After what seems like an eternity i am starting on a trial of steroids on wednesday for susspected PMR. I remember posting on here and getting lots of useful information from members who had symtoms which i could relate to. Im still not 100 sure i have this condition but will probably know more when iv been on steroids for a short while.
It was my endo who susspected PMR and asked my GP to start me on steroids, a had been presenting with typical PMR symtoms at my doctors but the dots were not joined and i was told i had fibro and M.E.
Another member on here told me of the PMR site which has been a godsend to me.
I am living in hope that i might soon start to feel better but also a little afraid of the medication and its side affects. Like most conditions if it does turn out to be PMR i am at the beginning of the journey.
Thanks for everryones help and will keep ypu updated of my progress.
Christine
Written by
yorkshiregirl44
To view profiles and participate in discussions please or .
Hi, I was started on steroids for suspected PMR, and all symptoms fitted. The effect was immediate and I was convinced that finally the doctor had worked out what was wrong with me - however, apparently I wasn't as better as I should have been and was referred to rheumatology. It seemed that as the steroids hadn't worked 100% it wasn't PMR but PMR onset of RA. The process of having to jump through all the hoops can seem interminable so I do hope you get a right prognosis soon
Hi, Sorry for delayed replly - I only bother to update mail every few days. I suggest you read all info regarding PMR and RA on the NHS website, here and on the NRSA website - I'm sure you;ll find more info0 there than I could ever know about. Good luck
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.