Hi @Thismorning83 I have been taking Mounjaro (MJ) since October last year, but I am lucky enough to get it on prescription, as I - obviously - qualify for it. In fact, I hadn't even mentioned it to my Diabetes team, they were the ones who advised me to start taking it.
{NB My Diabetes team are not attached to my GP's surgery, except that I have to get my prescription as normal, through my GP practice. The DT runs as a community, and specialist nurse, led, project, that is still funded through the NHS. They do, of course, keep my GP practice up to date with how I am doing.}
For my first month I was just taking the 2.5 that everyone is advised to start off with, but my next telephone appointment with the Diabetes team (DT) wasn't scheduled until after I was due to get my second pen. Before starting my first dose, the DT had sent me a booklet explaining a little about MJ, and the technique on how to administer it, and in that booklet, it said that MJ is given in monthly stages, adding an extra 2.5mg every month, until the maximum amount of 15mg per week, is reached.
So, I didn't realise during that first month that I was supposed to leave it up to my DT to decide if, and when, I should go up to the next dose, and, therefore, I just requested that my next prescription be for 5mg, which my GP practice agreed to without any extra questioning!
When I had my next - and the first - telephone appointment with the DT team since starting taking MJ, I told them how I had been during the first month of taking 2.5mg, and how I was now that I was taking the 5mg dose. The nurse I was talking to sounded a bit puzzled that I had increased my dosage to the 5mg dose of MJ. She told me that they are supposed to let me know when I should have the dose increased! However, as I was tolerating the second level well, she said I could stay on that dose for now, rather than having to go back to the 2.5 dose. So I asked her when she thought I should have my dose increased, she replied that most of their patients stay on that dose for at least 8 to 9 months, but that it, of course, depended on the individual patient.
Wanting to understand the whole process better, I delved into the whys, and why nots, a bit more. Apparently the slow start, and slow progression, are for safety reasons, and that when we read about 'celebrities' having quite strong adverse reactions to any of the WLpens, it is usually because they have increased their doses far to quickly! I have since then, read that hospitals have recently been seeing many more patients with severe kidney, bowel, and pancreas problems, amongst a range of other potentially dangerous symptoms, and that a large proportion of those nasty symptoms were due to them taking WL drugs, and especially to upping the doses far too quickly.
Therefore, it is very important to up one's doses very gradually, in order to let your different organs get slowly 'acclimatised' to the changes happening to them. I don't know if those of you who are funding your own MJ, have any chance to get advice from the people who you receive your MJ from? If not, I hope that your GP practice would agree to monitor, and advise you on when you should be changing the amount of MJ that you take? After all, if anyine in the UK takes too much of any of the WL drugs, it is almost certainly our NHS hospitals that are going to have to deal with the fallout.
Good luck OP, and please take care with your doses. 💐