TRENDING HASHTAG: #Vein Center

Blogs

  • New member needs advice

    Posted October 15, 2010 by Sharon Koller

    64,546 Views

    I'm unable to put on short stretch bandages of my arm & hand due to neuropathy.  It is impossible to get the right gradient doing by yourself.  My lymphedema is getting worse.  Any new products out there f Read More...

  • Let's get the LE dx and tx bill passed soon!

    Posted October 3, 2010 by Barbara Pilvin

    4,469 Views

    I've sent letters and my own story to anyone in or outside Congress who might, just might, read them and get motivated.  I know plenty of other people have done so as well.  Here's a reason for doing so that I Read More...

  • "Share Your Story" Campaign

    Posted September 19, 2010 by Jenny Sterner

    1 Comment 5,116 Views

    Dear HR 4662 Supporters, This update is devoted to announcing a new way in which you can help.  We are launching the “Share Your Lymphedema Story” campaign!  Complete information is below. I a Read More...

  • HR 4662 and the American Cancer Society

    Posted September 3, 2010 by Jenny Sterner

    1 Like 4,703 Views

    Hello, I heard that some people were having trouble with the links to the American Cancer Society.  There are two new ones below so hopefully no one will have any problems with these.  http://action.acscan. Read More...

  • Farrow Wraps

    Posted August 23, 2010 by Dale Rutala

    3 Comments 5,721 Views

    Hi, I am new to this site. I recently received information on a compression product called Farrow Wrap. It claims to be a short stretch compression wrap that is premade and you trim it to fit. I am recently certified and Read More...

  • HR 4662 - Lymphedema Cost Relief Bill on Capitol Hill

    Posted July 2, 2010 by Kathryn Krastin

    8 Comments 4,649 Views

    If you have been following me on my BEYOND WORDS LIVE radio show on BlogTalkRadio you will have heard several advocates speak out about the bill, what they have been doing in Washington, DC, and what still needs to be do Read More...

  • new to this site

    Posted April 26, 2010 by Kathy B

    13 Comments 3,839 Views

    Hello all, I'm new to this website.  I am a member of another LE website and find it very helpful.  I am hoping to find that here.  I am a bit taken back by everyone using real names and pictures. Read More...

  • Emotional Well-being

    Posted April 23, 2010 by Kathryn Krastin

    10 Comments 3,849 Views

    Hey, just wanted to share with you all a book that I discovered through a place called LYMPHEDEMA PRODUCTS, LLC.  (http://www.lymphedemaproducts.com) that focuses upon the emotional well-being of a lymphedema p Read More...

  • Employer is Changing Insurance Companies...

    Posted April 15, 2010 by Kathryn Krastin

    9 Comments 3,625 Views

     I hate change when one has been having a great response to Blue Cross Blue Shield in the past with the paying for lymphedema treatment costs and garments, pump, etc.  Now, my employer (due to cost factors) are Read More...

  • National Lymphedema Awareness Day - Radio Show

    Posted March 6, 2010 by Kathryn Krastin

    7 Comments 3,716 Views

     In case you missed the show, you can still hear the show at http://www.blogtalkradio.com/rlrn/2010/03/06/beyond-words-live-an-oral-history-project.   Please pass this  link to others to bring about Read More...