Hi does anyone know off any support groups for trochanteric bursitis please
Thank you
Hi does anyone know off any support groups for trochanteric bursitis please
Thank you
You might ask this question on the healthunlocked Lupus UK forum ....go to the link kara gave you & find lupus UK
My impression is that various types of bursitis is something we lupus patients do get - my bursitis is in my forefeet, but I've encountered trochanteric on our lupus uk forum
Any type of chronic Bursitis is a nightmare, but after years of suffering mine is more controlled
Good luck
This is often a feature of ankylosing spondylitis, so you may get some answers from a spondyloarthritis support group
I have steroid injections in my greater tracanta (hip) every 3 or 4 months.My pain consultant has never mentioned Lupus.He injects the tender points in my back caused by Fibromysalgia and Sponylosis of the spine.