#endoawareness

When I woke up from a coma on December 2011 I noticed that I started getting daily pelvic pain that wouldn’t go away, something that felt like cramps. I was stricken with the pain and thought it was odd that it got worse right after waking up from the coma, I mean I did get horrible cramps before but only around the days that I would get my period, even if I didn’t get my period I would still have my pain but it wasn’t daily like it was happening now.
To me it wasn’t normal and I fought doctors non-stop, until 2013 when I got diagnosed with Endometriosis. I never told my doctors that I had my pain escalate right after the coma, but I always thought maybe something happened to me that changed my body a bit or made me more sensitive to pain, but at the same time I wasn’t sure so I always kept it to myself.
Now that it’s been a couple of years after I got diagnosed and been through surgeries and other treatments I have noticed a change in pain patterns by keeping logs.

-For starters when I was a young teen I would get SEVERE cramps when I was on my period or days around it
-After the coma it was daily on the right side mainly
-Daily pain on mornings and night but not as much after noon to four
-Now it’s on both left and right and it’s severe in the mornings and at night but sometimes it slows down a lot, like I have no pain, but comes back once a day to get revenge on me.

I mean I don’t know if it’ll get better over time or worse, all I know it’s that it has been changing, and I don’t know if I am the only one.