I was diagnosed with Crohns disease 5 years ago and went into remission with Aza. I then decided to take my chances without medication and...it came back in my TI. I was put back onto steroids and aza in the short term but, having had side effects with Aza I enquired about the possibility of biological drugs and have chosen Adalimumab. Unfortunately, my consultant won't let me begin this treatment until I have neurological tests to find the cause of another symptom I have. I have developed pins and needles in my hands and feet with the occasional 'shaky', tremor- like fingers.
I have an 11 week (at least) wait for an appointment with the neurologist and have to live with my flare up until then. I am currently only taking budesonide but they don't appear to be having the desired affect!
I was wondering whether anyone else suffers similar issues during a flare up or as a result of medication?
Any comments are appreciated!
Thanks
Jenny
I have an 11 week (at least) wait for an appointment with the neurologist and have to live with my flare up until then. I am currently only taking budesonide but they don't appear to be having the desired affect!
I was wondering whether anyone else suffers similar issues during a flare up or as a result of medication?
Any comments are appreciated!
Thanks
Jenny