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  • Charlotte Marx
    Charlotte Marx is now friends with Annie Ross.
    • September 30, 2013
  • Jim Miller
    Jim Miller is now friends with Annie Ross.
    • April 13, 2012
  • Gwen Chinn
    Gwen Chinn is now friends with Annie Ross.
    • March 15, 2012
  • corcoran corinne
    corcoran corinne is now friends with Annie Ross.
    • March 12, 2012
  • Annie Ross
    Annie Ross I'm glad I found this site. I have been breast cancer free for two years but suffer from Lymphedema in my left arm and chest. I do the the self massage therapy twice a day and wear my Sleeve everyday. I really dont know very much about Lymphedema, glad...  moreI'm glad I found this site. I have been breast cancer free for two years but suffer from Lymphedema in my left arm and chest. I do the the self massage therapy twice a day and wear my Sleeve everyday. I really dont know very much about Lymphedema, glad to find other people with my problem so I can learn from them.  
    • March 12, 2012
    • Gwen Chinn and Patricia Chapman like this.
    • Annie Ross
      Gwen Chinn Hi Annie, I didn't know a lot about lympedema either until it caught up with me last year. I am a former LPN and worked many years in hospitals and clinics but rarely had seen anyone with lymphedema. My doctor connected me with a lymphedema clinic in my...  moreHi Annie, I didn't know a lot about lympedema either until it caught up with me last year. I am a former LPN and worked many years in hospitals and clinics but rarely had seen anyone with lymphedema. My doctor connected me with a lymphedema clinic in my area and boy, did I get an earful. It is good that...    
      • March 13, 2012
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  • Annie Ross
    Annie Ross has just joined the community. Say hello!
    • March 12, 2012
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Info

  • Classification Patient
  • Gender Female
  • Birthday September 26, 1969
  • Employer First American Title
  • Last Name Ross
  • First Name Annie

Friends

  • Jim Miller (sorry for the long post but I couldn't stop) About those compression garments we wear...I know personally how we all are sensitive to wearing our garments in public. Many posts and emails and other blogs are filled with comments about people unwilling to wear their garments "out" in public. Yup, it absolutely does set us apart as "special", that's for sure. So we  either don't wear the garment (dangerous) or keep it hidden even on the warmest of summer days.  I've had primary LE of the left leg for 45 years. I hid my LE garment for over 12 years, too uncomfortable to wear it in public. Then one summer day in 1980 I said to heck with what others think, I'm wearing shorts because I'm hot (no, not "that" hot! Sheesh!). I've worn shorts for every outdoor spring, summer and fall activity (hiking, cycling) ever since, showing off my garment, my big fat leg and my normal-looking muscled right leg. I got accustomed to the special looks and the questions. But most often there were no questions and no looks (that I could see). So what's my point? My point is that I'm realizing that uncomfortableness you all feel about wearing your garment in public is still there with me even after all these years of wearing a garment in public. Because now, you see, the LE has progressed into my once "good" right leg. Now I'm having to wear a thigh high Juzo on the right leg all the time to control the new LE. Yup. Sucks. And so what am I doing about it? I'm hiding it. Wearing long pants or taking it off when I'm going in shorts. Yes: I'm unable to go to the gym with both legs in a compression garment!  Until this week when I convinced myself all over again that nobody cares, nobody is interested, nobody really will notice that both of my legs are in compression garments instead of just one. It's like that little sticky on the refrigerator that says something like dance like nobody's watching. But I must confess, it took a great deal of - something I don't know what - for me to go to yoga class on Monday night and have both legs in garments.  So I feel your pain, people. Every one of you who is uncomfortable going out in public with your arm or your leg in compression garments. Because I'm right there feeling the same thing. And I'm very uncertain if the next time I go to yoga class or go to work out in the gym I'll not strip off the thigh high before I step out there. Silly? No. Challenging? Every day.
  • corcoran corinne I did not look into this. I was hoping someone had experience/knowledge with this surgery.That and my lymphedema was under control. Well that has changed and it is 'growing' yet again. I would love to get your feedback after you visit them. Here are two other links you may be interested in. Thanks for the post and hope to hear from you again.  http://drmarga.com/what-is-lymphedema.html http://www.nytimes.com/2011/06/21/health/21lymph.html?_r=1
  • Gwen Chinn I had a modified radical mastectomy nineteen years ago and did not have lymphedema until last summer. I have been followed recently in a lymphedema clinic near where I live and even though I have had to adapt and change how I do things from now on, I am glad I sought help when I did. I now wear a compression sleeve and try to stay positive.
  • Charlotte Marx
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