Does anyone else out there with CFS/ME have problems with taking antibiotics?Not only have I developed sensitivity to taking them but...I have had to have a short course of co-amoxiclav to treat a dental problem and its totally knocked me for six
I'm just totally exhausted...I seem to remember this was how my CFS/ME first started..first an infection then antibiotics and then feeling absolutely shattered, hot sweats and headaches all the fun that I usually get with the CFS/ME.Anyway just wanted to indulge in a bit of self-pity there

