Thanks Stealth. That's great to hear that your teeth etc are improving and generally you have yourself a good regime. Bone health is part of the mystery of my disease ups and downs. I had no fillings as a child, despite dreadful oral hygiene but from late teens on, which is when UC started, my dentist was always confused as to why I had weak teeth enamel and started needing fillings when I was now looking after my teeth and not having high acid foods in great quantities. I also had developed mild osteoepenia about
5 years ago but then the next bone scan, which coincided with a great 3 yr remission from UC on just 2 oral Lialda a day showed that it had resolved (I had also been doing weight bearing exercise in that time).
...and thank you for including that about
Kefir batches possibly having subtilits. I just have not been able to tolerate Kefir since I tried it on and off after I had UC and I had a massive reaction last year when I was in the c diff complicated flare, ate some and bowel just went crazy, bled more than I had in years. I wonder now if subtilis is a problem for me and then this could be part of the reason for my first bout of UC after proctitis. I had proctitis age 18, it cleared up perfectly with steroid enemas (1984, proper old fashioned liquid enemas) and I was never told that it might come back or any relation to UC. Age 21 I went to study in what was the Soviet Union, Kefir was a major part of the diet there and I would have had quite a bit, along with lots of bouts of food poisoning as sorry to say, it was unhygienic out there, particularly in our student hostel conditions. I came back to the West, went to the opposite end of the spectrum food-wise in France, got the worst bout of constipation ever and then, hello proctitis symptoms, then took me 3 months to be seen by a doctor by which time I had pan colitis.
I think you have done your DNA screen Stealth if I remember right? I am wondering if the reaction to this is going to depend on some SNPs, and SNPs beyond being homoz for c677t which I am. I was talking to a moderator on one of the MTHFR sites and she said that lots of people with the SLC19A1 SNP (folate transporter) report "tummy issues"
I suppose in theory I need to experiment by loading up with b. subtilis and see what happens. Would have to be off pred though to be able to see the reaction and if it puts me into another flare the GI will not be impressed. Maybe we'll have to be like the guy who infected himself with H Pylori to prove his point that it was implicated in stomach ulcers when no one would believe his research.
Edited to add:
Just been reading a bit more about
subtilis. It produces hyaluronan.
aem.asm.org/content/71/7/3747.full Hyaluronan or Hyaluronic acid has been tested a lot for help with osteoarthritis, some helped by it but no conclusive evidence. Just found a study "Hyaluronan Inhibits Dextran Sodium Sulfate-Induced Colitis in a Toll-Like Receptor Dependent Manner" Ling Zheng, Yan Zhang, Terrence Riehl, William Stenson
DSS colitis is what the poor mice get induced in them when they do colitis testing
So - if subtilis is getting killed off, that's one inflammatory substance in the body that you are going to miss...
Post Edited (London Lurker) : 4/5/2014 6:11:18 AM (GMT-6)