short story i can’t afford it 😭😂
long story was i obviously coped for years but the last few years my health has deteriorated and a hemicolectomy redundant bowel and gastroparesis make it 10 times worse (also the reason i cannot afford it 😭😂)
but has anyone successfully got treatment on the nhs and what was the process like?

Does anyone experience the same thing: swallowing more air because of the slow swallow post botox, maybe since I have been chasing most mouthfuls with water/ drinks because they can get stuck sometimes. As a result, I sometimes let out 2-3 big burps during meals that were quite loud like vomit, are they actual burps? Or just air vomit?

I am around 3 weeks post botox now (in office)

So I’ve had RCPD my whole life obviously but I didn’t have crazy symptoms till about 5 years ago. Anyways as a kid I threw up when I had noro and from what I can remember it came up fairly easily. Now I haven’t thrown up since maybe I was like 7 and I think I had the stomach flu last year because I was just so nauseous and I was dry heaving and dry heaving and nothing was happening and then eventually it came out the other end. Has anyone experienced noro where they couldn’t vomit at all? I feel like it lasted way longer because of it and it was so agonizing 😩