Well since my last post things have not improved, they have continued to get worse to the point that the GP under the advice of the Rheumy nurse that I spoke to have changed my pain meds three different times, now I am on Tramadol and Paracetamol so I spend quite a lot of my time asleep as I feel so drugged and out of it all the time. My legs hurt like hell, does anyone know where I can get spare parts as would gladly rip off legs for a new set. The swelling is expanding and the hospital got so pissed at the GP because even after I came out of lockdown and actually got an appointment at my GP practice, they refused to measure my legs for the stockings, saying they don't know how, even the practice nurse didn't know.
The Rheumy lot complained to the GP and the GP blamed the pharmacy saying they should measure my legs and send the measurements to them and then they will put the prescription through. From February they were asked to get these done to ease the pain/swelling in legs and the could not organise a piss up in a brewery. Eventually a district nurse was sent who then made me feel even more anxious as she just kept saying oh my they are so big and the right is a whole 5cm bigger than the left, how do you get around? I just had to explain I have been living in flip flops but the weather is changing and I can't walk around in flip flops forever, plus the indentations are sore and look unpleasant. That was the beginning of October, no stockings and now the GP has just sent me a text out of the blue saying they are not going to do what the Vasular and Rheumy team have asked they have referred me to the Lymphoedema team in a hospital miles away from my home and I can't drive at the moment because the of the swelling. Why this has been decided, no explanation.
So will call them tomorrow. Tired of being on steriods, although it has helped a lot and has reduced the swelling by half, just hope this ends soon as so fed up with the ifs, buts and maybes.