I'd like to know people's thoughts on this as well. I've wanted to for a while now but I guess I tell myself the ablelist bull.

I do. I fought it for a long time. I still fight using it unless I absolutely have to. It’s useful, but there are days when I need more than one extra point of balance.

I've never used a cane, but I do use a shower chair. 🚿💺. It is SO much safer, easier, and I feel like I get a little spa day bc I soak my feet in a little foot bath while I'm sitting there. Gotta make the most of it 😅 even if its POTS

I also fought it for a while and now have a cane. I have a chronic illness therapist who has really helped me with this. I always felt like buying / using mobility aids was a last resort or meant I had given up on a certain stage of life or freedom. Now I’ve learned that there are times where I may need to use my cane (or other items) and there are times where I don’t need to. I’ve also realized that my nervous system tends to respond well to having “help” sooner rather than later when I’m struggling. That’s just my experience though 💗

I used to use a stick stool which worked really well. Now a full time wheelchair user but have positioning which really helps to stop me passing out.

I don’t feel like a cane would help me enough I’m considering a wheelchair but whatever you think will be most beneficial for you go for it!!

I use a cane both for POTS and EDS symptoms. Helps give my hips and knees a break and with stability. Good if i randomly get dizzy as well!