cording problems
I have just joined this form and would like to help anyone through.
(History) I am a 67 year old housewife, I was diagnosed with left breast cancer end December 2015 and on the 8th January 2016 had mastectomy and the removal of 18 lymph nodes, prior to surgery was diagnosed as grade 3 aggressive but after surgery was taken down to grade 2 non aggressive, from the 18 lymph nodes only the first was infected. Since then I had chemotherapy, Radiotherapy and I am in my 8th Herceptin also having Anastrozole tablet daily.
Had very little side effects but the few I had were very aggressive, loss of hair, diarrhea (this is mainly because I take daily dosage of Metformin for diabetes) also afraid to go out of house for long hours , foot ache and swollen hand.
Soon after MX I was referred to Physiotherapy regarding the cording and at the beginning of July my arm started getting swollen (lymphedema!!!!) for which I was referred to a specialist physiotherapist who gave me the four bandage treatment and at the end of August went back to treat cording.
What happened during the four bandage treatment the cords got thicker and have one that cannot be snapped.... Presently have full arm movement but still lot of pressure on the underarm to my breast area. Spoken to my physio about this and she will try another 3 sessions and if the cord will not snapp have to do with this what left of my life.
Can anyone suggest what to do to remedy this
Many thanks and best regard to all in this fantastixc forum
Comments
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Welcome, MDAng!
I'm glad you found us. Actually snapping the cords, while it gives fairly immediate relief, is not the recommended treatment for cording. The recommendation is for a specific form of massage, but not every therapist is acquainted with the process. There's more information here:
http://www.stepup-speakout.org/Cording_and_Axillar...
Your therapist might be interested in the "Additional Information" links at the bottom of the page that lead to information specific for health care providers.
Please keep us posted!
Hugs,
Binney -
I've had three bouts of cording and have had none of them snapped. I've always done gentle massage and gentle stretching and each time it has gone away and I have regained full range of motion. There is not strong research on cording, though it is my contention that it is way more common than the breast surgeons think it is.
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I had cording as well several times in the first year after UMX and treatment esp after rads.
My therapist was able to take care of it with a lot of work...sending my best!
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I heard nothing about lymphedema or cording during my visits with oncologist/surgeon or radiation oncologist. When I first went to physical therapy for my lymphedema, I commented the therapist about the "void" left in my armpit where I assumed surgeon had removed lymph nodes. She gently corrected me: it wasn't a "void" in the armpit, those were two cords that had developed in the armpit, raising the skin and leaving a hollow between them. She was able to show me that they continued down into my upper arm. She did a lot of manual stretching in the area, saying that sometimes one could even hear them pop when they break. Mine would not break - and let me tell you she tried!!!! Ouch! She did get eventually get them stretched.
It was a surprise to me to realize the range of motion that I had lost in that arm. With her stretching manipulation and having me do arm exercises, I got my range of motion back. That was three years ago. Now, when I feel my arm tightening up and that pulling feeling in my armpit, I start back with the snow-angel stretches that she started me on: Lay on your back on the floor, arms at your side, palms up. Keeping arms in contact with the floor, raise them as high as you can overhead - like you are a child making a snow angel. Works for me!
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