Akylosing spondylitis

Hi guys

I'm Susie & after 25 years of suffering & complaining to GPs & specialists I have finally been diagnosed with AS which showed on an MRI that I have now fused in several places ๐Ÿ˜”

My dad has suffered with AS for years & now it looks like both my brothers have it also.

Im awaiting biological therapy treatment & am praying it works as I live with the pain constantly & just want an escape from it & some kind of a normal life back again. Anybody else living with AS & how's your pain & what treatments are you on to manage yours?

Thanks ๐Ÿ˜Š