My daughter felt better whilst on H Pylori protocol of drugs - perhaps similar effect. GP and paediatrician both at loss.
I think H1 are the standard allergy antihistamines.No, not really. Just standard antihistamines for allergies, but I don't think that's the same thing, is it? Those have no effect on my symptoms.
My CRP is almost always quite raised (between 11 and 30), and there's a lot of accumulated evidence that IL6 plays a causal role in CRP production. So reckon there a very high chance my IL6 production is raised too.
If your CRP isn't on the high side, then it would seem unlikely IL6 is a big player for you, so you might not expect to get any benefit from any IL6 inhibition effects of Zantac.
But yes, could be worth seeing if the H2 blocking effect has some benefits for you.
I am only planning on taking it as a test, 2-3 days is the described run in period, if it hasn't done anything by the end of the 3rd day, then I know it's not likely to.I take ranitidine. I hate having to take it. It reduces stomach acid, and the long term effects of this could be catastrophic.
1) This means, as far as I'm concerned, that I am at greater risk of getting an infection from eating something dodgy e.g. getting food poisoning.
2) Stomach acid is vital for breaking down food so that nutrients are properly extracted from food. Without sufficient stomach acid food will be inadequately broken down so nutrient deficiencies are likely to develop.
3) The small intestine is supposed to be near sterile. Reducing stomach acid increases the risk of dysbiosis.
Just do a google for "dangers of acid blockers" to find info on some highly undesirable effects of the things. For anyone who takes them, keeping duration of treatment to a minimum is a very good idea.
Interesting. An Internist rx'd Zantac along with zinc for me 25 years ago. I never asked why back then or had the internet to look it up. I took it (don't remember for how long), and it was during that time I started improving. I didn't know what to make of it but now you have me thinking.
I don't know what my CRP was at that time but it was not raised 11 years later when I was tested.
I really hope it has a positive outcome for you.
I was just curious. I don’t show any signs of iron imbalance either.No, I didn't even know it existed. Looking at the symptom profile, it doesn't seem a good fit for me. Why do you think it might be relevant?
I take ranitidine. I hate having to take it. It reduces stomach acid, and the long term effects of this could be catastrophic.
1) This means, as far as I'm concerned, that I am at greater risk of getting an infection from eating something dodgy e.g. getting food poisoning.
2) Stomach acid is vital for breaking down food so that nutrients are properly extracted from food. Without sufficient stomach acid food will be inadequately broken down so nutrient deficiencies are likely to develop.
3) The small intestine is supposed to be near sterile. Reducing stomach acid increases the risk of dysbiosis.
Just do a google for "dangers of acid blockers" to find info on some highly undesirable effects of the things. For anyone who takes them, keeping duration of treatment to a minimum is a very good idea.
Yes, may try this however PPIs are no good long term.she was on omeprazole, clarithromycin and metrodiazole (?)Being treated for H Pylori involves taking antibiotics as well as acid-blockers (ranitidine/Zantac or PPIs). It could have been the antibiotics that helped. Assuming that your daughter no longer takes the antibiotics, it should be easy enough to test whether or not it was the ranitidine/Zantac or the PPI which helped rather than the antibiotics because both drugs are available over the counter without prescription.
Thanks for the info.
I have acid issues, so does my Father. If I try them out, it would only be a short term trial.
I used it at night for a while - no noticeable effect (cimetidine).Ranitidine did nothing for me but cimetidine (another H2 antagonist) had a noticeable positive effect. I know two other people with CFS who benefitted from cimetidine. Unfortunately, the effects wear off over time.
Sure. I'm weird. Its important to say that. I have a lot of immune type symptoms. Flu-like. Lots of burning glands, headaches, feeling overheated. Very fluctuating pattern. If I overdo activity, I get PEM the next day (an exacerbation of all of the symptoms I just described), but I also get some immediate symptoms when I try to walk any distance - within around 10 minutes of starting. A sort of flushed sensation.@Woolie, are you willing to share your symptom profile or m.e. criteria you resonate with the most?
Yea, that's seems highish. One paper that did a really reliable assay on a large number of people found that IL6 levels above 4.45 pg/mL were in the 95th percentile.my il-6 has been tested by a research lab to be around 7
I've now been taking this stuff for 3 days @ 150mg a day with no noticeable effect, given it's reported it starts to act after 2 days I'm pronouncing this experiment a failure
TBH this is an expected result![]()
I've now been taking this stuff for 3 days @ 150mg a day with no noticeable effect, given it's reported it starts to act after 2 days I'm pronouncing this experiment a failure![]()
?The standard dose is 150 mg twice a day. You might want to try that for a while before giving up on this drug, since you had such good results initially.
I was under the impression the dosage was 150mg per day, not 300mg