Hello all (1st post) I’m a mother of 4 and have a huge diastasis recti. My oldest is 10 is 4.4 kg and all my babies after were 4 kg and an over.
My youngest is two years old but after having my 3rd baby I noticed a significant difference in the symptoms I was getting from the diastases recti, which were pain when with any pressure to the centre part of my belly, urine incontinence, lots of back and chest pain due to using other muscles in the body other than my core muscles and just general aches and pains all over my body for trying to compensate for such a weak core.
Since then, I contacted my GP and explained all my symptoms and he has referred me to a surgeon in one of the biggest hospitals in London and then had a CT scan which I haven’t heard back results from yet and now have a follow-up appointment with the surgeon. I’m extremely worried about my Results and what the plan is going forward but I’m hoping the CT scan showed the extent of the gap and that they are willing to preform the surgical procedure to put this right.
I’m not sure how much longer I can cope with the issues. Does anyone have any experience with the NHS and regards to a diastases recti or who had actually gone down the same route that I’m going down currently and if so what’s your experience?
😚