_2.png) [@SImone\_B](https://forum.livingwithpolyneuropathy.org/u/SImone_B)\
**Post date:** [June 8, 2013, 12:29am UTC](https://forum.livingwithpolyneuropathy.org/t/participants-needed-for-cmt-study/1391/2 "2013-06-08T00:29:02Z")

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Can count on me!!!