On Monday I had my FeNO test. It was with the really good asthma nurse at the surgery. There was a suggestion I could replace my Fostair 200/6 with the Forstair !00/6 so that I could be more flexible. At present I use half the dose in summer, full dose in winter. I am well, have been remarkably so for some time, so it is a good thing to refect on whether I could reduce my overall dosage. But then again it could be the dosage that is keeping me so well. It is a conundrum.
However, yesterday I received two text messages from the surgery, one saying they want to send me for a bone density test (yes, please!), and the second one suggesting I also start taking Risedronate to prevent development of osteoporosis. I am 73. My age was not cited as the main reason but that I have been on high doses of steroids over that last few years . (I know many on here are far higher than me). Nothing about me suggests my bone density is lowering, but of course you normally discover it if you start breaking bones, and I don't want that. So part of me is very appreciative they have flagged up a potential issue, but the other part is frightened of this drug.
Has anyone on here taken it, and how has it affected you if at all? I would be interested to hear. The whole thing came rather out of the blue.
I don't know much about risedronate, but while some bone protection is definitely good given steroids and age, would it make more sense to get the results of the test first if you're concerned about this specific drug? Or can you ask to discuss the reasoning with a GP? It might be that that's the best option for you anyway, but I feel like it might at least be helpful to know what their thinking is and what other options for bone protection are. (It definitely is good to have something in place before you break anything though - I have a friend in her 20s with severe osteoporosis and fractures from steroids because she asked and asked and asked for bone protection and was ignored).
Thank you, Lysistrata! I am not sure about this versus any other drug in this matter, but I fully intend to approach in the way you suggest. I just got the text message last night so I haven't got to it yet, but I really do need to know their thinking better. They did send a. link to the NHS medication explanation. My concern is two fold ( or thereabouts). My mother once was on such a drug. she lived in Sweden and I have no idea of the name, but this weekly protocol and the purpose sounds much the same. But it was probably 20-25 years ago. She got terrible stomach pain, worse each time she took one, so she really had to stop - and she never broke anything, thankfully, until she died. But my wariness certainly stems from that time. I do have a sensitive gut so that worries me. And there were at least 2 other things under side effects I need to understand better.
I took Fosamax once a week, apx 20 years ago. Each pill gave me more heartburn pain. I was then switched to once a month pill when that version was available. Each pill created worse heartburn. The month that I had 3 FULL days of heartburn, I could think of nothing else, breathing burned,…, barely slept…Nothing relieved it, was the last Fosamax that I took.
Side note, my Mom was also on Fosamax. Eventually she also stopped. We both had bone scans & there was bone rebuilt after using it.
Mom had a couple of minor bumps that resulted in breaks, Then one day her ankle shattered. She had a plate & 6 screws used in the repair. Mom has passed now, her ankle repair was well-done, but not without places where her shoe rubbed.