In regards to gallbladder and Lyme disease, I got my ME after glandular fever if that makes a difference? And also my parents are going to see a doctor today for me (I am too ill to attend) but have written them a letter explaining how I am so I will mention the gallbladder thing. Shell, sorry I don't know what do is, I have been seeing doctors on the NHS for the last four years and a few outside the NHS but with little improvement, I was diagnosed with ME after a bit less than a year of being ill I guess, I was diagnosed by an NHS doctor and I also diagnosed by another doctor outside the NHS. Something I realised from the night just had was I woke up and decided not to move at all and see if it didn't make me feel as sick (usually I wake up feeling completely sick so there is nothing I can do), and I didn't and managed to fall back to sleep and then in the morning around the time I would get up I moved my legs up a bit rather than being stretched out and stretched a bit myself which made me feel much worse pretty much straight away, but now once I am up a bit more I feel better, even though at night if I were to get up out of bed I would still feel awful.
In terms of enimas would that just be more alleviating the constipation?
And I am planning and have started to take action in regard to my anxiety but it has been a constant battle with it pretty much these four years but I am quietly confident. And I am sorry, what is an antiemetic?
I apologise that I have so many question etc.
Feel in no rush to answer or write at all if your are experiencing brain fog or anything, I don't want to be the reason any feels worse at all.