Survivorship questions and resources

Thanks Marg, I still have cording (two very minor cords) and am 7 months after surgery. I am lucky enough to have the full range of movement in my arm and when I feel it starting to tighten I have a little massage to try and loosen it up. My Lymphoedema nurse tried breaking it for me at the 4 month mark but it didn't work. Prior to that I had not been told about cording or how to deal with it and it was through this network and looking up you tube that I found information.I just tend to think I am incredibly lucky with it and I know that others are not so lucky.