I see all these posts lately about different things. Pancreatitis, Bacterial Ulcers among others. I start to question if the pains, burning etc that I have throughout my life are true symptoms of something new.
OR
are they results of current problems. I tend to put up with a lot of pain for some reason. Much more then I think most people would. Pain I dont have a problem with. Its the gasping for air that will bring me to the doctor first.
So for those who have diagnoses of things outside of CF......at what point did you decide, hey I should have this checked on. I dont have anything that last for weeks or months on end, but I have had things that can go for days.
I just do what I normally do to get through it. Maybe its a mental block about having to deal with another issue that prevents me from acknowleding it might be something. Maybe its the hassle of being so far from my clinic & knowing they will want me to trod all over NYC to the doctors they refer to.
Maybe its just normal. What is normal for me might be just that....NORMAL FOR ME.
This especially makes me wonder when people have all the usual testing done & nothing is found to clarify why/where the pain is coming from.
I dont think it will change the way I handle things. Unless it directly affects my CF or is more then the usual amount of pain I withstand......
Just curious is all!
OR
are they results of current problems. I tend to put up with a lot of pain for some reason. Much more then I think most people would. Pain I dont have a problem with. Its the gasping for air that will bring me to the doctor first.
So for those who have diagnoses of things outside of CF......at what point did you decide, hey I should have this checked on. I dont have anything that last for weeks or months on end, but I have had things that can go for days.
I just do what I normally do to get through it. Maybe its a mental block about having to deal with another issue that prevents me from acknowleding it might be something. Maybe its the hassle of being so far from my clinic & knowing they will want me to trod all over NYC to the doctors they refer to.
Maybe its just normal. What is normal for me might be just that....NORMAL FOR ME.
This especially makes me wonder when people have all the usual testing done & nothing is found to clarify why/where the pain is coming from.
I dont think it will change the way I handle things. Unless it directly affects my CF or is more then the usual amount of pain I withstand......
Just curious is all!