u/Kitchen-Doughnut-731

My pots symptoms are the absolute WORST whenever I eat something. Even if it’s a small meal or snack. Anyone know how to help this??

So the Mireena IUD has been my birth control method for 7 years now. I had stage 3 endo excised in August and I am feeling a lot better. However, I am still struggling with pelvic floor pain and spasms. Even with going to physical therapy since July. I am worried the IUD is causing my pelvic floor muscles to tighten especially because i am hyper mobile. However, it’s been so nice to not have a period for 7 years because it was so heavy and painful before. I have an appointment in a week to remove it but i am TERRIFIED my period will be terrible like it was 7 years ago. Or that I will experience way more endo flare ups. My dr says it would be helpful to get it out and see how i do with no BC for a month and track my cycle then try YAZ or SLYND. Any similar experiences or advice??? I would hate myself if i get it taken out and ruin my quality of life but maybe it will help my pelvic floor relax??? any experiences with endo on yaz, slyndd, or no bc??? HELP

So the Mireena IUD has been my birth control method for 7 years now. I had stage 3 endo excised in August and I am feeling a lot better. However, I am still struggling with pelvic floor pain and spasms. Even with going to physical therapy since July. I am worried the IUD is causing my pelvic floor muscles to tighten especially because i am hyper mobile. However, it’s been so nice to not have a period for 7 years because it was so heavy and painful before. I have an appointment in a week to remove it but i am TERRIFIED my period will be terrible like it was 7 years ago. Or that I will experience way more endo flare ups. My dr says it would be helpful to get it out and see how i do with no BC for a month and track my cycle then try YAZ or SLYND. Any similar experiences or advice??? I would hate myself if i get it taken out and ruin my quality of life but maybe it will help my pelvic floor relax??? any experiences with endo on yaz, slyndd, or no bc??? HELP

i was diagnosed with stage 3 endometriosis last year and underwent 2 surgeries and went in and out of medically induced menopause. this caused me to develop POTS which i was just diagnosed with. I have also been diagnosed with PMDD and hypermobility (may also have hEDs). Oh and i also am autistic. oh and my hormone levels are borderline normal, almost PCOS levels. Anyone have advise??? I am getting so overwhelmed and hopeless. I just want to be healthy. 😖 They’re all invisible illnesses / disabilities too so no one even understands the extent of pain and suffering i go through every day. What has helped you guys???