Has anyone got any experience of a wheelchair with lymphedema?
I’ve had multiple cellulitis infections, 20+, I am getting treatment though. Along with the lymphedema I’ve also had a stroke and I’ve got arthritis in my spine (AS).
I’ve some idea what it’s like as I spent over 14 months in a chair after the stroke, but I’m facing the notion of it being a more permanent thing now.
I can walk, but the distance I can cover is getting shorter, maybe 2 - 300 yards, and it’s getting harder. I’m really struggling with walking, but I’m also aware of the restrictions being in a chair will bring.
I’m just trying to understand how other people deal with a situation where mobility is a challenge.