My left arm has got larger and the skin is also lumpy. I was wondering if other people had the same problem. I have had lymphoedema for six years now. I don,t have an appointment with my clinic until the end of October. I can't wear a compression sleeve as I have poor circulation. I have had a few sessions on the Lymph assist but the machine was only on loan for a few weeks at my clinic.
Does anyone have the details for the Newcastle Support Group? Is it too late to get tickets for the conference? I don't even know where it is being held.