I had an endoscopy and colonoscopy. They showed nothing but made my symptoms more believable to doctors. I've had 3 surgeries for endo and will have another in a few months. The road is long and in my case surgery didnt put it into remission. Myfembree wasnt an option because it $1600 a month so my only choice is surgical menopause at 46.
1 day ago
First of all β finding the right care team is genuinely one of the hardest parts, so that's a big deal worth acknowledging! Here are some things that many people wish they'd known earlier in their endometriosis journey: Trust yourself and your symptoms
- Ultrasounds frequently miss endometriosis β so you're right to push Show Full Answer
First of all β finding the right care team is genuinely one of the hardest parts, so that's a big deal worth acknowledging! Here are some things that many people wish they'd known earlier in their endometriosis journey: Trust yourself and your symptoms
- Ultrasounds frequently miss endometriosis β so you're right to push further
- A laparoscopy is currently the gold standard for diagnosis, so pursuing that consult is the right move
- Keep a detailed symptom diary to bring to appointments β timing, severity, triggers Advocate loudly for yourself
- If a doctor dismisses your pain, it's okay to seek another opinion
- Bring notes, articles, or books to appointments β being informed helps doctors take you more seriously
- One MyEndometriosisTeam member saw 10 doctors before getting a proper diagnosis Build your care team broadly
A strong team can include:
- A gynecologist or specialized surgeon
- A pain specialist
- A hormone specialist if needed
Research shows combining treatments from different specialties leads to better outcomes. Be open and honest with your doctors about what's working and what isn't β including how Natazia and Myfembree are making you feel. Open communication really does shape the quality of care you receive.
You're already doing so many right things. Keep going! π
August 31