Despite all this piffle I have been staying in touch with the UC blogosphere. And in particular was provoked into thought by this post on the The Knife you See, and a comment a friend made to me about how far down the 'chronic illness' road I have travelled. At the start we have questions, many questions, and duly recieve answers. Answers that I think we believe. In time the answers don't seem to hold up. May be they stop working. Maybe new questions render them redundant. So, next come the questions that cannot be answered so readily. These questions begin to give us an insight to the methods of finding answers to our original questions. We find that the answers to our new questions are unobtainable or subject to new leaps of faith. A crisis of confidence occurs. If this were a religion we might be doubting our god. We are forced to find a new framework within which we can restore belief. I stopped asking questions and started to look for the answers myself. First from without, and finally within.
I still do not understand why my UC causes massive inflammation in my limbs. I have been told unequivocally by a rhuematology professor that this is the case. At the time when the gastro docs were assuring me the only stone left to turn had a stoma under it, the rheumy prof pretty much told me that was the only course of action. I had made a big fuss for a second opinion through which I had been referred to his care. He basically kicked me into the long grass. I was damn sure they were wrong then. I still am.
I am not anti-surgery. I am not anti-drugs. I have not lost all faith in western medicine. What I am is sure that this disease is so variable and varying that we have to break out of the regimented methods of dealing with it. So many people I know have had to take exactly the same journey: 5ASA's, preds, azathioprine, 6MP, Methatrexate, Infliximab... surgery? Colostomy? Ileostomy? Perhaps peppered with alternatives along the way. But look at the blogs. People finding success, and indeed failure, with so many combinations of approach. But different. Different. Different.
I was trying to find a way to express all this when I stumbled upon this in an interview with the venerable old Willie Nelson:
"I think everyone has to decide for themselves. I think there's a scripture in the Bible [Luke 4:23] that says: "Physician, heal thyself". I think we all have to look at ourselves and say OK, I think this would be good for me, or I don't think this would be good for me..."As it happens he was talking about marijuana! But I like the sentiment.

4 comments:
If this SCD Diet does work, I'll let you know an dif it doesn't I'll be hotting the 'pot' big time :D ...
Too early to say yet for me...30 days on the thing before I say for defo.
Did you try the magnesium supplment yet..I'm still doing research on that once, but again after over 30 days, I think there is defo a difference in inflamation in different bits of my body...not sure if the wheat grass or cod liver oil tablets made any difference at all ...I dropped them a few weeks back, but still have a supply to play with. Do some research on the SCD Diet and see what you think...it was a bit of an eye opener for me....and along with stress, I think food is a factor...funny thing is that with taking magnesium I seem to have the stress under control..now I think that is weird, but for me anyone, it seems to have helped
I love this post Rich! I am often confused by my IBD, I am left at crossroads more often than not. For the last 2 months I decided that I could no longer question myself. I could only do what I could do, what worked for some would never work for me no matter how hard I tried. I started out on Western medicine and left it when I was unwilling to subject my body to it any longer. I went to the opposite side. SCD, supplements, needles, moxa sticks and though I had sucess, the blood always returned. I then decided to take it both ways. A little western sulfazine, SCD, supplements, needles, stress control. And I found a healing balance. What works for some don't work for others. Balance and trial gave me relief from inflammation.
Hey Paula - I'm very interested in the outcome of the diet (got my fingers crossed for you). I'm also impressed with your determination: I'm not sure I could be disciplined enough to be that strict with my eating regime. But, as I've blogged before now - you end up doing whatever it takes. I do agree though; food is a factor (somehow or other!). I think I might look into the magnesium too.
Otherwise, yep, there's nothing for it but to smoke pot...
Hi Candice. You've pretty much nailed my MO there: trial and error to find that healing balance. I'm convinced it's different for all of us, that's why the UC is so hard to deal with.
Having to give a speech like that could make anyone's bowels sick. Glad you made it through it! I'm sure it was great!
Post a Comment