I initially bought 2 pounds from
www.bulkherbstore.com/PSP?s=psyllium of which I have about
1/2 a pound left. It seems that I'm using about
1 pound a month.
I ordered up a year's supply (12 pounds) a little over a week ago from
www.starwest-botanicals.com/product/2-psyllium-seed-powder.html which was much cheaper and shipping was free. Fortunately, I have a freezer in which to store it.
I started taking it during the worst of my flare and increased the dose to the two teaspoon level when things did not improve and as I noted earlier the flare dramatically improved at that point. My only unwanted side effect was an increase in gas initially. I also noticed that I got extra thirsty about
an hour after having the psyllium seed powder which was easily addressed with a glass of water.
Here is the clinical study that I tracked down before starting the psyllium seed powder (
www.ncbi.nlm.nih.gov/pubmed/10022641). Obviously, it did not help everyone but it seemed to do as well as mesalamine.
For some reason my flare did not respond to the prednisone like previous flares. My abdomen was in significant discomfort when I first started taking the prednisone and the discomfort went away in about
two days but it never controlled the bleeding and mucus. In the past the bleeding and mucus would vanish within two days of starting the prednisone and it was like a magic potion.
In mid-November, when I had my last exam with my GI he wanted me to have blood tests for preparation for taking immunosuppressive drugs and start my treatment down that course of action. I don't want to go there. I think my immune system is working perfectly fine and it's doing its best to defend my body but whatever is in my colon is able to survive the attack. In my case I think I have a spore based bacteria that comes out to play about
every six months since I flare every February/March and September/October. I don't think that the Asacol I'm taking is of any use. If its purpose is to keep me in remission then is sucks at it. The only reason that I keep taking it is because there are indications that it reduces the chances for cancer and my luck will probably be that it is only is applicable in those patients that maintain remission but I continue to take it.
I started to use the mesalamine enemas after the psyllium seed power had brought my flare down to just four stools a day. I don't think that my body likes the enemas because I get the same sensation a day after using one that I get just prior to a flare kicking up. I get this bubbly sensation throughout my rectum and lower colon. This produces lots of gas for the next couple of days. I have my next GI exam in early January (with a younger and hopefully more creative GI) and I will discuss the enema sensations with him at that time. In the mean time I will continue to take them twice a week just in case the gas production is related to using a new medicine.
Although the psyllium seed powder did a fantastic job getting me out of my flare, I won't be satisfied until I make it past February/March without flaring. Now I just need to wait and see.
LookingFortheCure, the three months just before my latest flare, I swear that my digestive system was working the best ever in my life and I was hopeful that I finally had this disease in check but that abruptly changed on September 24th when I started bleeding again. For me nothing had changed prior to its arrival. I was eating the same, I was exercising the same, and my stress level (or lack thereof) was the same. It just showed up as it typically does every fall. Hopefully you have better luck.