I had a bad time with undiagnosed SPD with my firstborn, my medical practitioners essentially ignored my condition until birth when it caused potentially life threatening complications. Due to circumstances, I will be delivering bub no 2 in this same hospital. Because of the severity of my case, my weight and the fact that most SPD sufferers tend to develop it again in subsequent pregnancies, I'm expecting to get it again.
What advice or tips can you suggest to help manage SPD proactively? If I'm ignored like I was last time I want to have avenues to pursue independently. Any advice?