Hello, i've had lymphoedma in my right arm for thirteen years. I have been managing my condition wearing made to measure compression stockings. My husband has been to taught to apply the compression bandages once a week which really improves the size initially. I also have a private MLD therapist once a month to move the fluid using massage, one that is registered through LSN. This can be quite expensive as you can all imagine. My question is would this MLD be available on the NHS. My lympoedma is non cancer related by the way.
Would welcome any feedback
Thanks in advance