If you MTS or think that you have MTS, then you can click on the following links to learn more.
- http://www.may-
thurnersyndrome.org/ - http://www.facebook.com/group.php?gid=109802252379583
- http://groups.google.com/group/mts-international-group
- http://groups.google.com/group/may-thurner-syndrome-support-group
- http://groups.google.com/group/annes-non-dvt-may-thurner-syndrome-group
To help with lymph edema drainage in the Fayetteville Area, you can contact Laurie Blair.
Hi Dee,
ReplyDeleteI hope you have received my comment explaining how links #2, #3, #4, and #5 above will not work unless the readers are already members of these groups. #1 is their best bet if they wish to join us. Great work...you've had this going for 3 years and I only just learned about it today. Where have I been?
Diane Peterson, Creator/Manager of MTS Resource Network since 2008
Now I see that you will not have received my first comment. I have the hang of this now. Great set up you have created here, and I appreciate your effort to advertise the MTS Resource Network. Together we will continue to spread the word of MTS and encourage our readers to persist in seeking appropriate medical intervention.
DeleteDiane Peterson