Connect with others who understand.

Sign up Log in
Resources
About MyEndometriosisTeam
Powered By
Real members of MyEndometriosisTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

Diagnosis/Gyno Recommendations/ Tips??

A MyEndometriosisTeam Member asked a question 💭
Phoenix, AZ

Hi everyone! I am new to this cite and excited to be able to use you all a recourse and build a network with you guys. I am 22 and experience chronic endometriosis pain. For a couple years I went vegan and was very strict with my diet. I then fell into a deep hole of hyper focussed workouts, eating regimens, caloric counting and weighing myself that soon became very unhealthy for my mental health. After some time, I believe myself to be at a healthy balance between positive body image and a… read more

December 20, 2019
•
View reactions
A MyEndometriosisTeam Member
December 21, 2019
A MyEndometriosisTeam Member

A heat pack is the most effective pain relief for me. It’s not super transportable, but it does wonders for my pain. I looked on the Nancy’s Nook Fb page (an educational group about endo that compiles a huge list of vetted endo specialists) and there are several doctors in Phoenix. I’ll try to upload a photo of their contact info. As far as surgery, I’m very pro surgery as long as it is an excision done by an expert. My first surgery did nothing but my second which was an excision helped me so so much.

December 21, 2019
A MyEndometriosisTeam Member

Hi! A product I use that really helps alot of my muscle tightness and cramping is Magnesium Lotion! You can get it at Sprouts, Whole Foods, or other health food stores for less than $10 and it is a hidden Gem! I just found it and take it with me everywhere. I find it more helpful than lidocain ointment :) I also go to pelvic floor physical therapy which has been a long process but I am finally starting to see results and its a good feeling. I had laproscopic surgery to remove my adhesions and clean up a ruptured endometrioma and TBH I was pain free for about 3-4 months before it started ceeeping back. 4 years later I have sharp pulling pains near my incision site going down to my pubic bone and my doctor believes adhesions have formed from that scar tissue. Dont get me wrong some women find relief from surgery, I just wasnt one of them. I hope you find relief soon! Good luck 😊

December 20, 2019
A MyEndometriosisTeam Member

If you click on the photos they will get more in focus!

December 21, 2019

Related content

View All

Should I Tell My Doctor About My Endo Diagnosis?

A MyEndometriosisTeam Member asked a question 💭
Kildare, IE

Staying In The Hosputal

A MyEndometriosisTeam Member asked a question 💭
Syracuse, NY

When Were You Diagnosed And What Age? Any Misdiagnoses Or Comments From Your Doctors?

A MyEndometriosisTeam Member asked a question 💭
Fulton, NY
Continue with Facebook
Continue with Google
By joining, you accept our Terms of Use, and acknowledge our collection, sharing, and use of your data in accordance with our Health Data Policy and Privacy policies.Your privacy is our priority Lock Icon
Already a Member? Log in