Symptoms present 6 months after treatment
Posted: Wed Apr 03, 2019 6:44 pm
Hello
Long story short, I've had my deal with helicobacter back in November and I took a treatment (Amoxicillin 2 g / day
Claritomichin 1 g / day for 7 days)
Ever since then, my symptoms oscillated around but remained around the same intensity and type, such as:
- Pain in the stern spread around after I eat / before I eat / In the morning .. basically it always appears after I eat and sometimes before I eat. Some days are better, some are very bad.
- Nausea
- Feeling very weak
- Diahreea sometimes
- Feeling bloated
- Not feeling hungry almost all the time, just very nauseous when hungry
- Chills in my jaw
I took two stool tests, when I stayed for both 2 weeks of PPIs, which came back negative.
I've been off PPIs for about 4 weeks now and I don't feel much difference in symptoms intensity or frequency since I switched off PPIs
My current doctor states that stool tests are accurate when they are taken from the right zone and she claims she has a lot of patients with false negatives from stool tests. She insists I do a breathing test.
Honestly, I hope this is true because it would explain everything that happened with my health post-treatment.
I did many tests and all came back good, including digestion tests.
Any thoughts?
Long story short, I've had my deal with helicobacter back in November and I took a treatment (Amoxicillin 2 g / day
Claritomichin 1 g / day for 7 days)
Ever since then, my symptoms oscillated around but remained around the same intensity and type, such as:
- Pain in the stern spread around after I eat / before I eat / In the morning .. basically it always appears after I eat and sometimes before I eat. Some days are better, some are very bad.
- Nausea
- Feeling very weak
- Diahreea sometimes
- Feeling bloated
- Not feeling hungry almost all the time, just very nauseous when hungry
- Chills in my jaw
I took two stool tests, when I stayed for both 2 weeks of PPIs, which came back negative.
I've been off PPIs for about 4 weeks now and I don't feel much difference in symptoms intensity or frequency since I switched off PPIs
My current doctor states that stool tests are accurate when they are taken from the right zone and she claims she has a lot of patients with false negatives from stool tests. She insists I do a breathing test.
Honestly, I hope this is true because it would explain everything that happened with my health post-treatment.
I did many tests and all came back good, including digestion tests.
Any thoughts?