Experiences with

Peptic ulcer disease

Some of these drugs subsequently found themselves a new role as PPIs, after research in 1982 by Barry Marshall and Robin Warren came to overturn the prevailing view that stress and lifestyle were the major causes of peptic ulcer disease, demonstrating an infectious cause from the common bacterium [i]

hello forum friends I’ve just bought some cytoplan betaine and pepsin. My thinking is to raise my stomach acid to help my body better absorb nutrients. I’m just wondering have any of you tried this, and has it helped? Thanks 💜

hello and thank you all for your help on my last post for acv. so if we snack between meals do I take some as well, the bottle says 8 oI think it's already helping this is my second day. the betaine pepsin will show up tomorrow I ordered so I'm eager to try it. I do snack a lot so I'm not sure if I

Smoking and Effects on the Stomach Smoking may affect the entire body, increasing the chances of developing several life-threatening ailments such as heart disease, emphysema, and lung cancer. Smoking leads to numerous diseases and several types of cancers of the digestive system, such as stomach

Does pepcid AC make RLS worse? Almost 38 weeks pregnant having horrible acid reflux. Intestines feel like they're on fire for hours leading to a giant throw up. Pepcid really helps but it makes my rls sooo bad which i can't afford because I only sleep 20-30 mins a day on a good day bc of my insomnia

Post from lady on here earlier caught my attention and I wonder if any of you knowledgable people can throw some light on this? I done the home test - some baking soda & water first thing and no burp at all which indicates low stomach acid. Thankfully I do not have discomfort but I’m concerned about

I have generally had IBS D or M, but recently it has changed to more constipation. About the same time I also was told by my doctor to take Pepcid in the morning and again before dinner. I can't remember exactly, but it does seem that the constipation started about the same time as I started taking

Had a major hick up day 4. The beginning of an anaphylaxis reaction. Chemo stopped. Rapid response team called and in my room in 2 minutes. Got IV benedryl, epinephrine, Pepcid. Things resolved pretty quick but the lymph nodes in my neck enlarged so they ordered an mri stat. In the evening had another

Hi everyone, So, my levothyroxine was put up to 88mcg at the end of November. I tested in March and results were: TSH 1.270 µUI/mL 0.380 - 5.330 T4 (free) 1.16 ng/dL 0.54 - 1.24 (88% through range) T3 (free) 3.79 pg/mL 2.50 - 3.90 (92% through range) I always test before 9am, fasted, no

Hi everyone o have my last transfer next month and wanted to try everything I can as this is my last attempt. I have downregulated for 3 months on zorodex as I have adenomyosis and endo. For the transfer, I will be taking prednisone 10mg twice daily and aspirin 150mg from cd2 and forward. I've also

hi there. So I’ve been getting dry eyes and a dry sore burning tongue and mouth. GP did ANA bloods which were negative. I was thinking sjogrens syndrome or lichen planus (as I also get bad mouth sores.) Anyway dentist has referred me to Birmingham dental hospital and I’m now thinking it could be burning

I'm currently under an endocrinologist, we discussed possible treatment also looking at other reasons why I'm tired(especially in afternoons) plus other usual symptoms associated with hypothyroidism, I've Ords & anti bodies & Doi2 deficiency. Currently on 100/125mcg alternate so far so good. In July

Hi, Can anyone clarify please how Hashimotos affects teeth/gums? Or is it the Levothyroxine that does it? Whenever I mention to dentist, she is oblivious to this/never heard of it.My teeth have always suffered. Countless fillings, extractions, sensitivity, poor enamel, teeth practically disappearing!

I had a gastroscopy last December and was told I have mild Gastritis/peptic ulcer disease/hiatal hernia. My recent Full Blood count: Mean cell volume 97.0 fL [83.0 - 101.0] Mean cell haemoglobin level 30.1 pg [27.0 - 32.0] both these values have been creeping up in the last few years.

Hi lovely people! My latest thyroid results were: TSH 1,27 (0,380-5,330μUI/mL) (18% through range) fT4 1,16 (0.38-1,40 ng/dL) (88% through range) fT3 3,79 (2,5-3,9pg/mL) (92% through range) Miraculously they finally tested fT3 for the first time, and I was so happy to see that I seem to be converting

Diagnosed barely 2 months ago and on brukinsa for a month now. Tolerated fairly well so far except for mouth sores. Used magic mouthwash for10 days and cleared things up pretty well I stopped it but still getting lumpy things in mouth. Also dull ache in back molar. Anyone having trouble with mouth sores

I have had terrible hives and angioedema for the past two days. I look like I've had lip injections. And my hands are both incredibly swollen. I'm itchy to the point of misery. I'm going to see my PCP this afternoon. I already take Claritin and Pepcid daily. I try not to attribute everything to

Quick question....anybody else experience a sore tongue and roof of mouth and gums with GCA? Along with mild numbness on lip and cheek area and the usual temporal headaches and scalp sensitivity?

please , anyone know if any meds help with mouth 👄 sores and the occasional genital sores / ulcers? I’ve had Lupus for five years now and this is the first time I’ve been troubled with them … so very painful 😣 Thanks for hopefully reading this.

My mouth keeps feeling sore, this affects my tongue, roof of mouth & gums, also feels sensitive & hot. I have several health issues including hypothyroidism, ME/CFS, fibromyalgia & hypertension so not sure if any of these could be the cause? Advice appreciated 🤞