Guest guest Posted May 3, 2011 Report Share Posted May 3, 2011 I believe that each and every Samter's patient is different and it is really a matter of trial and error as to what works for each individual. I have had the experience that doctors want to treat all patients the same and I have had to take things into my own hands along with what the doctors have told me to do and find all the right things that work for me. I have been off aspirin and prednisone since February and am doing great. I am still on Zyflo CR, Nasonex, Singulair, and Dulara. I have added sitting in a far infrared sauna daily to clean out toxins in my body, I do light yoga, I visit a chiropractor to help blood flow throughout my body and I take a variety of vitamins and minerals. I also sit in a bath of hot water and epsom salts a couple of times of week to sweat out toxins. These seem to work for me but not one of my physicians recommended any of these. It was up to me to try these things. I figured I needed to work in conjunction with my doctors if I wanted to get any real solutions and relief. Not being a very patient person, I had to force myself to take time with each of these things to see if they really did work. Results did not happen in the first few days. How long will all of this continue to work for me????that's the million dollar questions but for now it all seems good. I encourage everyone with the pain in the butt disease to try as many things as possible to find what works for you. It has taken me years of reading, researching, getting PO'd at doctors and finding new ones etc..... On another note: As many of us know Zyflo CR is very, very expensive. I happen to be one without insurance so it was imperative that I find a way to get assistance with this med. There is a program, Conerstone Cares, that has an application you can fill out and get assistance with this med. You can also do the same for Singulair and Nasonex, I just can't recall the name of that program at the moment. I wish the best of luck to everyone with this maddening and frustrating disease. Quote Link to comment Share on other sites More sharing options...
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