I thought it about time to offer something positive about my reflux issues.
You can skip to conclusion but thought history would help:
. I posted months ago about how a cardiologist said my upper chest pressure probably reflux. I spent weeks on PPI - helped sensation in throat but gave me awful regurgitation/reflux! Straightforward oesophageal Endoscopy didn’t show reflux but was told the endoscopy was only really to rule out tumours etc but I coukd still be suffering from reflux. I tried an ACE inhibitor - same problems.
I decided no more PPIs but it took weeks to adjust. Then I read about IBS ( again as gp thought I had it years ago when I upped my fibre and developed diarrhoea ).
My issue is I wasn’t getting indigestion with my reflux or pain - and IBS diagnosis requires pain. I just had lot of bloating and discomfort. I found I could not eat things I have enjoyed- eg my homemade chicken pie. Lasagne etc and found myself eating less in evening and nothing after 7, using bed risers which helped a bit but still had discomfort.
Conclusion/solution?
I decided I’d look at diet and have taken on LOw FOD map since September. In a way I was already getting there as know the things that are ok- like oats bananas etc.
I also knew I have difficulty with milk for years. So it was logical to cut out dairy from cooking too- no more sauces! But also cut out leeks ( onions give me migraine so use to eat leeks instead) . It means No wheat or gluten but also cut out vegetables I love like mushrooms and broccoli. I was sceptical but the results quite amazing - at least for now- after just couple of weeks the bloating reduced. I am eating lot of potatoes ( didn’t before) but have lost nearly a stone without even trying. I wasn’t trying to lose weight as not overweight but great to get rid of the bloating. I have less sensations in chest and probably some reflux still there but I feel so much better!
I have started to reintroduce foods- avocado fine, small it if sourdough bread. Pearl barley a big no no! So I’m posting this to say it is worth trying - everyone is different. There is loads on line about this approach. I found information on nhs website- happened to be Gloucestershire.
I now need to adapt to statins and find out why I have developed hypochromasia ( strange blood cells but that all happened in July after the virus and before my diet change).
I hope this helps some of you. Of course I don’t know whether I will relapse or not but am living in hope. Take care all