Cording / Axillary Web Syndrome (AWS)
Does anyone have experience with Cording, also called Axillary Web Syndrome (AWS)
I recently found a rope like structures under the skin in my armpit. I asked my radiation oncologist about and he explained it was called Cording and is scar tissue. I had a lumpectomy and few lymph nodes removed 6 months ago and I did not notice any cording. I am on my 3rd week of radiation and cording is now apparent.
Here is an article on cording:
https://www.breastcancer.org/treatment/side_effects/aws
The dr did give me some stretching exercises.
I am interested in hearing from others who have had cording and if you had any treatment for.
Laurie M
Interested in more discussions like this? Go to the Breast Cancer Support Group.
I had cording down my left arm and underneath my reconstruction. Many PT’s and doctors don’t know what it is. I asked for a pt prescription and found 2 lymphedema specialists at my ambulatory center. They told me I had way more cording than I thought. Exercise there and at home and massage to break it up.
They gave me a lot of twists and I am finding that my yoga practices include similar twists. They also had me use a rod over my head during the twists. It can come back. I am always uncomfortable on my left side but no pain.
A good PT will often print out the exercises or connect you to videos.
My cording stayed with me for quite some time. I have to exercise almost every day now (final surgery in April of 23). I don't see the cording but I have the tightness when I skip the stretching. I'm glad the web site was helpful
I saw an OT but she was a lymphedema specialist too. You’ll get there.
Thanks to everyone. My OT printed a page of exercises for me to practice daily. I am going to see her twice a week for 4 weeks. She also gave me a small piece of dycern to message my scars. I hope the cording will eventually go away. Right now, I feel slight improvements. It has been 8 weeks since my DMX.