from the partner side, i’ve been trying to understand what trigger finger feels like for my wife who has lupus. she’s been experiencing it lately and it’s been tough to see her struggle with everyday tasks. i’ve read that it’s common in people with rheumatoid arthritis, but not as much about lupus.
does anyone have experience with trigger finger and lupus? how did you manage it? my wife’s doc mentioned steroid injections, but we’re not sure if that’s the best option.
someone posted about this in a thread on gardening with lupus, and it got me thinking about how trigger finger affects daily life. any advice or personal experiences would be really helpful right now.