So not much has been going on here, just waiting for results to been seen by consultant and/an appointment to discuss results.
Today I received a letter to say the infliximab treatment is no longer work as a lot of antibodies had been found in my bloods. It seems I have to switch to Humira which has to be injected at home.
I didn't really want this treatment, not cos I have to inject that's not something to bother me, but I kind of just didn't want my home to feel too clinical, probably sounds stupid but that's just how I feel!!
I will wait to see when this gets sorted out and what advice/information I will be given. Not feeling very informed at the moment and like I don't have much choice 😐
Oh yeah I did go to Lego land at the weekend and my insides where very well behaved!! Had a great time there would like to go again when the kids are older so we can go on the rides 😄
