Hi I've had relapsing remitting MS for nearly ten years.
Just had a couple of questions for anyone else with same condition..
Have stopped taking injections of Beta Inteferon so we can ttc baby number 3. Does anyone know whether it is worth stopping and starting this? Can't really remember what the benefits of inteferon were..
Have been unable to bf my dds as fatigue gets the better of me and need to re start medication but would like to give it another go if we manage to have a 3rd. Anyone else manage it?
With dd1 I was categorised high risk and had to give birth on main ward and be monitored in totally tedious consultant appointments throughout with doctors who didn't know me or much about ms.
With dd2 I refused to see consultants sending midwife into spasms and ended up having her on the MLU but only because the ward ws full.
Will they go on medical history or previous birth history instead with a 3rd?