First Thank You all for this site! It has helped so much just knowing others are out there! Every post resistant with me in some way and lets me know my thoughts and feelings are legitimate (or understandable).
I'm (we're) 4 years post PP and I am wondering if there have been any Brain Studies on PP patients or medical follow up in general (besides this amazing forum of course). My (our) experience was to take the drug for 17 months come off of it and "resume" "normal" programming. I still go to my psychologist once a month, but that is all my doing because it helps.
Many post say "can't get back to normal", "less confident", "should I be feeling this way" etc
So I am wondering besides this site and the wonderful people behind it, is anyone doing anything as follow up after PP? I feel as though we PP mamas have been left to fend for ourselves after the initial diagnoses and drug regiment. It may be different in the UK. Here in the US it feels like "oh your fine now, stop talking about that, move on" and the dreaded "Let it Go" (darn you Frozen!)
Thanks for any insight into this question.
To all of you, keep fighting the good fight, you are worth it, your child is worth it, and all those who support you are worth it!