Hello all,
Just wanted to share my good news re I CAN HAVE THAT MRI! Woo hoo 😀
I have been waiting over 15 months for this. It had to take me paying private to see one of the top ankle surgeons who told me I must go back and insist to help with the RA deterioration in my ankles. It was in one now spread to the second ankle. Hoping the Xeljanz kicks in soon as so far all I have been experiencing is swollen stiff sore fingers and tender ankles.
The foot surgeon could not understand why my rheumatologist would not let me have an MRI, he said he is going to ask him. I was told by one of the drs at my local clinic it was too expensive, and by my rheumatologist that it would make no difference as I have RA an MRI would not change that. I went back to see the practice owner who pushed for me and it paid off.
Sorry to go on but I am pleased. I just don't understand how the young lady at work who says she has had three MRI in pretty quick succession. She did recommend I contact her hospital, however I do not live in East London.
Hope everyone is coping as well as can be. I haven't been posting much due to the RA which seems to have spread to fingers. One minute my hands were perfect the next day all was not good, how quick the RA spread or perhaps it’s the biologic? Who knows. Told the only way to fix is exercise! Easier said than done. As said, I need to be my own Dr and put on my persistent hat!
Stay well, gentle hugs, Hessie 🤗