Guest guest Posted April 5, 2010 Report Share Posted April 5, 2010 Hi My SCD Friends: Since it is my birthday today, I thought it fitting to post an update on my condition. I have not posted for a while, 'though I read the list digest daily. For those of you new to the list who don't know me, I was diagnosed in July of '08 with proctosigmoiditis, a form of UC limited to those anatomical areas. I was diagnosed only a month or so after I started to have symptoms that consisted of bleeding, progressing to gas and diarrhea. Luckily, I immediately found SCD and I started on Lialda, a form of mesalamine in extended release form that allows once a day dosing. I threw myself into SCD wholeheartedly and was very vigilant with it ( with some mistakes, of course). I also was taking Tamoxifen, an anti-estrogen, since I had had abnormal mammograms with some Atypical Ductal hyperplasia ( excess abnormal cells) on biopsy found in February of 2007. Currently, my OB-GYN has switched me to Evista, also an anti-estrogen, now that I am officially in menopause. It supposedly has less side effects than Tamoxifen. My last mammogram in February was NEGATIVE.( whopee!) After 3 months on SCD and Lialda, I became totally symptom free. I experimented with many SCD legal advanced foods. At the one year mark from diagnosis, I was taking my Lialda perhaps once or twice a week when I felt I needed it. I occasionally had some loose stool, but not that I was concerned about. At this time I saw my GI who was amazed that I wasn't taking my meds, and passed off this improvement to the fact that he said there is a small percentage of patients who get better on their own. I asked him for a script for LDN and brought him the U of PA study and he eventually refused. I obtained a prescription for LDN finally and started it September of '09. I totally discontinued my Lialda within the month and have had consistent stool since then. Recently I have been feeling so well that I actually forget to take my LDN and take it maybe every 3 days if I remember. I have been adding back non SCD foods into my diet that I have missed, like garbanzo beans and sweet potatoes but I do not have them every day. I still continue my daily yogurt ( 'cause I love it!) and I do follow SCD. However, I dine out now without being so paranoid and visit friends and don't bring my own food. I am doing fine. I consider myself in remission and healed. I did not eat the so- called SAD prior to my dx. I do not intend to start now. I will continue to add back in non SCD foods that I enjoyed before and I will experiment with non grain " grains " such as quinoa, which is actually a high protein seed used by the ancients. I am scheduled for a colonoscopy next year. I may wait another year, but I am curious to see what it would reveal. I don't agree with my GI that I got better on my own. I totally credit SCD for my healing and progress and I was lucky to find this group several months after from whom I learned so much. I share my SCD experience with anyone who will listen and have recommended SCD to many of my patients in my dental practice who have digestion issues. I hope that new people who are struggling will read this and be encouraged and I hope that all the 'old' people with whom I have corresponded will know how much I appreciated their support and cherished their friendship. Love and luck to all. Yours in health, Terry Rumas, D.M.D Proctosigmoiditis 6/08 SCD 7/08 LDN 3 times per week Evista Quote Link to comment Share on other sites More sharing options...
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