Only you can fight for you! But I will have your backs

Here's a honest truth, I am learning the more people with Endometriosis, also have lupus symptoms, the "researchers" are finding this connection, and trying to find out if Endometriosis is actually another form of lupus..wait for a flare up, see a arthritis, autoimmune doc, get a standing order to walk in for blood work, get your inflammation markers checked. Go from there, once you know you can fight it, or figure out what else may be going on with your body, cycst that have continued to grow, maybe become hard, anything is a possibility, the point to all is to rule out..go down the list..find out, get to the root of your illness, so you can get better, and have a more " Normal" life..that you shoukd be able to have.

Thank you, Katherine. I'm new to this platform and am really l💝ving all the stories, support, +resource info.

Ill try make this long story short, basically i have a large endometrioma on my left ovarie an plenty of tissue growth in the reproductive area and also my bowels. From the age of 23-25 i was not sexually active atall because of the pain. I now have a partner an have been sexually active an i sometimes get slight discomfort but its nothing to complain about. My issue is i have the marina coil fitted and i also have the nexplanon rod in my arm. These past few weeks, maybe just over a month i have all the symptoms of coming on my period ive had mild to severe cramps and dysomenorhea but nothing is showing, my abdomen is slightly swollen an it has veins showing, im sleeping alot, i have my bladder has been odd aswell. Ill have no feeling of needing to pee then out of nowhere im absolutly busting an have to run to the toilet! Im just curious because all this is new and different